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Genome-wide polygenic score to predict chronic kidney disease across ancestries.
Khan A, Turchin MC, Patki A, Srinivasasainagendra V, Shang N, Nadukuru R, Jones AC, Malolepsza E, Dikilitas O, Kullo IJ, Schaid DJ, Karlson E, Ge T, Meigs JB, Smoller JW, Lange C, Crosslin DR, Jarvik GP, Bhatraju PK, Hellwege JN, Chandler P, Torvik LR, Fedotov A, Liu C, Kachulis C, Lennon N, Abul-Husn NS, Cho JH, Ionita-Laza I, Gharavi AG, Chung WK, Hripcsak G, Weng C, Nadkarni G, Irvin MR, Tiwari HK, Kenny EE, Limdi NA, Kiryluk K. Khan A, et al. Nat Med. 2022 Jul;28(7):1412-1420. doi: 10.1038/s41591-022-01869-1. Epub 2022 Jun 16. Nat Med. 2022. PMID: 35710995 Free PMC article.
On the frequency of copy number variants.
Ionita-Laza I, Laird NM, Raby BA, Weiss ST, Lange C. Ionita-Laza I, et al. Bioinformatics. 2008 Oct 15;24(20):2350-5. doi: 10.1093/bioinformatics/btn421. Epub 2008 Aug 8. Bioinformatics. 2008. PMID: 18689430 Free PMC article.
Estimating the number of unseen variants in the human genome.
Ionita-Laza I, Lange C, M Laird N. Ionita-Laza I, et al. Proc Natl Acad Sci U S A. 2009 Mar 31;106(13):5008-13. doi: 10.1073/pnas.0807815106. Epub 2009 Mar 10. Proc Natl Acad Sci U S A. 2009. PMID: 19276111 Free PMC article.
Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus.
Fan J, Ionita-Laza I, McQueen MB, Devlin B, Purcell S, Faraone SV, Allen MH, Bowden CL, Calabrese JR, Fossey MD, Friedman ES, Gyulai L, Hauser P, Ketter TB, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel JK, Sachs GS, Thase ME, Molay FB, Escamilla MA, Nimgaonkar VL, Sklar P, Laird NM, Smoller JW. Fan J, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):29-37. doi: 10.1002/ajmg.b.30942. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19308960 Free PMC article.
87 results