Archive 1999-2008

1. Alonso S, Izagirre N, Smith-Zubiaga I, Gardeazabal J, Díaz-Ramón JL, Díaz-Pérez JL, Zelenika D, Boyano MD, Smit N, de la Rúa C, Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans. BMC Evol Biol, 2008, 8p. 74. 
2. Barrett JC, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmada MM, Bitton A, Dassopoulos T, Datta LW, Green T, Griffiths AM, Kistner EO, Murtha MT, Regueiro MD, Rotter JI, Schumm LP, Steinhart AH, Targan SR, Xavier RJ, [NIDDK IBD Genetics Consortium] , Libioulle C, Sandor C, Lathrop M, Belaiche J, Dewit O, Gut I, Heath S, Laukens D, Mni M, Rutgeerts P, Van Gossum A, Zelenika D, Franchimont D, Hugot JP, de Vos M, Vermeire S, Louis E, [Belgian-French IBD Consortium] , [Wellcome Trust Case Control Consortium] , Cardon LR, Anderson CA, Drummond H, Nimmo E, Ahmad T, Prescott NJ, Onnie CM, Fisher SA, Marchini J, Ghori J, Bumpstead S, Gwilliam R, Tremelling M, Deloukas P, Mansfield J, Jewell D, Satsangi J, Mathew CG, Parkes M, Georges M, Daly MJ, Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet, 2008, 40 (8): p. 955-962. 
3. Bellis C, Cox HC, Ovcaric M, Begley KN, Lea RA, Quinlan S, Burgner D, Heath SC, Blangero J, Griffiths LR, Linkage disequilibrium analysis in the genetically isolated Norfolk Island population. Heredity, 2008, 100 (4): p. 366-373. 
4. Bellis C, Cox HC, Dyer TD, Charlesworth JC, Begley KN, Quinlan S, Lea RA, Heath SC, Blangero J, Griffiths LR, Linkage mapping of CVD risk traits in the isolated Norfolk Island population. Hum Genet, 2008, 124 (5): p. 543-552. 
5. Bennett DA, Xu P, Clarke R, Zondervan K, Parish S, Palmer A, Cardon L, Peto R, Lathrop M, Collins R, International Study of Infarct Survival Collaborators , The exon 1-8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom population. Eur J Hum Genet, 2008, 16 (4): p. 480-486. 
6. Bonnin I, Rousset M, Madur D, Sourdille P, Dupuits C, Brunel D, Goldringer I, FT genome A and D polymorphisms are associated with the variation of earliness components in hexaploid wheat. Theor Appl Genet, 2008, 116 (3): p. 383-394. 
7. Bouzigon E, Corda E, Aschard H, Dizier MH, Boland A, Bousquet J, Chateigner N, Gormand F, Just J, Le Moual N, Scheinmann P, Siroux V, Vervloet D, Zelenika D, Pin I, Kauffmann F, Lathrop M, Demenais F, Effect of 17q21 variants and smoking exposure in early-onset asthma. N Engl J Med, 2008, 359 (19): p. 1985-1994. 
8. Caulfield MJ, Munroe PB, O'Neill D, Witkowska K, Charchar FJ, Doblado M, Evans S, Eyheramendy S, Onipinla A, Howard P, Shaw-Hawkins S, Dobson RJ, Wallace C, Newhouse SJ, Brown M, Connell JM, Dominiczak A, Farrall M, Lathrop GM, Samani NJ, Kumari M, Marmot M, Brunner E, Chambers J, Elliott P, Kooner J, Laan M, Org E, Veldre G, Viigimaa M, Cappuccio FP, Ji C, Iacone R, Strazzullo P, Moley KH, Cheeseman C, SLC2A9 is a high-capacity urate transporter in humans. PLoS Med, 2008, 5 (10): p. e197. 
9. Chaouachi M, Chupeau G, Berard A, McKhann H, Romaniuk M, Giancola S, Laval V, Bertheau Y, Brunel D, A high-throughput multiplex method adapted for GMO detection. J Agric Food Chem, 2008, 56 (24): p. 11596-11606. 
10. Chaouachi M, El Malki R, Berard A, Romaniuk M, Laval V, Brunel D, Bertheau Y, Development of a real-time PCR method for the differential detection and quantification of four solanaceae in GMO analysis: potato (Solanum tuberosum), tomato (Solanum lycopersicum), eggplant (Solanum melongena), and pepper (Capsicum annuum). J Agric Food Chem, 2008, 56 (6): p. 1818-1828. 
11. Claus S, Fischer J, Mégarbané H, Mégarbané A, Jobard F, Debret R, Peyrol S, Saker S, Devillers M, Sommer P, Damour O, A p.C217R mutation in fibulin-5 from cutis laxa patients is associated with incomplete extracellular matrix formation in a skin equivalent model. J Invest Dermatol, 2008, 128 (6): p. 1442-1450. 
12. Danoy P, Michiels S, Dessen P, Pignat C, Boulet T, Monet M, Bouchardy C, Lathrop M, Sarasin A, Benhamou S, Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers. Int J Cancer, 2008, 123 (2): p. 457-463. 
13. de Alencar Figueiredo LF, Calatayud C, Dupuits C, Billot C, Rami JF, Brunel D, Perrier X, Courtois B, Deu M, Glaszmann JC, Phylogeographic evidence of crop neodiversity in sorghum. Genetics, 2008, 179 (2): p. 997-1008. 
14. Desrivières S, Krause K, Dyer A, Frank J, Blomeyer D, Lathrop M, Mann K, Banaschewski T, Laucht M, Schumann G, Nucleotide sequence variation within the PI3K p85 alpha gene associates with alcohol risk drinking behaviour in adolescents. PLoS ONE, 2008, 3 (3): p. e1769. 
15. Druet T, Fritz S, Boussaha M, Ben-Jemaa S, Guillaume F, Derbala D, Zelenika D, Lechner D, Charon C, Boichard D, Gut IG, Eggen A, Gautier M, Fine mapping of quantitative trait loci affecting female fertility in dairy cattle on BTA03 using a dense single-nucleotide polymorphism map. Genetics, 2008, 178 (4): p. 2227-2235. 
16. Guilloud-Bataille M, Bouzigon E, Annesi-Maesano I, Bousquet J, Charpin D, Gormand F, Hochez J, Just J, Lemainque A, Le Moual N, Matran R, Neukirch F, Oryszczyn MP, Paty E, Pin I, Vervloet D, Kauffmann F, Lathrop M, Demenais F, Dizier MH, Evidence for linkage of a new region (11p14) to eczema and allergic diseases. Hum Genet, 2008, 122 (6): p. 605-614. 
17. Haliloglu G, Jobard F, Oguz KK, Anlar B, Akalan N, Coskun T, Sass JO, Fischer J, Topcu M, L-2-hydroxyglutaric aciduria and brain tumors in children with mutations in the L2HGDH gene: neuroimaging findings. Neuropediatrics, 2008, 39 (2): p. 119-122. 
18. Haseneyer G, Ravel C, Dardevet M, Balfourier F, Sourdille P, Charmet G, Brunel D, Sauer S, Geiger HH, Graner A, Stracke S, High level of conservation between genes coding for the GAMYB transcription factor in barley (Hordeum vulgare L.) and bread wheat (Triticum aestivum L.) collections. Theor Appl Genet, 2008, 117 (3): p. 321-331. 
19. Heath SC, Gut IG, Brennan P, McKay JD, Bencko V, Fabianova E, Foretova L, Georges M, Janout V, Kabesch M, Krokan HE, Elvestad MB, Lissowska J, Mates D, Rudnai P, Skorpen F, Schreiber S, Soria JM, Syvänen AC, Meneton P, Herçberg S, Galan P, Szeszenia-Dabrowska N, Zaridze D, Génin E, Cardon LR, Lathrop M, Investigation of the fine structure of European populations with applications to disease association studies. Eur J Hum Genet, 2008, 16 (12): p. 1413-1429. 
20. Hung RJ, McKay JD, Gaborieau V, Boffetta P, Hashibe M, Zaridze D, Mukeria A, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Mates D, Bencko V, Foretova L, Janout V, Chen C, Goodman G, Field JK, Liloglou T, Xinarianos G, Cassidy A, McLaughlin J, Liu G, Narod S, Krokan HE, Skorpen F, Elvestad MB, Hveem K, Vatten L, Linseisen J, Clavel-Chapelon F, Vineis P, Bueno-de-Mesquita HB, Lund E, Martinez C, Bingham S, Rasmuson T, Hainaut P, Riboli E, Ahrens W, Benhamou S, Lagiou P, Trichopoulos D, Holcátová I, Merletti F, Kjaerheim K, Agudo A, Macfarlane G, Talamini R, Simonato L, Lowry R, Conway DI, Znaor A, Healy C, Zelenika D, Boland A, Delepine M, Foglio M, Lechner D, Matsuda F, Blanche H, Gut I, Heath S, Lathrop M, Brennan P, A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature, 2008, 452 (7187): p. 633-637. 
21. Kaufman JM, Ostertag A, Saint-Pierre A, Cohen-Solal M, Boland A, Van Pottelbergh I, Toye K, de Vernejoul MC, Martinez M, Genome-wide linkage screen of bone mineral density (BMD) in European pedigrees ascertained through a male relative with low BMD values: evidence for quantitative trait loci on 17q21-23, 11q12-13, 13q12-14, and 22q11. J Clin Endocrinol Metab, 2008, 93 (10): p. 3755-3762. 
22. Kayser M, Liu F, Janssens AC, Rivadeneira F, Lao O, van Duijn K, Vermeulen M, Arp P, Jhamai MM, van Ijcken WF, den Dunnen JT, Heath S, Zelenika D, Despriet DD, Klaver CC, Vingerling JR, de Jong PT, Hofman A, Aulchenko YS, Uitterlinden AG, Oostra BA, van Duijn CM, Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene. Am J Hum Genet, 2008, 82 (2): p. 411-423. 
23. Kim CA, Delépine M, Boutet E, El Mourabit H, Le Lay S, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O'Rahilly S, Dugail I, Capeau J, Lathrop M, Magré J, Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. J Clin Endocrinol Metab, 2008, 93 (4): p. 1129-1134. 
24. Kurreeman FA, Rocha D, Houwing-Duistermaat J, Vrijmoet S, Teixeira VH, Migliorini P, Balsa A, Westhovens R, Barrera P, Alves H, Vaz C, Fernandes M, Pascual-Salcedo D, Michou L, Bombardieri S, Radstake T, van Riel P, van de Putte L, Lopes-Vaz A, Prum B, Bardin T, Gut I, Cornelis F, Huizinga TW, Petit-Teixeira E, Toes RE, European Consortium on Rheumatoid Arthritis Families , Replication of the tumor necrosis factor receptor-associated factor 1/complement component 5 region as a susceptibility locus for rheumatoid arthritis in a European family-based study. Arthritis Rheum, 2008, 58 (9): p. 2670-2674. 
25. Le Stunff C, Dechartres A, Mariot V, Lotton C, Trainor C, Miraglia Del Giudice E, Meyre D, Bieche I, Laurendeau I, Froguel P, Zelenika D, Fallin D, Lathrop M, Roméo PH, Bougnères P, Association analysis indicates that a variant GATA-binding site in the PIK3CB promoter is a Cis-acting expression quantitative trait locus for this gene and attenuates insulin resistance in obese children. Diabetes, 2008, 57 (2): p. 494-502. 
26. Limou S, Coulonges C, Foglio M, Heath S, Diop G, Leclerc S, Hirtzig T, Spadoni JL, Therwath A, Lambeau G, Gut I, Zagury JF, Exploration of associations between phospholipase A2 gene family polymorphisms and AIDS progression using the SNPlextrade mark method. Biomed Pharmacother, 2008, 62 (1): p. 31-40. 
27. Liu Y, Padgett D, Takahashi M, Li H, Sayeed A, Teichert RW, Olivera BM, McArdle JJ, Green WN, Lin W, Essential roles of the acetylcholine receptor {gamma}-subunit in neuromuscular synaptic patterning. Development, 2008, 135 (11): p. 1957-1967. 
28. López S, Buil A, Ordoñez J, Souto JC, Almasy L, Lathrop M, Blangero J, Blanco-Vaca F, Fontcuberta J, Soria JM, Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels. Eur J Hum Genet, 2008, 16 (11): p. 1372-1379. 
29. Mandon-Pépin B, Touraine P, Kuttenn F, Derbois C, Rouxel A, Matsuda F, Nicolas A, Cotinot C, Fellous M, Genetic investigation of four meiotic genes in women with premature ovarian failure. Eur J Endocrinol, 2008, 158 (1): p. 107-115. 
30. Maouche S, Poirier O, Godefroy T, Olaso R, Gut I, Collet JP, Montalescot G, Cambien F, Performance comparison of two microarray platforms to assess differential gene expression in human monocyte and macrophage cells. BMC Genomics, 2008, 9p. 302. 
31. McKay JD, Hung RJ, Gaborieau V, Boffetta P, Chabrier A, Byrnes G, Zaridze D, Mukeria A, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Mates D, Bencko V, Foretova L, Janout V, McLaughlin J, Shepherd F, Montpetit A, Narod S, Krokan HE, Skorpen F, Elvestad MB, Vatten L, Njølstad I, Axelsson T, Chen C, Goodman G, Barnett M, Loomis MM, Lubiñski J, Matyjasik J, Lener M, Oszutowska D, Field J, Liloglou T, Xinarianos G, Cassidy A, [EPIC Study] , Vineis P, Clavel-Chapelon F, Palli D, Tumino R, Krogh V, Panico S, González CA, Ramón Quirós J, Martínez C, Navarro C, Ardanaz E, Larrañaga N, Kham KT, Key T, Bueno-de-Mesquita HB, Peeters PH, Trichopoulou A, Linseisen J, Boeing H, Hallmans G, Overvad K, Tjønneland A, Kumle M, Riboli E, Zelenika D, Boland A, Delepine M, Foglio M, Lechner D, Matsuda F, Blanche H, Gut I, Heath S, Lathrop M, Brennan P, Lung cancer susceptibility locus at 5p15.33. Nat Genet, 2008, 40 (12): p. 1404-1406. 
