Robert James Morell

Dr. Robert James Morell

orcid

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2001 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
JBJulie M. Bork
Julie M. Bork
LPLinda Peters
Linda Peters
SRSaima Riazuddin
Saima Riazuddin
SBSteve L. Bernstein
Steve L. Bernstein
ZAZubair M. Ahmed
Zubair M. Ahmed
RMRobert James Morell
Robert James Morell

19 November 1998 in New England Journal of Medicine
Verified
Journal Article
Open access
PDF file
RMRobert James Morell
Robert James Morell
HKHung Jeff Kim
Hung Jeff Kim
LHLinda J. Hood
Linda J. Hood
LGLeah Goforth
Leah Goforth
KFKaren Friderici
Karen Friderici
JDJan Dumon
Jan Dumon
Mutations in the GJB2 gene cause one form of nonsyndromic recessive deafness. Among Mediterranean Europeans, more than 80 percent of cases of nonsyndromic recessive deafness result from inheritance of the 30delG mutant allele of GJB2. We assessed the contribution of mutations in GJB2 to the prevalence of the condition among Ashkenazi Jews.

1 January 2001 in Cell
Verified
Journal Article
Closed access
EWEdward R Wilcox
Edward R Wilcox
QBQuianna L Burton
Quianna L Burton
SNSadaf Naz
Sadaf Naz
SRSaima Riazuddin
Saima Riazuddin
TSTenesha N Smith
Tenesha N Smith
TFThomas B Friedman
Thomas B Friedman

29 May 1998 in Science
Verified
Journal Article
Open access
PDF file
AWAihui Wang
Aihui Wang
YLYong Liang
Yong Liang
RFRobert A. Fridell
Robert A. Fridell
FPFrank J. Probst
Frank J. Probst
EWEdward R. Wilcox
Edward R. Wilcox
TFThomas B. Friedman
Thomas B. Friedman
DFNB3 , a locus for nonsyndromic sensorineural recessive deafness, maps to a 3-centimorgan interval on human chromosome 17p11.2, a region that shows conserved synteny with mouse shaker-2 . A human unconventional myosin gene, MYO15 , was identified by combining functional and positional cloning approaches in searching for shaker-2 and DFNB3 . MYO15 has at least 50 exons spanning 36 kilobases. Sequence analyses of these exons in affected individuals from three unrelated DFNB3 families revealed two missense mutations and one nonsense mutation that cosegregated with congenital recessive deafness.

1 July 2001 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
ZAZubair M. Ahmed
Zubair M. Ahmed
SRSaima Riazuddin
Saima Riazuddin
SBSteve L. Bernstein
Steve L. Bernstein
ZAZahoor Ahmed
Zahoor Ahmed
SKShaheen Khan
Shaheen Khan
EWEdward R. Wilcox
Edward R. Wilcox

15 October 2015 in Nature Communications
Verified
Journal Article
Open access
PDF file
JBJoseph C. Burns
Joseph C. Burns
MKMichael C. Kelly
Michael C. Kelly
MHMichael Hoa
Michael Hoa
RMRobert James Morell
Robert James Morell
MKMatthew Kelley
Matthew Kelley
In the inner ear, cochlear and vestibular sensory epithelia utilize grossly similar cell types to transduce different stimuli: sound and acceleration. Each individual sensory epithelium is composed of highly heterogeneous populations of cells based on physiological and anatomical criteria. However, limited numbers of each cell type have impeded transcriptional characterization. Here we generated transcriptomes for 301 single cells from the utricular and cochlear sensory epithelia of newborn mice to circumvent this challenge. Cluster analysis indicates distinct profiles for each of the major sensory epithelial cell types, as well as less-distinct sub-populations. Asynchrony within utricles allows reconstruction of the temporal progression of cell-type-specific differentiation and suggests possible plasticity among cells at the sensory–nonsensory boundary. Comparisons of cell types from utricles and cochleae demonstrate divergence between auditory and vestibular cells, despite a common origin. These results provide significant insights into the developmental processes that form unique inner ear cell types.