Jessica B. Mandell

University of Washington — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

17h-index5.0kcitations36works4.32yr avg
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Research Topics

BRCA gene mutations in cancer(23), DNA Repair Mechanisms(10), Cancer Genomics and Diagnostics(7), Genomic variations and chromosomal abnormalities(6), Nutrition, Genetics, and Disease(6)

Publications36 total

Genetic regulation of the estrogen receptor and inherited predisposition to breast cancer
Proceedings of the National Academy of Sciences·2025Open Access
Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms
Journal of Medical Genetics·2025· 3 citedOpen Access
<i>TP53</i> missense allele predisposing to high risk of breast cancer but not pediatric cancers
JNCI Journal of the National Cancer Institute·2024· 4 cited
Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes
Genome Research·2024· 10 citedOpen Access
Data from Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer
2023Open Access
Supplementary Tables 1-4, Figure 1 from Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer
2023Open Access
Data from Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer
2023Open Access
Supplementary Tables 1-4, Figure 1 from Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer
2023Open Access
Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes
JAMA Otolaryngology–Head & Neck Surgery·2023· 31 citedOpen Access
CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in <i>BRCA1</i> and other tumour suppressor genes
Journal of Medical Genetics·2020· 29 citedOpen Access
Characterization of splice-altering mutations in inherited predisposition to cancer
Proceedings of the National Academy of Sciences·2019· 46 citedOpen Access
Genetic Predisposition to Breast Cancer Due to Mutations Other Than <i>BRCA1</i> and <i>BRCA2</i> Founder Alleles Among Ashkenazi Jewish Women
JAMA Oncology·2017· 63 citedOpen Access
Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53
International Journal of Cancer·2017· 40 citedOpen Access
Haplotype analyses of the c.1027C&gt;T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2
Breast Cancer Research and Treatment·2016· 12 citedOpen Access
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease
Molecular Case Studies·2016· 15 citedOpen Access
Abstract AS09: Germline mutations in cancer susceptibility genes in BRCA1 and BRCA2 negative families with ovarian and breast cancer
Clinical Cancer Research·2015· 1 cited
Germline mutations in cancer susceptibility genes in brca1 and brca2 negative families with ovarian and breast cancer
Gynecologic Oncology·2014· 1 cited
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·2014· 339 citedOpen Access
Corrigendum to: Loss of function germline mutations in RAD51D in women with ovarian carcinoma [Gynecol Oncol 127: 552–555, 2012]
Gynecologic Oncology·2013· 4 cited
Next generation sequencing to identify inherited mutations in all breast cancer genes in three breast cancer cohorts
Journal of the American College of Surgeons·2013
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Frequent Co-authors

Mary‐Claire King(27), Tom Walsh(23), Silvia Casadei(15), Ming K. Lee(12), Sunday M. Stray(10), Barbara M. Norquist(10), Süleyman Gülsüner(10), Elizabeth M. Swisher(8), Joan H. Marks(5), Ephrat Levy‐Lahad(5), J Stamatoyannopoulos(5), Amal Abu Rayyan(5), M. Lee(5), Robin L. Bennett(4), Kathy Agnew(4), Sarah B. Pierce(4), Ming K. Lee(4), Christopher C. Pennil(3), Paul Renbaum(3), Amnon Lahad(2)