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Items: 33

1.

A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.

Choquet H, Paylakhi S, Kneeland SC, Thai KK, Hoffmann TJ, Yin J, Kvale MN, Banda Y, Tolman NG, Williams PA, Schaefer C, Melles RB, Risch N, John SWM, Nair KS, Jorgenson E.

Nat Commun. 2018 Jun 11;9(1):2278. doi: 10.1038/s41467-018-04555-4.

2.

Common Mitochondrial Haplogroups and Cutaneous Squamous Cell Carcinoma Risk.

Jorgenson E, Choquet H, Yin J, Asgari MM.

Cancer Epidemiol Biomarkers Prev. 2018 Apr 25. doi: 10.1158/1055-9965.EPI-18-0236. [Epub ahead of print]

PMID:
29695379
3.

A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure.

Choquet H, Thai KK, Yin J, Hoffmann TJ, Kvale MN, Banda Y, Schaefer C, Risch N, Nair KS, Melles R, Jorgenson E.

Nat Commun. 2017 Dec 13;8(1):2108. doi: 10.1038/s41467-017-01913-6.

4.

Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.

Jorgenson E, Thai KK, Hoffmann TJ, Sakoda LC, Kvale MN, Banda Y, Schaefer C, Risch N, Mertens J, Weisner C, Choquet H.

Mol Psychiatry. 2017 Sep;22(9):1359-1367. doi: 10.1038/mp.2017.101. Epub 2017 May 9.

5.

Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.

Choquet H, Trapani E, Goitre L, Trabalzini L, Akers A, Fontanella M, Hart BL, Morrison LA, Pawlikowska L, Kim H, Retta SF.

Free Radic Biol Med. 2016 Mar;92:100-109. doi: 10.1016/j.freeradbiomed.2016.01.008. Epub 2016 Jan 19.

6.

Genetics of cerebral cavernous malformations: current status and future prospects.

Choquet H, Pawlikowska L, Lawton MT, Kim H.

J Neurosurg Sci. 2015 Sep;59(3):211-20. Epub 2015 Apr 22. Review.

7.

Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.

Choquet H, Pawlikowska L, Nelson J, McCulloch CE, Akers A, Baca B, Khan Y, Hart B, Morrison L, Kim H; Brain Vascular Malformation Consortium (BVMC) Study.

Cerebrovasc Dis. 2014;38(6):433-40. doi: 10.1159/000369200. Epub 2014 Dec 3.

8.

Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation.

Choquet H, Nelson J, Pawlikowska L, McCulloch CE, Akers A, Baca B, Khan Y, Hart B, Morrison L, Kim H.

Cerebrovasc Dis. 2014;37(1):57-63. doi: 10.1159/000356839. Epub 2013 Dec 21.

9.

Examination of rare missense variants in the CHRNA5-A3-B4 gene cluster to level of response to alcohol in the San Diego Sibling Pair study.

Choquet H, Joslyn G, Lee A, Kasberger J, Robertson M, Brush G, Schuckit MA, White R, Jorgenson E.

Alcohol Clin Exp Res. 2013 Aug;37(8):1311-6. doi: 10.1111/acer.12099. Epub 2013 Mar 4.

PMID:
23458267
10.

Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population.

Choquet H, Kasberger J, Hamidovic A, Jorgenson E.

PLoS One. 2013;8(2):e57857. doi: 10.1371/journal.pone.0057857. Epub 2013 Feb 25.

11.

Genetic analysis of a population heavy drinking phenotype identifies risk variants in whites.

Hamidovic A, Goodloe RJ, Young TR, Styn MA, Mukamal KJ, Choquet H, Kasberger JL, Buxbaum SG, Papanicolaou GJ, White W, Volcik K, Spring B, Hitsman B, Levy D, Jorgenson E.

J Clin Psychopharmacol. 2013 Apr;33(2):206-10. doi: 10.1097/JCP.0b013e318287009a.

12.

Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human.

Ichimura A, Hirasawa A, Poulain-Godefroy O, Bonnefond A, Hara T, Yengo L, Kimura I, Leloire A, Liu N, Iida K, Choquet H, Besnard P, Lecoeur C, Vivequin S, Ayukawa K, Takeuchi M, Ozawa K, Tauber M, Maffeis C, Morandi A, Buzzetti R, Elliott P, Pouta A, Jarvelin MR, Körner A, Kiess W, Pigeyre M, Caiazzo R, Van Hul W, Van Gaal L, Horber F, Balkau B, Lévy-Marchal C, Rouskas K, Kouvatsi A, Hebebrand J, Hinney A, Scherag A, Pattou F, Meyre D, Koshimizu TA, Wolowczuk I, Tsujimoto G, Froguel P.

