Nathaniel D. Miller

Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: Evidence for <i>HMX2</i> and <i>HMX3</i> as candidate genes in hearing and vestibular function

Nathaniel D. Miller, Melonie A. Nance, Elizabeth Wohler et al. · American Journal of Medical Genetics Part A · 2009 · 46 citations · Full text

Genetics, Pathology, Molecular Genetics +18

Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio

Jason C. Ting, Elisha Roberson, Nathaniel D. Miller et al. · Human Mutation · 2007 · 46 citations

Origin Effects, Genetics, Human Polymorphism +17

Promoter, alternative splice forms, and genomic structure of protocadherin 15

Kumar N. Alagramam, Nathaniel D. Miller, Nithin D. Adappa et al. · Genomics · 2007 · 23 citations · Full text

Transcriptional Regulation, Natural Sciences, Genetics +7

Estimating Genome-Wide Copy Number Using Allele-Specific Mixture Models

Wenyi Wang, Benilton S. Carvalho, Nathaniel D. Miller et al. · Journal of Computational Biology · 2008 · 18 citations · Full text

Probe Effects, Genetics, Genomics +20