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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2010 | 4 |
2011 | 1 |
2013 | 1 |
2024 | 0 |
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7 results
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Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.
N Engl J Med. 2010 Dec 2;363(23):2220-7. doi: 10.1056/NEJMoa1002926. Epub 2010 Oct 13.
N Engl J Med. 2010.
PMID: 20942659
Free PMC article.
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.
Science. 2007 Jun 8;316(5830):1488-91. doi: 10.1126/science.1142447. Epub 2007 May 3.
Science. 2007.
PMID: 17478681
Free PMC article.
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Emerging LDL therapies: Using human genetics to discover new therapeutic targets for plasma lipids.
Cohen JC.
Cohen JC.
J Clin Lipidol. 2013 May-Jun;7(3 Suppl):S1-5. doi: 10.1016/j.jacl.2013.03.005. Epub 2013 Mar 26.
J Clin Lipidol. 2013.
PMID: 23642322
Free PMC article.
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Identification by whole-genome resequencing of gene defect responsible for severe hypercholesterolemia.
Rios J, Stein E, Shendure J, Hobbs HH, Cohen JC.
Rios J, et al.
Hum Mol Genet. 2010 Nov 15;19(22):4313-8. doi: 10.1093/hmg/ddq352. Epub 2010 Aug 18.
Hum Mol Genet. 2010.
PMID: 20719861
Free PMC article.
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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.
Nature. 2010 Mar 18;464(7287):409-12. doi: 10.1038/nature08801. Epub 2010 Feb 21.
Nature. 2010.
PMID: 20173736
Free PMC article.
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Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans.
Deo RC, Wilson JG, Xing C, Lawson K, Kao WH, Reich D, Tandon A, Akylbekova E, Patterson N, Mosley TH Jr, Boerwinkle E, Taylor HA Jr.
Deo RC, et al.
PLoS One. 2011 Jan 24;6(1):e14581. doi: 10.1371/journal.pone.0014581.
PLoS One. 2011.
PMID: 21283670
Free PMC article.
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A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels.
Xing C, Cohen JC, Boerwinkle E.
Xing C, et al.
Am J Hum Genet. 2010 Mar 12;86(3):440-6. doi: 10.1016/j.ajhg.2010.01.025. Epub 2010 Feb 11.
Am J Hum Genet. 2010.
PMID: 20152958
Free PMC article.
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