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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
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 03, 2024
. (Total: 63769 Documents since 2012)
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Navigating equity in global access to genome therapy expanding access to potentially transformative therapies and benefiting those in need requires global policy changes.
Tsung-Ling Lee et al. Front Genet 2024 151381172
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Germline Testing in Patients With Breast Cancer: ASCO-Society of Surgical Oncology Guideline.
Isabelle Bedrosian et al. J Clin Oncol 2024 42(5) 584-604
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Medicolegal and insurance issues regarding BRCA1 and BRCA2 gene tests in high income countries.
Riccardo Oliva et al. Int J Gynecol Cancer 2024
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Evaluation of the Genetic Background of Patients with Niemann-Pick Disease.
Fatemeh Alipouran et al. Rep Biochem Mol Biol 2024 12(3) 386-392
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A multinational survey of potential participant perspectives on ocular gene therapy.
Alexis Ceecee Britten-Jones et al. Gene Ther 2024
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All you Need is Trust? Public Perspectives on Consenting to Participate in Genomic Research in the Sri Lankan District of Colombo.
Krishani Jayasinghe et al. Asian Bioeth Rev 2024 16(2) 281-302
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A Communication and Decision-Making Framework for Pediatric Precision Medicine.
Brittany L Greene et al. Pediatrics 2024
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Development of a Low Cost Semiquantitative Polymerase Chain Reaction Assay for Molecular Diagnosis of Williams Syndrome.
Dinali M Ranaweera et al. Clin Lab 2024 70(3)
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On the ethics of informed consent in genetic data collected before 1997.
Martin Zieger et al. Nature 2024 627(8003) 271
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Mainstreaming genomic testing: pre-test counselling and informed consent.
Michaela Cormack et al. Med J Aust 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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Direct-to-Consumer Genetic Tests and Canadian Genetic Counselors: A Pilot Exploration of Professional Roles in Response to Novel Biotechnologies.
Cassandra E Haley et al. Genes (Basel) 2024 15(2)
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Implementation of rapid genomic sequencing in safety-net neonatal intensive care units: protocol for the VIrtual GenOme CenteR (VIGOR) proof-of-concept study.
Alissa M D'Gama et al. BMJ Open 2024 14(2) e080529
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Redefining informed consent form in cell and gene therapy trials.
Varsha Dalal et al. Perspect Clin Res 2024 15(1) 4-9
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Clinical value of positive CNVs results by NIPT without fetal ultrasonography-identified structural anomalies.
Changhong Wang et al. Mol Genet Genomic Med 2024 12(1) e2352
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Patient survey on cancer genomic medicine in Japan under the national health insurance system.
Hidenori Kage et al. Cancer Sci 2024
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Development and assessment of educational materials for spinal muscular atrophy carrier screening in the Plain community.
Carly Eichten et al. J Genet Couns 2024
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Management considerations for clinically relevant findings on expanded carrier screening in a sperm donor applicant population.
Lauren Isley et al. F S Rep 2024 4(4) 384-389
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Informed consent for whole genome sequencing in mainstream clinics: logistical constraints and possible solutions
A Chaouch et al, EJHG, January 4, 2024
Ethical considerations for genetic research in low-income countries: perceptions of informed consent, data sharing, and expectations in Nicaragua.
Iris S Delgado et al. Eur J Hum Genet 2023
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Looking ahead: ethical and social challenges of somatic gene therapy for sickle cell disease in Africa.
Nchangwi Syntia Munung et al. Gene Ther 2023
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The Lived Experience of Pediatric Gene Therapy - A Scoping Review.
Laura Kimberly et al. Hum Gene Ther 2023
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Consideration and Disclosure of Group Risks in Genomics and Other Data-Centric Research: Does the Common Rule Need Revision?
Carolyn Riley Chapman et al. Am J Bioeth 2023 1-14
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Danish Prostate Cancer Consortium Study 1 (DPCC-1) protocol: Multicentre prospective validation of the urine-based three-microRNA biomarker model uCaP.
Jacob Fredsøe et al. BMJ Open 2023 13(11) e077020
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Call to Action for Advancing Equitable Genomic Newborn Screening.
Anne L Ersig et al. Public Health Genomics 2023
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Screening uptake of colonoscopy versus fecal immunochemical testing in first-degree relatives of patients with non-syndromic colorectal cancer: A multicenter, open-label, parallel-group, randomized trial (ParCoFit study).
Natalia González-López et al. PLoS Med 2023 20(10) e1004298
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"There should be one spot that you can go:" BRCA mutation carriers' perspectives on cancer risk management and a hereditary cancer registry.
J Hynes et al. J Community Genet 2023
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Women's experiences with non-invasive prenatal testing in Switzerland: a qualitative analysis.
Mirriam Tyebally Fang et al. BMC Med Ethics 2023 24(1) 85
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Specific measures for data-intensive health research without consent: a systematic review of soft law instruments and academic literature.
Julie-Anne R Smit et al. Eur J Hum Genet 2023
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Public attitudes towards genomic data sharing: results from a provincial online survey in Canada.
Holly Etchegary et al. BMC Med Ethics 2023 24(1) 81
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 03, 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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