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Items: 1 to 20 of 68

1.

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

Zekavat SM, Ruotsalainen S, Handsaker RE, Alver M, Bloom J, Poterba T, Seed C, Ernst J, Chaffin M, Engreitz J, Peloso GM, Manichaikul A, Yang C, Ryan KA, Fu M, Johnson WC, Tsai M, Budoff M, Ramachandran VS, Cupples LA, Rotter JI, Rich SS, Post W, Mitchell BD, Correa A, Metspalu A, Wilson JG, Salomaa V, Kellis M, Daly MJ, Neale BM, McCarroll S, Surakka I, Esko T, Ganna A, Ripatti S, Kathiresan S, Natarajan P; NHLBI TOPMed Lipids Working Group.

Nat Commun. 2018 Jul 4;9(1):2606. doi: 10.1038/s41467-018-04668-w.

2.

A response to "Likelihood ratio as weight of evidence: A closer look" by Lund and Iyer.

Gittelson S, Berger CEH, Jackson G, Evett IW, Champod C, Robertson B, Curran JM, Taylor D, Weir BS, Coble MD, Buckleton JS.

Forensic Sci Int. 2018 Jul;288:e15-e19. doi: 10.1016/j.forsciint.2018.05.025. Epub 2018 May 22.

PMID:
29857959
3.

Reply to Kardos et al.: Estimation of inbreeding depression from SNP data.

Yengo L, Zhu Z, Wray NR, Weir BS, Yang J, Robinson MR, Visscher PM.

Proc Natl Acad Sci U S A. 2018 Mar 13;115(11):E2494-E2495. doi: 10.1073/pnas.1718598115. Epub 2018 Feb 21. No abstract available.

PMID:
29467293
4.

Multi-allelic exact tests for Hardy-Weinberg equilibrium that account for gender.

Graffelman J, Weir BS.

Mol Ecol Resour. 2018 May;18(3):461-473. doi: 10.1111/1755-0998.12748. Epub 2018 Jan 22.

5.

Whole genome sequence analyses of brain imaging measures in the Framingham Study.

Sarnowski C, Satizabal CL, DeCarli C, Pitsillides AN, Cupples LA, Vasan RS, Wilson JG, Bis JC, Fornage M, Beiser AS, DeStefano AL, Dupuis J, Seshadri S; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; TOPMed Neurocognitive Working Group.

Neurology. 2018 Jan 16;90(3):e188-e196. doi: 10.1212/WNL.0000000000004820. Epub 2017 Dec 27.

6.

On the testing of Hardy-Weinberg proportions and equality of allele frequencies in males and females at biallelic genetic markers.

Graffelman J, Weir BS.

Genet Epidemiol. 2018 Feb;42(1):34-48. doi: 10.1002/gepi.22079. Epub 2017 Oct 25.

7.

Detection and quantification of inbreeding depression for complex traits from SNP data.

Yengo L, Zhu Z, Wray NR, Weir BS, Yang J, Robinson MR, Visscher PM.

Proc Natl Acad Sci U S A. 2017 Aug 8;114(32):8602-8607. doi: 10.1073/pnas.1621096114. Epub 2017 Jul 26.

8.

A Unified Characterization of Population Structure and Relatedness.

Weir BS, Goudet J.

Genetics. 2017 Aug;206(4):2085-2103. doi: 10.1534/genetics.116.198424. Epub 2017 May 26.

9.

A genome-wide study of Hardy-Weinberg equilibrium with next generation sequence data.

Graffelman J, Jain D, Weir B.

Hum Genet. 2017 Jun;136(6):727-741. doi: 10.1007/s00439-017-1786-7. Epub 2017 Apr 3.

10.

SeqArray-a storage-efficient high-performance data format for WGS variant calls.

Zheng X, Gogarten SM, Lawrence M, Stilp A, Conomos MP, Weir BS, Laurie C, Levine D.

Bioinformatics. 2017 Aug 1;33(15):2251-2257. doi: 10.1093/bioinformatics/btx145.

PMID:
28334390
11.

The factor of 10 in forensic DNA match probabilities.

Gittelson S, Moretti TR, Onorato AJ, Budowle B, Weir BS, Buckleton J.

Forensic Sci Int Genet. 2017 May;28:178-187. doi: 10.1016/j.fsigen.2017.02.007. Epub 2017 Feb 16.

PMID:
28273509
12.

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.

