Nicole L. Hoppman‐Chaney

Identification of single gene deletions at 15q13.3: further evidence that <i><scp>CHRNA7</scp></i> causes the 15q13.3 microdeletion syndrome phenotype

Nicole L. Hoppman‐Chaney, KE Wain, PR Seger et al. · Clinical Genetics · 2012 · 132 citations

Developmental Biology, Single Gene Deletions, Microdeletion Syndrome Phenotype +15

Evaluation of Oligonucleotide Sequence Capture Arrays and Comparison of Next-Generation Sequencing Platforms for Use in Molecular Diagnostics

Nicole L. Hoppman‐Chaney, Lisa M. Peterson, Eric W. Klee et al. · Clinical Chemistry · 2010 · 44 citations · Full text

Partial hexasomy for the Prader–Willi–Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome

Nicole L. Hoppman‐Chaney, D. Brian Dawson, Lai P. Nguyen et al. · American Journal of Medical Genetics Part A · 2010 · 43 citations

In‐frame multi‐exon deletion of <i>SMC1A</i> in a severely affected female with Cornelia de Lange Syndrome

Nicole L. Hoppman‐Chaney, Jin Sung Jang, Jin Jen et al. · American Journal of Medical Genetics Part A · 2011 · 25 citations