32. McKhann HI, Gery C, Bérard A, Lévêque S, Zuther E, Hincha DK, De Mita S, Brunel D, Téoulé E, Natural variation in CBF gene sequence, gene expression and freezing tolerance in the Versailles core collection of Arabidopsis thaliana. BMC Plant Biol, 2008, 8p. 105. 
33. Paris M, Roux F, Bérard A, Reboud X, The effects of the genetic background on herbicide resistance fitness cost and its associated dominance in Arabidopsis thaliana. Heredity, 2008, 101 (6): p. 499-506. 
34. Poupon R, Ping C, Chrétien Y, Corpechot C, Chazouillères O, Simon T, Heath SC, Matsuda F, Poupon RE, Housset C, Barbu V, Genetic factors of susceptibility and of severity in primary biliary cirrhosis. J Hepatol, 2008, 49 (6): p. 1038-1045. 
35. Rønneberg JA, Tost J, Solvang HK, Alnaes GI, Johansen FE, Brendeford EM, Yakhini Z, Gut IG, Lønning PE, Børresen-Dale AL, Gabrielsen OS, Kristensen VN, GSTP1 promoter haplotypes affect DNA methylation levels and promoter activity in breast carcinomas. Cancer Res, 2008, 68 (14): p. 5562-5571. 
36. Sabater-Lleal M, Buil A, Souto JC, Alamsy L, Borrell M, Lathrop M, Blangero J, Fontcuberta J, Soria JM, A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels. Hum Genet, 2008, 124 (1): p. 81-88. 
37. Saint-Martin C, Bouteiller D, Stevanin G, Popescu C, Charon C, Ruberg M, Baulac S, Leguern E, Labauge P, Depienne C, Refinement of the 2p11.1-q12.2 locus responsible for cortical tremor associated with epilepsy and exclusion of candidate genes. Neurogenetics, 2008, 9 (1): p. 69-71. 
38. Sakuntabhai A, Ndiaye R, Casadémont I, Peerapittayamonkol C, Rogier C, Tortevoye P, Tall A, Paul R, Turbpaiboon C, Phimpraphi W, Trape JF, Spiegel A, Heath S, Mercereau-Puijalon O, Dieye A, Julier C, Genetic determination and linkage mapping of Plasmodium falciparum malaria related traits in Senegal. PLoS ONE, 2008, 3 (4): p. e2000. 
39. Sass JO, Jobard F, Topçu M, Mahfoud A, Werlé E, Cure S, Al-Sannaa N, Alshahwan SA, Bataillard M, Cimbalistiene L, Grolik C, Kemmerich V, Omran H, Sztriha L, Tabache M, Fischer J, L: -2-Hydroxyglutaric aciduria: Identification of ten novel mutations in the L2HGDH gene. J Inherit Metab Dis, 2008. 
40. Schumann G, Johann M, Frank J, Preuss U, Dahmen N, Laucht M, Rietschel M, Rujescu D, Lourdusamy A, Clarke TK, Krause K, Dyer A, Depner M, Wellek S, Treutlein J, Szegedi A, Giegling I, Cichon S, Blomeyer D, Heinz A, Heath S, Lathrop M, Wodarz N, Soyka M, Spanagel R, Mann K, Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior. Arch Gen Psychiatry, 2008, 65 (7): p. 826-838. 
41. Schweiger M, Schoiswohl G, Lass A, Radner FP, Haemmerle G, Malli R, Graier W, Cornaciu I, Oberer M, Salvayre R, Fischer J, Zechner R, Zimmermann R, The C-terminal region of human adipose triglyceride lipase affects enzyme activity and lipid droplet binding. J Biol Chem, 2008, 283 (25): p. 17211-17220. 
42. Simon M, Loudet O, Durand S, Bérard A, Brunel D, Sennesal FX, Durand-Tardif M, Pelletier G, Camilleri C, Quantitative trait loci mapping in five new large recombinant inbred line populations of Arabidopsis thaliana genotyped with consensus single-nucleotide polymorphism markers. Genetics, 2008, 178 (4): p. 2253-2264. 
43. Tarnow L, Groop PH, Hadjadj S, Kazeem G, Cambien F, Marre M, Forsblom C, Parving HH, Trégouët D, Thévard A, Farrall M, Gut I, Gauguier D, Cox R, Matsuda F, Lathrop M, Vionnet N, [EURAGEDIC Consortium] , European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy. Nephrol Dial Transplant, 2008, 23 (1): p. 161-168. 
44. Thiery G, Anselmi E, Audebourg A, Darii E, Abarbri M, Terris B, Tabet JC, Gut IG, Improvements of TArgeted multiplex mass spectrometry IMaging. Proteomics, 2008, 8 (18): p. 3725-3734. 
45. Tocharoentanaphol C, Promso S, Zelenika D, Lowhnoo T, Tongsima S, Sura T, Chantratita W, Matsuda F, Mooney S, Sakuntabhai A, Evaluation of resequencing on number of tag SNPs of 13 atherosclerosis-related genes in Thai population. J Hum Genet, 2008, 53 (1): p. 74-86. 
46. Trégouet DA, Groop PH, McGinn S, Forsblom C, Hadjadj S, Marre M, Parving HH, Tarnow L, Telgmann R, Godefroy T, Nicaud V, Rousseau R, Parkkonen M, Hoverfält A, Gut I, Heath S, Matsuda F, Cox R, Kazeem G, Farrall M, Gauguier D, Brand-Herrmann SM, Cambien F, Lathrop M, Vionnet N, [EURAGEDIC Consortium] , G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes. Diabetes, 2008, 57 (10): p. 2843-2850. 
47. Wallace C, Newhouse SJ, Braund P, Zhang F, Tobin M, Falchi M, Ahmadi K, Dobson RJ, Marçano AC, Hajat C, Burton P, Deloukas P, Brown M, Connell JM, Dominiczak A, Lathrop GM, Webster J, Farrall M, Spector T, Samani NJ, Caulfield MJ, Munroe PB, Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. Am J Hum Genet, 2008, 82 (1): p. 139-149. 
48. Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, Heath SC, Timpson NJ, Najjar SS, Stringham HM, Strait J, Duren WL, Maschio A, Busonero F, Mulas A, Albai G, Swift AJ, Morken MA, Narisu N, Bennett D, Parish S, Shen H, Galan P, Meneton P, Hercberg S, Zelenika D, Chen WM, Li Y, Scott LJ, Scheet PA, Sundvall J, Watanabe RM, Nagaraja R, Ebrahim S, Lawlor DA, Ben-Shlomo Y, Davey-Smith G, Shuldiner AR, Collins R, Bergman RN, Uda M, Tuomilehto J, Cao A, Collins FS, Lakatta E, Lathrop GM, Boehnke M, Schlessinger D, Mohlke KL, Abecasis GR, Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet, 2008, 40 (2): p. 161-169. 
49. Zalloua PA, Azar ST, Delépine M, Makhoul NJ, Blanc H, Sanyoura M, Lavergne A, Stankov K, Lemainque A, Baz P, Julier C, WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon. Hum Mol Genet, 2008, 17 (24): p. 4012-4021. 
50. [SEARCH Collaborative Group] , Link E, Parish S, Armitage J, Bowman L, Heath S, Matsuda F, Gut I, Lathrop M, Collins R, SLCO1B1 variants and statin-induced myopathy--a genomewide study. N Engl J Med, 2008, 359 (8): p. 789-799. 
51. [STAR Consortium] , Saar K, Beck A, Bihoreau MT, Birney E, Brocklebank D, Chen Y, Cuppen E, Demonchy S, Dopazo J, Flicek P, Foglio M, Fujiyama A, Gut IG, Gauguier D, Guigo R, Guryev V, Heinig M, Hummel O, Jahn N, Klages S, Kren V, Kube M, Kuhl H, Kuramoto T, Kuroki Y, Lechner D, Lee YA, Lopez-Bigas N, Lathrop GM, Mashimo T, Medina I, Mott R, Patone G, Perrier-Cornet JA, Platzer M, Pravenec M, Reinhardt R, Sakaki Y, Schilhabel M, Schulz H, Serikawa T, Shikhagaie M, Tatsumoto S, Taudien S, Toyoda A, Voigt B, Zelenika D, Zimdahl H, Hubner N, SNP and haplotype mapping for genetic analysis in the rat. Nat Genet, 2008, 40 (5): p. 560-566. 
52. Bouslam N, Bouhouche A, Benomar A, Hanein S, Klebe S, Azzedine H, Giandomenico SD, Boland-Augé A, Santorelli FM, Durr A, Brice A, Yahyaoui M, Stevanin G, A novel locus for autosomal recessive spastic ataxia on chromosome 17p. Hum Genet, 2007, 121 (3-4): p. 413-420. 
53. Bouzigon E, Ulgen A, Dizier MH, Siroux V, Lathrop M, Kauffmann F, Pin I, Demenais F, Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA families. Hum Genet, 2007, 121 (6): p. 711-719. 
54. Bouzigon E, Siroux V, Dizier MH, Lemainque A, Pison C, Lathrop M, Kauffmann F, Demenais F, Pin I, Scores of asthma and asthma severity reveal new regions of linkage in EGEA study families. Eur Respir J, 2007, 30 (2): p. 253-259. 
55. Chelbi ST, Mondon F, Jammes H, Buffat C, Mignot TM, Tost J, Busato F, Gut I, Rebourcet R, Laissue P, Tsatsaris V, Goffinet F, Rigourd V, Carbonne B, Ferré F, Vaiman D, Expressional and epigenetic alterations of placental serine protease inhibitors: SERPINA3 is a potential marker of preeclampsia. Hypertension, 2007, 49 (1): p. 76-83. 
56. Danoy P, Sonoda E, Lathrop M, Takeda S, Matsuda F, A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. Biochem Biophys Res Commun, 2007, 352 (3): p. 763-768. 
57. De Mita S, Ronfort J, McKhann HI, Poncet C, El Malki R, Bataillon T, Investigation of the demographic and selective forces shaping the nucleotide diversity of genes involved in nod factor signaling in Medicago truncatula. Genetics, 2007, 177 (4): p. 2123-2133. 
58. Dejeux E, Audard V, Cavard C, Gut IG, Terris B, Tost J, Rapid identification of promoter hypermethylation in hepatocellular carcinoma by pyrosequencing of etiologically homogeneous sample pools. J Mol Diagn, 2007, 9 (4): p. 510-520. 
59. Dixon AL, Liang L, Moffatt MF, Chen W, Heath S, Wong KC, Taylor J, Burnett E, Gut I, Farrall M, Lathrop GM, Abecasis GR, Cookson WO, A genome-wide association study of global gene expression. Nat Genet, 2007, 39 (10): p. 1202-1207. 
60. Dizier MH, Bouzigon E, Guilloud-Bataille M, Siroux V, Lemainque A, Boland A, Lathrop M, Demenais F, Evidence for gene x smoking exposure interactions in a genome-wide linkage screen of asthma and bronchial hyper-responsiveness in EGEA families. Eur J Hum Genet, 2007, 15 (7): p. 810-815. 
61. Elleuch N, Bouslam N, Hanein S, Lossos A, Hamri A, Klebe S, Meiner V, Birouk N, Lerer I, Grid D, Bacq D, Tazir M, Zelenika D, Argov Z, Durr A, Yahyaoui M, Benomar A, Brice A, Stevanin G, Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families. Neurogenetics, 2007, 8 (4): p. 307-315. 
62. Fischer J, Lefèvre C, Morava E, Mussini JM, Laforêt P, Negre-Salvayre A, Lathrop M, Salvayre R, The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy. Nat Genet, 2007, 39 (1): p. 28-30. 
63. Fradin D, Heath S, Lathrop M, Bougnères P, Quantitative trait loci for fasting glucose in young Europeans replicate previous findings for type 2 diabetes in 2q23-24 and other locations. Diabetes, 2007, 56 (6): p. 1742-1745. 
64. Gautier M, Faraut T, Moazami-Goudarzi K, Navratil V, Foglio M, Grohs C, Boland A, Garnier JG, Boichard D, Lathrop GM, Gut IG, Eggen A, Genetic and haplotypic structure in 14 European and African cattle breeds. Genetics, 2007, 177 (2): p. 1059-1070. 
65. Hadjadj S, Tarnow L, Forsblom C, Kazeem G, Marre M, Groop PH, Parving HH, Cambien F, Tregouet DA, Gut IG, Théva A, Gauguier D, Farrall M, Cox R, Matsuda F, Lathrop M, Hager-Vionnet N, [EURAGEDIC (European Rational A , Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations. J Am Soc Nephrol, 2007, 18 (4): p. 1284-1291. 
66. Hanein S, Dürr A, Ribai P, Forlani S, Leutenegger AL, Nelson I, Babron MC, Elleuch N, Depienne C, Charon C, Brice A, Stevanin G, A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3. Hum Genet, 2007, 122 (3-4): p. 261-273. 
67. Klebe S, Durr A, Bouslam N, Grid D, Paternotte C, Depienne C, Hanein S, Bouhouche A, Elleuch N, Azzedine H, Poea-Guyon S, Forlani S, Denis E, Charon C, Hazan J, Brice A, Stevanin G, Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description. Am J Med Genet B Neuropsychiatr Genet, 2007, 144B (7): p. 854-861. 
68. Lesueur F, Lefèvre C, Has C, Guilloud-Bataille M, Oudot T, Mahé E, Lahfa M, Mansouri S, Mosharraf-Olmolk H, Sobel E, Heath S, Lathrop M, Dizier MH, Prud'Homme JF, Fischer J, Confirmation of psoriasis susceptibility loci on chromosome 6p21 and 20p13 in French families. J Invest Dermatol, 2007, 127 (6): p. 1403-1409. 
69. Lesueur F, Oudot T, Heath S, Foglio M, Lathrop M, Prud'homme JF, Fischer J, ADAM33, a new candidate for psoriasis susceptibility. PLoS ONE, 2007, 2 (9): p. e906. 
70. Lesueur F, Bouadjar B, Lefèvre C, Jobard F, Audebert S, Lakhdar H, Martin L, Tadini G, Karaduman A, Emre S, Saker S, Lathrop M, Fischer J, Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13. J Invest Dermatol, 2007, 127 (4): p. 829-834. 
