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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.
Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations.
Horimoto ARVR, Boyken LA, Blue EE, Grinde KE, Nafikov RA, Sohi HK, Nato AQ Jr, Bis JC, Brusco LI, Morelli L, Ramirez A, Dalmasso MC, Temple S, Satizabal C, Browning SR, Seshadri S, Wijsman EM, Thornton TA.
Horimoto ARVR, et al. Among authors: grinde ke.
HGG Adv. 2023 May 20;4(3):100207. doi: 10.1016/j.xhgg.2023.100207. eCollection 2023 Jul 13.
HGG Adv. 2023.
PMID: 37333771
Free PMC article.
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Genetic ancestry, differential gene expression, and survival in pediatric B-cell acute lymphoblastic leukemia.
Barragan FA, Mills LJ, Raduski AR, Marcotte EL, Grinde KE, Spector LG, Williams LA.
Barragan FA, et al. Among authors: grinde ke.
Cancer Med. 2023 Feb;12(4):4761-4772. doi: 10.1002/cam4.5266. Epub 2022 Sep 20.
Cancer Med. 2023.
PMID: 36127808
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. Among authors: grinde ke.
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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Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African Americans.
Raffield LM, Lu AT, Szeto MD, Little A, Grinde KE, Shaw J, Auer PL, Cushman M, Horvath S, Irvin MR, Lange EM, Lange LA, Nickerson DA, Thornton TA, Wilson JG, Wheeler MM; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Hematology & Hemostasis Working Group; Zakai NA, Reiner AP.
Raffield LM, et al. Among authors: grinde ke.
J Thromb Haemost. 2020 Jun;18(6):1335-1347. doi: 10.1111/jth.14741. Epub 2020 Feb 20.
J Thromb Haemost. 2020.
PMID: 31985870
Free PMC article.
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Genome-wide Significance Thresholds for Admixture Mapping Studies.
Grinde KE, Brown LA, Reiner AP, Thornton TA, Browning SR.
Grinde KE, et al.
Am J Hum Genet. 2019 Mar 7;104(3):454-465. doi: 10.1016/j.ajhg.2019.01.008. Epub 2019 Feb 14.
Am J Hum Genet. 2019.
PMID: 30773276
Free PMC article.
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Generalizing polygenic risk scores from Europeans to Hispanics/Latinos.
Grinde KE, Qi Q, Thornton TA, Liu S, Shadyab AH, Chan KHK, Reiner AP, Sofer T.
Grinde KE, et al.
Genet Epidemiol. 2019 Feb;43(1):50-62. doi: 10.1002/gepi.22166. Epub 2018 Oct 15.
Genet Epidemiol. 2019.
PMID: 30368908
Free PMC article.
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Illustrating, Quantifying, and Correcting for Bias in Post-hoc Analysis of Gene-Based Rare Variant Tests of Association.
Grinde KE, Arbet J, Green A, O'Connell M, Valcarcel A, Westra J, Tintle N.
Grinde KE, et al.
Front Genet. 2017 Sep 14;8:117. doi: 10.3389/fgene.2017.00117. eCollection 2017.
Front Genet. 2017.
PMID: 28959274
Free PMC article.
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