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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 30, 2024
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Query Trace:
A framework for the evaluation and reporting of incidental findings in clinical genomic testing.
Carolyn M Brown et al. Eur J Hum Genet 2024
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A framework for the evaluation and reporting of incidental findings in clinical genomic testing
CM Brown et al, EJHG, April 2, 2024
Secondary (additional) findings from the 100,000 Genomes Project: disease manifestation, healthcare outcomes and costs of disclosure
J Nolan et al, Genetics in Medicine, December 19, 2023
Ten Years of Incidental, Secondary, and Actionable Findings.
Sharon Plon et al. N Engl J Med 2023 389(19) 1813-1814
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Research participants' perception of ethical issues in stroke genomics and neurobiobanking research in Africa.
Ayodele Jegede et al. medRxiv 2023
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[Genomic newborn screening-research approaches, challenges, and opportunities].
Heiko Brennenstuhl et al. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2023
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Experiences of adults living with refractory epilepsy and their views and expectations on receiving results from whole genome sequencing.
Cynthia Addona et al. Epilepsy Res 2023 196107221
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Opportunistic genetic screening increases the diagnostic yield and is medically valuable for care of patients and their relatives with hereditary cancer.
Sara Fernández-Castillejo et al. J Med Genet 2023
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ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
DT Miller et al, Genetics in Medicine, June 22, 2023
Challenges in the clinical understanding of genetic testing in birth defects and pediatric diseases.
Tina O Findley et al. Transl Pediatr 2023 12(5) 1028-1040
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Clinically actionable incidental and secondary parental genomic findings after proband exome sequencing: yield and dilemmas
LB Salmon et al, Genet Med Open, May 2023
Evaluation of pre-test counselling offered for non-invasive prenatal testing (NIPT) as a primary screening tool.
Ho Yin Diana Lee et al. J Obstet Gynaecol 2023 43(1) 2204959
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Single Gene Non-invasive Prenatal Screening (NIPS-SGD) for Autosomal Dominant Conditions in a High-risk Cohort.
Sophie Adams et al. Prenatal diagnosis 2023
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Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart Association
AP Landsrtom et al, Circ Genomics & Prec Med, March 27, 2023
Whole genome sequencing versus chromosomal microarray analysis in prenatal diagnosis.
Ping Hu et al. American journal of obstetrics and gynecology 2023
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Expanded carrier screening for reproductive risk assessment: An evidence-based practice guideline from the National Society of Genetic Counselors.
Katelynn G Sagaser et al. Journal of genetic counseling 2023
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Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care.
Cuppen Edwin et al. JCO precision oncology 2022 6e2200245
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Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disorders.
Carrasco Estela et al. Journal of medical genetics 2022
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REFINEMENT OF NEWBORN SCREENING FOR CYSTIC FIBROSIS WITH NEXT GENERATION SEQUENCING.
Rock Michael J et al. Pediatric pulmonology 2022
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Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.
Bowling Kevin M et al. Genome medicine 2022 14(1) 131
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Incidental Findings from Deep Phenotyping Research in Psychiatry: Legal and Ethical Considerations.
Kim Amanda et al. Cambridge quarterly of healthcare ethics : CQ : the international journal of healthcare ethics committees 2022 31(4) 482-486
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Incidental Findings in Study Participants: What Is the Researcher's Obligation?
Schaare Donna et al. Genes 2022 13(10)
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Parental Preferences about Policy Options Regarding Disclosure of Incidental Genetic Findings in Newborn Screening: Using Videos and the Internet to Educate and Obtain Input.
Farrell Michael H et al. International journal of neonatal screening 2022 8(4)
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Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance.
Howell Susan et al. Journal of genetic counseling 2022
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Patient Understanding of Tumor Genomic Testing: A Quality Improvement Effort.
Senter Leigha et al. JCO oncology practice 2022 OP2200316
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Clinical implementation of genetic testing in adults for hereditary hematologic malignancy syndromes.
Ansar Safa et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
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Perspectives and experiences of researchers regarding feedback of incidental genomic research findings: A qualitative study.
Ochieng Joseph et al. PloS one 2022 17(8) e0273657
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When Silence Disrupts
RC Hunt et al, NEJM, August 24, 2022
Genomic tools for health: Secondary findings as findings to be shared
SA Miner et al, Genetics in Medicine, August 18, 2022
Genetic testing and screening in children.
Moore Aideen M et al. Paediatrics & child health 2022 27(4) 243-253
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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
,
National Center on Birth Defects and Developmental Disabilities
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