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A genome-wide association study identifies novel risk loci for type 2 diabetes
R Sladek, G Rocheleau, J Rung, C Dina, L Shen, D Serre, P Boutin, ...
Nature 445 (7130), 881-885, 2007
37382007
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
K Clement, C Vaisse, N Lahlou, S Cabrol, V Pelloux, D Cassuto, ...
Nature 392 (6674), 398-401, 1998
31421998
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
J Dupuis, C Langenberg, I Prokopenko, R Saxena, N Soranzo, ...
Nature genetics 42 (2), 105-116, 2010
25172010
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
BF Voight, LJ Scott, V Steinthorsdottir, AP Morris, C Dina, RP Welch, ...
Nature genetics 42 (7), 579-589, 2010
21522010
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC ...
Nature genetics 44 (9), 981-990, 2012
21432012
Variation in FTO contributes to childhood obesity and severe adult obesity
C Dina, D Meyre, S Gallina, E Durand, A Körner, P Jacobson, ...
Nature genetics 39 (6), 724-726, 2007
19412007
Common variants near MC4R are associated with fat mass, weight and risk of obesity
RJF Loos, CM Lindgren, S Li, E Wheeler, JH Zhao, I Prokopenko, ...
Nature genetics 40 (6), 768-775, 2008
15642008
Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population
K Hara, P Boutin, Y Mori, K Tobe, C Dina, K Yasuda, T Yamauchi, S Otabe, ...
Diabetes 51 (2), 536-540, 2002
10982002
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
10302019
Genomewide search for type 2 diabetes–susceptibility genes in French Whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and …
N Vionnet, S Dupont, S Gallina, S Francke, S Dotte, F De Matos, E Durand, ...
The American Journal of Human Genetics 67 (6), 1470-1480, 2000
9442000
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Nature genetics 46 (3), 234-244, 2014
8972014
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
HJ Watson, Z Yilmaz, LM Thornton, C Hübel, JRI Coleman, HA Gaspar, ...
Nature genetics 51 (8), 1207-1214, 2019
7812019
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
D Meyre, J Delplanque, JC Chèvre, C Lecoeur, S Lobbens, S Gallina, ...
Nature genetics 41 (2), 157-159, 2009
7582009
Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels …
F Vasseur, N Helbecque, C Dina, S Lobbens, V Delannoy, S Gaget, ...
Human molecular genetics 11 (21), 2607-2614, 2002
7502002
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
R Saxena, MF Hivert, C Langenberg, T Tanaka, JS Pankow, ...
Nature genetics 42 (2), 142-148, 2010
7422010
An expanded genome-wide association study of type 2 diabetes in Europeans
RA Scott, LJ Scott, R Mägi, L Marullo, KJ Gaulton, M Kaakinen, ...
Diabetes 66 (11), 2888-2902, 2017
7212017
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk
N Bouatia-Naji, A Bonnefond, C Cavalcanti-Proença, T Sparsø, ...
Nature genetics 41 (1), 89-94, 2009
6872009
Parental origin of sequence variants associated with complex diseases
A Kong, V Steinthorsdottir, G Masson, G Thorleifsson, P Sulem, ...
Nature 462 (7275), 868-874, 2009
6562009
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia
J Rung, S Cauchi, A Albrechtsen, L Shen, G Rocheleau, ...
Nature genetics 41 (10), 1110-1115, 2009
5462009
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ...
Nature genetics 45 (9), 1044-1049, 2013
5402013
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