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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 14, 2008
Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic womenBronson E Oosterhuis, K Steven LaForge, Dmitri Proudnikov, et al.Human Genetics|April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesLane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.Proceedings of the National Academy of Sciences of the United States of America|June 28, 2018
Sex-chromosome dosage effects on gene expression in humansArmin Raznahan, Neelroop N Parikshak, Vijay Chandran, et al.JCI Insight|November 2, 2019
NK cell defects in X-linked pigmentary reticulate disorderPetro Starokadomskyy, Katelynn M Wilton, Konrad Krzewski, et al.American Journal of Medical Genetics. Part A|November 26, 2010
UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patientsNicole de Leeuw, Saskia Bulk, Andrew Green, et al.The Journal of Investigative Dermatology|November 25, 2003
Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomataAmalia Martinez-Mir, Benjamin Glaser, Gary S Chuang, et al.BMC Proceedings|December 19, 2009
Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysisSu-Wei Chang, Seung Hoan Choi, Ke Li, et al.Genetic Epidemiology|October 6, 2005
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mappingNathan A Ellis, Tomas Kirchhoff, Nandita Mitra, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 29, 2015
Deficits in Trabecular Bone Microarchitecture in Young Women With Type 1 Diabetes MellitusNaiemh Abdalrahaman, Christie McComb, John E Foster, et al.American Journal of Human Genetics|April 17, 2007
CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosisXiaochong Gao, Derek Gordon, Dongping Zhang, et al.Pageof 13