Kingshuk Das

Invitae (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

14h-index1.9kcitations27works0.02yr avg
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Research Topics

Cancer Genomics and Diagnostics(7), BRCA gene mutations in cancer(6), Genetic factors in colorectal cancer(5), Genomics and Rare Diseases(5), NF-κB Signaling Pathways(3)

Publications27 total

Integrated germline and somatic cancer testing provides opportunity to identify cancer risk and resolve variant origins.
Journal of Clinical Oncology·2022
Yield and Utility of Germline Testing Following Tumor Sequencing in Patients With Cancer
JAMA Network Open·2020· 122 citedOpen Access
Diagnostic yield and clinical utility of germline genetic testing following somatic testing in breast cancer patients.
Journal of Clinical Oncology·2020
Diagnostic yield of germline genetic testing following tumor testing in prostate cancer patients.
Journal of Clinical Oncology·2020· 1 cited
Expansion of germline genetic testing criteria for prostate cancer yields findings across all stages of disease.
Journal of Clinical Oncology·2020
Effect of access to germline genetic testing on pancreatic cancer precision treatment across disease stage and ethnicity.
Journal of Clinical Oncology·2020
Clinical utility of germline genetic testing after tumor genomic testing in colorectal cancer patients.
Journal of Clinical Oncology·2020
Genomic Adequacy from Solid Tumor Core Needle Biopsies of ex Vivo Tissue and in Vivo Lung Masses: Prospective Study
Radiology·2016· 37 cited
Increased prevalence of two mitochondrial DNA polymorphisms in functional disease: Are we describing different parts of an energy-depleted elephant?
Mitochondrion·2015· 25 cited
Instability of a dinucleotide repeat in the 3′‐untranslated region (UTR) of the microsomal prostaglandin E synthase‐1 (<i>mPGES</i>‐1) gene in microsatellite instability‐high (MSI‐H) colorectal carcinoma
Molecular Oncology·2015· 1 citedOpen Access
region (UTR) of the microsomal prostaglandin E synthase-1 (mPGES-1) gene in microsatellite instability-high (MSI-H) colorectal carcinoma
2015
Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders
JAMA·2014· 971 citedOpen Access
Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory
Genetics in Medicine·2014· 134 citedOpen Access
Nanofilaments on glioblastoma exosomes revealed by peak force microscopy
Journal of The Royal Society Interface·2014· 64 citedOpen Access
Translational utility of next-generation sequencing
Genomics·2013· 35 cited
Molecular Testing: Regulatory Issues
2012
Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing
Expert Review of Molecular Diagnostics·2012· 95 citedOpen Access
Clinical Utility of Pharmacogenetic Biomarkers in Cardiovascular Therapeutics: a Challenge for Clinical Implementation
Pharmacogenomics·2012· 31 citedOpen Access
71 Two common mtDNA polymorphisms are associated with sudden infant death syndrome (SIDS)
Mitochondrion·2010
Evaluation of a Novel Chromogenic Agar Medium for Isolation and Differentiation of Vancomycin-Resistant <i>Enterococcus faecium</i> and <i>Enterococcus faecalis</i> Isolates
Journal of Clinical Microbiology·2007· 38 citedOpen Access
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Frequent Co-authors

Wayne W. Grody(7), Robert L. Nussbaum(7), Sarah M. Nielsen(7), Nhu Ngo(7), Edward D. Esplin(7), Stephen E. Lincoln(6), Scott T. Michalski(6), Shan Yang(6), Joshua L. Deignan(5), Frank S Ong(4), Daniel Esteban Pineda Alvarez(4), Anju Agarwal(3), Natalia Lerner(3), Nywana Sizemore(3), Hane Lee(2), Samuel P. Strom(2), Éric Vilain(2), Stanley F. Nelson(2), Jane Kuo(2), Kenneth E. Bernstein(2)