Cohen JC - Search Results

1

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C, Blow MJ, Cohen JC, Rubin EM, Pennacchio LA. Visel A, et al. Among authors: cohen jc. Nature. 2010 Mar 18;464(7287):409-12. doi: 10.1038/nature08801. Epub 2010 Feb 21. Nature. 2010. PMID: 20173736 Free PMC article.

2

Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels.

Pennacchio LA, Olivier M, Hubacek JA, Krauss RM, Rubin EM, Cohen JC. Pennacchio LA, et al. Among authors: cohen jc. Hum Mol Genet. 2002 Nov 15;11(24):3031-8. doi: 10.1093/hmg/11.24.3031. Hum Mol Genet. 2002. PMID: 12417524

3

Lack of MEF2A mutations in coronary artery disease.

Weng L, Kavaslar N, Ustaszewska A, Doelle H, Schackwitz W, Hébert S, Cohen JC, McPherson R, Pennacchio LA. Weng L, et al. Among authors: cohen jc. J Clin Invest. 2005 Apr;115(4):1016-20. doi: 10.1172/JCI24186. J Clin Invest. 2005. PMID: 15841183 Free PMC article.

4

A common allele on chromosome 9 associated with coronary heart disease.

McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, Roberts R, Cox DR, Hinds DA, Pennacchio LA, Tybjaerg-Hansen A, Folsom AR, Boerwinkle E, Hobbs HH, Cohen JC. McPherson R, et al. Among authors: cohen jc. Science. 2007 Jun 8;316(5830):1488-91. doi: 10.1126/science.1142447. Epub 2007 May 3. Science. 2007. PMID: 17478681 Free PMC article.

5

Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease.

Romeo S, Kozlitina J, Xing C, Pertsemlidis A, Cox D, Pennacchio LA, Boerwinkle E, Cohen JC, Hobbs HH. Romeo S, et al. Among authors: cohen jc. Nat Genet. 2008 Dec;40(12):1461-5. doi: 10.1038/ng.257. Epub 2008 Sep 25. Nat Genet. 2008. PMID: 18820647 Free PMC article.

6

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

Romeo S, Pennacchio LA, Fu Y, Boerwinkle E, Tybjaerg-Hansen A, Hobbs HH, Cohen JC. Romeo S, et al. Among authors: cohen jc. Nat Genet. 2007 Apr;39(4):513-6. doi: 10.1038/ng1984. Epub 2007 Feb 25. Nat Genet. 2007. PMID: 17322881 Free PMC article.

7

Relationship between genetic variation at PPP1R3B and levels of liver glycogen and triglyceride.

Stender S, Smagris E, Lauridsen BK, Kofoed KF, Nordestgaard BG, Tybjaerg-Hansen A, Pennacchio LA, Dickel DE, Cohen JC, Hobbs HH. Stender S, et al. Among authors: cohen jc. Hepatology. 2018 Jun;67(6):2182-2195. doi: 10.1002/hep.29751. Epub 2018 Apr 19. Hepatology. 2018. PMID: 29266543 Free PMC article.

8

Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.

Romeo S, Yin W, Kozlitina J, Pennacchio LA, Boerwinkle E, Hobbs HH, Cohen JC. Romeo S, et al. Among authors: cohen jc. J Clin Invest. 2009 Jan;119(1):70-9. doi: 10.1172/JCI37118. Epub 2008 Dec 15. J Clin Invest. 2009. PMID: 19075393 Free PMC article.

9

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.

Garg V, Kathiriya IS, Barnes R, Schluterman MK, King IN, Butler CA, Rothrock CR, Eapen RS, Hirayama-Yamada K, Joo K, Matsuoka R, Cohen JC, Srivastava D. Garg V, et al. Among authors: cohen jc. Nature. 2003 Jul 24;424(6947):443-7. doi: 10.1038/nature01827. Epub 2003 Jul 6. Nature. 2003. PMID: 12845333

10

Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple loci.

Stender S, Kozlitina J, Nordestgaard BG, Tybjærg-Hansen A, Hobbs HH, Cohen JC. Stender S, et al. Among authors: cohen jc. Nat Genet. 2017 Jun;49(6):842-847. doi: 10.1038/ng.3855. Epub 2017 Apr 24. Nat Genet. 2017. PMID: 28436986 Free PMC article.

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