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Shanaka R. Gunawardena

Observed names: Gunawardena, Shanaka, Gunawardena, Shanaka R., Shanaka Gunawardena
Observed institutions: University of Southern California, University of Minnesota, Mayo Clinic, The University of Melbourne, University of Toronto, University of Kansas Medical Center
OpenAlex ID: A5040988985
Identification of Lynch Syndrome Among Patients With Colorectal Cancer
2012 · Leticia Moreira, Francesc Balaguer, et al. · JAMA · 556
Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study
2012 · Aung Ko Win, Joanne P. Young, et al. · Journal of Clinical Oncology · 333
Cancer Risks forMLH1andMSH2Mutation Carriers
2012 · James G. Dowty, Aung K. Win, et al. · Human Mutation · 244
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes
2017 · Melissa S. DeRycke, Shanaka Gunawardena, et al. · Molecular Genetics & Genomic Medicine · 45
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Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2013 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al. · Cancer Epidemiology Biomarkers & Prevention · 40
Mutations of SMAD4 account for both LAPS and Myhre syndromes
2012 · Noralane M. Lindor, Shanaka R. Gunawardena, et al. · American Journal of Medical Genetics Part A · 29
NOM1 Targets Protein Phosphatase I to the Nucleolus
2007 · Shanaka R. Gunawardena, Brian L. Ruis, et al. · Journal of Biological Chemistry · 24
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Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations
2012 · Noralane M. Lindor, Tom C. Smyrk, et al. · Familial Cancer · 5
Data from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
Data from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
Supplementary Figure 2 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
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Description of supplementary files from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
Supplementary Tables from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
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Supplementary Figure 1 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
Supplementary Figure 1 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
PDF
Supplementary Tables from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
Supplementary Figure 2 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
Description of supplementary files from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
2023 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al.
PDF
Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study
2020 · Winship, Ingrid, Young, Graeme P., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Identification of Lynch Syndrome Among Patients With Colorectal Cancer
2020 · Moreno, Victor, Gallinger, Steven, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Abstract 2548: Targeted sequencing to identify rare variants in colorectal cancer.
2013 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al. · Cancer Research
Identification of Risk Genes through Whole Exome Sequencing in the Colon Cancer Family Registry
2012 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al. · Genetic Epidemiology
Abstract 2742: Assessment of next generation platforms and use of duplicate runs for whole exome sequencing
2011 · Melissa S. DeRycke, Shanaka R. Gunawardena, et al. · Cancer Research
Works count: 26
Citation count: 1,276
H-index: 7
I10-index: 7
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