Sarika U. Peters

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

Trilochan Sahoo, Daniela del Gaudio, Jennifer R. German et al. · Nature Genetics · 2008 · 664 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Autism and other neuropsychiatric symptoms are prevalent in individuals with <i>MeCP2</i> duplication syndrome

Melissa B. Ramocki, Sarika U. Peters, Y. Jane Tavyev et al. · Annals of Neurology · 2009 · 301 citations · Full text

Life Sciences, Genetics, Pediatrics +17

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

Jonathan S. Berg, Nicola Brunetti‐Pierri, Sarika U. Peters et al. · Genetics in Medicine · 2007 · 191 citations

Medicine, Genetics, Pediatrics +13

A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations

Jennifer Gentile, Wen‐Hann Tan, Lucia T. Horowitz et al. · Journal of Developmental & Behavioral Pediatrics · 2010 · 167 citations

Education, Human Development, Pediatrics +17

Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype–phenotype correlations

Trilochan Sahoo, Carlos A. Bacino, Jennifer R. German et al. · European Journal of Human Genetics · 2007 · 149 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15