Kristin Herman

Autism Profiles of Males With Fragile X Syndrome

Susan Harris, David Hessl, Beth L. Goodlin‐Jones et al. · American Journal on Mental Retardation · 2008 · 388 citations

Autism Profiles, Disability, Diagnosis +17

Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational histories

Kara E. Koehler, Christina Boulton, Heather E. Collins et al. · Nature Genetics · 1996 · 170 citations

Chromatin, Different Recombinational Histories, Developmental Biology +10

Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

Scott C. Bell, Justine Rousseau, Huashan Peng et al. · The American Journal of Human Genetics · 2019 · 87 citations · Full text

Neurodevelopmental Disorders, Human Neurons, Synaptic Plasticity +11

A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and Deafness

Margaret J. Kovach, Jing‐Ping Lin, Simeon A. Boyadjiev et al. · The American Journal of Human Genetics · 1999 · 83 citations · Full text

Mendelian Disorder, Genetic Disorder, Pmp22 Gene Is +8

Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders

Hui Guo, Elisa Bettella, Paul C. Marcogliese et al. · Nature Communications · 2019 · 59 citations · Full text