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Iris Schrijver
PeerJ Author & Reviewer
485 Points

Contributions by role

Author 435
Preprint Author 35
Reviewer 15

Contributions by subject area

Genetics
Otorhinolaryngology
Pathology
Pediatrics
Medical Genetics
Health Policy
Psychiatry and Psychology
Public Health
Ethical Issues
Science and Medical Education
Molecular Biology
Biotechnology

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

Editing Journals

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