Schick UM, Jain D, Hodonsky CJ, Morrison JV, Davis JP, Brown L, Sofer T, Conomos MP, Schurmann C, McHugh CP, Nelson SC, Vadlamudi S, Stilp A, Plantinga A, Baier L, Bien SA, Gogarten SM, Laurie CA, Taylor KD, Liu Y, Auer PL, Franceschini N, Szpiro A, Rice K, Kerr KF, Rotter JI, Hanson RL, Papanicolaou G, Rich SS, Loos RJ, Browning BL, Browning SR, Weir BS, Laurie CC, Mohlke KL, North KE, Thornton TA, Reiner AP.

Am J Hum Genet. 2016 Feb 4;98(2):229-42. doi: 10.1016/j.ajhg.2015.12.003. Epub 2016 Jan 21.

13.

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.

Conomos MP, Laurie CA, Stilp AM, Gogarten SM, McHugh CP, Nelson SC, Sofer T, Fernández-Rhodes L, Justice AE, Graff M, Young KL, Seyerle AA, Avery CL, Taylor KD, Rotter JI, Talavera GA, Daviglus ML, Wassertheil-Smoller S, Schneiderman N, Heiss G, Kaplan RC, Franceschini N, Reiner AP, Shaffer JR, Barr RG, Kerr KF, Browning SR, Browning BL, Weir BS, Avilés-Santa ML, Papanicolaou GJ, Lumley T, Szpiro AA, North KE, Rice K, Thornton TA, Laurie CC.

Am J Hum Genet. 2016 Jan 7;98(1):165-84. doi: 10.1016/j.ajhg.2015.12.001.

14.

Model-free Estimation of Recent Genetic Relatedness.

Conomos MP, Reiner AP, Weir BS, Thornton TA.

Am J Hum Genet. 2016 Jan 7;98(1):127-48. doi: 10.1016/j.ajhg.2015.11.022.

15.

Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.

Williams SR, Hsu FC, Keene KL, Chen WM, Nelson S, Southerland AM, Madden EB, Coull B, Gogarten SM, Furie KL, Dzhivhuho G, Rowles JL, Mehndiratta P, Malik R, Dupuis J, Lin H, Seshadri S, Rich SS, Sale MM, Worrall BB; METASTROKE, The Genomics and Randomized Trials Network (GARNET) Collaborative Research Group; METASTROKE The Genomics and Randomized Trials Network GARNET Collaborative Research Group.

Neurology. 2016 Jan 26;86(4):351-9. doi: 10.1212/WNL.0000000000002319. Epub 2015 Dec 30.

16.

SNPs and SNVs in forensic science.

Weir BS, Zheng X.

Forensic Sci Int Genet Suppl Ser. 2015 Dec;5:e267-e268. doi: 10.1016/j.fsigss.2015.09.106. Epub 2015 Oct 1.

17.

Eigenanalysis of SNP data with an identity by descent interpretation.

Zheng X, Weir BS.

Theor Popul Biol. 2016 Feb;107:65-76. doi: 10.1016/j.tpb.2015.09.004. Epub 2015 Oct 23.

18.

Dominance genetic variation contributes little to the missing heritability for human complex traits.

Zhu Z, Bakshi A, Vinkhuyzen AA, Hemani G, Lee SH, Nolte IM, van Vliet-Ostaptchouk JV, Snieder H; LifeLines Cohort Study, Esko T, Milani L, Mägi R, Metspalu A, Hill WG, Weir BS, Goddard ME, Visscher PM, Yang J.

Am J Hum Genet. 2015 Mar 5;96(3):377-85. doi: 10.1016/j.ajhg.2015.01.001. Epub 2015 Feb 12.

19.

Letter to editor in response to editorial by Risinger et al.

Buckleton J, Evett I, Weir B.

Sci Justice. 2014 Dec;54(6):510. doi: 10.1016/j.scijus.2014.07.003. Epub 2014 Aug 27. No abstract available.

PMID:
25498943
20.

Genetic variants associated with development of TMD and its intermediate phenotypes: the genetic architecture of TMD in the OPPERA prospective cohort study.

Smith SB, Mir E, Bair E, Slade GD, Dubner R, Fillingim RB, Greenspan JD, Ohrbach R, Knott C, Weir B, Maixner W, Diatchenko L.

J Pain. 2013 Dec;14(12 Suppl):T91-101.e1-3. doi: 10.1016/j.jpain.2013.09.004.

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