نتائج البحث - "Brigette Tippin Davis"

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دورية أكاديمية

Quantitative Analysis of BRCA1 and BRCA2 Germline Splicing Variants Using a Novel RNA-Massively Parallel Sequencing Assay

المؤلفون: Suzette Farber-Katz, Vickie Hsuan, Sitao Wu, Tyler Landrith, Huy Vuong, Dong Xu, Bing Li, Jayne Hoo, Stephanie Lam, Sarah Nashed, Deborah Toppmeyer, Phillip Gray, Ginger Haynes, Hsiao-Mei Lu, Aaron Elliott, Brigette Tippin Davis, Rachid Karam

المصدر: Frontiers in Oncology, Vol 8 (2018)

مصطلحات موضوعية: genetic testing, hereditary breast and ovarian cancer, HBOC, BRCA1, BRCA2, RNA, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fonc.2018.00286/full; https://doaj.org/toc/2234-943X

URL الوصول: https://doaj.org/article/ac330a471ac74523a1d861cc1c74206b

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Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer

المؤلفون: Jill S. Dolinsky, Brigette Tippin Davis, David E. Goldgar, Tina Pesaran, Jenna Lilyquist, Jie Na, Holly LaDuca, Amal Yussuf, Nancy Niguidula, Elizabeth C. Chao, Chunling Hu, Hermela Shimelis, Steven N. Hart, Siddhartha Yadav, Fergus J. Couch, Kun Y. Lee, Stephanie Gutierrez, Eric C. Polley

المصدر: JNCI Journal of the National Cancer Institute

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f878a957b7b1952845553924295cf4
https://doi.org/10.1093/jnci/djaa167

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Validation of a prostate cancer polygenic risk score

المؤلفون: Shuwei Li, Robert Hoiness, Siqun Lilly Zheng, Brian T. Helfand, Mary Helen Black, Jun Wei, Jefferey Chen, Jianfeng Xu, Kathleen E. Wiley, Stephanie Gutierrez, Brigette Tippin-Davis, Min-Tzu Lo, Hsiao Mei Lu, William B. Isaacs, Holly LaDuca, Zhuqing Shi, Marta Gielzak

المصدر: The Prostate

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Genotype, Urology, polygenic, Single-nucleotide polymorphism, urologic and male genital diseases, Logistic regression, Polymorphism, Single Nucleotide, Risk Assessment, 03 medical and health sciences, Prostate cancer, 0302 clinical medicine, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Family history, Aged, Genetic association, business.industry, High-Throughput Nucleotide Sequencing, Prostatic Neoplasms, Original Articles, Middle Aged, prostate cancer, medicine.disease, Confidence interval, 030104 developmental biology, Oncology, Quartile, Case-Control Studies, 030220 oncology & carcinogenesis, Original Article, Polygenic risk score, Neoplasm Grading, business, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeae415641ec22d8b744367012fae5dd
https://doi.org/10.1002/pros.24058

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A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients

المصدر: Genetics in Medicine

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Oncology, medicine.medical_specialty, Genes, BRCA2, Genes, BRCA1, cancer predisposition, Breast Neoplasms, 030105 genetics & heredity, Article, Cohort Studies, 03 medical and health sciences, Neoplasms, Internal medicine, clinical validity, Biomarkers, Tumor, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Germ-Line Mutation, Genetics (clinical), Aged, Genetic testing, Ovarian Neoplasms, medicine.diagnostic_test, BRCA1 Protein, Genetic heterogeneity, business.industry, Melanoma, Cancer, Middle Aged, multigene panel, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, testing criteria, Lynch syndrome, Human genetics, 030104 developmental biology, hereditary cancer, Mutation, Cohort, Female, business, Ovarian cancer

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b95de2404409940db6205b678a73e8a
https://doi.org/10.1038/s41436-019-0633-8

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Abstract P6-08-08: Concurrent DNA and RNA genetic testing identifies more patients with hereditary breast cancer than DNA testing alone

المصدر: Cancer Research. 80:P6-08

مصطلحات موضوعية: Oncology, Cancer Research, medicine.medical_specialty, medicine.diagnostic_test, business.industry, PALB2, Cancer, medicine.disease, MLH1, MSH6, Breast cancer, MSH2, Internal medicine, medicine, business, CHEK2, Genetic testing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a50932ad25e8a5992a3fd2a38eb880ba
https://doi.org/10.1158/1538-7445.sabcs19-p6-08-08

