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Ming K. Lee

University of California, Santa Barbara · US
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Area of research
Genetics · Reproductive Medicine
Research interest
Research interests include Medicine, Biology, Oncology, Germline, Breast cancer, and Ovarian cancer.
h-index
citations
4,221
works
13
NIH funding
primary concept
email

Recent publications

Inherited predisposition to malignant mesothelioma and overall survival following platinum chemotherapy
Proceedings of the National Academy of Sciences 2019cited by 156position: middledoi
Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study
Clinical Cancer Research 2017cited by 233position: middledoi
Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy
Biology of Blood and Marrow Transplantation 2016cited by 50position: middledoi
Inherited Mutations in Women With Ovarian Carcinoma
JAMA Oncology 2015cited by 760position: middledoi
Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy
Nature Genetics 2015cited by 358position: middledoi
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies
Blood 2015cited by 218position: middledoi
Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy‐related leukemia
Cancer 2015cited by 170position: middledoi
Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
New England Journal of Medicine 2014cited by 696position: middledoi
Population-based screening for breast and ovarian cancer risk due to<i>BRCA1</i>and<i>BRCA2</i>
Proceedings of the National Academy of Sciences 2014cited by 345position: middledoi
Inherited predisposition to breast cancer among African American women
Breast Cancer Research and Treatment 2014cited by 150position: middledoi
Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network
Cell 2013cited by 566position: middledoi
Validation and Implementation of Targeted Capture and Sequencing for the Detection of Actionable Mutation, Copy Number Variation, and Gene Rearrangement in Clinical Cancer Specimens
Journal of Molecular Diagnostics 2013cited by 279position: middledoi
Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease
The American Journal of Human Genetics 2013cited by 240position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Mary‐Claire King · Hebrew University of Jerusalem9 papers (2013–2019)Barbara Neistadt · University of Colorado Denver4 papers (2014–2016)Jane E. Churpek · University of Wisconsin–Madison4 papers (2013–2016)Süleyman Gülsüner · Hebrew University of Jerusalem4 papers (2015–2019)Rafael Márquez · Museo Nacional de Ciencias Naturales4 papers (2014–2016)Colin C. Pritchard · Seattle University3 papers (2013–2015)Silvia Casadei · University of Washington3 papers (2014–2017)Lucy A. Godley · Northwestern University3 papers (2015–2016)Elizabeth M. Swisher · University of Washington2 papers (2015–2017)Matthew M. Churpek · University of Wisconsin–Madison2 papers (2014–2015)Sioḃán Keel · University of Washington2 papers (2015–2016)Jane Churpek · University of Wisconsin System2 papers (2014–2019)Dezheng Huo · Chicago Department of Public Health2 papers (2014–2015)Maria I. Harrell · LabCorp (United States)2 papers (2015–2017)Heather A. Lankes · NRG Oncology2 papers (2015–2017)Akiko Shimamura · Harvard University2 papers (2015–2016)Barbara M. Norquist · University of Washington2 papers (2015–2017)Nilsa C. Ramirez · University of North Carolina at Pembroke2 papers (2015–2017)Olufunmilayo I. Olopade · Chicago Department of Public Health2 papers (2014–2015)Robert A. Burger · Mersana Therapeutics (United States)2 papers (2015–2017)
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