Nature. 2012 Feb 19;483(7389):350-4. doi: 10.1038/nature10798.

PMID:
22343897
13.

Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity.

Creemers JW, Choquet H, Stijnen P, Vatin V, Pigeyre M, Beckers S, Meulemans S, Than ME, Yengo L, Tauber M, Balkau B, Elliott P, Jarvelin MR, Van Hul W, Van Gaal L, Horber F, Pattou F, Froguel P, Meyre D.

Diabetes. 2012 Feb;61(2):383-90. doi: 10.2337/db11-0305. Epub 2011 Dec 30.

14.

Gene-centric analysis of serum cotinine levels in African and European American populations.

Hamidovic A, Goodloe RJ, Bergen AW, Benowitz NL, Styn MA, Kasberger JL, Choquet H, Young TR, Meng Y, Palmer C, Pletcher M, Kertesz S, Hitsman B, Spring B, Jorgenson E.

Neuropsychopharmacology. 2012 Mar;37(4):968-74. doi: 10.1038/npp.2011.280. Epub 2011 Nov 16.

15.

Genetics of Obesity: What have we Learned?

Choquet H, Meyre D.

Curr Genomics. 2011 May;12(3):169-79. doi: 10.2174/138920211795677895.

16.

Molecular basis of obesity: current status and future prospects.

Choquet H, Meyre D.

Curr Genomics. 2011 May;12(3):154-68. doi: 10.2174/138920211795677921.

17.

Genetic and functional characterization of PCSK1.

Choquet H, Stijnen P, Creemers JW.

Methods Mol Biol. 2011;768:247-53. doi: 10.1007/978-1-61779-204-5_13.

PMID:
21805247
18.

Lack of association of CD36 SNPs with early onset obesity: a meta-analysis in 9,973 European subjects.

Choquet H, Labrune Y, De Graeve F, Hinney A, Hebebrand J, Scherag A, Lecoeur C, Tauber M, Balkau B, Elliot P, Jarvelin MR, Walley AJ, Besnard P, Froguel P, Meyre D.

Obesity (Silver Spring). 2011 Apr;19(4):833-9. doi: 10.1038/oby.2010.226. Epub 2010 Oct 21.

19.

Genomic insights into early-onset obesity.

Choquet H, Meyre D.

Genome Med. 2010 Jun 23;2(6):36. doi: 10.1186/gm157.

20.

Meta-analysis and functional effects of the SLC30A8 rs13266634 polymorphism on isolated human pancreatic islets.

Cauchi S, Del Guerra S, Choquet H, D'Aleo V, Groves CJ, Lupi R, McCarthy MI, Froguel P, Marchetti P.

Mol Genet Metab. 2010 May;100(1):77-82. doi: 10.1016/j.ymgme.2010.01.001. Epub 2010 Jan 15.

PMID:
20138556
21.

Prevalence of loss-of-function FTO mutations in lean and obese individuals.

Meyre D, Proulx K, Kawagoe-Takaki H, Vatin V, Gutiérrez-Aguilar R, Lyon D, Ma M, Choquet H, Horber F, Van Hul W, Van Gaal L, Balkau B, Visvikis-Siest S, Pattou F, Farooqi IS, Saudek V, O'Rahilly S, Froguel P, Sedgwick B, Yeo GS.

Diabetes. 2010 Jan;59(1):311-8. doi: 10.2337/db09-0703. Epub 2009 Oct 15.

22.

The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects.

Choquet H, Cavalcanti-Proença C, Lecoeur C, Dina C, Cauchi S, Vaxillaire M, Hadjadj S, Horber F, Potoczna N, Charpentier G, Ruiz J, Hercberg S, Maimaitiming S, Roussel R, Boenhnke M, Jackson AU, Patsch W, Krempler F, Voight BF, Altshuler D, Groop L, Thorleifsson G, Steinthorsdottir V, Stefansson K, Balkau B, Froguel P, Meyre D.

Hum Mol Genet. 2009 Jul 1;18(13):2495-501. doi: 10.1093/hmg/ddp169. Epub 2009 Apr 18.

PMID:
19377085
23.

TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia.