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Comprehensive Paired Tumor/Germline Testing for Lynch Syndrome: Bringing Resolution to the Diagnostic Process

المصدر: Journal of Clinical Oncology

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Oncology, Cancer Research, medicine.medical_specialty, Genetic Testing for Cancer, DNA Mutational Analysis, Germline, 03 medical and health sciences, 0302 clinical medicine, Predictive Value of Tests, Internal medicine, Biomarkers, Tumor, medicine, Humans, Genetic Predisposition to Disease, Promoter Regions, Genetic, Germ-Line Mutation, Aged, Retrospective Studies, business.industry, Reproducibility of Results, Diagnostic test, ORIGINAL REPORTS, DNA Methylation, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Endometrial Neoplasms, 030104 developmental biology, 030220 oncology & carcinogenesis, Female, Microsatellite Instability, MutL Protein Homolog 1, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd3843d83c1490e469a734034178320b
https://doi.org/10.1200/jco.18.00696

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Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes

المؤلفون: Meagan Farmer, Brandon Smith, Kara N. Maxwell, Brigette Tippin-Davis, Julia Burdette, Danielle McKenna, Ashley A. Cass, Sinead Charpentier, Sitao Wu, Emily Dalton, Melissa Parra, Susanne Fox, Aaron Elliott, Holly LaDuca, Cathryn Koptiuch, Susan M. Domchek, Elizabeth Hoodfar, Robert Pilarski, Dong Xu, Khateriaa Pyrtel, Kara J. Milliron, Michele Fennessy, Gayle Patel, Lily Hoang, Morgan M Depas, Tina Pesaran, Rachid Karam, Meredith Seidel, Ann Bunnell, Huy Gia Vuong, Deborah Wham, Bing Li, Ragene Rivera, Jennie Vagher, Nichole A. Morman, Aarani Arulmoli, Sara Pirzadeh-Miller, Hsiao-Mei Lu, Jessica Profato, Joy Rae-Radecki Crandall, Elizabeth C. Chao, Ruth Baxter, Shraddha Gaonkar, Ginger Haynes, Amanda Ganzak, Deepika Nathan, Jennifer L. Geurts, Blair R. Conner, Tyler Landrith, Rebekah Krukenberg, John J. Lee, Christopher Heinlen, Bhuvan Molparia

المصدر: npj Precision Oncology, Vol 4, Iss 1, Pp 1-9 (2020)
NPJ Precision Oncology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d16807d808110f22b027a699b83d981
https://doi.org/10.1038/s41698-020-0109-y

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8

Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer

المصدر: JAMA network open. 2(10)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1255e7ea8e8731fbb1469d2b0d9634f
https://pubmed.ncbi.nlm.nih.gov/31642931

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9

Multigene Hereditary Cancer Panels Reveal High-Risk Pancreatic Cancer Susceptibility Genes

المؤلفون: Hermela Shimelis, Steven N. Hart, Jill S. Dolinsky, Chunling Hu, Kun Y. Lee, Eric C. Polley, Holly LaDuca, David E. Goldgar, Jenna Lilyquist, Abigail Thomas, Brigette Tippin Davis, Tina Pesaran, Fergus J. Couch, Mary Helen Black, Jie Na

المصدر: JCO precision oncology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8731a85f7f64e72674a0497e991088db
https://pubmed.ncbi.nlm.nih.gov/31497750

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False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care

المؤلفون: Kate Krempely, Stephany Tandy-Connor, Holly LaDuca, Brigette Tippin Davis, Stephanie Gutierrez, Jenna Guiltinan, Patrick Reineke, Phillip Gray

المصدر: Genetics in Medicine

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, false positive, Alcohol Drinking, Concordance, Population, MEDLINE, clinical confirmation direct-to-consumer, 030105 genetics & heredity, Article, 03 medical and health sciences, Direct-To-Consumer Screening and Testing, False positive paradox, Medicine, Humans, Medical physics, Attention, Genetic Testing, education, Genotyping, raw data, Genetics (clinical), classification discrepancy, Genetic testing, Aged, education.field_of_study, Internet, medicine.diagnostic_test, business.industry, United States Food and Drug Administration, Genetic Variation, Genomics, Middle Aged, United States, 030104 developmental biology, Medical genetics, Female, Patient Care, Raw data, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c88377214ed8f13df0475ec2ced55dcf
http://europepmc.org/articles/PMC6301953

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