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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 18, 2024
. (Total: 63623 Documents since 2012)
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all[original query]>>Hereditary Cancer[Category]
Impact of Family History and Germline Genetic Risk Single Nucleotide Polymorphisms on Long-Term Outcomes of Favorable-Risk Prostate Cancer.
Florian Rumpf et al. J Urol 2024 101097JU0000000000003927
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Uptake of screening and risk-reducing recommendations among women with hereditary breast and ovarian cancer syndrome due to pathogenic BRCA1/2 variants evaluated at a large urban comprehensive cancer center.
Hadeel Assad et al. Breast Cancer Res Treat 2024
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Clinical features of prostate cancer by polygenic risk score.
Christina Spears et al. Fam Cancer 2024
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Colorectal Cancer Risk between Mendelian and Non-Mendelian Inheritance.
Elizabeth A Hibler et al. Clin Colon Rectal Surg 2024 37(3) 140-145
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Factors Influencing Adherence to the Risk Management Program for Women With a Genetic Predisposition to Breast Cancer: Real-World Data from a French Multicenter Program.
Ke Zhou et al. Oncologist 2024
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Population-based BRCA germline mutation screening in the Han Chinese identifies individuals at risk of BRCA mutation-related cancer: experience from a clinical diagnostic center from greater Shanghai area.
Zhiyuan Wu et al. BMC Cancer 2024 24(1) 411
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Oncologists' perceptions of tumor genomic profiling and barriers to communicating secondary hereditary risks to African American cancer patients.
Michael J Hall et al. BMC Cancer 2024 24(1) 412
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Olaparib not cost-effective as maintenance therapy for platinum-sensitive, BRCA1/2 germline-mutated metastatic pancreatic cancer.
Tarun Mehra et al. PLoS One 2024 19(4) e0301271
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BRCA awareness and testing experience in the UK Jewish population: a qualitative study.
Katrina Sarig et al. J Med Genet 2024
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Hereditary Cancer Syndrome Carriers: Feeling Left in the Corner.
Celia Diez de Los Rios de la Serna et al. Semin Oncol Nurs 2024 151624
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Variants in BRCA1/2 in a hospital-based cohort in Chile and national literature review.
Fernanda J Martin et al. Ecancermedicalscience 2024 181683
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Integration of pathologic characteristics, genetic risk and lifestyle exposure for colorectal cancer survival assessment
J Xin et al, Nature Comm, April 8, 2024
Strategies to improve implementation of cascade testing in hereditary cancer syndromes: a systematic review
J Chiang et al, NPJ Genomic Medicine, April 5, 2024
A scoping review of web-based, interactive, personalized decision-making tools available to support breast cancer treatment and survivorship care.
Kaitlyn M Wojcik et al. J Cancer Surviv 2024
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IMPACT OF ENDOSCOPIC TREATMENT IN SEVERE DUODENAL POLYPOSIS: A NATIONAL STUDY IN FAMILIAL ADENOMATOUS POLYPOSIS PATIENTS.
Pierrine Le Bras et al. Clin Gastroenterol Hepatol 2024
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Difficulties in disclosing secondary findings by facilities performing comprehensive germline genetic testing for rare diseases in Japan.
Kana Hiromoto et al. Congenit Anom (Kyoto) 2024
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The BRCA mutation spectrum among breast and ovarian cancers in India: highlighting the need to screen BRCA1 185delAG among South Indians.
Ajoy Oommen John et al. Eur J Hum Genet 2024
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Challenges and opportunities for Lynch syndrome cascade testing in the United States.
Lauren E Passero et al. Fam Cancer 2024
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What to Know About Lynch Syndrome
ThedaCare Genetic Counseling, March 2024
The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?
Natalia Campacci et al. Front Psychol 2024 151306388
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Codesign of Lynch Choices : Using implementation science to create a clinically deliverable patient decision support website to transform cancer genetics care pathways.
Kelly Kohut et al. Psychooncology 2024 33(3) e6330
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Low Rates of Colorectal Cancer Screening in Our Patients' First-Degree Relatives: Are We Failing Them?
Anyelin Almanzar et al. Dis Colon Rectum 2024
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Family health beliefs and cascade genetic testing in Asian families with hereditary cancer risk: "Okay, now what?".
Leena Tran et al. J Genet Couns 2024
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The dynamic buffering of social support on depressive symptoms and cancer worries in patients seeking cancer genetic counseling.
Sally Ho et al. J Cancer Surviv 2024
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A Scoping Review of Personalized, Interactive, Web-Based Clinical Decision Tools Available for Breast Cancer Prevention and Screening in the United States.
Dalya Kamil et al. MDM Policy Pract 2024 9(1) 23814683241236511
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Knowledge, perceptions, attitudes, and barriers pertaining to genetic literacy among surgeons: a scoping review.
Zuhaib M Mir et al. Can J Surg 2024 67(2) E118-E127
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Lynch Syndrome Ups Risk for Colorectal, Other Cancers
E Herlache, Cancer Care, March 2024
Cascade screening in HBOC and Lynch syndrome: guidelines and procedures in a UK centre.
D Gareth Evans et al. Fam Cancer 2024
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Genetic counselors' and community clinicians' implementation and perceived barriers to informed consent during pre-test counseling for hereditary cancer risk.
Alexandra Capasso et al. J Genet Couns 2024
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Family Recall of and Response to Germline Pathologic Variants Found on Paired Tumor-Germline Sequencing in Pediatric Oncology.
Michelle F Jacobs et al. JCO Precis Oncol 2024 8e2300539
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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