M. Benzinou

发表

Common nonsynonymous variants in PCSK1 confer risk of obesity

T. Hansen, O. Pedersen, T. Jørgensen, 2008, Nature Genetics.

Xylazine-induced reduction of tissue sensitivity to insulin leads to acute hyperglycemia in diabetic and normoglycemic monkeys

B. Wang, Xiaoliang Wang, Y. Wang, 2013, BMC Anesthesiology.

A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature

B. Heude, D. Meyre, C. Mein, 2009, Annals of human genetics.

Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations.

T. Hansen, O. Pedersen, T. Jørgensen, 2008, Human molecular genetics.

Evaluating the Association of FAAH Common Gene Variation with Childhood, Adult Severe Obesity and Type 2 Diabetes in the French Population

P. Boutin, B. Balkau, G. Charpentier, 2008, Obesity Facts.

Bardet-Biedl Syndrome Gene Variants Are Associated With Both Childhood and Adult Common Obesity in French Caucasians

B. Balkau, D. Meyre, P. Froguel, 2006, Diabetes.

Bardet-Biedl Syndrome Gene Variants Are Associated With Both Childhood and Adult Common Obesity in

B. Balkau, D. Meyre, P. Froguel, 2006 .

Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q.

K. Clément, C. Dina, D. Meyre, 2004, Diabetes.

Genetic variants of Adam17 differentially regulate TGFβ signaling to modify vascular pathology in mice and humans

Marie M. Lee, R. Coffey, R. Akhurst, 2014, Proceedings of the National Academy of Sciences.

Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Juan Arbelaez, R. Akhurst, C. Hughes, 2012, Nature Communications.

Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity

B. Heude, D. Meyre, P. Froguel, 2009, Obesity.

Proteinuria in Cynomolgus macaques (Macaca fascicularis) with Spontaneously Developed Metabolic Disorder and Diabetes: Transcriptome Analysis of Biopsy Kidney

K. Chng, Sheng Guo, Xuan Chen, 2014 .

Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14

A. Balmain, R. Akhurst, D. Jablons, 2015, Front. Genet..

Replication Attempt: “Effect of BMAP-28 Antimicrobial Peptides on Leishmania Major Promastigote and Amastigote Growth: Role of Leishmanolysin in Parasite Survival”

Elizabeth Iorns, William Gunn, Ana Rodriguez, 2014, PloS one.

Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity

B. Heude, D. Meyre, P. Froguel, 2009, Obesity.

Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Juan Arbelaez, R. Akhurst, C. Hughes, 2012, Nature Communications.