Andrea Oza

4PUBLICATIONS
24CO-AUTHORS
NeurogeneticsLinguistic structures (incl. phonology, morphology and syntax)Gene expression (incl. microarray and other genome-wide approaches)Decision making
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Publications (4)

|Jan 25, 2021
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients.

Sacha Laurent, Corinne Gehrig, Thierry Nouspikel

|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

|Oct 13, 2018
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss.

Andrea M Oza, Marina T DiStefano, Sarah E Hemphill

|Sep 08, 2018
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion.

Ahmad N Abou Tayoun, Tina Pesaran, Marina T DiStefano

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Frequent Collaborators

3 joint publications

Heidi L Rehm

3 joint publications

Sami S Amr

3 joint publications

Ahmad N Abou Tayoun

1 joint publications

Jun Shen