Bouhaha R, Choquet H, Meyre D, Abid Kamoun H, Ennafaa H, Baroudi T, Sassi R, Vaxillaire M, Elgaaied A, Froguel P, Cauchi S.

Pathol Biol (Paris). 2010 Dec;58(6):426-9. doi: 10.1016/j.patbio.2009.01.003. Epub 2009 Mar 14.

PMID:
19286335
24.

Common nonsynonymous variants in PCSK1 confer risk of obesity.

Benzinou M, Creemers JW, Choquet H, Lobbens S, Dina C, Durand E, Guerardel A, Boutin P, Jouret B, Heude B, Balkau B, Tichet J, Marre M, Potoczna N, Horber F, Le Stunff C, Czernichow S, Sandbaek A, Lauritzen T, Borch-Johnsen K, Andersen G, Kiess W, Körner A, Kovacs P, Jacobson P, Carlsson LM, Walley AJ, Jørgensen T, Hansen T, Pedersen O, Meyre D, Froguel P.

Nat Genet. 2008 Aug;40(8):943-5. doi: 10.1038/ng.177. Epub 2008 Jul 6.

PMID:
18604207
25.

The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies.

Cauchi S, Nead KT, Choquet H, Horber F, Potoczna N, Balkau B, Marre M, Charpentier G, Froguel P, Meyre D.

BMC Med Genet. 2008 May 22;9:45. doi: 10.1186/1471-2350-9-45.

26.

Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value.

Cauchi S, Meyre D, Durand E, Proença C, Marre M, Hadjadj S, Choquet H, De Graeve F, Gaget S, Allegaert F, Delplanque J, Permutt MA, Wasson J, Blech I, Charpentier G, Balkau B, Vergnaud AC, Czernichow S, Patsch W, Chikri M, Glaser B, Sladek R, Froguel P.

PLoS One. 2008 May 7;3(5):e2031. doi: 10.1371/journal.pone.0002031.

27.

Effects of TCF7L2 polymorphisms on obesity in European populations.

Cauchi S, Choquet H, Gutiérrez-Aguilar R, Capel F, Grau K, Proença C, Dina C, Duval A, Balkau B, Marre M, Potoczna N, Langin D, Horber F, Sørensen TI, Charpentier G, Meyre D, Froguel P.

Obesity (Silver Spring). 2008 Feb;16(2):476-82. doi: 10.1038/oby.2007.77.

28.

Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study.

Cauchi S, Proença C, Choquet H, Gaget S, De Graeve F, Marre M, Balkau B, Tichet J, Meyre D, Vaxillaire M, Froguel P; D.E.S.I.R. Study Group.

J Mol Med (Berl). 2008 Mar;86(3):341-8. doi: 10.1007/s00109-007-0295-x. Epub 2008 Jan 22.

PMID:
18210030
29.

TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population.

Cauchi S, Meyre D, Choquet H, Deghmoun S, Durand E, Gaget S, Lecoeur C, Froguel P, Levy-Marchal C.

BMC Med Genet. 2007 Jun 25;8:37.

30.

TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis.

Cauchi S, El Achhab Y, Choquet H, Dina C, Krempler F, Weitgasser R, Nejjari C, Patsch W, Chikri M, Meyre D, Froguel P.

J Mol Med (Berl). 2007 Jul;85(7):777-82. Epub 2007 May 3.

PMID:
17476472
31.

No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects.

Cauchi S, Vaxillaire M, Choquet H, Durand E, Duval A, Polak M, Froguel P.

Diabetologia. 2007 Jan;50(1):214-6. Epub 2006 Nov 9. No abstract available.

PMID:
17093940
32.

TCF7L2 variation predicts hyperglycemia incidence in a French general population: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study.

Cauchi S, Meyre D, Choquet H, Dina C, Born C, Marre M, Balkau B, Froguel P; DESIR Study Group.

Diabetes. 2006 Nov;55(11):3189-92. Erratum in: Diabetes. 2006 Dec;55(12):3635.

33.

Transcription factor TCF7L2 genetic study in the French population: expression in human beta-cells and adipose tissue and strong association with type 2 diabetes.

Cauchi S, Meyre D, Dina C, Choquet H, Samson C, Gallina S, Balkau B, Charpentier G, Pattou F, Stetsyuk V, Scharfmann R, Staels B, Frühbeck G, Froguel P.

Diabetes. 2006 Oct;55(10):2903-8.

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