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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2021 | 2 |
2022 | 2 |
2023 | 1 |
2024 | 1 |
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Adjusting for principal components can induce spurious associations in genome-wide association studies in admixed populations.
bioRxiv [Preprint]. 2024 Apr 3:2024.04.02.587682. doi: 10.1101/2024.04.02.587682.
bioRxiv. 2024.
PMID: 38617337
Free PMC article.
Preprint.
Fast, accurate local ancestry inference with FLARE.
Browning SR, Waples RK, Browning BL.
Browning SR, et al.
Am J Hum Genet. 2023 Feb 2;110(2):326-335. doi: 10.1016/j.ajhg.2022.12.010. Epub 2023 Jan 6.
Am J Hum Genet. 2023.
PMID: 36610402
Free PMC article.
Item in Clipboard
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Li Z, Li X, Zhou H, Gaynor SM, Selvaraj MS, Arapoglou T, Quick C, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Auer PL, Bielak LF, Bis JC, Blackwell TW, Blangero J, Boerwinkle E, Bowden DW, Brody JA, Cade BE, Conomos MP, Correa A, Cupples LA, Curran JE, de Vries PS, Duggirala R, Franceschini N, Freedman BI, Göring HHH, Guo X, Kalyani RR, Kooperberg C, Kral BG, Lange LA, Lin BM, Manichaikul A, Manning AK, Martin LW, Mathias RA, Meigs JB, Mitchell BD, Montasser ME, Morrison AC, Naseri T, O'Connell JR, Palmer ND, Peyser PA, Psaty BM, Raffield LM, Redline S, Reiner AP, Reupena MS, Rice KM, Rich SS, Smith JA, Taylor KD, Taub MA, Vasan RS, Weeks DE, Wilson JG, Yanek LR, Zhao W; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; TOPMed Lipids Working Group; Rotter JI, Willer CJ, Natarajan P, Peloso GM, Lin X.
Li Z, et al.
Nat Methods. 2022 Dec;19(12):1599-1611. doi: 10.1038/s41592-022-01640-x. Epub 2022 Oct 27.
Nat Methods. 2022.
PMID: 36303018
Free PMC article.
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AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos.
Granot-Hershkovitz E, Sun Q, Argos M, Zhou H, Lin X, Browning SR, Sofer T.
Granot-Hershkovitz E, et al.
HGG Adv. 2022 Feb 24;3(2):100096. doi: 10.1016/j.xhgg.2022.100096. eCollection 2022 Apr 14.
HGG Adv. 2022.
PMID: 35300209
Free PMC article.
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Protocol for detecting introgressed archaic variants with SPrime.
Zhou Y, Browning SR.
Zhou Y, et al.
STAR Protoc. 2021 May 19;2(2):100550. doi: 10.1016/j.xpro.2021.100550. eCollection 2021 Jun 18.
STAR Protoc. 2021.
PMID: 34095864
Free PMC article.
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Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
Lin BM, Grinde KE, Brody JA, Breeze CE, Raffield LM, Mychaleckyj JC, Thornton TA, Perry JA, Baier LJ, de Las Fuentes L, Guo X, Heavner BD, Hanson RL, Hung YJ, Qian H, Hsiung CA, Hwang SJ, Irvin MR, Jain D, Kelly TN, Kobes S, Lange L, Lash JP, Li Y, Liu X, Mi X, Musani SK, Papanicolaou GJ, Parsa A, Reiner AP, Salimi S, Sheu WH, Shuldiner AR, Taylor KD, Smith AV, Smith JA, Tin A, Vaidya D, Wallace RB, Yamamoto K, Sakaue S, Matsuda K, Kamatani Y, Momozawa Y, Yanek LR, Young BA, Zhao W, Okada Y, Abecasis G, Psaty BM, Arnett DK, Boerwinkle E, Cai J, Yii-Der Chen I, Correa A, Cupples LA, He J, Kardia SL, Kooperberg C, Mathias RA, Mitchell BD, Nickerson DA, Turner ST, Vasan RS, Rotter JI, Levy D, Kramer HJ, Köttgen A, Nhlbi Trans-Omics For Precision Medicine TOPMed Consortium, TOPMed Kidney Working Group, Rich SS, Lin DY, Browning SR, Franceschini N.
Lin BM, et al.
EBioMedicine. 2021 Jan;63:103157. doi: 10.1016/j.ebiom.2020.103157. Epub 2021 Jan 6.
EBioMedicine. 2021.
PMID: 33418499
Free PMC article.
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