Sarah Alliman

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Angela L. Duker, Blake C. Ballif, Erawati V. Bawle et al. · European Journal of Human Genetics · 2010 · 320 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

Lisa G. Shaffer, Justine Coppinger, Sarah Alliman et al. · Prenatal Diagnosis · 2008 · 186 citations

Life Sciences, Genetics, Obstetrics +15

Whole‐genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

Justine Coppinger, Sarah Alliman, Allen N. Lamb et al. · Prenatal Diagnosis · 2009 · 173 citations

Life Sciences, Genetics, Molecular Genetics +17

Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array‐based comparative genomic hybridization

Aguinaldo Bonalumi Filho, Josiane Souza, Fábio R. Faucz et al. · American Journal of Medical Genetics Part A · 2011 · 82 citations

Life Sciences, Biology, Genetics +16

The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes

Lisa G. Shaffer, Justine Coppinger, S. Annie Morton et al. · Prenatal Diagnosis · 2011 · 44 citations

Life Sciences, Genetics, Molecular Genetics +17