Sunyaev S - Search Results

1

Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis.

Diogo D, Kurreeman F, Stahl EA, Liao KP, Gupta N, Greenberg JD, Rivas MA, Hickey B, Flannick J, Thomson B, Guiducci C, Ripke S, Adzhubey I, Barton A, Kremer JM, Alfredsson L; Consortium of Rheumatology Researchers of North America; Rheumatoid Arthritis Consortium International; Sunyaev S, Martin J, Zhernakova A, Bowes J, Eyre S, Siminovitch KA, Gregersen PK, Worthington J, Klareskog L, Padyukov L, Raychaudhuri S, Plenge RM. Diogo D, et al. Among authors: sunyaev s. Am J Hum Genet. 2013 Jan 10;92(1):15-27. doi: 10.1016/j.ajhg.2012.11.012. Epub 2012 Dec 20. Am J Hum Genet. 2013. PMID: 23261300 Free PMC article.

2

Impact of selection, mutation rate and genetic drift on human genetic variation.

Sunyaev S, Kondrashov FA, Bork P, Ramensky V. Sunyaev S, et al. Hum Mol Genet. 2003 Dec 15;12(24):3325-30. doi: 10.1093/hmg/ddg359. Epub 2003 Oct 21. Hum Mol Genet. 2003. PMID: 14570704

3

Small fitness effect of mutations in highly conserved non-coding regions.

Kryukov GV, Schmidt S, Sunyaev S. Kryukov GV, et al. Among authors: sunyaev s. Hum Mol Genet. 2005 Aug 1;14(15):2221-9. doi: 10.1093/hmg/ddi226. Epub 2005 Jun 30. Hum Mol Genet. 2005. PMID: 15994173

4

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.

Kryukov GV, Pennacchio LA, Sunyaev SR. Kryukov GV, et al. Am J Hum Genet. 2007 Apr;80(4):727-39. doi: 10.1086/513473. Epub 2007 Mar 8. Am J Hum Genet. 2007. PMID: 17357078 Free PMC article.

5

Medical sequencing at the extremes of human body mass.

Ahituv N, Kavaslar N, Schackwitz W, Ustaszewska A, Martin J, Hebert S, Doelle H, Ersoy B, Kryukov G, Schmidt S, Yosef N, Ruppin E, Sharan R, Vaisse C, Sunyaev S, Dent R, Cohen J, McPherson R, Pennacchio LA. Ahituv N, et al. Among authors: sunyaev s. Am J Hum Genet. 2007 Apr;80(4):779-91. doi: 10.1086/513471. Epub 2007 Mar 5. Am J Hum Genet. 2007. PMID: 17357083 Free PMC article.

6

Common single-nucleotide polymorphisms act in concert to affect plasma levels of high-density lipoprotein cholesterol.

Spirin V, Schmidt S, Pertsemlidis A, Cooper RS, Cohen JC, Sunyaev SR. Spirin V, et al. Among authors: sunyaev sr. Am J Hum Genet. 2007 Dec;81(6):1298-303. doi: 10.1086/522497. Am J Hum Genet. 2007. PMID: 17952847 Free PMC article.

7

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.

Gorlov IP, Gorlova OY, Sunyaev SR, Spitz MR, Amos CI. Gorlov IP, et al. Am J Hum Genet. 2008 Jan;82(1):100-12. doi: 10.1016/j.ajhg.2007.09.006. Am J Hum Genet. 2008. PMID: 18179889 Free PMC article.

8

Power of deep, all-exon resequencing for discovery of human trait genes.

Kryukov GV, Shpunt A, Stamatoyannopoulos JA, Sunyaev SR. Kryukov GV, et al. Proc Natl Acad Sci U S A. 2009 Mar 10;106(10):3871-6. doi: 10.1073/pnas.0812824106. Epub 2009 Feb 6. Proc Natl Acad Sci U S A. 2009. PMID: 19202052 Free PMC article.

9

Pooled association tests for rare variants in exon-resequencing studies.

Price AL, Kryukov GV, de Bakker PI, Purcell SM, Staples J, Wei LJ, Sunyaev SR. Price AL, et al. Am J Hum Genet. 2010 Jun 11;86(6):832-8. doi: 10.1016/j.ajhg.2010.04.005. Epub 2010 May 13. Am J Hum Genet. 2010. PMID: 20471002 Free PMC article.

10

Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.

Jordan DM, Kiezun A, Baxter SM, Agarwala V, Green RC, Murray MF, Pugh T, Lebo MS, Rehm HL, Funke BH, Sunyaev SR. Jordan DM, et al. Among authors: sunyaev sr. Am J Hum Genet. 2011 Feb 11;88(2):183-92. doi: 10.1016/j.ajhg.2011.01.011. Am J Hum Genet. 2011. PMID: 21310275 Free PMC article.

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