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Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions.
Yu F, Lu J, Liu X, Gazave E, Chang D, Raj S, Hunter-Zinck H, Blekhman R, Arbiza L, Van Hout C, Morrison A, Johnson AD, Bis J, Cupples LA, Psaty BM, Muzny D, Yu J, Gibbs RA, Keinan A, Clark AG, Boerwinkle E. Yu F, et al. Among authors: van hout c. PLoS One. 2015 Mar 25;10(3):e0121644. doi: 10.1371/journal.pone.0121644. eCollection 2015. PLoS One. 2015. PMID: 25807536 Free PMC article.
Exome Sequencing of 21 Bardet-Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians.
Day SE, Muller YL, Koroglu C, Kobes S, Wiedrich K, Mahkee D, Kim HI, Van Hout C, Gosalia N, Ye B; Regeneron Genetics Center; Shuldiner AR, Knowler WC, Hanson RL, Bogardus C, Baier LJ. Day SE, et al. Among authors: van hout c. Obesity (Silver Spring). 2021 Apr;29(4):748-754. doi: 10.1002/oby.23115. Epub 2021 Feb 22. Obesity (Silver Spring). 2021. PMID: 33616283 Free PMC article.
Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population.
Humphries EM, Ahn K, Kember RL, Lopes FL, Mocci E, Peralta JM, Blangero J, Glahn DC, Goes FS, Zandi PP, Kochunov P, Van Hout C, Shuldiner AR, Pollin TI, Mitchell BD, Bucan M, Hong LE, McMahon FJ, Ament SA. Humphries EM, et al. Among authors: van hout c. Mol Psychiatry. 2023 Dec;28(12):5262-5271. doi: 10.1038/s41380-023-02014-1. Epub 2023 Mar 7. Mol Psychiatry. 2023. PMID: 36882501 Free PMC article.
Functional characterization of a novel p.Ser76Thr variant in IGFBP4 that associates with body mass index in American Indians.
Muller YL, Saporito M, Day S, Bandesh K, Koroglu C, Kobes S, Knowler WC, Hanson RL; Regeneron Genetics Center; Van Hout CV, Shuldiner AR, Bogardus C, Baier LJ. Muller YL, et al. Among authors: van hout cv. Eur J Hum Genet. 2022 Oct;30(10):1159-1166. doi: 10.1038/s41431-022-01129-3. Epub 2022 Jun 10. Eur J Hum Genet. 2022. PMID: 35688891 Free PMC article.
Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia.
Salzer-Sheelo L, Fellner A, Orenstein N, Bazak L, Lev-El Halabi N, Daue M, Smirin-Yosef P, Van Hout CV, Fellig Y, Ruhrman-Shahar N, Staples J, Magal N, Shuldiner AR, Mitchell BD, Nevo Y, Pollin TI, Gonzaga-Jauregui C, Basel-Salmon L. Salzer-Sheelo L, et al. Among authors: van hout cv. Eur J Neurol. 2022 Apr;29(4):1174-1180. doi: 10.1111/ene.15218. Epub 2022 Jan 7. Eur J Neurol. 2022. PMID: 34935254
Genetic and functional evidence links a missense variant in B4GALT1 to lower LDL and fibrinogen.
Montasser ME, Van Hout CV, Miloscio L, Howard AD, Rosenberg A, Callaway M, Shen B, Li N, Locke AE, Verweij N, De T, Ferreira MA, Lotta LA, Baras A, Daly TJ, Hartford SA, Lin W, Mao Y, Ye B, White D, Gong G, Perry JA, Ryan KA, Fang Q, Tzoneva G, Pefanis E, Hunt C, Tang Y, Lee L; Regeneron Genetics Center Collaboration‡; Sztalryd-Woodle C, Mitchell BD, Healy M, Streeten EA, Taylor SI, O'Connell JR, Economides AN, Della Gatta G, Shuldiner AR. Montasser ME, et al. Among authors: van hout cv. Science. 2021 Dec 3;374(6572):1221-1227. doi: 10.1126/science.abe0348. Epub 2021 Dec 2. Science. 2021. PMID: 34855475
A missense variant Arg611Cys in LIPE which encodes hormone sensitive lipase decreases lipolysis and increases risk of type 2 diabetes in American Indians.
Muller YL, Sutherland J, Nair AK, Koroglu C, Kobes S, Knowler WC, Van Hout CV; Regeneron Genetics Center; Shuldiner AR, Hanson RL, Bogardus C, Baier LJ. Muller YL, et al. Among authors: van hout cv. Diabetes Metab Res Rev. 2022 Mar;38(3):e3504. doi: 10.1002/dmrr.3504. Epub 2021 Oct 28. Diabetes Metab Res Rev. 2022. PMID: 34655148
44 results