71. Libioulle C, Louis E, Hansoul S, Sandor C, Farnir F, Franchimont D, Vermeire S, Dewit O, de Vos M, Dixon A, Demarche B, Gut I, Heath S, Foglio M, Liang L, Laukens D, Mni M, Zelenika D, Gossum AV, Rutgeerts P, Belaiche J, Lathrop M, Georges M, Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4. PLoS Genet, 2007, 3 (4): p. e58. 
72. Marçano AC, Burke B, Gungadoo J, Wallace C, Kaisaki PJ, Woon PY, Farrall M, Clayton D, Brown M, Dominiczak A, Connell JM, Webster J, Lathrop M, Caulfield M, Samani N, Gauguier D, Munroe PB, Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension. J Med Genet, 2007, 44 (9): p. 603-605. 
73. Mauger F, Bauer K, Calloway CD, Semhoun J, Nishimoto T, Myers TW, Gelfand DH, Gut IG, DNA sequencing by MALDI-TOF MS using alkali cleavage of RNA/DNA chimeras. Nucleic Acids Res, 2007, 35 (8): p. e62. 
74. Menzel S, Garner C, Gut I, Matsuda F, Yamaguchi M, Heath S, Foglio M, Zelenika D, Boland A, Rooks H, Best S, Spector TD, Farrall M, Lathrop M, Thein SL, A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. Nat Genet, 2007, 39 (10): p. 1197-1199. 
75. Menzel S, Jiang J, Silver N, Gallagher J, Cunningham J, Surdulescu G, Lathrop M, Farrall M, Spector TD, Thein SL, The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans. Blood, 2007, 110 (10): p. 3624-3626. 
76. Michiels S, Danoy P, Dessen P, Bera A, Boulet T, Bouchardy C, Lathrop M, Sarasin A, Benhamou S, Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers. Carcinogenesis, 2007, 28 (8): p. 1731-1739. 
77. Moffatt MF, Kabesch M, Liang L, Dixon AL, Strachan D, Heath S, Depner M, von Berg A, Bufe A, Rietschel E, Heinzmann A, Simma B, Frischer T, Willis-Owen SA, Wong KC, Illig T, Vogelberg C, Weiland SK, von Mutius E, Abecasis GR, Farrall M, Gut IG, Lathrop GM, Cookson WO, Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature, 2007, 448 (7152): p. 470-473. 
78. Mollet J, Giurgea I, Schlemmer D, Dallner G, Chretien D, Delahodde A, Bacq D, de Lonlay P, Munnich A, Rötig A, Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders. J Clin Invest, 2007, 117 (3): p. 765-772. 
79. Partonen T, Treutlein J, Alpman A, Frank J, Johansson C, Depner M, Aron L, Rietschel M, Wellek S, Soronen P, Paunio T, Koch A, Chen P, Lathrop M, Adolfsson R, Persson ML, Kasper S, Schalling M, Peltonen L, Schumann G, Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression. Ann Med, 2007, 39 (3): p. 229-238. 
80. Thein SL, Menzel S, Peng X, Best S, Jiang J, Close J, Silver N, Gerovasilli A, Ping C, Yamaguchi M, Wahlberg K, Ulug P, Spector TD, Garner C, Matsuda F, Farrall M, Lathrop M, Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Proc Natl Acad Sci U S A, 2007, 104 (27): p. 11346-11351. 
81. Thiery G, Shchepinov MS, Southern EM, Audebourg A, Audard V, Terris B, Gut IG, Multiplex target protein imaging in tissue sections by mass spectrometry--TAMSIM. Rapid Commun Mass Spectrom, 2007, 21 (6): p. 823-829. 
82. Tost J, Jammes H, Dupont JM, Buffat C, Robert B, Mignot TM, Mondon F, Carbonne B, Siméoni U, Grangé G, Kerjean A, Ferré F, Gut IG, Vaiman D, Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region. Nucleic Acids Res, 2007, 35 (2): p. 701. 
83. Tost J, Gut IG, DNA methylation analysis by pyrosequencing. Nat Protoc, 2007, 2 (9): p. 2265-2275. 
84. Tournev I, Royer B, Szepetowski P, Guergueltcheva V, Radionova M, Velizarova R, Yonova M, Lathrop M, Jamali S, Petkov R, Raycheva M, Genton P, Familial generalized epilepsy in Bulgarian Roma. Epileptic Disord, 2007, 9 (3): p. 300-306. 
85. Vasilescu A, Terashima Y, Enomoto M, Heath S, Poonpiriya V, Gatanaga H, Do H, Diop G, Hirtzig T, Auewarakul P, Lauhakirti D, Sura T, Charneau P, Marullo S, Therwath A, Oka S, Kanegasaki S, Lathrop M, Matsushima K, Zagury JF, Matsuda F, A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients. Proc Natl Acad Sci U S A, 2007, 104 (9): p. 3354-3359. 
86. Wahlberg P, Strömstedt L, Tordoir X, Foglio M, Heath S, Lechner D, Hellström AR, Tixier-Boichard M, Lathrop M, Gut IG, Andersson L, A high-resolution linkage map for the Z chromosome in chicken reveals hot spots for recombination. Cytogenet Genome Res, 2007, 117 (1-4): p. 22-29. 
87. Zeggini E, Weedon MN, Lindgren CM, Frayling TM, Elliott KS, Lango H, Timpson NJ, Perry JR, Rayner NW, Freathy RM, Barrett JC, Shields B, Morris AP, Ellard S, Groves CJ, Harries LW, Marchini JL, Owen KR, Knight B, Cardon LR, Walker M, Hitman GA, Morris AD, Doney AS, [Wellcome Trust Case Control Co , McCarthy MI, Hattersley AT, Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science, 2007, 316 (5829): p. 1336-1341. 
88. Bell JT, Wallace C, Dobson R, Wiltshire S, Mein C, Pembroke J, Brown M, Clayton D, Samani N, Dominiczak A, Webster J, Lathrop GM, Connell J, Munroe P, Caulfield M, Farrall M, Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension. Hum Mol Genet, 2006, 15 (8): p. 1365-1374. 
89. Brenner D, Labreuche J, Touboul PJ, Schmidt-Petersen K, Poirier O, Perret C, Schönfelder J, Combadière C, Lathrop M, Cambien F, Brand-Herrmann SM, Amarenco P, [GENIC Investigators] , Cytokine polymorphisms associated with carotid intima-media thickness in stroke patients. Stroke, 2006, 37 (7): p. 1691-1696. 
90. Ciesek S, Hadem J, Fischer J, Manns MP, Strassburg CP, A rare cause of nonalcoholic fatty liver disease. Ann Intern Med, 2006, 145 (2): p. 154-155. 
91. Clarke R, Xu P, Bennett D, Lewington S, Zondervan K, Parish S, Palmer A, Clark S, Cardon L, Peto R, Lathrop M, Collins R, [International Study of Infarct , Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study. PLoS Genet, 2006, 2 (7): p. e107. 
92. Delmaghani S, del Castillo FJ, Michel V, Leibovici M, Aghaie A, Ron U, Van Laer L, Ben-Tal N, Van Camp G, Weil D, Langa F, Lathrop M, Avan P, Petit C, Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nat Genet, 2006, 38 (7): p. 770-778. 
93. Do H, Vasilescu A, Diop G, Hirtzig T, Coulonges C, Labib T, Heath SC, Spadoni JL, Therwath A, Lathrop M, Matsuda F, Zagury JF, Associations of the IL2Ralpha, IL4Ralpha, IL10Ralpha, and IFN (gamma) R1 cytokine receptor genes with AIDS progression in a French AIDS cohort. Immunogenetics, 2006, 58 (2-3): p. 89-98. 
94. Drouaud J, Camilleri C, Bourguignon PY, Canaguier A, Bérard A, Vezon D, Giancola S, Brunel D, Colot V, Prum B, Quesneville H, Mézard C, Variation in crossing-over rates across chromosome 4 of Arabidopsis thaliana reveals the presence of meiotic recombination "hot spots". Genome Res, 2006, 16 (1): p. 106-114. 
95. Etain B, Mathieu F, Rietschel M, Maier W, Albus M, McKeon P, Roche S, Kealey C, Blackwood D, Muir W, Bellivier F, Henry C, Dina C, Gallina S, Gurling H, Malafosse A, Preisig M, Ferrero F, Cichon S, Schumacher J, Ohlraun S, Borrmann-Hassenbach M, Propping P, Abou Jamra R, Schulze TG, Marusic A, Dernovsek ZM, Giros B, Bourgeron T, Lemainque A, Bacq D, Betard C, Charon C, Nöthen MM, Lathrop M, Leboyer M, Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14. Mol Psychiatry, 2006, 11 (7): p. 685-694. 
96. Fontanière S, Tost J, Wierinckx A, Lachuer J, Lu J, Hussein N, Busato F, Gut I, Wang ZQ, Zhang CX, Gene expression profiling in insulinomas of Men1 {beta}-cell mutant mice reveals early genetic and epigenetic events involved in pancreatic {beta}-cell tumorigenesis. Endocr Relat Cancer, 2006, 13 (4): p. 1223-1236. 
97. Fradin D, Heath S, Lepercq J, Lathrop M, Bougnères P, Identification of distinct quantitative trait Loci affecting length or weight variability at birth in humans. J Clin Endocrinol Metab, 2006, 91 (10): p. 4164-4170. 
98. Giancola S, McKhann HI, Bérard A, Camilleri C, Durand S, Libeau P, Roux F, Reboud X, Gut IG, Brunel D, Utilization of the three high-throughput SNP genotyping methods, the GOOD assay, Amplifluor and TaqMan, in diploid and polyploid plants. Theor Appl Genet, 2006, 112 (6): p. 1115-1124. 
99. Keavney B, Danesh J, Parish S, Palmer A, Clark S, Youngman L, Delépine M, Lathrop M, Peto R, Collins R, Fibrinogen and coronary heart disease: test of causality by 'Mendelian randomization'. Int J Epidemiol, 2006, 35 (4): p. 935-943. 
100. Khachidze M, Buil A, Viel KR, Porter S, Warren D, Machiah DK, Soria JM, Souto JC, Ameri A, Lathrop M, Blangero J, Fontcuberta J, Warren ST, Almasy L, Howard TE, Genetic determinants of normal variation in coagulation factor (F) IX levels: genome-wide scan and examination of the FIX structural gene. J Thromb Haemost, 2006, 4 (7): p. 1537-1545. 
101. Klebe S, Azzedine H, Durr A, Bastien P, Bouslam N, Elleuch N, Forlani S, Charon C, Koenig M, Melki J, Brice A, Stevanin G, Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3. Brain, 2006, 129 (Pt 6): p. 1456-1462. 
102. Lefèvre C, Bouadjar B, Ferrand V, Tadini G, Mégarbané A, Lathrop M, Prud'homme JF, Fischer J, Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3. Hum Mol Genet, 2006, 15 (5): p. 767-776. 
103. Mauger F, Jaunay O, Chamblain V, Reichert F, Bauer K, Gut IG, Gelfand DH, SNP genotyping using alkali cleavage of RNA/DNA chimeras and MALDI time-of-flight mass spectrometry. Nucleic Acids Res, 2006, 34 (3): p. e18. 
104. Menchari Y, Camilleri C, Michel S, Brunel D, Dessaint F, Le Corre V, Délye C, Weed response to herbicides: regional-scale distribution of herbicide resistance alleles in the grass weed Alopecurus myosuroides. New Phytol, 2006, 171 (4): p. 861-874. 
105. Munroe PB, Wallace C, Xue MZ, Marçano AC, Dobson RJ, Onipinla AK, Burke B, Gungadoo J, Newhouse SJ, Pembroke J, Brown M, Dominiczak AF, Samani NJ, Lathrop M, Connell J, Webster J, Clayton D, Farrall M, Mein CA, Caulfield M, [Medical Research Council Briti , Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study. Hypertension, 2006, 48 (1): p. 105-111. 
106. Ostrowski MF, David J, Santoni S, McKhann H, Reboud X, Le Corre V, Camilleri C, Brunel D, Bouchez D, Faure B, Bataillon T, Evidence for a large-scale population structure among accessions of Arabidopsis thaliana: possible causes and consequences for the distribution of linkage disequilibrium. Mol Ecol, 2006, 15 (6): p. 1507-1517. 
107. Padmanabhan S, Wallace C, Munroe PB, Dobson R, Brown M, Samani N, Clayton D, Farrall M, Webster J, Lathrop M, Caulfield M, Dominiczak AF, Connell JM, Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study. Hypertension, 2006, 47 (3): p. 603-608. 
108. Ravel C, Praud S, Murigneux A, Linossier L, Dardevet M, Balfourier F, Dufour P, Brunel D, Charmet G, Identification of Glu-B1-1 as a candidate gene for the quantity of high-molecular-weight glutenin in bread wheat (Triticum aestivum L.) by means of an association study. Theor Appl Genet, 2006, 112 (4): p. 738-743. 
109. Remacha AF, Souto JC, Soria JM, Buil A, Sardà MP, Lathrop M, Blangero J, Almasy L, Fontcuberta J, Genomewide linkage analysis of soluble transferrin receptor plasma levels. Ann Hematol, 2006, 85 (1): p. 25-28. 
110. Ribai P, Stevanin G, Bouslam N, Pontier B, Nelson I, Fontaine B, Dussert C, Charon C, Durr A, Brice A, A new phenotype linked to SPG27 and refinement of the critical region on chromosome. J Neurol, 2006, 253 (6): p. 714-719. 
111. Roll P, Rudolf G, Pereira S, Royer B, Scheffer IE, Massacrier A, Valenti MP, Roeckel-Trevisiol N, Jamali S, Beclin C, Seegmuller C, Metz-Lutz MN, Lemainque A, Delepine M, Caloustian C, de Saint Martin A, Bruneau N, Depétris D, Mattéi MG, Flori E, Robaglia-Schlupp A, Lévy N, Neubauer BA, Ravid R, Marescaux C, Berkovic SF, Hirsch E, Lathrop M, Cau P, Szepetowski P, SRPX2 mutations in disorders of language cortex and cognition. Hum Mol Genet, 2006, 15 (7): p. 1195-1207. 
112. Rothenbuhler A, Fradin D, Heath S, Lefevre H, Bouvattier C, Lathrop M, Bougnères P, Weight-adjusted genome scan analysis for mapping quantitative trait Loci for menarchal age. J Clin Endocrinol Metab, 2006, 91 (9): p. 3534-3537. 
