Anne B. Skvorak

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Fiona E. Karet, Karin E. Finberg, Raoul D. Nelson et al. · Nature Genetics · 1999 · 681 citations

Renal Function, Molecular Physiology, Biochemistry +8

Mutation in Transcription Factor <i>POU4F3</i> Associated with Inherited Progressive Hearing Loss in Humans

Oz Vahava, Robert J. Morell, Eric D. Lynch et al. · Science · 1998 · 348 citations

Mapping and Characterization of a Novel Cochlear Gene in Human and in Mouse: A Positional Candidate Gene for a Deafness Disorder, DFNA9

Nahid G. Robertson, Anne B. Skvorak, Yi Yin et al. · Genomics · 1997 · 141 citations

Developmental Biology, Genetics, Audiology +15

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness

Anne B. Skvorak · Human Molecular Genetics · 1999 · 74 citations

Genetics, Molecular Biology, Gene Characterization +24

An Ancient Conserved Gene Expressed in the Human Inner Ear: Identification, Expression Analysis, and Chromosomal Mapping of Human and Mouse Antiquitin (ATQ1)

Anne B. Skvorak, Nahid G. Robertson, Yi Yin et al. · Genomics · 1997 · 35 citations

Mouse Antiquitin, Developmental Biology, Genetics +5