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PeerJ Author & Reviewer

485 Points

Contributions by role

Contributions by subject area

Iris Schrijver

PeerJ Author & Reviewer

Summary

Iris Schrijver, M.D. holds specialty certification in Clinical Molecular Genetics and Clinical Pathology. She directs the diagnostic Molecular Pathology laboratory at Stanford University Medical Center and Lucile Packard Children's Hospital. Her research interests include the genetic basis and genotype-phenotype correlations in cystic fibrosis and hereditary hearing loss, and the development and application of diagnostic innovations.

Medical Genetics Molecular Biology Pathology

Editorial Board Member

PeerJ - the Journal of Life & Environmental Sciences

Past or current institution affiliations

Stanford University

Work details

Adjuct Professor of Pathology

Stanford University

Pathology

PeerJ Contributions

Articles 4
Preprints 1

October 11, 2016

Comparative functional characterization of novel non-syndromic GJB2 gene variant p.Gly45Arg and lethal syndromic variant p.Gly45Glu

Juan Rodriguez-Paris, Jörg Waldhaus, Jeenal A. Gordhandas, Lynn Pique, Iris Schrijver

https://doi.org/10.7717/peerj.2494 PubMed 27761313

March 10, 2016

An exploration of key issues and potential solutions that impact physician wellbeing and professional fulfillment at an academic center

Iris Schrijver, Keri J.S. Brady, Mickey Trockel

https://doi.org/10.7717/peerj.1783 PubMed 26989621

May 8, 2014

Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss

Lynn M. Pique, Marie-Luise Brennan, Colin J. Davidson, Frederick Schaefer, John Greinwald Jr, Iris Schrijver

https://doi.org/10.7717/peerj.384 PubMed 24860705

July 2, 2013

Feasibility of using microbeads with holographic barcodes to track DNA specimens in the clinical molecular laboratory

Jason D. Merker, Naomi O’Grady, Linda Gojenola, Mai Dao, Ross Lenta, Joanne M. Yeakley, Iris Schrijver

https://doi.org/10.7717/peerj.91 PubMed 23862106

March 7, 2014 - Version: 1

Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss

Lynn M Pique, Marie-Luise Brennan, Colin J Davidson, Frederick Schaefer, John Greinwald Jr., Iris Schrijver

https://doi.org/10.7287/peerj.preprints.275v1