113. Roux F, Giancola S, Durand S, Reboud X, Building of an experimental cline with Arabidopsis thaliana to estimate herbicide fitness cost. Genetics, 2006, 173 (2): p. 1023-1031. 
114. Senée V, Chelala C, Duchatelet S, Feng D, Blanc H, Cossec JC, Charon C, Nicolino M, Boileau P, Cavener DR, Bougnères P, Taha D, Julier C, Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. Nat Genet, 2006, 38 (6): p. 682-687. 
115. Shmulewitz D, Heath SC, Blundell ML, Han Z, Sharma R, Salit J, Auerbach SB, Signorini S, Breslow JL, Stoffel M, Friedman JM, Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia. Proc Natl Acad Sci U S A, 2006, 103 (10): p. 3502-3509. 
116. Tost J, Gut IG, DNA analysis by mass spectrometry-past, present and future. J Mass Spectrom, 2006, 41 (8): p. 981-995. 
117. Tost J, El Abdalaoui H, Gut IG, Serial pyrosequencing for quantitative DNA methylation analysis. Biotechniques, 2006, 40 (6): p. 721-2, 724, 726. 
118. Tost J, Jammes H, Dupont JM, Buffat C, Robert B, Mignot TM, Mondon F, Carbonne B, Siméoni U, Grangé G, Kerjean A, Ferré F, Gut IG, Vaiman D, Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region. Nucleic Acids Res, 2006, 34 (19): p. 5438-5448. 
119. Vionnet N, Tregouët D, Kazeem G, Gut I, Groop PH, Tarnow L, Parving HH, Hadjadj S, Forsblom C, Farrall M, Gauguier D, Cox R, Matsuda F, Heath S, Thévard A, Rousseau R, Cambien F, Marre M, Lathrop M, Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin gene. Diabetes, 2006, 55 (11): p. 3166-3174. 
120. Wallace C, Xue MZ, Newhouse SJ, Marcano AC, Onipinla AK, Burke B, Gungadoo J, Dobson RJ, Brown M, Connell JM, Dominiczak A, Lathrop GM, Webster J, Farrall M, Mein C, Samani NJ, Caulfield MJ, Clayton DG, Munroe PB, Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension. Am J Hum Genet, 2006, 79 (2): p. 323-331. 
121. Abbas A, Vasilescu A, Do H, Hendel H, Maachi M, Goutalier FX, Regulier EG, Rappaport J, Matsuda F, Therwath A, Aucouturier P, Zagury JF, Analysis of IGG and IGG4 in HIV-1 seropositive patients and correlation with biological and genetic markers. Biomed Pharmacother, 2005, 59 (1-2): p. 38-46. 
122. Almasy L, Soria JM, Souto JC, Warren DM, Buil A, Borrell M, Muñoz X, Sala N, Lathrop M, Fontcuberta J, Blangero J, A locus on chromosome 2 influences levels of tissue factor pathway inhibitor: results from the GAIT study. Arterioscler Thromb Vasc Biol, 2005, 25 (7): p. 1489-1492. 
123. Besson V, Nalesso V, Herpin A, Bizot JC, Messaddeq N, Romand R, Puech A, Blanquet V, Hérault Y, Training and aging modulate the loss-of-balance phenotype observed in a new ENU-induced allele of Otopetrin1. Biol Cell, 2005, 97 (10): p. 787-798. 
124. Bouslam N, Benomar A, Azzedine H, Bouhouche A, Namekawa M, Klebe S, Charon C, Durr A, Ruberg M, Brice A, Yahyaoui M, Stevanin G, Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28). Ann Neurol, 2005, 57 (4): p. 567-571. 
125. Brown JH, Bihoreau MT, Hoffmann S, Kränzlin B, Tychinskaya I, Obermüller N, Podlich D, Boehn SN, Kaisaki PJ, Megel N, Danoy P, Copley RR, Broxholme J, Witzgall R, Lathrop M, Gretz N, Gauguier D, Missense mutation in sterile alpha motif of novel protein SamCystin is associated with polycystic kidney disease in (cy/+) rat. J Am Soc Nephrol, 2005, 16 (12): p. 3517-3526. 
126. Castanet M, Sura-Trueba S, Chauty A, Carré A, de Roux N, Heath S, Léger J, Lyonnet S, Czernichow P, Polak M, Linkage and mutational analysis of familial thyroid dysgenesis demonstrate genetic heterogeneity implicating novel genes. Eur J Hum Genet, 2005, 13 (2): p. 232-239. 
127. de Parseval N, Diop G, Blaise S, Helle F, Vasilescu A, Matsuda F, Heidmann T, Comprehensive search for intra- and inter-specific sequence polymorphisms among coding envelope genes of retroviral origin found in the human genome: genes and pseudogenes. BMC Genomics, 2005, 6p. 117. 
128. Delague V, Chouery E, Corbani S, Ghanem I, Aamar S, Fischer J, Levy-Lahad E, Urtizberea JA, Mégarbané A, Molecular study of WISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: identification of two novel mutations, and description of a founder effect. Am J Med Genet A, 2005, 138 (2): p. 118-126. 
129. Diop G, Spadoni JL, Do H, Hirtzig T, Coulonges C, Labib T, Issing W, Rappaport J, Therwath A, Lathrop M, Matsuda F, Zagury JF, Genomic approach of AIDS pathogenesis: exhaustive genotyping of the TNFR1 gene in a French AIDS cohort. Biomed Pharmacother, 2005, 59 (8): p. 474-480. 
130. Dizier MH, Bouzigon E, Guilloud-Bataille M, Bétard C, Bousquet J, Charpin D, Gormand F, Hochez J, Just J, Lemainque A, Le Moual N, Matran R, Neukirch F, Oryszczyn MP, Paty E, Pin I, Vervloet D, Kauffmann F, Lathrop M, Demenais F, Annesi-Maesano I, Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma. Genes Immun, 2005, 6 (2): p. 95-102. 
131. Do H, Vasilescu A, Diop G, Hirtzig T, Heath SC, Coulonges C, Rappaport J, Therwath A, Lathrop M, Matsuda F, Zagury JF, Exhaustive genotyping of the CEM15 (APOBEC3G) gene and absence of association with AIDS progression in a French cohort. J Infect Dis, 2005, 191 (2): p. 159-163. 
132. Duchatelet S, Ostergaard E, Cortes D, Lemainque A, Julier C, Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes. Hum Mol Genet, 2005, 14 (1): p. 1-5. 
133. Elder JT, Abecasis G, Allen M, Barker JNWN, Burden D, Capon F, Christophers E, Fischer J, Giardina E, Gudjonsson JE, Hüffmeier U, Jenish S, Karason A, Kere J, Nair RP, Novelli G, Prud'homme JF, Qin ZS, Samuelsson L, Sanchez F, Saarialho-Kere U, Stahle M, Stuart P, Tillman D, Traupe H, Trembath R, Valdimarsson H, Veal C, Voorhees JJ, Weichenthal M, [Cluster 17 Collaboration] , Fine mapping of the psoriasis susceptibility gene PSORS1: a reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6. J Invest Dermatol, 2005, 124 (5): p. 921-930. 
134. Gut IG, Taylor GR, Day INM, Mass Spectrometry for High-Throughput Genotyping . Guide to mutation detection, John Wiley & sons, 2005p. 117-122. 
135. Khau Van Kien P, Mathieu F, Zhu L, Lalande A, Betard C, Lathrop M, Brunotte F, Wolf JE, Jeunemaitre X, Mapping of familial thoracic aortic aneurysm/dissection with patent ductus arteriosus to 16p12.2-p13.13. Circulation, 2005, 112 (2): p. 200-206. 
136. McKenzie CA, Sinsheimer JS, Adeyemo AA, Cox RD, Southam L, Hugill A, Bouzekri N, Lathrop M, Forrester TE, Cooper RS, Ward R, SNP haplotypes in the angiotensin I-converting enzyme (ACE) gene: analysis of Nigerian family data using gamete competition models. Ann Hum Genet, 2005, 69 (Pt 2): p. 227-232. 
137. Newhouse SJ, Wallace C, Dobson R, Mein C, Pembroke J, Farrall M, Clayton D, Brown M, Samani N, Dominiczak A, Connell JM, Webster J, Lathrop GM, Caulfield M, Munroe PB, Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. Hum Mol Genet, 2005, 14 (13): p. 1805-1814. 
138. Ohmura K, Johnsen A, Ortiz-Lopez A, Desany P, Roy M, Besse W, Rogus J, Bogue M, Puech A, Lathrop M, Mathis D, Benoist C, Variation in IL-1beta gene expression is a major determinant of genetic differences in arthritis aggressivity in mice. Proc Natl Acad Sci U S A, 2005, 102 (35): p. 12489-12494. 
139. Pelet A, de Pontual L, Clément-Ziza M, Salomon R, Mugnier C, Matsuda F, Lathrop M, Munnich A, Feingold J, Lyonnet S, Abel L, Amiel J, Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease. J Med Genet, 2005, 42 (3): p. e18. 
140. Pujol RM, Gilaberte M, Toll A, Florensa L, Lloreta J, González-Enseñat MA, Fischer J, Azon A, Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome. Br J Dermatol, 2005, 153 (4): p. 838-841. 
141. Roux F, Camilleri C, Giancola S, Brunel D, Reboud X, Epistatic interactions among herbicide resistances in Arabidopsis thaliana: the fitness cost of multiresistance. Genetics, 2005, 171 (3): p. 1277-1288. 
142. Roux F, Camilleri C, Bérard A, Reboud X, Multigenerational versus single generation studies to estimate herbicide resistance fitness cost in Arabidopsis thaliana. Evolution Int J Org Evolution, 2005, 59 (10): p. 2264-2269. 
143. Sakuntabhai A, Turbpaiboon C, Casadémont I, Chuansumrit A, Lowhnoo T, Kajaste-Rudnitski A, Kalayanarooj SM, Tangnararatchakit K, Tangthawornchaikul N, Vasanawathana S, Chaiyaratana W, Yenchitsomanus PT, Suriyaphol P, Avirutnan P, Chokephaibulkit K, Matsuda F, Yoksan S, Jacob Y, Lathrop GM, Malasit P, Desprès P, Julier C, A variant in the CD209 promoter is associated with severity of dengue disease. Nat Genet, 2005, 37 (5): p. 507-513. 
144. Schleinitz N, Fischer J, Sanchez A, Veit V, Harle JR, Pelissier JF, Two new mutations of the ABHD5 gene in a new adult case of Chanarin Dorfman syndrome: an uncommon lipid storage disease. Arch Dermatol, 2005, 141 (6): p. 798-800. 
145. Seboun E, Lemainque A, Jackson CE, Amish brittle hair syndrome gene maps to 7p14.1. Am J Med Genet A, 2005, 134 (3): p. 290-294. 
146. Soria JM, Almasy L, Souto JC, Buil A, Lathrop M, Blangero J, Fontcuberta J, A genome search for genetic determinants that influence plasma fibrinogen levels. Arterioscler Thromb Vasc Biol, 2005, 25 (6): p. 1287-1292. 
147. Souto JC, Blanco-Vaca F, Soria JM, Buil A, Almasy L, Ordoñez-Llanos J, Martín-Campos JM, Lathrop M, Stone W, Blangero J, Fontcuberta J, A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project. Am J Hum Genet, 2005, 76 (6): p. 925-933. 
148. Spanagel R, Pendyala G, Abarca C, Zghoul T, Sanchis-Segura C, Magnone MC, Lascorz J, Depner M, Holzberg D, Soyka M, Schreiber S, Matsuda F, Lathrop M, Schumann G, Albrecht U, The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption. Nat Med, 2005, 11 (1): p. 35-42. 
149. Tost J, Gut IG, Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications. Clin Biochem, 2005, 38 (4): p. 335-350. 
150. Valdes AM, Thomson G, Graham J, Zarghami M, McNeney B, Kockum I, Smith A, Lathrop M, Steenkiste AR, Dorman JS, Noble JA, Hansen JA, Pugliese A, Lernmark A, [Swedish Childhood Study Group] , [Diabetes Incidence in Sweden S , [Type 1 Diabetes Component of t , D6S265*15 marks a DRB1*15, DQB1*0602 haplotype associated with attenuated protection from type 1 diabetes mellitus. Diabetologia, 2005, 48 (12): p. 2540-2543. 
151. Windsor L, Puschendorf M, Allcock R, Scott A, Sayer D, Kucharzak R, Gut I, McCann V, Davis E, Witt C, Christiansen F, Price P, Does a central MHC gene in linkage disequilibrium with HLA-DRB1*0401 affect susceptibility to type 1 diabetes? Genes Immun, 2005, 6 (4): p. 298-304. 
152. Yamazaki K, McGovern D, Ragoussis J, Paolucci M, Butler H, Jewell D, Cardon L, Takazoe M, Tanaka T, Ichimori T, Saito S, Sekine A, Iida A, Takahashi A, Tsunoda T, Lathrop M, Nakamura Y, Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. Hum Mol Genet, 2005, 14 (22): p. 3499-3506. 
153. Allcock RJ, Windsor L, Gut IG, Kucharzak R, Sobre L, Lechner D, Garnier JG, Baltic S, Christiansen FT, Price P, High-Density SNP genotyping defines 17 distinct haplotypes of the TNF block in the Caucasian population: implications for haplotype tagging. Hum Mutat, 2004, 24 (6): p. 517-525. 
154. Auwerx J, Avner P, Baldock R, Ballabio A, Balling R, Barbacid M, Berns A, Bradley A, Brown S, Carmeliet P, Chambon P, Cox R, Davidson D, Davies K, Duboule D, Forejt J, Granucci F, Hastie N, de Angelis MH, Jackson I, Kioussis D, Kollias G, Lathrop M, Lendahl U, Malumbres M, von Melchner H, Müller W, Partanen J, Ricciardi-Castagnoli P, Rigby P, Rosen B, Rosenthal N, Skarnes B, Stewart AF, Thornton J, Tocchini-Valentini G, Wagner E, Wahli W, Wurst W, The European dimension for the mouse genome mutagenesis program. Nat Genet, 2004, 36 (9): p. 925-927. 
