Karl V. Voelkerding

Biochemistry, Genetics and Molecular Biology · Life Sciences

40h-index37.9kcitations120works2.02yr avg
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Research Topics

Genomics and Rare Diseases(32), Cancer Genomics and Diagnostics(20), Molecular Biology Techniques and Applications(19), Genetic factors in colorectal cancer(13), Genomic variations and chromosomal abnormalities(12)

Publications120 total

Genomic Reporting Practices Across 5 Molecular Disciplines: A Study From the College of American Pathologists
Archives of Pathology & Laboratory Medicine·2024· 2 citedOpen Access
Implementation, Evolution, and Laboratory Performance of Methods-Based Proficiency Testing for Next-Generation Sequencing Detection of Germline Sequence Variants
Archives of Pathology & Laboratory Medicine·2023· 2 citedOpen Access
Four-Year Laboratory Performance of the First College of American Pathologists In Silico Next-Generation Sequencing Bioinformatics Proficiency Testing Surveys
Archives of Pathology & Laboratory Medicine·2022· 7 citedOpen Access
Creation of an Expert Curated Variant List for Clinical Genomic Test Development and Validation
Journal of Molecular Diagnostics·2021· 7 citedOpen Access
Creation of an Expert Curated Variant List for Clinical Genomic Test Development and Validation: A ClinGen and GeT-RM Collaborative Project
2021· 1 citedOpen Access
Laboratory and Clinical Implications of Incidental and Secondary Germline Findings During Tumor Testing
Archives of Pathology & Laboratory Medicine·2021· 26 citedOpen Access
A Primer on Chimeric Antigen Receptor T-cell Therapy: What Does It Mean for Pathologists?
Archives of Pathology & Laboratory Medicine·2020· 2 citedOpen Access
CXXC5 variant in an immunodeficient patient with a progressive loss of hematopoietic cells
Journal of Allergy and Clinical Immunology·2020· 3 cited
Abstract 2119: Gene mapping in high-risk chronic lymphocytic leukemia pedigree identifies risk locus at chromosome 2q22.1
Cancer Research·2020
Development and Validation of Targeted Next-Generation Sequencing Panels for Detection of Germline Variants in Inherited Diseases
UNC Libraries·2020Open Access
Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease
UNC Libraries·2020Open Access
Frontline Science: Cxxc5 expression alters cell cycle and myeloid differentiation of mouse hematopoietic stem and progenitor cells
Journal of Leukocyte Biology·2020· 20 cited
Issue Information
Cytometry Part B Clinical Cytometry·2019Open Access
Evaluation of Mass Cytometry in the Clinical Laboratory
Cytometry Part B Clinical Cytometry·2019· 10 citedOpen Access
Designing and Implementing NGS Tests for Inherited Disorders
Journal of Molecular Diagnostics·2018· 29 cited
Bioinformatics Tools in Clinical Genomics
2018
Ikaros family zinc finger 1 regulates dendritic cell development and function in humans
Nature Communications·2018· 78 citedOpen Access
Response to Biesecker and Harrison
Genetics in Medicine·2018· 7 citedOpen Access
Novel <i>PLP1</i> Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical Phenotypes
Child Neurology Open·2018· 2 citedOpen Access
Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines
Journal of Molecular Diagnostics·2017· 450 cited
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Frequent Co-authors

Jacob Durtschi(17), Carl T. Wittwer(11), Shale Dames(8), Rebecca L. Margraf(8), Madhuri Hegde(6), Nazneen Aziz(5), Birgit Funke(5), Emily Coonrod(5), Attila Kumánovics(5), Ira M. Lubin(4), Jason D. Merker(4), Martin G. Reese(4), Karen E. Weck(4), Mark G. Herrmann(4), Harry R. Hill(4), Mark Yandell(4), Michael Seipp(4), Daniel F. Klessig(4), David Bick(3), Wayne W. Grody(3)