400
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365
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35
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Iris Schrijver
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.
Institution affiliations
Work details
Articles published in PeerJ
October 11th, 2016
Juan Rodriguez-Paris, Jörg Waldhaus, Jeenal A. Gordhandas, Lynn Pique, Iris Schrijver
March 10th, 2016
Iris Schrijver, Keri J.S. Brady, Mickey Trockel
Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss
May 8th, 2014
Lynn M. Pique, Marie-Luise Brennan, Colin J. Davidson, Frederick Schaefer, John Greinwald Jr, Iris Schrijver
July 2nd, 2013
Jason D. Merker, Naomi O’Grady, Linda Gojenola, Mai Dao, Ross Lenta, Joanne M. Yeakley, Iris Schrijver
Preprints
Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss
March 7th, 2014
Lynn M Pique, Marie-Luise Brennan, Colin J Davidson, Frederick Schaefer, John Greinwald Jr., Iris Schrijver