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Neurology. Genetics|February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disordersE Robert Wassman, Karen S Ho, Diana Bertrand, et al.
Plos One|January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD populationNori Matsunami, Dexter Hadley, Charles H Hensel, et al.
Oncogene|December 5, 1996
An 80 Kb P1 clone from chromosome 3p21.3 suppresses tumor growth in vivoM C Todd, R H Xiang, D K Garcia, et al.
Molecular Psychiatry|March 2, 2011
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorderL Priebe, F A Degenhardt, S Herms, et al.
Human Genetics|November 10, 2001
Linkage of body mass index to chromosome 20 in Utah pedigreesS C Hunt, V Abkevich, C H Hensel, et al.
Molecular Autism|January 29, 2014
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control populationNori Matsunami, Charles H Hensel, Lisa Baird, et al.
American Journal of Human Genetics|April 17, 2002
A major predisposition locus for severe obesity, at 4p15-p14Steven Stone, Victor Abkevich, Steven C Hunt, et al.
The British Journal of Dermatology|October 29, 2011
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldnessF F Brockschmidt, S Heilmann, J A Ellis, et al.
Translational Psychiatry|July 8, 2015
Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample setsF Degenhardt, L Priebe, S Meier, et al.
American Journal of Human Genetics|November 8, 2003
Predisposition locus for major depression at chromosome 12q22-12q23.2Victor Abkevich, Nicola J Camp, Charles H Hensel, et al.
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