Jessica B. Mandell

发表

Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

T. Walsh, M. King, Ming K. Lee, 2006, JAMA.

Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2

M. King, Jessica B. Mandell, J. H. Marks, 2003, Science.

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

T. Walsh, M. King, Ming K. Lee, 2010, Proceedings of the National Academy of Sciences.

Spectrum of Mutations in BRCA 1 , BRCA 2 , CHEK 2 , and TP 53 in Families at High Risk of Breast Cancer

T. Walsh, M. King, Ming K. Lee, 2006 .

Characterization of splice-altering mutations in inherited predisposition to cancer

T. Walsh, M. King, Ming K. Lee, 2019, Proceedings of the National Academy of Sciences.

Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria

Michael S. Bereman, M. King, M. MacCoss, 2011, Proceedings of the National Academy of Sciences.

Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women

T. Walsh, M. King, Ming K. Lee, 2017, JAMA oncology.

CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes

T. Walsh, M. King, S. Casadei, 2020, Journal of Medical Genetics.

Germline mutations in cancer susceptibility genes in brca1 and brca2 negative families with ovarian and breast cancer

T. Walsh, M. King, Ming K. Lee, 2014 .

Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2

M. King, Ming K. Lee, Jessica B. Mandell, 2014, Proceedings of the National Academy of Sciences.

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.

Kenneth Offit, Tom Walsh, T. Walsh, 2005, Human molecular genetics.

Loss of function germline mutations in RAD51D in women with ovarian carcinoma.

Rochelle L. Garcia, T. Walsh, M. King, 2012, Gynecologic oncology.

Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53

Tom Walsh, Mohammad Salahat, T. Walsh, 2017, International journal of cancer.

Genetic counselors: translating genomic science into clinical practice.

Jessica B. Mandell, R. Bennett, J. H. Marks, 2003, The Journal of clinical investigation.

Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.

T. Walsh, M. King, J. Stamatoyannopoulos, 2011, Cancer research.

Association of Genetic Diagnoses of Childhood-Onset Hearing Loss With Cochlear Implant Outcomes.

T. Walsh, M. King, D. Horn, 2023, JAMA otolaryngology-- head & neck surgery.

Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease

Tom Walsh, Augusto Morales, T. Walsh, 2016, Cold Spring Harbor molecular case studies.

Genetic counseling throughout the life cycle.

Jessica B. Mandell, R. Bennett, J. H. Marks, 2003, The Journal of clinical investigation.

Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2

T. Walsh, M. King, O. Olopade, 2016, Breast Cancer Research and Treatment.

Contribution of InheritedMutations in the BRCA 2-Interacting Protein PALB 2 to Familial Breast Cancer

T. Walsh, M. King, J. Stamatoyannopoulos, 2011 .

Contribution of InheritedMutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer

T. Walsh, M. King, J. Stamatoyannopoulos, 2011 .