Selected publications
- Understanding inherited risk in unselected newly diagnosed patients with endometrial cancer. Obstetrical and Gynecological Survey. 2019 Comment GET IT
- Correction: Toward automation of germline variant curation in clinical cancer genetics (Genetics in Medicine, (2019), 10.1038/s41436-019-0463-8). Genetics in Medicine. 2019 Article GET IT
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Toward automation of germline variant curation in clinical cancer genetics.
Genetics in Medicine.
2019
Academic Article
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Times cited: 1 -
Prospective Evaluation of Germline Alterations in Patients With Exocrine Pancreatic Neoplasms.
Journal of the National Cancer Institute.
2018
Academic Article
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Times cited: 24 -
Mutation detection in patients with advanced cancer by universal sequencing of cancer-related genes in tumor and normal DNA vs guideline-based germline testing.
JAMA - Journal of the American Medical Association.
2017
Academic Article
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Times cited: 78 -
A recurrent ERCC3 truncating mutation confers moderate risk for breast cancer.
Cancer Discovery.
2016
Academic Article
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Times cited: 14 -
Collaborative science in the next-generation sequencing era: A viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes.
Briefings in Bioinformatics.
2016
Academic Article
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Times cited: 2 -
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
American Journal of Human Genetics.
2016
Academic Article
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Times cited: 40