Sunyaev S - Search Results

1

Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations.

Gazal S, Loh PR, Finucane HK, Ganna A, Schoech A, Sunyaev S, Price AL. Gazal S, et al. Among authors: sunyaev s. Nat Genet. 2018 Nov;50(11):1600-1607. doi: 10.1038/s41588-018-0231-8. Epub 2018 Oct 8. Nat Genet. 2018. PMID: 30297966 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

A limited role for balancing selection.

Asthana S, Schmidt S, Sunyaev S. Asthana S, et al. Among authors: sunyaev s. Trends Genet. 2005 Jan;21(1):30-2. doi: 10.1016/j.tig.2004.11.001. Trends Genet. 2005. PMID: 15680511

4

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

5

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.

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

Hypermutable non-synonymous sites are under stronger negative selection.

Schmidt S, Gerasimova A, Kondrashov FA, Adzhubei IA, Adzuhbei IA, Kondrashov AS, Sunyaev S. Schmidt S, et al. Among authors: sunyaev s. PLoS Genet. 2008 Nov;4(11):e1000281. doi: 10.1371/journal.pgen.1000281. Epub 2008 Nov 28. PLoS Genet. 2008. PMID: 19043566 Free PMC article.

8

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.

9

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.

Pasaniuc B, Rohland N, McLaren PJ, Garimella K, Zaitlen N, Li H, Gupta N, Neale BM, Daly MJ, Sklar P, Sullivan PF, Bergen S, Moran JL, Hultman CM, Lichtenstein P, Magnusson P, Purcell SM, Haas DW, Liang L, Sunyaev S, Patterson N, de Bakker PI, Reich D, Price AL. Pasaniuc B, et al. Among authors: sunyaev s. Nat Genet. 2012 May 20;44(6):631-5. doi: 10.1038/ng.2283. Nat Genet. 2012. PMID: 22610117 Free PMC article.

10

Exome sequencing and the genetic basis of complex traits.

Kiezun A, Garimella K, Do R, Stitziel NO, Neale BM, McLaren PJ, Gupta N, Sklar P, Sullivan PF, Moran JL, Hultman CM, Lichtenstein P, Magnusson P, Lehner T, Shugart YY, Price AL, de Bakker PI, Purcell SM, Sunyaev SR. Kiezun A, et al. Nat Genet. 2012 May 29;44(6):623-30. doi: 10.1038/ng.2303. Nat Genet. 2012. PMID: 22641211 Free PMC article.

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