Robert J. Morell

Overview

Best Publications

• Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness

  Morell Rj;Kim Hj;Hood Lj;Goforth L

  747
  Citations

• Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

  Julie M. Bork;Linda M. Peters;Saima Riazuddin;Saima Riazuddin;Steve L. Bernstein

  642
  Citations

• Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

  Edward R Wilcox;Quianna L Burton;Sadaf Naz;Saima Riazuddin;Saima Riazuddin

  556
  Citations

• Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene

  Frank J. Probst;Robert A. Fridell;Yehoash Raphael;Thomas L. Saunders

  544
  Citations

• Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3

  Aihui Wang;Yong Liang;Robert A. Fridell;Frank J. Probst

  523
  Citations

• Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

  Zubair M. Ahmed;Saima Riazuddin;Steve L. Bernstein;Zahoor Ahmed

  479
  Citations

• Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

  Oz Vahava;Robert Morell;Eric D. Lynch;Sigal Weiss

  430
  Citations

• A dysbiotic microbiome triggers T H 17 cells to mediate oral mucosal immunopathology in mice and humans.

  Nicolas Dutzan;Nicolas Dutzan;Tetsuhiro Kajikawa;Loreto Abusleme;Loreto Abusleme;Teresa Greenwell-Wild

  343
  Citations

• CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

  L.M. Astuto;J.M. Bork;M.D. Weston;J.W. Askew

  255
  Citations

• Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)

  M. Zhu;T. Yang;S. Wei;A.T. DeWan

  253
  Citations

• Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

  Emma M. Jenkinson;Atteeq U. Rehman;Tom Walsh;Jill Clayton-Smith

  245
  Citations

• Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

  Atteeq Ur Rehman;Atteeq Ur Rehman;Robert J. Morell;Inna A. Belyantseva;Shahid Y. Khan

  240
  Citations

• Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear

  Joseph C. Burns;Michael C. Kelly;Michael Hoa;Robert J. Morell

  233
  Citations

• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

  Zubair M. Ahmed;Robert J. Morell;Saima Riazuddin;Andrea Gropman

  233
  Citations

• Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2

  Julie M. Schultz;Yandan Yang;Ariel J. Caride;Adelaida G. Filoteo

  207
  Citations

• Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.

  Arti Pandya;Kathleen S. Arnos;Xia J. Xia;Katherine O. Welch

  196
  Citations

• Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.

  Sadaf Naz;Chantal M. Giguere;David C. Kohrman;Kristina L. Mitchem

  167
  Citations

• Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.

  Ayala Lagziel;Zubair M. Ahmed;Julie M. Schultz;Robert J. Morell

  160
  Citations

• Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

  Linda M. Peters;David W. Anderson;Andrew J. Griffith;Kenneth M. Grundfast

  138
  Citations

• Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

  Guntram Borck;Atteeq Ur Rehman;Atteeq Ur Rehman;Kwanghyuk Lee;Hans Martin Pogoda

  134
  Citations