155. Bell CG, Benzinou M, Siddiq A, Lecoeur C, Dina C, Lemainque A, Clément K, Basdevant A, Guy-Grand B, Mein CA, Meyre D, Froguel P, Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q. Diabetes, 2004, 53 (7): p. 1857-1865. 
156. Borck G, Rio M, Sanlaville D, Redon R, Molinari F, Bacq D, Raoul O, Cormier-Daire V, Lyonnet S, Amiel J, Le Merrer M, de Blois MC, Prieur M, Vekemans M, Carter NP, Munnich A, Colleaux L, Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation. Clin Genet, 2004, 66 (2): p. 122-127. 
157. Bouzigon E, Dizier MH, Krähenbühl C, Lemainque A, Annesi-Maesano I, Betard C, Bousquet J, Charpin D, Gormand F, Guilloud-Bataille M, Just J, Le Moual N, Maccario J, Matran R, Neukirch F, Oryszczyn MP, Paty E, Pin I, Rosenberg-Bourgin M, Vervloet D, Kauffmann F, Lathrop M, Demenais F, Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families. Hum Mol Genet, 2004, 13 (24): p. 3103-3113. 
158. Buil A, Soria JM, Souto JC, Almasy L, Lathrop M, Blangero J, Fontcuberta J, Protein C levels are regulated by a quantitative trait locus on chromosome 16: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project. Arterioscler Thromb Vasc Biol, 2004, 24 (7): p. 1321-1325. 
159. Caux F, Selma ZB, Laroche L, Prud'homme JF, Fischer J, CGI-58/ABHD5 gene is mutated in Dorfman-Chanarin syndrome. Am J Med Genet A, 2004, 129A (2): p. 214. 
160. Dupont JM, Tost J, Jammes H, Gut IG, De novo quantitative bisulfite sequencing using the pyrosequencing technology. Anal Biochem, 2004, 333 (1): p. 119-127. 
161. Eckhardt F, Beck S, Gut IG, Berlin K, Future potential of the Human Epigenome Project. Expert Rev Mol Diagn, 2004, 4 (5): p. 609-618. 
162. Gut IG, DNA analysis by MALDI-TOF mass spectrometry. Hum Mutat, 2004, 23 (5): p. 437-441. 
163. Gut IG, Lathrop GM, Duplicating SNPs. Nat Genet, 2004, 36 (8): p. 789-790. 
164. Hao GP, Wu ZY, Cao MQ, Pelletier G, Brunel D, Huang CL, Yang Q, [Nucleotide polymorphism in the drought induced transcription factor CBF4 region of Arabidopsis thaliana and its molecular evolution analyses] Yi Chuan Xue Bao, 2004, 31 (12): p. 1415-1425. 
165. Kaisaki PJ, Delépine M, Woon PY, Sebag-Montefiore L, Wilder SP, Menzel S, Vionnet N, Marion E, Riveline JP, Charpentier G, Schurmans S, Levy JC, Lathrop M, Farrall M, Gauguier D, Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome. Diabetes, 2004, 53 (7): p. 1900-1904. 
166. Keavney B, Palmer A, Parish S, Clark S, Youngman L, Danesh J, McKenzie C, Delépine M, Lathrop M, Peto R, Collins R, [International Studies of Infar , Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease risk. Int J Epidemiol, 2004, 33 (5): p. 1002-1013. 
167. Lagier-Tourenne C, Boltshauser E, Breivik N, Gribaa M, Bétard C, Barbot C, Koenig M, Homozygosity mapping of a third Joubert syndrome locus to 6q23. J Med Genet, 2004, 41 (4): p. 273-277. 
168. Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D, A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24. Brain, 2004, 127 (Pt 9): p. 1979-1992. 
169. Lefèvre C, Bouadjar B, Karaduman A, Jobard F, Saker S, Ozguc M, Lathrop M, Prud'homme JF, Fischer J, Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis. Hum Mol Genet, 2004, 13 (20): p. 2473-2482. 
170. Liao G, Wang J, Guo J, Allard J, Cheng J, Ng A, Shafer S, Puech A, McPherson JD, Foernzler D, Peltz G, Usuka J, In silico genetics: identification of a functional element regulating H2-Ealpha gene expression. Science, 2004, 306 (5696): p. 690-695. 
171. McKhann HI, Camilleri C, Bérard A, Bataillon T, David JL, Reboud X, Le Corre V, Caloustian C, Gut IG, Brunel D, Nested core collections maximizing genetic diversity in Arabidopsis thaliana. Plant J, 2004, 38 (1): p. 193-202. 
172. Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Morais D, Lathrop M, Petit C, Moreno F, A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci. J Med Genet, 2004, 41 (2): p. e14. 
173. Rakyan VK, Hildmann T, Novik KL, Lewin J, Tost J, Cox AV, Andrews TD, Howe KL, Otto T, Olek A, Fischer J, Gut IG, Berlin K, Beck S, DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project. PLoS Biol, 2004, 2 (12): p. e405. 
174. Rapley R, Harbron S, Gut IG, An overview of genotyping and single nucleotide polymorphisms (SNP) . Molecular Analysis and Genome Discovery, J Wiley & Sons, 2004p. 43-69. 
175. Reboud X, Lecorre V, Scarcelli N, Roux F, David JL, Bataillon T, Camilleri C, Brunel D, McKhann HI, Cronk QCB, Whitton J, Ree RH, Taylor IEP, Natural variation among accessions of Arabidopsis thaliana: beyond the flowering date what morphological traits are relevant to study adaptation? . Plant Adaptation: Molecular Genetics and Ecology, NRC Research Press, 2004p. 135-142. 
176. Rudolf G, Thérèse Bihoreau M, F Godfrey R, P Wilder S, D Cox R, Lathrop M, Marescaux C, Gauguier D, Polygenic control of idiopathic generalized epilepsy phenotypes in the genetic absence rats from Strasbourg (GAERS). Epilepsia, 2004, 45 (4): p. 301-308. 
177. Senée V, Vattem KM, Delépine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C, Michaud JL, Bin-Abbas B, Taha D, Zabel B, Franceschini P, Topaloglu AK, Lathrop GM, Barrett TG, Nicolino M, Wek RC, Julier C, Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity. Diabetes, 2004, 53 (7): p. 1876-1883. 
178. Srinivasan R, Hadzi? N, Fischer J, Knisely AS, Steatohepatitis and unsuspected micronodular cirrhosis in Dorfman-Chanarin syndrome with documented ABHD5 mutation. J Pediatr, 2004, 144 (5): p. 662-665. 
179. Stevanin G, Hahn V, Lohmann E, Bouslam N, Gouttard M, Soumphonphakdy C, Welter ML, Ollagnon-Roman E, Lemainque A, Ruberg M, Brice A, Durr A, Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. Arch Neurol, 2004, 61 (8): p. 1242-1248. 
180. Stevanin G, Bouslam N, Thobois S, Azzedine H, Ravaux L, Boland A, Schalling M, Broussolle E, Dürr A, Brice A, Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. Ann Neurol, 2004, 55 (1): p. 97-104. 
181. Topçu M, Jobard F, Halliez S, Coskun T, Yalçinkayal C, Gerceker FO, Wanders RJ, Prud'homme JF, Lathrop M, Ozguc M, Fischer J, L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1. Hum Mol Genet, 2004, 13 (22): p. 2803-2811. 
182. Tost J, Gut IG, Genotyping Single Nucleotide Polymorphisms by Mass Spectrometry . Advances in Mass Spectrometry, Elsevier Science, 2004, 16p. 123-143. 
183. Tost J, Kucharzak R, Lechner D, Gut IG, Weissensteiner T, Griffin AM, Griffin HG, The GOOD Assay: A purification free assay for genotyping by MALDI mass spectrometry . PCR Technology, Current Innovations, CRC Press, 2004p. 121-130. 
184. Tsunoda T, Lathrop GM, Sekine A, Yamada R, Takahashi A, Ohnishi Y, Tanaka T, Nakamura Y, Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome. Hum Mol Genet, 2004, 13 (15): p. 1623-1632. 
185. Vasilescu A, Heath SC, Diop G, Do H, Hirtzig T, Hendel H, Bertin-Maghit S, Rappaport J, Therwath A, Lathrop GM, Matsuda F, Zagury JF, Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS. Immunogenetics, 2004, 56 (1): p. 56-60. 
186. Wilder SP, Bihoreau MT, Argoud K, Watanabe TK, Lathrop M, Gauguier D, Integration of the rat recombination and EST maps in the rat genomic sequence and comparative mapping analysis with the mouse genome. Genome Res, 2004, 14 (4): p. 758-765. 
187. Alizadeh M, Babron MC, Birebent B, Matsuda F, Quelvennec E, Liblau R, Cournu-Rebeix I, Momigliano-Richiardi P, Sequeiros J, Yaouanq J, Genin E, Vasilescu A, Bougerie H, Trojano M, Martins Silva B, Maciel P, Clerget-Darpoux F, Clanet M, Edan G, Fontaine B, Semana G, Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients. Ann Neurol, 2003, 54 (1): p. 119-122. 
188. Allen M, Heinzmann A, Noguchi E, Abecasis G, Broxholme J, Ponting CP, Bhattacharyya S, Tinsley J, Zhang Y, Holt R, Jones EY, Lench N, Carey A, Jones H, Dickens NJ, Dimon C, Nicholls R, Baker C, Xue L, Townsend E, Kabesch M, Weiland SK, Carr D, von Mutius E, Adcock IM, Barnes PJ, Lathrop GM, Edwards M, Moffatt MF, Cookson WO, Positional cloning of a novel gene influencing asthma from chromosome 2q14. Nat Genet, 2003, 35 (3): p. 258-263. 
189. Almasy L, Soria JM, Souto JC, Coll I, Bacq D, Faure A, Mateo J, Borrell M, Muñoz X, Sala N, Stone WH, Lathrop M, Fontcuberta J, Blangero J, [Genetic Analysis of Idiopathic , A quantitative trait locus influencing free plasma protein S levels on human chromosome 1q: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) project. Arterioscler Thromb Vasc Biol, 2003, 23 (3): p. 508-511. 
190. Bucheton B, Abel L, El-Safi S, Kheir MM, Pavek S, Lemainque A, Dessein AJ, A major susceptibility locus on chromosome 22q12 plays a critical role in the control of kala-azar. Am J Hum Genet, 2003, 73 (5): p. 1052-1060. 
191. Caulfield M, Munroe P, Pembroke J, Samani N, Dominiczak A, Brown M, Benjamin N, Webster J, Ratcliffe P, O'Shea S, Papp J, Taylor E, Dobson R, Knight J, Newhouse S, Hooper J, Lee W, Brain N, Clayton D, Lathrop GM, Farrall M, Connell J, [MRC British Genetics of Hypert , Genome-wide mapping of human loci for essential hypertension. Lancet, 2003, 361 (9375): p. 2118-2123. 
192. Chimienti F, Hogg RC, Plantard L, Lehmann C, Brakch N, Fischer J, Huber M, Bertrand D, Hohl D, Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda. Hum Mol Genet, 2003, 12 (22): p. 3017-3024. 
193. de Roux N, Genin E, Carel JC, Matsuda F, Chaussain JL, Milgrom E, Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc Natl Acad Sci U S A, 2003, 100 (19): p. 10972-10976. 
194. Delmaghani S, Aghaie A, Compain-Nouaille S, Ataie A, Lemainque A, Zeinali S, Lathrop M, Weil D, Petit C, DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1. Eur J Hum Genet, 2003, 11 (10): p. 816-818. 
195. Faivre L, Le Merrer M, Al-Gazali LI, Ausems MG, Bitoun P, Bacq D, Maroteaux P, Munnich A, Cormier-Daire V, Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3. J Med Genet, 2003, 40 (4): p. 282-284. 
196. Feldmann J, Callebaut I, Raposo G, Certain S, Bacq D, Dumont C, Lambert N, Ouachée-Chardin M, Chedeville G, Tamary H, Minard-Colin V, Vilmer E, Blanche S, Le Deist F, Fischer A, de Saint Basile G, Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3). Cell, 2003, 115 (4): p. 461-473. 
197. Fitch KR, McGowan KA, van Raamsdonk CD, Fuchs H, Lee D, Puech A, Hérault Y, Threadgill DW, Hrabé de Angelis M, Barsh GS, Genetics of dark skin in mice. Genes Dev, 2003, 17 (2): p. 214-228. 
198. Heath SC, Green PJ, Hjort NL, Richardson S, Genetic linkage analysis using Markov chain Monte Carlo techniques . Highly Structured Stochastic Systems, Oxford University Press, 2003p. 363-378. 
199. Heilig R, Eckenberg R, Petit JL, Fonknechten N, Da Silva C, Cattolico L, Levy M, Barbe V, de Berardinis V, Ureta-Vidal A, Pelletier E, Vico V, Anthouard V, Rowen L, Madan A, Qin S, Sun H, Du H, Pepin K, Artiguenave F, Robert C, Cruaud C, Brüls T, Jaillon O, Friedlander L, Samson G, Brottier P, Cure S, Ségurens B, Anière F, Samain S, Crespeau H, Abbasi N, Aiach N, Boscus D, Dickhoff R, Dors M, Dubois I, Friedman C, Gouyvenoux M, James R, Madan A, Mairey-Estrada B, Mangenot S, Martins N, Ménard M, Oztas S, Ratcliffe A, Shaffer T, Trask B, Vacherie B, Bellemere C, Belser C, Besnard-Gonnet M, Bartol-Mavel D, Boutard M, Briez-Silla S, Combette S, Dufossé-Laurent V, Ferron C, Lechaplais C, Louesse C, Muselet D, Magdelenat G, Pateau E, Petit E, Sirvain-Trukniewicz P, Trybou A, Vega-Czarny N, Bataille E, Bluet E, Bordelais I, Dubois M, Dumont C, Guérin T, Haffray S, Hammadi R, Muanga J, Pellouin V, Robert D, Wunderle E, Gauguet G, Roy A, Sainte-Marthe L, Verdier J, Verdier-Discala C, Hillier L, Fulton L, McPherson J, Matsuda F, Wilson R, Scarpelli C, Gyapay G, Wincker P, Saurin W, Quétier F, Waterston R, Hood L, Weissenbach J, The DNA sequence and analysis of human chromosome 14. Nature, 2003, 421 (6923): p. 601-607. 
