
Everyone deserves a diagnosis
The Family Heart Foundation, July 18, 2022
Incorporating family history of disease improves polygenic risk scores in diverse populations
MLA Hujeol et al, Cell Genomics, July 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
Chronic Kidney Disease Basics
CDC, March 2022


Patted Aishwarya et al. The Journal of the Association of Physicians of India 2022 70(4) 11-12
Common data elements to standardize genomics studies in cerebral palsy.

Wilson Yana A et al. Developmental medicine and child neurology 2022
Heterozygous and Homozygous Variants in SORL1 Gene in Alzheimer's Disease Patients: Clinical, Neuroimaging and Neuropathological Findings.

Alvarez-Mora Maria Isabel et al. International journal of molecular sciences 2022 23(8)
Polygenic risk score as a possible tool for identifying familial monogenic causes of complex diseases.

Lu Tianyuan et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
Preconception leisure-time physical activity and family history of stroke and myocardial infarction associate with preterm delivery: findings from a Norwegian cohort.

Engen Tone et al. BMC pregnancy and childbirth 2022 22(1) 341
Prenatal genetic counseling practices regarding recommendations for cancer genetic counseling: A retrospective chart review from two academic institutions.

Saba Lisa F et al. Journal of genetic counseling 2022
Prevalence of Americans reporting a family history of cancer indicative of increased cancer risk: Estimates from the 2015 National Health Interview Survey.

Kumerow Marie T et al. Preventive medicine 2022 107062
Increased Number Of Colorectal Interval Cancers In Lynch Syndrome After The SARS-CoV-2 Pandemic. A Survey-based Study.

Russo Michele, et al. Digestive diseases (Basel, Switzerland) 2022 0 0.
Cost-effectiveness of artificial intelligence for screening colonoscopy: a modelling study.

Areia Miguel et al. The Lancet. Digital health 2022
Thrombosis Risk History and D-dimer Levels in Asymptomatic Individuals with Prader-Willi Syndrome.

Matesevac Lisa et al. Journal of clinical medicine 2022 11(7)
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About Family Health History PHGKB
Family Health History PHGKB is an online, continuously updated, searchable database of information and publications relevant to the role of family health history in healthcare and disease prevention....more
Content Summary
- CDC Information (60)
- NIH Information (21)
- COVID-19 (15)
- CDC Publications (22)
- Human Genome Epidemiologic Studies (3640)
- Human Genomics Translation/Implementation Studies (1815)
- Genomic Tests Evidence Synthesis (146)
- Genomic Tests Guidelines (67)
- Tier-Classified Guidelines (32)
- Non-Genomics Precision Health (35)
- Pathogen Advanced Molecular Detection (1)
- State Public Health Genomics Programs (112)
- Reviews/Commentaries (546)
- Tools/Methods (43)
- Ethical/Legal and Social Issues (ELSI) (33)
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Jul 25, 2022
- Page last updated:Aug 10, 2022
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