Jun Shen

5PUBLICATIONS
34CO-AUTHORS
NeurogeneticsInfant and child healthLinguistic structures (incl. phonology, morphology and syntax)Cardiology (incl. cardiovascular diseases)
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Publications (5)

|Jan 05, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing.

Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth

|Jun 08, 2019
A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children.

A Eliot Shearer, Jun Shen, Sami Amr

|Jun 05, 2019
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel.

Jun Shen, Andrea M Oza, Ignacio Del Castillo

|Apr 24, 2015
Gene Expression by Mouse Inner Ear Hair Cells during Development.

Déborah I Scheffer, Jun Shen, David P Corey

|Jan 23, 2015
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.

Ahmed A Alfares, Melissa A Kelly, Gregory McDermott

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