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European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy.
Tarnow L, Groop PH, Hadjadj S, Kazeem G, Cambien F, Marre M, Forsblom C, Parving HH, Trégouët D, Thévard A, Farrall M, Gut I, Gauguier D, Cox R, Matsuda F, Lathrop M, Vionnet N; EURAGEDIC Consortium. Tarnow L, et al. Among authors: lathrop m. Nephrol Dial Transplant. 2008 Jan;23(1):161-8. doi: 10.1093/ndt/gfm501. Epub 2007 Aug 17. Nephrol Dial Transplant. 2008. PMID: 17704113
Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin gene.
Vionnet N, Tregouët D, Kazeem G, Gut I, Groop PH, Tarnow L, Parving HH, Hadjadj S, Forsblom C, Farrall M, Gauguier D, Cox R, Matsuda F, Heath S, Thévard A, Rousseau R, Cambien F, Marre M, Lathrop M. Vionnet N, et al. Among authors: lathrop m. Diabetes. 2006 Nov;55(11):3166-74. doi: 10.2337/db06-0271. Diabetes. 2006. PMID: 17065357
Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations.
Hadjadj S, Tarnow L, Forsblom C, Kazeem G, Marre M, Groop PH, Parving HH, Cambien F, Tregouet DA, Gut IG, Théva A, Gauguier D, Farrall M, Cox R, Matsuda F, Lathrop M, Hager-Vionnet N; EURAGEDIC (European Rational Approach for Genetics of Diabetic Complications) Study Group. Hadjadj S, et al. Among authors: lathrop m. J Am Soc Nephrol. 2007 Apr;18(4):1284-91. doi: 10.1681/ASN.2006101102. Epub 2007 Mar 21. J Am Soc Nephrol. 2007. PMID: 17376814
Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome.
Kaisaki PJ, Delépine M, Woon PY, Sebag-Montefiore L, Wilder SP, Menzel S, Vionnet N, Marion E, Riveline JP, Charpentier G, Schurmans S, Levy JC, Lathrop M, Farrall M, Gauguier D. Kaisaki PJ, et al. Among authors: lathrop m. Diabetes. 2004 Jul;53(7):1900-4. doi: 10.2337/diabetes.53.7.1900. Diabetes. 2004. PMID: 15220217
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension.
Marçano AC, Burke B, Gungadoo J, Wallace C, Kaisaki PJ, Woon PY, Farrall M, Clayton D, Brown M, Dominiczak A, Connell JM, Webster J, Lathrop M, Caulfield M, Samani N, Gauguier D, Munroe PB. Marçano AC, et al. Among authors: lathrop m. J Med Genet. 2007 Sep;44(9):603-5. doi: 10.1136/jmg.2007.049718. Epub 2007 Jun 8. J Med Genet. 2007. PMID: 17557929 Free PMC article.
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.
Thein SL, Menzel S, Peng X, Best S, Jiang J, Close J, Silver N, Gerovasilli A, Ping C, Yamaguchi M, Wahlberg K, Ulug P, Spector TD, Garner C, Matsuda F, Farrall M, Lathrop M. Thein SL, et al. Among authors: lathrop m. Proc Natl Acad Sci U S A. 2007 Jul 3;104(27):11346-51. doi: 10.1073/pnas.0611393104. Epub 2007 Jun 25. Proc Natl Acad Sci U S A. 2007. PMID: 17592125 Free PMC article.
657 results