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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)
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Last data update: Apr 30, 2024
. (Total: 63724 Documents since 2012)
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An approach to identify gene-environment interactions and reveal new biological insight in complex traits
Examining Sex Differences in Autism Heritability.
Sven Sandin et al. JAMA Psychiatry 2024
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Many roads to a gene-environment interaction.
Kenneth E Westerman et al. Am J Hum Genet 2024 111(4) 626-635
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Familial aggregation and heritability of childhood-onset and adult-onset type 1 diabetes: a Swedish register-based cohort study.
Yuxia Wei et al. Lancet Diabetes Endocrinol 2024
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Socioecologic Factors and Racial Differences in Breast Cancer Multigene Prognostic Scores in US Women.
Ashwini Z Parab et al. JAMA Netw Open 2024 7(4) e244862
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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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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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Contextual factors influencing the equitable implementation of precision medicine in routine cancer care in Belgium.
Tugce Schmitt et al. Eur J Public Health 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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Polypharmacy and precision medicine.
Kenji Fujita et al. Camb Prism Precis Med 2024 1e22
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Spondyloarthritis in first-degree relatives and spouses of patients with inflammatory bowel disease: A nationwide population-based cohort study from Sweden.
Sarita Shrestha et al. J Crohns Colitis 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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The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?
Roel H P Wouters et al. Psychiatr Genet 2024 34(2) 31-36
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Consumer attitudes and preferences toward psychiatric genetic counselling and educational resources: A scoping review.
Tessa Gatt-Rutter et al. Patient Educ Couns 2024 123108229
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The Potential and Challenges of Genomics Informed Precision Care for Substance Use Disorders.
Rose Mary Xavier et al. J Psychosoc Nurs Ment Health Serv 2024 62(3) 11-14
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Being precise with anticoagulation to reduce adverse drug reactions: are we there yet?
Benjamin Cross et al. Pharmacogenomics J 2024 24(2) 7
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Polygenic risk scores, radiation treatment exposures and subsequent cancer risk in childhood cancer survivors.
Todd M Gibson et al. Nat Med 2024
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The Finnish Adoptive Family Study of Schizophrenia: differences in somatic diseases and conditions between adoptees with high or low genetic risk for schizophrenia spectrum disorders.
Emma Karjalainen et al. Nord J Psychiatry 2024 1-7
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Genetics of chronic respiratory disease.
Ian Sayers et al. Nat Rev Genet 2024
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Health-Related quality of life and DNA Methylation-Based aging biomarkers among survivors of childhood cancer.
Noel-Marie Plonski et al. J Natl Cancer Inst 2024
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Describing patterns of familial cancer risk in subfertile men using population pedigree data.
Joemy M Ramsay et al. Hum Reprod 2024
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Sex Differences in Diagnosis, Treatment, and Cardiovascular Outcomes in Homozygous Familial Hypercholesterolemia.
Janneke W C M Mulder et al. JAMA Cardiol 2024
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Genetic and non-genetic predictors of risk for opioid dependence.
Peter J Na et al. Psychol Med 2024 1-8
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Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues.
Kate Sahan et al. J Med Ethics 2024
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Assessing the utility of measurement methods applied in economic evaluations of pharmacogenomics applications.
Vasileios Fragoulakis et al. Pharmacogenomics 2024
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Use of drugs with pharmacogenomics (PGx)-based dosing guidelines in a Danish cohort of persons with chronic kidney disease, both on dialysis and not on dialysis: Perspectives for prescribing optimization.
Niels Westergaard et al. Basic Clin Pharmacol Toxicol 2024
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It’s time to admit that genes are not the blueprint for life The view of biology often presented to the public is oversimplified and out of date.
D Noble, Nature book Review, February 5, 2024
Unraveling Complexities in Genetically Elusive Long QT Syndrome.
Babken Asatryan et al. Circ Arrhythm Electrophysiol 2024 e012356
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Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit.
Kyle B Brothers et al. Ethics Hum Res 2024 46(1) 43-48
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The Impact of Integration of a Genetic Clinic Into a Pediatric Cardiac Unit.
Ayman Elfky et al. Cureus 2024 15(12) e50941
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 30, 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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