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Genome-wide copy number variations in a large cohort of bantu African children.
Yilmaz F, Null M, Astling D, Yu HC, Cole J, Santorico SA, Hallgrimsson B, Manyama M, Spritz RA, Hendricks AE, Shaikh TH. Yilmaz F, et al. Among authors: hendricks ae. BMC Med Genomics. 2021 May 17;14(1):129. doi: 10.1186/s12920-021-00978-z. BMC Med Genomics. 2021. PMID: 34001112 Free PMC article.
Progress in methods for rare variant association.
Santorico SA, Hendricks AE. Santorico SA, et al. Among authors: hendricks ae. BMC Genet. 2016 Feb 3;17 Suppl 2(Suppl 2):6. doi: 10.1186/s12863-015-0316-7. BMC Genet. 2016. PMID: 26866487 Free PMC article.
RAREsim: A simulation method for very rare genetic variants.
Null M, Dupuis J, Sheinidashtegol P, Layer RM, Gignoux CR, Hendricks AE. Null M, et al. Among authors: hendricks ae. Am J Hum Genet. 2022 Apr 7;109(4):680-691. doi: 10.1016/j.ajhg.2022.02.009. Epub 2022 Mar 16. Am J Hum Genet. 2022. PMID: 35298919 Free PMC article.
Summix: A method for detecting and adjusting for population structure in genetic summary data.
Arriaga-MacKenzie IS, Matesi G, Chen S, Ronco A, Marker KM, Hall JR, Scherenberg R, Khajeh-Sharafabadi M, Wu Y, Gignoux CR, Null M, Hendricks AE. Arriaga-MacKenzie IS, et al. Among authors: hendricks ae. Am J Hum Genet. 2021 Jul 1;108(7):1270-1282. doi: 10.1016/j.ajhg.2021.05.016. Epub 2021 Jun 21. Am J Hum Genet. 2021. PMID: 34157305 Free PMC article.
Opportunities and challenges for the use of common controls in sequencing studies.
Wojcik GL, Murphy J, Edelson JL, Gignoux CR, Ioannidis AG, Manning A, Rivas MA, Buyske S, Hendricks AE. Wojcik GL, et al. Among authors: hendricks ae. Nat Rev Genet. 2022 Nov;23(11):665-679. doi: 10.1038/s41576-022-00487-4. Epub 2022 May 17. Nat Rev Genet. 2022. PMID: 35581355 Free PMC article. Review.
Insight into genetic regulation of miRNA in mouse brain.
Kordas G, Rudra P, Hendricks A, Saba L, Kechris K. Kordas G, et al. BMC Genomics. 2019 Nov 13;20(1):849. doi: 10.1186/s12864-019-6110-6. BMC Genomics. 2019. PMID: 31722663 Free PMC article.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
Tachmazidou I, Süveges D, Min JL, Ritchie GRS, Steinberg J, Walter K, Iotchkova V, Schwartzentruber J, Huang J, Memari Y, McCarthy S, Crawford AA, Bombieri C, Cocca M, Farmaki AE, Gaunt TR, Jousilahti P, Kooijman MN, Lehne B, Malerba G, Männistö S, Matchan A, Medina-Gomez C, Metrustry SJ, Nag A, Ntalla I, Paternoster L, Rayner NW, Sala C, Scott WR, Shihab HA, Southam L, St Pourcain B, Traglia M, Trajanoska K, Zaza G, Zhang W, Artigas MS, Bansal N, Benn M, Chen Z, Danecek P, Lin WY, Locke A, Luan J, Manning AK, Mulas A, Sidore C, Tybjaerg-Hansen A, Varbo A, Zoledziewska M, Finan C, Hatzikotoulas K, Hendricks AE, Kemp JP, Moayyeri A, Panoutsopoulou K, Szpak M, Wilson SG, Boehnke M, Cucca F, Di Angelantonio E, Langenberg C, Lindgren C, McCarthy MI, Morris AP, Nordestgaard BG, Scott RA, Tobin MD, Wareham NJ; SpiroMeta Consortium; GoT2D Consortium; Burton P, Chambers JC, Smith GD, Dedoussis G, Felix JF, Franco OH, Gambaro G, Gasparini P, Hammond CJ, Hofman A, Jaddoe VWV, Kleber M, Kooner JS, Perola M, Relton C, Ring SM, Rivadeneira F, Salomaa V, Spector TD, Stegle O, Toniolo D, Uitterlinden AG; arcOGEN Consortium; Understanding Society Scientific Group; UK10K Consortium; Barroso… See abstract for full author list ➔ Tachmazidou I, et al. Among authors: hendricks ae. Am J Hum Genet. 2017 Jun 1;100(6):865-884. doi: 10.1016/j.ajhg.2017.04.014. Epub 2017 May 25. Am J Hum Genet. 2017. PMID: 28552196 Free PMC article.
Correction for multiple testing in a gene region.
Hendricks AE, Dupuis J, Logue MW, Myers RH, Lunetta KL. Hendricks AE, et al. Eur J Hum Genet. 2014 Mar;22(3):414-8. doi: 10.1038/ejhg.2013.144. Epub 2013 Jul 10. Eur J Hum Genet. 2014. PMID: 23838599 Free PMC article.
75 results