Iris Schrijver

University of North Carolina at Chapel Hill — United States

Neuroscience · Life Sciences

38h-index5.3kcitations129works0.02yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(22), Cystic Fibrosis Research Advances(20), Genomics and Rare Diseases(18), Connexins and lens biology(17), Cancer Genomics and Diagnostics(14)

Publications129 total

A panoramic view of the accuracy of molecular genetic testing
UNC Libraries·2024Open Access
Potential pitfalls in multiplex PCR-based next-generation sequencing: a case-based report
Journal of Clinical Pathology·2022
A Curriculum for Genomic Education of Molecular Genetic Pathology Fellows
Journal of Molecular Diagnostics·2021· 6 cited
Development and Characterization of Reference Materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 Genetic Testing
UNC Libraries·2020Open Access
Developing Gene-Specific Meta-Predictor of Variant Pathogenicity
2017· 2 citedOpen Access
Comparative functional characterization of novel non-syndromic<i>GJB2</i>gene variant p.Gly45Arg and lethal syndromic variant p.Gly45Glu
PeerJ·2016· 8 citedOpen Access
A panoramic view of the accuracy of molecular genetic testing
Genetics in Medicine·2016· 2 citedOpen Access
Cystic fibrosis newborn screening programs: implications of the CFTR variant spectrum in nonwhite patients
Genetics in Medicine·2016· 50 citedOpen Access
An exploration of key issues and potential solutions that impact physician wellbeing and professional fulfillment at an academic center
PeerJ·2016· 61 citedOpen Access
Pathology in the Medical Profession?: Taking the Pulse of Physician Wellness and Burnout
Archives of Pathology & Laboratory Medicine·2016· 56 citedOpen Access
Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic Fibrosis
Journal of Molecular Diagnostics·2016· 33 citedOpen Access
The Spectrum of CFTR Variants in Nonwhite Cystic Fibrosis Patients
Journal of Molecular Diagnostics·2015· 116 cited
Cystic Fibrosis
Journal of Molecular Diagnostics·2015· 81 cited
Lymph node involvement by mycosis fungoides and Sézary syndrome mimicking angioimmunoblastic T-cell lymphoma
Human Pathology·2015· 5 cited
The Evolving Role of the Laboratory Professional in the Age of Genome Sequencing
Journal of Molecular Diagnostics·2015· 15 citedOpen Access
Genomics in the Clinic: Ethical and Policy Challenges in Clinical Next-Generation Sequencing Programs at Early Adopter USA Institutions
Personalized Medicine·2015· 3 cited
A randomized study of temozolomide or temozolomide and capecitabine in patients with advanced pancreatic neuroendocrine tumors: A trial of the ECOG-ACRIN Cancer Research Group (E2211).
Journal of Clinical Oncology·2015· 114 cited
Assessment of epithelial sodium channel variants in nonwhite cystic fibrosis patients with non-diagnostic CFTR genotypes
Journal of Cystic Fibrosis·2015· 4 citedOpen Access
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss
BMC Genomics·2014· 39 citedOpen Access
Variation in pre-PCR processing of FFPE samples leads to discrepancies in <i>BRAF</i> and <i>EGFR</i> mutation detection: a diagnostic RING trial
Journal of Clinical Pathology·2014· 43 citedOpen Access
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Frequent Co-authors

James L. Zehnder(8), Lynn Pique(6), Juan Rodriguez‐Paris(5), Phyllis Gardner(5), Karen E. Weck(4), Uta Francke(4), Nazneen Aziz(3), Wayne W. Grody(3), Karl V. Voelkerding(3), Thomas Brenn(3), Heinz Furthmayr(3), Narasimhan Nagan(3), Teri A. Longacre(3), Martin Kharrazi(3), Margaret A. Kenna(2), Heidi L. Rehm(2), Desirée du Sart(2), Lies H. Hoefsloot(2), Jane S. Gibson(2), Debra G. B. Leonard(2)