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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: 63770 Documents since 2012)
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The Health History of First-Degree Relatives' Dyslipidemia Can Affect Preferences and Intentions following the Return of Genomic Results for Monogenic Familial Hypercholesterolemia.
Tomoharu Tokutomi et al. Genes (Basel) 2024 15(3)
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Efficacy of Community Health Worker-Delivered Family Health History-Based Breast Cancer Education and Services Among Chinese Americans.
Bertille Assoumou et al. J Cancer Educ 2024
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Influence of family history on penetrance of hereditary cancers in a population setting.
Leigh Jackson et al. EClinicalMedicine 2023 64102159
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Experts say Found’s story highlights the extraordinary complexity of the problem for pregnant people living with SCD – and the critical importance of receiving proper, specialized care as early as possible. This is especially true now that medical advances in care and disease-modifying therapies have helped many people living with SCD survive well through their reproductive years. For parents-to-be, that means awareness is key. Individuals with SCD are at higher risk than the general population for preeclampsia, as Found discovered; but those with preeclampsia can go on to develop a condition called eclampsia, which can lead to seizures and even coma. People with SCD are also at higher risk for sepsis and blood clots. And there are risks for the fetus, such as lower-than-normal growth in the womb, preterm delivery, and stillbirth.
K Miller, Self, September 2023
Does the amount of family history matter? Perspectives of adult adoptees.
Alyssa Williams et al. J Genet Couns 2023
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Are You Up to Date on Your Preventive Care?
CDC, July 2023
Family and personal history of cancer in the All of Us research program for precision medicine.
Lauryn Keeler Bruce et al. PLoS One 2023 18(7) e0288496
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Barriers and facilitators to genetic testing for breast and ovarian cancer amongst Black African women in Luton (UK).
Valencia Kabeya et al. J Genet Couns 2023
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Talking About Your Family History of Cancer
CDC, July 2023
Family history can help identify health risks, but many Latino people know little about theirs
L Medrano, American Heart News, June 2023
Extended Family Outreach in Hereditary Cancer Using Web-Based Genealogy, Direct-to-Consumer Ancestry Genetics, and Social Media: Mixed Methods Process Evaluation of the ConnectMyVariant Intervention.
Annie T Chen et al. JMIR Cancer 9e43126
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Predicting personal cardiovascular disease risk based on family health history: Development of expert-based family criteria for the general population.
Tetske Dijkstra et al. European journal of human genetics : EJHG 2023
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Predicting personal cardiovascular disease risk based on family health history: Development of expert-based family criteria for the general population
T DIjsktra et al, EJHG, March 27, 2023
Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?
Thomas May et al. Family practice 2023
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Expanding Family Health History to Include Family Medication History
SB Haga et al, J Per Med, Feb 2023
The Michigan Genetic Hereditary Testing (MiGHT) study's innovative approaches to promote uptake of clinical genetic testing among cancer patients: a study protocol for a 3-arm randomized controlled trial.
Lynette Hammond Gerido et al. Trials 2023 24(1) 105
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Increasing Use and Impact of Family Health History in Medically Underserved Populations: Work in Progress
G Wood et al, CDC Blog Post, December 20, 2022
Barriers to family history collection among Spanish-speaking primary care patients: a BRIDGE qualitative study.
Liebermann Erica et al. PEC innovation 2022 1
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Calculating variant penetrance from family history of disease and average family size in population-scale data.
Spargo Thomas P et al. Genome medicine 2022 14(1) 141
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Implementation-effectiveness trial of systematic family health history based risk assessment and impact on clinical disease prevention and surveillance activities.
Wu R Ryanne et al. BMC health services research 2022 22(1) 1486
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Hypertrophic Cardiomyopathy (HCM) and Family Health History of Sudden Death
CDC, December 2022
Prevalence of familial autoimmune diseases in juvenile idiopathic arthritis: results from the international Pharmachild registry.
van Straalen Joeri W et al. Pediatric rheumatology online journal 2022 20(1) 103
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Systematic comparison of family history and polygenic risk across 24 common diseases.
Mars Nina et al. American journal of human genetics 2022
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A Cluster Randomized Trial of a Family Health History Platform to Identify and Manage Patients at Increased Risk for Colorectal Cancer.
Voils Corrine I et al. Journal of general internal medicine 2022
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When It Comes to Breast Cancer, Sometimes It’s All in the Family
G Miller, CDC Cancer, Blog, October 2022
The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study
D Rasooly et al, Public Health Genomics, October 6, 2022
FHH Quick App Review: How Can a Quality Review Process Assist Primary Care Providers in Choosing a Family Health History App for Patient Care?
GM Wood et al, Genes, August 2022
Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing Approach.
Shi Jianlin et al. JMIR medical informatics 2022 10(8) e37842
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Why Family Health History is Important if You or Your Child has Learning or Attention Problems
CDC, June 13, 2022
Family history tools for primary care: A systematic review.
Miroševic Špela et al. The European journal of general practice 2022 28(1) 75-86
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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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