200. Hoh J, Matsuda F, Peng X, Markovic D, Lathrop MG, Ott J, SNP haplotype tagging from DNA pools of two individuals. BMC Bioinformatics, 2003, 4p. 14. 
201. Jobard F, Bouadjar B, Caux F, Hadj-Rabia S, Has C, Matsuda F, Weissenbach J, Lathrop M, Prud'homme JF, Fischer J, Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. Hum Mol Genet, 2003, 12 (8): p. 925-935. 
202. Keavney B, Parish S, Palmer A, Clark S, Youngman L, Danesh J, McKenzie C, Delépine M, Lathrop M, Peto R, Collins R, [International Studies of Infar , Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E epsilon2/epsilon3/epsilon4 genotype. Lancet, 2003, 361 (9355): p. 396-398. 
203. Kim-Saijo M, Akamizu T, Ikuta K, Iida Y, Ohmori K, Matsubara K, Matsuda Y, Suzuki M, Matsuda F, Nakao K, Generation of a transgenic animal model of hyperthyroid Graves' disease. Eur J Immunol, 2003, 33 (9): p. 2531-2538. 
204. Lagier-Tourenne C, Tranebaerg L, Chaigne D, Gribaa M, Dollfus H, Silvestri G, Bétard C, Warter JM, Koenig M, Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31. Eur J Hum Genet, 2003, 11 (10): p. 770-778. 
205. Lefévre C, Audebert S, Jobard F, Bouadjar B, Lakhdar H, Boughdene-Stambouli O, Blanchet-Bardon C, Heilig R, Foglio M, Weissenbach J, Lathrop M, Prud'homme JF, Fischer J, Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2. Hum Mol Genet, 2003, 12 (18): p. 2369-2378. 
206. Leutenegger AL, Prum B, Génin E, Verny C, Lemainque A, Clerget-Darpoux F, Thompson EA, Estimation of the inbreeding coefficient through use of genomic data. Am J Hum Genet, 2003, 73 (3): p. 516-523. 
207. Magré J, Delépine M, Van Maldergem L, Robert JJ, Maassen JA, Meier M, Panz VR, Kim CA, Tubiana-Rufi N, Czernichow P, Seemanova E, Buchanan CR, Lacombe D, Vigouroux C, Lascols O, Kahn CR, Capeau J, Lathrop M, Prevalence of mutations in AGPAT2 among human lipodystrophies. Diabetes, 2003, 52 (6): p. 1573-1578. 
208. Marrakchi S, Audebert S, Bouadjar B, Has C, Lefèvre C, Munro C, Cure S, Jobard F, Morlot S, Hohl D, Prud'homme JF, Zahaf A, Turki H, Fischer J, Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda. J Invest Dermatol, 2003, 120 (3): p. 351-355. 
209. Masmoudi S, Tlili A, Majava M, Ghorbel AM, Chardenoux S, Lemainque A, Zina ZB, Moala J, Männikkö M, Weil D, Lathrop M, Ala-Kokko L, Drira M, Petit C, Ayadi H, Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1. Eur J Hum Genet, 2003, 11 (2): p. 185-188. 
210. Matsuda F, Honjo T, Alt FW, Neuberger M, The human immunoglobulin heavy-chain loci in human . Molecular Biology of B Cells, Academic Press, 2003p. 1-18. 
211. Matsuda F, [Organization and evolution of the human immunoglobulin heavy-chain loci] Seikagaku, 2003, 75 (4): p. 271-278. 
212. Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Armenta D, Lathrop M, Petit C, Moreno F, A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29. Hum Genet, 2003, 112 (1): p. 24-28. 
213. Moreno-Pelayo MA, Modamio-Høybjør S, Mencía A, del Castillo I, Chardenoux S, Fernández-Burriel M, Lathrop M, Petit C, Moreno F, DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23. J Med Genet, 2003, 40 (11): p. 832-836. 
214. Ruf RG, Fuchshuber A, Karle SM, Lemainque A, Huck K, Wienker T, Otto E, Hildebrandt F, Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p. J Am Soc Nephrol, 2003, 14 (7): p. 1897-1900. 
215. Sauer S, Gut IG, Extension of the GOOD assay for genotyping single nucleotide polymorphisms by matrix-assisted laser desorption/ionization mass spectrometry. Rapid Commun Mass Spectrom, 2003, 17 (12): p. 1265-1272. 
216. Soria JM, Almasy L, Souto JC, Buil A, Martinez-Sanchez E, Mateo J, Borrell M, Stone WH, Lathrop M, Fontcuberta J, Blangero J, A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility. Blood, 2003, 101 (1): p. 163-167. 
217. Souto JC, Almasy L, Soria JM, Buil A, Stone W, Lathrop M, Blangero J, Fontcuberta J, Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project. Thromb Haemost, 2003, 89 (3): p. 468-474. 
218. Takahashi M, Matsuda F, Margetic N, Lathrop M, Automated identification of single nucleotide polymorphisms from sequencing data. J Bioinform Comput Biol, 2003, 1 (2): p. 253-265. 
219. Tost J, Schatz P, Schuster M, Berlin K, Gut IG, Analysis and accurate quantification of CpG methylation by MALDI mass spectrometry. Nucleic Acids Res, 2003, 31 (9): p. e50. 
220. Tost J, Dunker J, Gut IG, Analysis and quantification of multiple methylation variable positions in CpG islands by Pyrosequencing. Biotechniques, 2003, 35 (1): p. 152-156. 
221. Vasilescu A, Heath SC, Ivanova R, Hendel H, Do H, Mazoyer A, Khadivpour E, Goutalier FX, Khalili K, Rappaport J, Lathrop GM, Matsuda F, Zagury JF, Genomic analysis of Th1-Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression. Genes Immun, 2003, 4 (6): p. 441-449. 
222. Wijsman EM, Rosenthal EA, Hall D, Blundell ML, Sobin C, Heath SC, Williams R, Brownstein MJ, Gogos JA, Karayiorgou M, Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q. Mol Psychiatry, 2003, 8 (7): p. 695-705, 643. 
223. Yang Y, Zhang J, Hoh J, Matsuda F, Xu P, Lathrop M, Ott J, Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA. Proc Natl Acad Sci U S A, 2003, 100 (12): p. 7225-7230. 
224. Bakija-Konsuo A, Basta-Juzbasic A, Rudan I, Situm M, Nardelli-Kovacic M, Levanat S, Fischer J, Hohl D, Loncaric D, Seiwert S, Campbell H, Mal de Meleda: genetic haplotype analysis and clinicopathological findings in cases originating from the island of Mljet (Meleda), Croatia. Dermatology, 2002, 205 (1): p. 32-39. 
225. Boland A, Magnon C, Filetti S, Bidart JM, Schlumberger M, Yeh P, Perricaudet M, Transposition of the thyroid iodide uptake and organification system in nonthyroid tumor cells by adenoviral vector-mediated gene transfers. Thyroid, 2002, 12 (1): p. 19-26. 
226. Brand E, Chatelain N, Paillard F, Tiret L, Visvikis S, Lathrop M, Soubrier F, Demenais F, Detection of putative functional angiotensinogen (AGT) gene variants controlling plasma AGT levels by combined segregation-linkage analysis. Eur J Hum Genet, 2002, 10 (11): p. 715-723. 
227. Chumakov I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio M, Abderrahim H, Bougueleret L, Barry C, Tanaka H, La Rosa P, Puech A, Tahri N, Cohen-Akenine A, Delabrosse S, Lissarrague S, Picard FP, Maurice K, Essioux L, Millasseau P, Grel P, Debailleul V, Simon AM, Caterina D, Dufaure I, Malekzadeh K, Belova M, Luan JJ, Bouillot M, Sambucy JL, Primas G, Saumier M, Boubkiri N, Martin-Saumier S, Nasroune M, Peixoto H, Delaye A, Pinchot V, Bastucci M, Guillou S, Chevillon M, Sainz-Fuertes R, Meguenni S, Aurich-Costa J, Cherif D, Gimalac A, Van Duijn C, Gauvreau D, Ouellette G, Fortier I, Raelson J, Sherbatich T, Riazanskaia N, Rogaev E, Raeymaekers P, Aerssens J, Konings F, Luyten W, Macciardi F, Sham PC, Straub RE, Weinberger DR, Cohen N, Cohen D, Ouelette G, Realson J, Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc Natl Acad Sci U S A, 2002, 99 (21): p. 13675-13680. 
228. Cox R, Bouzekri N, Martin S, Southam L, Hugill A, Golamaully M, Cooper R, Adeyemo A, Soubrier F, Ward R, Lathrop GM, Matsuda F, Farrall M, Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. Hum Mol Genet, 2002, 11 (23): p. 2969-2977. 
229. Faivre L, Mégarbané A, Alswaid A, Zylberberg L, Aldohayan N, Campos-Xavier B, Bacq D, Legeai-Mallet L, Bonaventure J, Munnich A, Cormier-Daire V, Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2. Hum Genet, 2002, 110 (4): p. 366-370. 
230. Ferreiro A, Monnier N, Romero NB, Leroy JP, Bönnemann C, Haenggeli CA, Straub V, Voss WD, Nivoche Y, Jungbluth H, Lemainque A, Voit T, Lunardi J, Fardeau M, Guicheney P, A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene. Ann Neurol, 2002, 51 (6): p. 750-759. 
231. Han Z, Heath SC, Shmulewitz D, Li W, Auerbach SB, Blundell ML, Lehner T, Ott J, Stoffel M, Friedman JM, Breslow JL, Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia. Am J Med Genet, 2002, 110 (3): p. 234-242. 
232. Heathcote K, Rajab A, Magré J, Syrris P, Besti M, Patton M, Délépine M, Lathrop M, Capeau J, Jeffery S, Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci. Diabetes, 2002, 51 (4): p. 1291-1293. 
233. Houldsworth J, Heath SC, Bosl GJ, Studer L, Chaganti RS, Expression profiling of lineage differentiation in pluripotential human embryonal carcinoma cells. Cell Growth Differ, 2002, 13 (6): p. 257-264. 
234. Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T, [Paris Autism Research Internat , Linkage and association of the glutamate receptor 6 gene with autism. Mol Psychiatry, 2002, 7 (3): p. 302-310. 
235. Jobard F, Lefèvre C, Karaduman A, Blanchet-Bardon C, Emre S, Weissenbach J, Ozgüc M, Lathrop M, Prud'homme JF, Fischer J, Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1. Hum Mol Genet, 2002, 11 (1): p. 107-113. 
236. Kaisaki PJ, Sebag-Montefiore LM, Brown JH, Magre J, Lathrop M, Capeau J, Gauguier D, Localization, cDNA sequence and genomic organization of the rat seipin gene (Bscl2) and sequence analysis in inbred rat models of Type 2 diabetes mellitus. Cytogenet Genome Res, 2002, 98 (1): p. 71-74. 
237. Kauffmann F, Dizier MH, Oryszczyn MP, Le Moual N, Siroux V, Annesi-Maesano I, Bousquet J, Charpin D, Feingold J, Gormand F, Grimfeld A, Hochez J, Lathrop M, Matran R, Neukirch F, Paty E, Pin I, Demenais F, Epidemiologic study of the genetics and environment of asthma, bronchial hyperresponsiveness, and atopy. Chest, 2002, 121 (3 Suppl): p. 27S. 
238. Lechner D, Lathrop GM, Gut IG, Large-scale genotyping by mass spectrometry: experience, advances and obstacles. Curr Opin Chem Biol, 2002, 6 (1): p. 31-38. 
239. Liu H, Abecasis GR, Heath SC, Knowles A, Demars S, Chen YJ, Roos JL, Rapoport JL, Gogos JA, Karayiorgou M, Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci U S A, 2002, 99 (26): p. 16859-16864. 
240. Liu H, Heath SC, Sobin C, Roos JL, Galke BL, Blundell ML, Lenane M, Robertson B, Wijsman EM, Rapoport JL, Gogos JA, Karayiorgou M, Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci U S A, 2002, 99 (6): p. 3717-3722. 
241. Mahé E, Lahfa M, Mansouri S, Mosharraf-Olmolk H, Le Rebours J, Prud'Homme JF, Fischer J, Physicians' response to a letter to confirm diagnosis in a genetic study of psoriasis. Eur J Dermatol, 2002, 12 (1): p. 66-69. 
242. Mandon-Pépin B, Derbois C, Matsuda F, Cotinot C, Wolgemuth DJ, Smith K, McElreavey K, Nicolas A, Fellous M, [Human infertility: meiotic genes as potential candidates] Gynecol Obstet Fertil, 2002, 30 (10): p. 817-821. 
243. Medlej-Hashim M, Mustapha M, Chouery E, Weil D, Parronaud J, Salem N, Delague V, Loiselet J, Lathrop M, Petit C, Mégarbané A, Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. Eur J Hum Genet, 2002, 10 (6): p. 391-394. 
244. Molinari F, Rio M, Meskenaite V, Encha-Razavi F, Augé J, Bacq D, Briault S, Vekemans M, Munnich A, Attié-Bitach T, Sonderegger P, Colleaux L, Truncating neurotrypsin mutation in autosomal recessive nonsyndromic mental retardation. Science, 2002, 298 (5599): p. 1779-1781. 
245. Mollet G, Salomon R, Gribouval O, Silbermann F, Bacq D, Landthaler G, Milford D, Nayir A, Rizzoni G, Antignac C, Saunier S, The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin. Nat Genet, 2002, 32 (2): p. 300-305. 
246. Moore EE, Presnell S, Garrigues U, Guilbot A, LeGuern E, Smith D, Yao L, Whitmore TE, Gilbert T, Palmer TD, Horner PJ, Kuestner RE, Expression of IL-17B in neurons and evaluation of its possible role in the chromosome 5q-linked form of Charcot-Marie-Tooth disease. Neuromuscul Disord, 2002, 12 (2): p. 141-150. 
247. Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C, DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34. Eur J Hum Genet, 2002, 10 (3): p. 210-212. 
248. Mustapha M, Chouery E, Torchard-Pagnez D, Nouaille S, Khrais A, Sayegh FN, Mégarbané A, Loiselet J, Lathrop M, Petit C, Weil D, A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25. Hum Genet, 2002, 110 (4): p. 348-350. 
249. Nervi S, Nicodeme S, Gartioux C, Atlan C, Lathrop M, Reviron D, Naquet P, Matsuda F, Imbert J, Vialettes B, No association between lck gene polymorphisms and protein level in type 1 diabetes. Diabetes, 2002, 51 (11): p. 3326-3330. 
