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M

Ming K. Lee

University of Washington(US)

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98

Papers

17.3K

Citations

48

h-index

68

i10-index

Ming K. Lee is an academic researcher from University of Washington. The author has contributed to research in topics: BRCA gene mutations in cancer & Cancer Genomics and Diagnostics & Ovarian cancer diagnosis and treatment. The author has an h-index of 48, co-authored 84 publications.

ORCID: 0000-0002-4529-9259

Research Topics

BRCA gene mutations in cancer Cancer Genomics and Diagnostics Ovarian cancer diagnosis and treatment Hearing, Cochlea, Tinnitus, Genetics DNA Repair Mechanisms

Papers by this author

works

Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas

2013 · Clinical Cancer Research · 1,018 citations

https://doi.org/10.1158/1078-0432.ccr-13-2287

Kathryn P. Pennington Tom Walsh Maria I. Harrell Ming K. Lee

Validation and Implementation of Targeted Capture and Sequencing for the Detection of Actionable Mutation, Copy Number Variation, and Gene Rearrangement in Clinical Cancer Specimens

2013 · Journal of Molecular Diagnostics · 276 citations

https://doi.org/10.1016/j.jmoldx.2013.08.004

Colin C. Pritchard Stephen J. Salipante Karen M. Koehler Christina Smith

Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study

2017 · Clinical Cancer Research · 230 citations

https://doi.org/10.1158/1078-0432.ccr-17-1327

Barbara M. Norquist Mark F. Brady Maria I. Harrell Tom Walsh

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

2011 · Genome biology · 201 citations

https://doi.org/10.1186/gb-2011-12-9-r89

Zippora Brownstein Lilach M. Friedman Hashem Shahin Varda Oron‐Karni

Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population

2006 · Human Genomics · 54 citations

https://doi.org/10.1186/1479-7364-2-4-203

Tom Walsh Amal Rayan Judeh Abu Sa’ed Hashem Shahin

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene <scp> <i>ATOH1</i> </scp>

2020 · Clinical Genetics · 28 citations

https://doi.org/10.1111/cge.13817

Zippora Brownstein Süleyman Gülsüner Tom Walsh Fábio Tadeu Arrojo Martins

Research topics

topics

BRCA gene mutations in cancer

Cancer Genomics and Diagnostics

Ovarian cancer diagnosis and treatment

Hearing, Cochlea, Tinnitus, Genetics

DNA Repair Mechanisms

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