Michael A. Schmidt

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

Holly N. Cukier, Nicole Dueker, Susan H. Slifer et al. · Molecular Autism · 2014 · 328 citations · Full text

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

Joshua C. Bis, Xueqiu Jian, Brian W. Kunkle et al. · Molecular Psychiatry · 2018 · 257 citations · Full text

Physical Mapping of a Translocation Breakpoint in Neurofibromatosis

Jane W. Fountain, Margaret R. Wallace, M BRUCE et al. · Science · 1989 · 141 citations

Fragile X Syndrome: Diagnosis, Treatment, and Research

Michael A. Schmidt · JAMA · 1997 · 96 citations

Genetics, Genetic Epidemiology, Wright Brothers +20

Cases of neurofibromatosis with rearrangements of chromosome 17 involving band 17q11.2

Michael A. Schmidt, Virginia V. Michels, Gordon W. Dewald et al. · American Journal of Medical Genetics · 1987 · 88 citations

Recklinghausen Neurofibromatosis, Mendelian Disorder, Cytogenetics +11