Biblio

Found 27 results
Filters: Author is Froguel, Philippe  [Clear All Filters]
2013
Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T et al..  2013.  Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.. Nat Genet. 45(2):145-54.
Berndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka DC, Day FR et al..  2013.  Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.. Nat Genet. 45(5):501-12.
Bottolo L, Chadeau-Hyam M, Hastie DI, Zeller T, Liquet B, Newcombe P, Yengo L, Wild PS, Schillert A, Ziegler A et al..  2013.  GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm.. PLoS Genet. 9(8):e1003657.
den Hoed M, Eijgelsheim M, Esko T, Brundel BJJM, Peal DS, Evans DM, Nolte IM, Segrè AV, Holm H, Handsaker RE et al..  2013.  Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.. Nat Genet. 45(6):621-31.
Horikoshi M, Yaghootkar H, Mook-Kanamori DO, Sovio U, Taal RH, Hennig BJ, Bradfield JP, St Pourcain B, Evans DM, Charoen P et al..  2013.  New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.. Nat Genet. 45(1):76-82.
Walters RG, Coin LJM, Ruokonen A, de Smith AJ, El-Sayed Moustafa JS, Jacquemont S, Elliott P, Esko T, Hartikainen A-L, Laitinen J et al..  2013.  Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.. PLoS One. 8(3):e58048.
2012
Clark SJ, Falchi M, Olsson B, Jacobson P, Cauchi S, Balkau B, Marre M, Lantieri O, Andersson JC, Jernås M et al..  2012.  Association of sirtuin 1 (SIRT1) gene SNPs and transcript expression levels with severe obesity.. Obesity (Silver Spring). 20(1):178-85.
Ichimura A, Hirasawa A, Poulain-Godefroy O, Bonnefond A, Hara T, Yengo L, Kimura I, Leloire A, Liu N, Iida K et al..  2012.  Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human.. Nature. 483(7389):350-4.
Bradfield JP, Taal RH, Timpson NJ, Scherag A, Lecoeur C, Warrington NM, Hypponen E, Holst C, Valcarcel B, Thiering E et al..  2012.  A genome-wide association meta-analysis identifies new childhood obesity loci.. Nat Genet. 44(5):526-31.
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME et al..  2012.  A genome-wide association search for type 2 diabetes genes in African Americans.. PLoS One. 7(1):e29202.
Froguel P, Ndiaye N C, Bonnefond A, Bouatia-Naji N, Dechaume A, Siest G, Herbeth B, Falchi M, Bottolo L, Guéant-Rodriguez R-M et al..  2012.  A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels.. PLoS One. 7(3):e32327.
Creemers JWM, Choquet H, Stijnen P, Vatin V, Pigeyre M, Beckers S, Meulemans S, Than ME, Yengo L, Tauber M et al..  2012.  Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity.. Diabetes. 61(2):383-90.
Ali Khan A, Rodriguez A, Sebert S, Kaakinen M, Cauchi S, Froguel P, Hartikainen A-L, Pouta A, Järvelin M-R.  2012.  The interplay of variants near LEKR and CCNL1 and social stress in relation to birth size.. PLoS One. 7(6):e38216.
Scott RA, Lagou V, Welch RP, Wheeler E, Montasser ME, Luan J'an, Mägi R, Strawbridge RJ, Rehnberg E, Gustafsson S et al..  2012.  Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.. Nat Genet. 44(9):991-1005.
van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X et al..  2012.  Seventy-five genetic loci influencing the human red blood cell.. Nature. 492(7429):369-75.