250. Novak U, Oppliger Leibundgut E, Hager J, Mühlematter D, Jotterand M, Besse C, Leupin N, Ratschiller D, Papp J, Kearsey G, Aebi S, Graber H, Jaggi R, Lüthi JM, Meyer-Monard S, Lathrop M, Tobler A, Fey MF, A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL). Blood, 2002, 100 (5): p. 1787-1794. 
251. Rogner UC, Danoy P, Matsuda F, Moore GE, Stanier P, Avner P, SNPs in the CpG island of NAP1L2: a possible link between DNA methylation and neural tube defects? Am J Med Genet, 2002, 110 (3): p. 208-214. 
252. Sauer S, Gut IG, Genotyping single-nucleotide polymorphisms by matrix-assisted laser-desorption/ionization time-of-flight mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci, 2002, 782 (1-2): p. 73-87. 
253. Sauer S, Gelfand DH, Boussicault F, Bauer K, Reichert F, Gut IG, Facile method for automated genotyping of single nucleotide polymorphisms by mass spectrometry. Nucleic Acids Res, 2002, 30 (5): p. e22. 
254. Soria JM, Almasy L, Souto JC, Bacq D, Buil A, Faure A, Martínez-Marchán E, Mateo J, Borrell M, Stone W, Lathrop M, Fontcuberta J, Blangero J, A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. Am J Hum Genet, 2002, 70 (3): p. 567-574. 
255. Soubrier F, Martin S, Alonso A, Visvikis S, Tiret L, Matsuda F, Lathrop GM, Farrall M, High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity. Eur J Hum Genet, 2002, 10 (9): p. 553-561. 
256. Takahashi M, Kubo T, Mizoguchi A, Carlson CG, Endo K, Ohnishi K, Spontaneous muscle action potentials fail to develop without fetal-type acetylcholine receptors. EMBO Rep, 2002, 3 (7): p. 674-681. 
257. Takahashi M, Matsuda F, Margetic N, Lathrop M, Automated identification of single nucleotide polymorphisms from sequencing data. Proc IEEE Comput Soc Bioinform Conf, 2002, 1p. 87-93. 
258. Tost J, Gut IG, Genotyping single nucleotide polymorphisms by mass spectrometry. Mass Spectrom Rev, 2002, 21 (6): p. 388-418. 
259. Tost J, Brandt O, Boussicault F, Derbala D, Caloustian C, Lechner D, Gut IG, Molecular haplotyping at high throughput. Nucleic Acids Res, 2002, 30 (19): p. e96. 
260. Van Maldergem L, Magré J, Khallouf TE, Gedde-Dahl T Jr, Delépine M, Trygstad O, Seemanova E, Stephenson T, Albott CS, Bonnici F, Panz VR, Medina JL, Bogalho P, Huet F, Savasta S, Verloes A, Robert JJ, Loret H, De Kerdanet M, Tubiana-Rufi N, Mégarbané A, Maassen J, Polak M, Lacombe D, Kahn CR, Silveira EL, D'Abronzo FH, Grigorescu F, Lathrop M, Capeau J, O'Rahilly S, Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy. J Med Genet, 2002, 39 (10): p. 722-733. 
261. Vickers MA, Green FR, Terry C, Mayosi BM, Julier C, Lathrop M, Ratcliffe PJ, Watkins HC, Keavney B, Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein. Cardiovasc Res, 2002, 53 (4): p. 1029-1034. 
262. Vuillaume I, Devos D, Schraen-Maschke S, Dina C, Lemainque A, Vasseur F, Bocquillon G, Devos P, Kocinski C, Marzys C, Destée A, Sablonnière B, A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1. Ann Neurol, 2002, 52 (5): p. 666-670. 
263. Zhou J, Ashouian N, Delepine M, Matsuda F, Chevillard C, Riblet R, Schildkraut CL, Birshtein BK, The origin of a developmentally regulated Igh replicon is located near the border of regulatory domains for Igh replication and expression. Proc Natl Acad Sci U S A, 2002, 99 (21): p. 13693-13698. 
264. Zwaenepoel I, Mustapha M, Leibovici M, Verpy E, Goodyear R, Liu XZ, Nouaille S, Nance WE, Kanaan M, Avraham KB, Tekaia F, Loiselet J, Lathrop M, Richardson G, Petit C, Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proc Natl Acad Sci U S A, 2002, 99 (9): p. 6240-6245. 
265. Bihoreau MT, Sebag-Montefiore L, Godfrey RF, Wallis RH, Brown JH, Danoy PA, Collins SC, Rouard M, Kaisaki PJ, Lathrop M, Gauguier D, A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps. Genomics, 2001, 75 (1-3): p. 57-69. 
266. Brüls T, Gyapay G, Petit JL, Artiguenave F, Vico V, Qin S, Tin-Wollam AM, Da Silva C, Muselet D, Mavel D, Pelletier E, Levy M, Fujiyama A, Matsuda F, Wilson R, Rowen L, Hood L, Weissenbach J, Saurin W, Heilig R, A physical map of human chromosome 14. Nature, 2001, 409 (6822): p. 947-948. 
267. Caraballo R, Pavek S, Lemainque A, Gastaldi M, Echenne B, Motte J, Genton P, Cersósimo R, Humbertclaude V, Fejerman N, Monaco AP, Lathrop MG, Rochette J, Szepetowski P, Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome. Am J Hum Genet, 2001, 68 (3): p. 788-794. 
268. Denecker G, Declercq W, Geuijen CA, Boland A, Benabdillah R, van Gurp M, Sory MP, Vandenabeele P, Cornelis GR, Yersinia enterocolitica YopP-induced apoptosis of macrophages involves the apoptotic signaling cascade upstream of bid. J Biol Chem, 2001, 276 (23): p. 19706-19714. 
269. Fischer J, Bouadjar B, Heilig R, Huber M, Lefèvre C, Jobard F, Macari F, Bakija-Konsuo A, Ait-Belkacem F, Weissenbach J, Lathrop M, Hohl D, Prud'homme JF, Mutations in the gene encoding SLURP-1 in Mal de Meleda. Hum Mol Genet, 2001, 10 (8): p. 875-880. 
270. Greco L, Babron MC, Corazza GR, Percopo S, Sica R, Clot F, Fulchignoni-Lataud MC, Zavattari P, Momigliano-Richiardi P, Casari G, Gasparini P, Tosi R, Mantovani V, De Virgiliis S, Iacono G, D'Alfonso A, Selinger-Leneman H, Lemainque A, Serre JL, Clerget-Darpoux F, Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families. Ann Hum Genet, 2001, 65 (Pt 1): p. 35-41. 
271. Guilbot A, Williams A, Ravisé N, Verny C, Brice A, Sherman DL, Brophy PJ, LeGuern E, Delague V, Bareil C, Mégarbané A, Claustres M, A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease. Hum Mol Genet, 2001, 10 (4): p. 415-421. 
272. Gut IG, Pharmakogenetik und Massenspektrometrie Medizinische Genetik, 2001, 13p. 281-284. 
273. Gut IG, Automation in genotyping of single nucleotide polymorphisms. Hum Mutat, 2001, 17 (6): p. 475-492. 
274. Holm P, Julier C, Kockum I, Senée V, Blanc H, Papp J, Åkesson K, Bartsocas C, de Leiva A, Dahlquist G, Ronningen , Lathrop GM, Luthman H, Pociot F, Nerup J, [European Consortium for IDDM S , A genomewide scan for type 1-diabetes susceptibility in Scandinavian families: identification of new loci with evidence of interactions. Am J Hum Genet, 2001, 69 (6): p. 1301-1313. 
275. Ji H, Gauguier D, Ohmura K, Gonzalez A, Duchatelle V, Danoy P, Garchon HJ, Degott C, Lathrop M, Benoist C, Mathis D, Genetic influences on the end-stage effector phase of arthritis. J Exp Med, 2001, 194 (3): p. 321-330. 
276. Kauffmann F, Dizier MH, Annesi-Maesano I, Bousquet J, Charpin D, Demenais F, Ecochard D, Feingold J, Gormand F, Grimfeld A, Lathrop M, Matran R, Neukirch F, Paty E, Pison C, Scheinmann P, Vervloet D, Lockhart A, [Epidemiological study of genetic and environmental factors in asthma, bronchial hyperresponsiveness and atopy. Protocol and potential selection bias] Rev Epidemiol Sante Publique, 2001, 49 (4): p. 343-356. 
277. Kyo K, Muto T, Nagawa H, Lathrop GM, Nakamura Y, Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease. J Hum Genet, 2001, 46 (1): p. 5-20. 
278. Laurin N, Brown JP, Lemainque A, Duchesne A, Huot D, Lacourcière Y, Drapeau G, Verreault J, Raymond V, Morissette J, Paget disease of bone: mapping of two loci at 5q35-qter and 5q31. Am J Hum Genet, 2001, 69 (3): p. 528-543. 
279. Lefèvre C, Blanchet-Bardon C, Jobard F, Bouadjar B, Stalder JF, Cure S, Hoffmann A, Prud'Homme JF, Fischer J, Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefèvre syndrome. J Invest Dermatol, 2001, 117 (6): p. 1657-1661. 
280. Lefèvre C, Jobard F, Caux F, Bouadjar B, Karaduman A, Heilig R, Lakhdar H, Wollenberg A, Verret JL, Weissenbach J, Ozgüc M, Lathrop M, Prud'homme JF, Fischer J, Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome. Am J Hum Genet, 2001, 69 (5): p. 1002-1012. 
281. Magré J, Delépine M, Khallouf E, Gedde-Dahl T Jr, Van Maldergem L, Sobel E, Papp J, Meier M, Mégarbané A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, Bourut C, Czernichow P, Huet F, Grigorescu F, de Kerdanet M, Lacombe D, Labrune P, Lanza M, Loret H, Matsuda F, Navarro J, Nivelon-Chevalier A, Polak M, Robert JJ, Tric P, Tubiana-Rufi N, Vigouroux C, Weissenbach J, Savasta S, Maassen JA, Trygstad O, Bogalho P, Freitas P, Medina JL, Bonnicci F, Joffe BI, Loyson G, Panz VR, Raal FJ, O'Rahilly S, Stephenson T, Kahn CR, Lathrop M, Capeau J, [BSCL Working Group] , Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nat Genet, 2001, 28 (4): p. 365-370. 
282. McKenzie CA, Abecasis GR, Keavney B, Forrester T, Ratcliffe PJ, Julier C, Connell JM, Bennett F, McFarlane-Anderson N, Lathrop GM, Cardon LR, Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE). Hum Mol Genet, 2001, 10 (10): p. 1077-1084. 
283. Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, Tokooya K, Jore BS, Lopez M, Pandita RK, Lia M, Carrion D, Xu H, Schorle H, Kobler JB, Scambler P, Wynshaw-Boris A, Skoultchi AI, Morrow BE, Kucherlapati R, TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell, 2001, 104 (4): p. 619-629. 
284. Sylvius N, Tesson F, Gayet C, Charron P, Bénaïche A, Peuchmaurd M, Duboscq-Bidot L, Feingold J, Beckmann JS, Bouchier C, Komajda M, A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16. Am J Hum Genet, 2001, 68 (1): p. 241-246. 
285. Vidailhet M, Tassin J, Durif F, Nivelon-Chevallier A, Agid Y, Brice A, Dürr A, A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q. Neurology, 2001, 56 (9): p. 1213-1216. 
286. Wiltshire S, Hattersley AT, Hitman GA, Walker M, Levy JC, Sampson M, O'Rahilly S, Frayling TM, Bell JI, Lathrop GM, Bennett A, Dhillon R, Fletcher C, Groves CJ, Jones E, Prestwich P, Simecek N, Rao PV, Wishart M, Bottazzo GF, Foxon R, Howell S, Smedley D, Cardon LR, Menzel S, McCarthy MI, A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q. Am J Hum Genet, 2001, 69 (3): p. 553-569. 
287. Anderson LV, Harrison RM, Pogue R, Vafiadaki E, Pollitt C, Davison K, Moss JA, Keers S, Pyle A, Shaw PJ, Mahjneh I, Argov Z, Greenberg CR, Wrogemann K, Bertorini T, Goebel HH, Beckmann JS, Bashir R, Bushby KM, Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Neuromuscul Disord, 2000, 10 (8): p. 553-559. 
288. Bishop T, Sham P, Lathrop GM, Weeks DE, Methods for mapping complex disease traits . Analysis of Multifactorial Diseases, BIOS Scientific Publishers Ltd, 2000p. 15-36. 
289. Boland A, Ricard M, Opolon P, Bidart JM, Yeh P, Filetti S, Schlumberger M, Perricaudet M, Adenovirus-mediated transfer of the thyroid sodium/iodide symporter gene into tumors for a targeted radiotherapy. Cancer Res, 2000, 60 (13): p. 3484-3492. 
290. Boland A, Cornelis GR, Interaction of Yersinia with host cells. Subcell Biochem, 2000, 33p. 343-382. 
291. Bouadjar B, Benmazouzia S, Prud'homme JF, Cure S, Fischer J, Clinical and genetic studies of 3 large, consanguineous, Algerian families with Mal de Meleda. Arch Dermatol, 2000, 136 (10): p. 1247-1252. 
292. Combes MC, Andrzejewski S, Anthony F, Bertrand B, Rovelli P, Graziosi G, Lashermes P, Characterization of microsatellite loci in Coffea arabica and related coffee species. Mol Ecol, 2000, 9 (8): p. 1178-1180. 
293. Delépine M, Nicolino M, Barrett T, Golamaully M, Lathrop GM, Julier C, EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. Nat Genet, 2000, 25 (4): p. 406-409. 
294. Dizier MH, Besse-Schmittler C, Guilloud-Bataille M, Annesi-Maesano I, Boussaha M, Bousquet J, Charpin D, Degioanni A, Gormand F, Grimfeld A, Hochez J, Hyne G, Lockhart A, Luillier-Lacombe M, Matran R, Meunier F, Neukirch F, Pacheco Y, Parent V, Paty E, Pin I, Pison C, Scheinmann P, Thobie N, Vervloet D, Kauffmann F, Feingold J, Lathrop M, Demenais F, Genome screen for asthma and related phenotypes in the French EGEA study. Am J Respir Crit Care Med, 2000, 162 (5): p. 1812-1818. 
