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Ryan J. Carlson
Observed names:
Carlson, Ryan James,
Ryan Carlson,
Ryan J Carlson
Institution:
University of Washington
Observed institutions:
National Institutes of Health,
University of Washington,
National Institute of Allergy and Infectious Diseases
ORCID:
0000-0001-8311-481X
Observed ORCID:
0000-0001-8311-481X
OpenAlex ID:
A5050573001
Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number
2016
·
Jonathan J Lyons
, Xiaomin Yu
, et al.
·
Nature Genetics
·
394
Genomic analysis of inherited hearing loss in the Palestinian population
2020
·
Amal Abu Rayyan
, Lara Kamal
, et al.
·
Proceedings of the National Academy of Sciences
·
65
PDF
Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes
2023
·
Ryan J. Carlson
, Tom Walsh
, et al.
·
JAMA Otolaryngology–Head & Neck Surgery
·
40
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1
2020
·
Zippora Brownstein
, Suleyman Gulsuner
, et al.
·
Clinical Genetics
·
31
PDF
Gene Therapy for Hearing Loss: Which Genes Next?
2025
·
Ryan J. Carlson
, Shahar Taiber
, et al.
·
Otology & Neurotology
·
15
Emerging complexities of the mouse as a model for human hearing loss
2022
·
Ryan J. Carlson
, Karen B. Avraham
·
Proceedings of the National Academy of Sciences
·
14
Detection of phosphoglucomutase-3 deficiency by lectin-based flow cytometry
2017
·
Ryan J. Carlson
, Michelle R. Bond
, et al.
·
Journal of Allergy and Clinical Immunology
·
12
PDF
Behavioral characterization of the cochlear amplifier lesion due to loss of function of stereocilin (STRC) in human subjects
2023
·
Charlotte Benoit
, Ryan J. Carlson
, et al.
·
Hearing Research
·
5
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder
2021
·
Ryan J. Carlson
, Alicia Quesnel
, et al.
·
Otology & Neurotology
·
4
Diagnostic Yield in Childhood-Onset Hearing Loss: A Meta-Analysis and Systematic Review
2026
·
Shahar Taiber
, Ryan J. Carlson
, et al.
·
Life
·
2
PDF
A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss
2023
·
Amal Aburayyan
, Ryan J Carlson
, et al.
·
Human Molecular Genetics
·
1
PDF
Merkel Cell Carcinoma
2017
·
Ryan J. Carlson
, Paul Nghiem
·
CRC Press eBooks
·
1
Letter to the Editor Regarding “hearing Preservation and Spatial Hearing Outcomes After Cochlear Implantation in Children With Tmprss3 Mutations”
2023
·
Ryan J. Carlson
, Jay Rubinstein
·
Otology & Neurotology
PDF
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Works count:
14
Citation count:
584
H-index:
7
I10-index:
7
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