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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.
A comparison of gene region simulation methods.
Hendricks AE, Dupuis J, Gupta M, Logue MW, Lunetta KL. Hendricks AE, et al. PLoS One. 2012;7(7):e40925. doi: 10.1371/journal.pone.0040925. Epub 2012 Jul 18. PLoS One. 2012. PMID: 22815869 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.
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.
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.
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.
73 results