Richard J. Schroer

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

Andrew J. Sharp, Heather C. Mefford, Kelly Li et al. · Nature Genetics · 2008 · 588 citations

Mendelian Disorder, Genetic Disorder, Psychiatric Genetics +9

Autism and maternally derived aberrations of chromosome 15q

Richard J. Schroer, Mary C. Phelan, Ron C. Michaelis et al. · American Journal of Medical Genetics · 1998 · 372 citations

High frequency of neurexin 1β signal peptide structural variants in patients with autism

Jinong Feng, Richard J. Schroer, Yan Jin et al. · Neuroscience Letters · 2006 · 263 citations

Neurexin 1β, Molecular Neuroscience, Syndromic Autism +9

Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders

Luigi Boccuto, Maria Lauri, Sara M. Sarasua et al. · European Journal of Human Genetics · 2012 · 243 citations · Full text

Psychiatry, Autism Spectrum Disorders, Syndromic Autism +9

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for <i>UBE3A</i>

Yong‐hui Jiang, Trilochan Sahoo, Ron C. Michaelis et al. · American Journal of Medical Genetics Part A · 2004 · 158 citations