Concepedia

Stephanie Newton

SN

6

Publications

410

Citations

6

H-Index

2009

Active since

Affiliations

Center for Human Genetics(Current)

Boston University

Stephanie Newton is an author at Center for Human Genetics specializing in molecular genetics, genetics, and medicine.

Top concepts

Publications per year

2009–2010

6

Publications

6

A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export

Chen Zhang, Jeff M. Milunsky, Stephanie Newton et al. · Journal of Neuroscience · 2009 · 186 citations · Full text

A complex maternal rearrangement results in a pure 10.8 Mb duplication of the 5q13.1–q14.1 region in an affected son

Ying Zou, Stephanie Newton, Jeff M. Milunsky · American Journal of Medical Genetics Part A · 2010 · 71 citations

Novel de novo <i>PCDH19</i> mutations in three unrelated females with epilepsy female restricted mental retardation syndrome

Seema M. Jamal, Raveen Basran, Stephanie Newton et al. · American Journal of Medical Genetics Part A · 2010 · 55 citations

A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (<i>AUTS2</i>) gene in a patient with autism

Xinli Huang, Ying Zou, Tom A. Maher et al. · American Journal of Medical Genetics Part A · 2010 · 49 citations

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Neonatal ventral hippocampus lesion induces increase in no levels which is attenuated by subchronic haloperidol treatment

José Vicente Negrete‐Díaz, Eduardo Baltazar‐Gaytán, María Elena Bringas et al. · Synapse · 2010 · 30 citations

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