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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 21, 2024
. (Total: 63914 Documents since 2012)
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Implementing genetic testing in diabetes: Knowledge, perceptions of healthcare professionals, and barriers in a developing country.
Williams O Balogun et al. Popul Med 2024 6
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The role of community engagement in promoting research participants' understanding of pharmacogenomic research results: Perspectives of stakeholders involved in HIV/AIDS research and treatment.
Sylvia Nabukenya et al. PLoS One 2024 19(4) e0299081
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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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A Bayesian approach for investigating the pharmacogenetics of combination antiretroviral therapy in people with HIV.
Wei Jin et al. Biostatistics 2024
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Development of an Electronic Decision Aid Tool to Facilitate Mainstream Genetic Testing in Ovarian Cancer Patients.
Kristen M Shannon et al. Oncologist 2024
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Perceptions and Attitudes Toward Genetic Counselors and Genetic Testing Among Certified Professional Midwives in Vermont: A Modified Grounded Theory Study.
Jazmine L Gabriel et al. Qual Health Res 2023 10497323231222395
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Patient-Level Exposure to Actionable Pharmacogenomic Medications in a Nationally Representative Insurance Claims Database.
Monica L Bianchini et al. J Pers Med 2023 13(11)
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Patient decision aids in mainstreaming genetic testing for women with ovarian cancer: A prospective cohort study.
Monika Sobocan et al. BJOG 2023
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Patient decision support resources inform decisions about cancer susceptibility genetic testing and risk management: a systematic review of patient impact and experience.
Kelly Kohut et al. Front Health Serv 2023 31092816
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The effects of decision aids for genetic counselling among people considering genetic testing: A systematic review.
Sek Ying Chair et al. J Clin Nurs 2023
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"There's gonna be a lot more heartache". Coping with a BRCA1/2 alteration: A qualitative reflexive thematic analysis.
Nikolett Zs Warner et al. Eur J Oncol Nurs 2023 64102328
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Genetic Testing for Adrenal Tumors-What the Contemporary Surgeon Should Know.
Maria F Bates et al. Surgical oncology clinics of North America 2023 32(2) 303-313
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Inherited causes of exocrine pancreatic insufficiency in pediatric patients: clinical presentation and laboratory testing.
Tatiana N Yuzyuk et al. Critical reviews in clinical laboratory sciences 2023 1-16
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Impact of Genetic Disorders in the Surgical Management of Congenital Heart Disease.
Elizabeth H Stephens et al. World journal for pediatric & congenital heart surgery 2023 21501351221139837
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Direct-to-consumer testing - benefits for consumers, people with disease and public health.
Rolf Hinzmann et al. Clinical chemistry and laboratory medicine 2023
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Association of apolipoprotein E epsilon 4 and cognitive impairment in adults living with human immunodeficiency virus: a meta-analysis.
Tingting Mu et al. Chinese medical journal 2023 135(22) 2677-2686
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Pathogenic Variants in Adult-Onset Cancer Predisposition Genes in Pediatric Cancer: Prevalence and Impact on Tumor Molecular Features and Clinical Management.
Rose B McGee et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2023
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Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.
Estefanía Martinez-Barrios et al. International journal of legal medicine 2023
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Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest.
Brendan J Floyd et al. Circulation. Genomic and precision medicine 2023
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Association of Genetic Diagnoses of Childhood-Onset Hearing Loss With Cochlear Implant Outcomes.
Carlson Ryan J et al. JAMA otolaryngology-- head & neck surgery 2023
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Diagnostic and therapeutic algorithms for monogenic autoinflammatory diseases presenting with recurrent fevers among adults.
Delplanque Marion et al. Rheumatology (Oxford, England) 2022
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Pharmacogenetics of CYP2A6, CYP2B6, and UGT2B7 in the Context of HIV Treatments in African Populations.
Ford Graeme R et al. Journal of personalized medicine 2022 12(12)
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Person-based co-design of a decision aid template for people with a genetic predisposition to cancer.
Morton Kate et al. Frontiers in digital health 2022 41039701
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Pharmacogenomics driven decision support prototype with machine learning: A framework for improving patient care.
Kidwai-Khan Farah et al. Frontiers in big data 2022 51059088
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A deliberative public engagement study on heritable human genome editing among South Africans: Study results.
Thaldar Donrich et al. PloS one 2022 17(11) e0275372
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Antibody response durability following three-dose COVID-19 vaccination in people with HIV receiving suppressive ART
HR LaPointe et al, MEDRXIV, November 7, 2022
Views of reproductive genetic carrier screening participants regarding screening for genes associated with non-syndromic hearing loss.
Freeman Lucinda et al. Prenatal diagnosis 2022
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Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review.
Young Alison Luk et al. European journal of human genetics : EJHG 2022
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Pharmacogenetics of HIV therapy: State of the art in Latin American countries.
Velozo Camila de Almeida et al. Genetics and molecular biology 2022 45(3 Suppl 1) e20220120
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Impact of Genetic Testing on Hearing Interventions.
Brodie Kara D et al. The Laryngoscope 2022
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 21, 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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