Contribution à la cartographie du génome humain. Application à l'étude de maladies mendéliennes et multifactorielles = Contribution to mapping the human genome. Applicaiton to genetic analysis of mendelian and multifactorial diseasesJulier, Cécile; Lathrop, Mark.1992, 178 p.Thesis

Control of fetal hemoglobin: new insights emerging from genomics and clinical implicationsLAY THEIN, Swee; MENZEL, Stephan; LATHROP, Mark et al.Human molecular genetics (Print). 2009, Vol 18, issn 0964-6906, R216-R223, NS2Article

Identification of distinct quantitative trait loci affecting length or weight variability at birth in humansFRADIN, Delphine; HEATH, Simon; LEPERCQ, Jacques et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 10, pp 4164-4170, issn 0021-972X, 7 p.Article

Mapping complex disease traits with global gene expressionCOOKSON, William; LIMING LIANG; ABECASIS, Concalo et al.Nature reviews. Genetics (Print). 2009, Vol 10, Num 3, pp 184-194, issn 1471-0056, 11 p.Article

A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any AgeAHSAN, Habibul; HALPERN, Jerry; ROY, Shantanu et al.Cancer epidemiology, biomarkers & prevention. 2014, Vol 23, Num 4, pp 658-669, issn 1055-9965, 12 p.Article

Genome-wide association study of lung function decline in adults with and without asthmaIMBODEN, Medea; BOUZIGON, Emmanuelle; NADIF, Rachel et al.Journal of allergy and clinical immunology. 2012, Vol 129, Num 5, pp 1218-1228, issn 0091-6749, 11 p.Article

Risk Taking and the Adolescent Reward System: A Potential Common Link to Substance AbuseSCHNEIDER, Sophia; PETERS, Jan; HEINZ, Andreas et al.The American journal of psychiatry. 2012, Vol 169, Num 1, pp 39-46, issn 0002-953X, 8 p.Article

KNG1 Ile581Thr and susceptibility to venous thrombosisMORANGE, Pierre-Emmanuel; OUDOT-MELLAKH, Tiphaine; LATHROP, Mark et al.Blood. 2011, Vol 117, Num 13, pp 3692-3694, issn 0006-4971, 3 p.Article

Perilipin Deficiency and Autosomal Dominant Partial LipodystrophyGANDOTRA, Sheetal; LE DOUR, Caroline; SEMPLE, Robert K et al.The New England journal of medicine. 2011, Vol 364, Num 8, pp 740-748, issn 0028-4793, 9 p.Article

C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S―independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studiesBUIL, Alfonso; TREGOUËT, David-Alexandre; ALESSI, Marie-Christine et al.Blood. 2010, Vol 115, Num 23, pp 4644-4650, issn 0006-4971, 7 p.Article

Genome-wide association study identifies five susceptibility loci for gliomaSHETE, Sanjay; HOSKING, Fay J; HOANG-XUAN, Khe et al.Nature genetics. 2009, Vol 41, Num 8, pp 899-904, issn 1061-4036, 6 p.Article

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 populationBENNETT, Derrick A; PENG XU; CLARKE, Robert et al.European journal of human genetics. 2008, Vol 16, Num 4, pp 480-486, issn 1018-4813, 7 p.Article

Implication du gene SRPX2 dans des pathologies de l'aire rolandique = Involvement of SRPX2 gene in disorders of the rolandic and perisylvian speech areasROLL, Patrice; RUDOLF, Gabrielle; ROYER, Barbara et al.Epilepsies (Montrouge). 2007, Vol 19, Num 2, pp 87-90, issn 1149-6576, 4 p.Article

Mapping of familial thoracic aortic aneurysm/dissection with patent ductus arteriosus to 16p12.2-p13.13KHAU VAN KIEN, Philippe; MATHIEU, Flavie; LIMIN ZHU et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 2, pp 200-206, issn 0009-7322, 7 p.Article

Polygenic control of idiopathic Generalized epilepsy phenotypes in the genetic absence rats from strasbourg (GAERS)RUDOLF, Gabrielle; BIHOREAU, Marie Thérèse; GODFREY, Richard F et al.Epilepsia (Copenhagen). 2004, Vol 45, Num 4, pp 301-308, issn 0013-9580, 8 p.Article

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 susceptibilitySORIA, José Manuel; ALMASY, Laura; BLANGERO, John et al.Blood. 2003, Vol 101, Num 1, pp 163-167, issn 0006-4971, 5 p.Article

Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndromeJOBARD, Florence; BOUADJAR, Bakar; CAUX, Frédéric et al.Human molecular genetics (Print). 2003, Vol 12, Num 8, pp 925-935, issn 0964-6906, 11 p.Article

Prevalence of mutations in AGPAT2 among human lipodystrophiesMAGRE, Jocelyne; DELEPINE, Marc; SEEMANOVA, Eva et al.Diabetes (New York, NY). 2003, Vol 52, Num 6, pp 1573-1578, issn 0012-1797, 6 p.Article

A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic diseaseSORIA, José Manuel; ALMASY, Laura; LATHROP, Mark et al.American journal of human genetics. 2002, Vol 70, Num 3, pp 567-574, issn 0002-9297Article

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1JOBARD, Florence; LEFEVRE, Caroline; KARADUMAN, Aysen et al.Human molecular genetics (Print). 2002, Vol 11, Num 1, pp 107-113, issn 0964-6906Article

A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic mapsBIHOREAU, Marie-Thérèse; SEBAG-MONTEFIORE, Liam; GAUGUIER, Dominique et al.Genomics (San Diego, Calif.). 2001, Vol 75, Num 1-3, pp 57-69, issn 0888-7543Article

Genetic and environmental influences on left ventricular mass : A family studyGARNER, Chad; LECOMTE, Edith; VISVIKIS, Sophie et al.Hypertension (Dallas, Tex. 1979). 2000, Vol 36, Num 5, pp 740-746, issn 0194-911XArticle

Human leukocyte antigen class II variants and adult-onset asthma: does occupational allergen exposure play a role?SMIT, Lidwien A. M; STRACHAN, David P; HEEDERIK, Dick et al.The European respiratory journal. 2014, Vol 44, Num 5, pp 1234-1242, issn 0903-1936, 9 p.Article

SHANK1 Deletions in Males with Autism Spectrum DisorderSATO, Daisuke; LIONEL, Anath C; MICHAUD, Jacques L et al.American journal of human genetics. 2012, Vol 90, Num 5, pp 879-887, issn 0002-9297, 9 p.Article

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseMOMOZAWA, Yukihide; MNI, Myriam; FINKEL, Yigael et al.Nature genetics. 2011, Vol 43, Num 1, pp 43-47, issn 1061-4036, 5 p.Article