295. Dürr A, Tassin J, Vidailhet M, Durif F, Jedynak P, Agid Y, Brice A, D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus. Ann Neurol, 2000, 48 (1): p. 127-128. 
296. Escary JL, Bottius E, Prince N, Reyes C, Fiawoumo Y, Caloustian C, Bruls T, Fujiyama A, Cooper RS, Adeyemo AA, Lathrop GM, Weissenbach J, Gyapay G, Foglio M, Beckmann JS, A first high-density map of 981 biallelic markers on human chromosome 14. Genomics, 2000, 70 (2): p. 153-164. 
297. Escary JL, Cecillon M, Maciazek J, Lathrop M, Tournier-Lasserve E, Joutel A, Mutational analysis of GLUT1 (SLC2A1) in glut-1 deficiency syndrome; dong wang; pamela kranz-eble; darryl C. De vivo; (Article was originally published in human mutation 16:224-231, 2000) Hum Mutat, 2000, 16 (6): p. 527. 
298. Escary JL, Cécillon M, Maciazek J, Lathrop M, Tournier-Lasserve E, Joutel A, Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content. Hum Mutat, 2000, 16 (6): p. 518-526. 
299. Fischer J, Faure A, Bouadjar B, Blanchet-Bardon C, Karaduman A, Thomas I, Emre S, Cure S, Ozgüc M, Weissenbach J, Prud'homme JF, Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity. Am J Hum Genet, 2000, 66 (3): p. 904-913. 
300. Garner C, Lecomte E, Visvikis S, Abergel E, Lathrop M, Soubrier F, Genetic and environmental influences on left ventricular mass. A family study. Hypertension, 2000, 36 (5): p. 740-746. 
301. Kaisaki PJ, Rouard M, Danoy PA, Wallis RH, Collins SC, Rice M, Levy ER, Lathrop M, Bihoreau MT, Gauguier D, Detailed comparative gene map of rat chromosome 1 with mouse and human genomes and physical mapping of an evolutionary chromosomal breakpoint. Genomics, 2000, 64 (1): p. 32-43. 
302. Keavney B, McKenzie C, Parish S, Palmer A, Clark S, Youngman L, Delépine M, Lathrop M, Peto R, Collins R, Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators. Lancet, 2000, 355 (9202): p. 434-442. 
303. Lathrop GM, Julier C, Matsuda F, Gut IG, Durand M, La génomique et les maladies Biofutur, 2000, 206p. 82-85. 
304. McCarthy LC, Bihoreau MT, Kiguwa SL, Browne J, Watanabe TK, Hishigaki H, Tsuji A, Kiel S, Webber C, Davis ME, Knights C, Smith A, Critcher R, Huxtall P, Hudson JR Jr, Ono T, Hayashi H, Takagi T, Nakamura Y, Tanigami A, Goodfellow PN, Lathrop GM, James MR, A whole-genome radiation hybrid panel and framework map of the rat genome. Mamm Genome, 2000, 11 (9): p. 791-795. 
305. Nandrot E, Dufour EM, Provost AC, Péquignot MO, Bonnel S, Gogat K, Marchant D, Rouillac C, Sépulchre de Condé B, Bihoreau MT, Shaver C, Dufier JL, Marsac C, Lathrop M, Menasche M, Abitbol MM, Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis. Neurobiol Dis, 2000, 7 (6 Pt B): p. 586-599. 
306. Puech A, Saint-Jore B, Merscher S, Russell RG, Cherif D, Sirotkin H, Xu H, Factor S, Kucherlapati R, Skoultchi AI, Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region. Proc Natl Acad Sci U S A, 2000, 97 (18): p. 10090-10095. 
307. Richard I, Roudaut C, Marchand S, Baghdiguian S, Herasse M, Stockholm D, Ono Y, Suel L, Bourg N, Sorimachi H, Lefranc G, Fardeau M, Sébille A, Beckmann JS, Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice. J Cell Biol, 2000, 151 (7): p. 1583-1590. 
308. Romana M, Kéclard L, Froger A, Lavocat E, Saint-Martin C, Berchel C, Mérault G, Diverse genetic mechanisms operate to generate atypical betaS haplotypes in the population of Guadeloupe. Hemoglobin, 2000, 24 (2): p. 77-87. 
309. Salih MA, Maisonobe T, Kabiraj M, al Rayess M, al-Turaiki MH, Akbar M, Tahan A, Urtizberea JA, Grid D, Hamadouche T, Guilbot A, Brice A, Leguern E, Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity. Neuromuscul Disord, 2000, 10 (1): p. 10-15. 
310. Sauer S, Lechner D, Berlin K, Plançon C, Heuermann A, Lehrach H, Gut IG, Full flexibility genotyping of single nucleotide polymorphisms by the GOOD assay. Nucleic Acids Res, 2000, 28 (23): p. E100. 
311. Sauer S, Lechner D, Berlin K, Lehrach H, Escary JL, Fox N, Gut IG, A novel procedure for efficient genotyping of single nucleotide polymorphisms. Nucleic Acids Res, 2000, 28 (5): p. E13. 
312. Tassin J, Dürr A, Bonnet AM, Gil R, Vidailhet M, Lücking CB, Goas JY, Durif F, Abada M, Echenne B, Motte J, Lagueny A, Lacomblez L, Jedynak P, Bartholomé B, Agid Y, Brice A, Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations? Brain, 2000, 123 ( Pt 6)p. 1112-1121. 
313. Watanabe TK, Ono T, Okuno S, Mizoguchi-Miyakita A, Yamasaki Y, Kanemoto N, Hishigaki H, Oga K, Takahashi E, Irie Y, Bihoreau MT, James MR, Lathrop GM, Takagi T, Nakamura Y, Tanigami A, Characterization of newly developed SSLP markers for the rat. Mamm Genome, 2000, 11 (4): p. 300-305. 
314. Akamizu T, Moriyama K, Miura M, Saijo M, Matsuda F, Nakao K, Characterization of recombinant monoclonal antithyrotropin receptor antibodies (TSHRAbs) derived from lymphocytes of patients with Graves' disease: epitope and binding study of two stimulatory TSHRAbs. Endocrinology, 1999, 140 (4): p. 1594-1601. 
315. Anderson LV, Davison K, Moss JA, Young C, Cullen MJ, Walsh J, Johnson MA, Bashir R, Britton S, Keers S, Argov Z, Mahjneh I, Fougerousse F, Beckmann JS, Bushby KM, Dysferlin is a plasma membrane protein and is expressed early in human development. Hum Mol Genet, 1999, 8 (5): p. 855-861. 
316. Andrew LJ, Brancolini V, de la Pena LS, Devoto M, Caeiro F, Marchegiani R, Reginato A, Gaucher A, Netter P, Gillet P, Loeuille D, Prockop DJ, Carr A, Wordsworth BF, Lathrop M, Butcher S, Considine E, Everts K, Nicod A, Walsh S, Williams CJ, Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease. Am J Hum Genet, 1999, 64 (1): p. 136-145. 
317. Berlin K, Gut IG, Analysis of negatively 'charge tagged' DNA by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Rapid Commun Mass Spectrom, 1999, 13 (17): p. 1739-1743. 
318. Bouhouche A, Benomar A, Birouk N, Mularoni A, Meggouh F, Tassin J, Grid D, Vandenberghe A, Yahyaoui M, Chkili T, Brice A, LeGuern E, A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3. Am J Hum Genet, 1999, 65 (3): p. 722-727. 
319. Cox RD, Southam L, Hashim Y, Horton V, Mehta Z, Taghavi J, Lathrop M, Turner R, UKPDS 31: Hepatocyte nuclear factor-1alpha (the MODY3 gene) mutations in late onset Type II diabetic patients in the United Kingdom. United Kingdom prospective diabetes study. Diabetologia, 1999, 42 (1): p. 120-121. 
320. Cuisset L, Drenth JP, Berthelot JM, Meyrier A, Vaudour G, Watts RA, Scott DG, Nicholls A, Pavek S, Vasseur C, Beckmann JS, Delpech M, Grateau G, Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44. Am J Hum Genet, 1999, 65 (4): p. 1054-1059. 
321. Deltour L, Foglio MH, Duester G, Impaired retinol utilization in Adh4 alcohol dehydrogenase mutant mice. Dev Genet, 1999, 25 (1): p. 1-10. 
322. Deltour L, Foglio MH, Duester G, Metabolic deficiencies in alcohol dehydrogenase Adh1, Adh3, and Adh4 null mutant mice. Overlapping roles of Adh1 and Adh4 in ethanol clearance and metabolism of retinol to retinoic acid. J Biol Chem, 1999, 274 (24): p. 16796-16801. 
323. Drenth JP, Cuisset L, Grateau G, Vasseur C, van de Velde-Visser SD, de Jong JG, Beckmann JS, van der Meer JW, Delpech M, Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group. Nat Genet, 1999, 22 (2): p. 178-181. 
324. Escary JL, Choy HA, Reue K, Wang XP, Castellani LW, Glass CK, Lusis AJ, Schotz MC, Paradoxical effect on atherosclerosis of hormone-sensitive lipase overexpression in macrophages. J Lipid Res, 1999, 40 (3): p. 397-404. 
325. Farrall M, Keavney B, McKenzie C, Delépine M, Matsuda F, Lathrop GM, Fine-mapping of an ancestral recombination breakpoint in DCP1. Nat Genet, 1999, 23 (3): p. 270-271. 
326. Giraudeau F, Apiou F, Amarger V, Kaisaki PJ, Bihoreau MT, Lathrop M, Vergnaud G, Gauguier D, Linkage and physical mapping of rat microsatellites derived from minisatellite loci. Mamm Genome, 1999, 10 (4): p. 405-409. 
327. Guilbot A, Ravisé N, Bouhouche A, Coullin P, Birouk N, Maisonobe T, Kuntzer T, Vial C, Grid D, Brice A, LeGuern E, Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1. Eur J Hum Genet, 1999, 7 (8): p. 849-859. 
328. Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, Leguern E, The autosomal recessive form of CMT disease linked to 5q31-q33. Ann N Y Acad Sci, 1999, 883p. 56-59. 
329. Herasse M, Ono Y, Fougerousse F, Kimura E, Stockholm D, Beley C, Montarras D, Pinset C, Sorimachi H, Suzuki K, Beckmann JS, Richard I, Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events. Mol Cell Biol, 1999, 19 (6): p. 4047-4055. 
330. Kato N, Hyne G, Bihoreau MT, Gauguier D, Lathrop GM, Rapp JP, Complete genome searches for quantitative trait loci controlling blood pressure and related traits in four segregating populations derived from Dahl hypertensive rats. Mamm Genome, 1999, 10 (3): p. 259-265. 
331. Kauffmann F, Dizier MH, Annesi-Maesano I, Bousquet J, Charpin D, Demenais F, Ecochard D, Feingold J, Gormand F, Grimfeld A, Lathrop M, Matran R, Neukirch F, Paty E, Pin I, Pison C, Scheinmann P, Vervloet D, Lockhart A, EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy)-- descriptive characteristics. Clin Exp Allergy, 1999, 29 Suppl 4p. 17-21. 
332. Kyo K, Parkes M, Takei Y, Nishimori H, Vyas P, Satsangi J, Simmons J, Nagawa H, Baba S, Jewell D, Muto T, Lathrop GM, Nakamura Y, Association of ulcerative colitis with rare VNTR alleles of the human intestinal mucin gene, MUC3. Hum Mol Genet, 1999, 8 (2): p. 307-311. 
333. Marinov M, Matise TC, Lathrop GM, Weeks DE, A comparison of two algorithms, MultiMap and gene mapping system, for automated construction of genetic linkage maps. Genet Epidemiol, 1999, 17 Suppl 1p. S649-54. 
334. Mustapha M, Weil D, Chardenoux S, Elias S, El-Zir E, Beckmann JS, Loiselet J, Petit C, An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol Genet, 1999, 8 (3): p. 409-412. 
335. Pallarès N, Lefebvre S, Contet V, Matsuda F, Lefranc MP, The human immunoglobulin heavy variable genes. Exp Clin Immunogenet, 1999, 16 (1): p. 36-60. 
336. Poza JJ, Sáenz A, Martínez-Gil A, Cheron N, Cobo AM, Urtasun M, Martí-Massó JF, Grid D, Beckmann JS, Prud'homme JF, López de Munain A, Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. Ann Neurol, 1999, 45 (2): p. 182-188. 
337. Ring HZ, Chang H, Guilbot A, Brice A, LeGuern E, Francke U, The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q. Hum Genet, 1999, 104 (4): p. 326-332. 
338. Sakuntabhai A, Ruiz-Perez V, Carter S, Jacobsen N, Burge S, Monk S, Smith M, Munro CS, O'Donovan M, Craddock N, Kucherlapati R, Rees JL, Owen M, Lathrop GM, Monaco AP, Strachan T, Hovnanian A, Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nat Genet, 1999, 21 (3): p. 271-277. 
339. Shinkura R, Kitada K, Matsuda F, Tashiro K, Ikuta K, Suzuki M, Kogishi K, Serikawa T, Honjo T, Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kappa b-inducing kinase. Nat Genet, 1999, 22 (1): p. 74-77. 
340. Southam L, Ashfield R, Cox R, Lathrop M, Ashcroft SJ, Human islets of Langerhans express the delta(C) isoform of calcium/calmodulin-dependent protein kinase II. Diabetes Metab Res Rev, 1999, 15 (4): p. 243-246. 
341. Watanabe TK, Bihoreau MT, McCarthy LC, Kiguwa SL, Hishigaki H, Tsuji A, Browne J, Yamasaki Y, Mizoguchi-Miyakita A, Oga K, Ono T, Okuno S, Kanemoto N, Takahashi E, Tomita K, Hayashi H, Adachi M, Webber C, Davis M, Kiel S, Knights C, Smith A, Critcher R, Miller J, Thangarajah T, Day PJ, Hudson JR Jr, Irie Y, Takagi T, Nakamura Y, Goodfellow PN, Lathrop GM, Tanigami A, James MR, A radiation hybrid map of the rat genome containing 5,255 markers. Nat Genet, 1999, 22 (1): p. 27-36.