
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
Advances in Breast Cancer-Screening and Treatment Get Personal
NIH News in Health, February 2022
Accounting for age of onset and family history improves power in genome-wide association studies.
Pedersen Emil M et al. American journal of human genetics 2022 2


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)
Tumor BRCA Testing in Epithelial Ovarian Cancers: Past and Future-Five-Years' Single-Institution Experience of 762 Consecutive Patients.

Fumagalli Caterina et al. Cancers 2022 14(7)
Association of Family History of Cancer with Clinical and Pathological Outcomes for Prostate Cancer Patients on Active Surveillance.

Jibara Ghalib A et al. The Journal of urology 2022 101097JU0000000000002668
Diagnostic validity and clinical utility of genetic testing for hypertrophic cardiomyopathy: a systematic review and meta-analysis.

Christian Susan et al. Open heart 2022 9(1)
Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome.

Guan Bao et al. Frontiers in oncology 2022 12774202
Interventions to improve delivery of cancer genetics services in the United States: A scoping review.

Bednar Erica M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
BRCA mutations: Implications of genetic testing in ovarian cancer.

Talwar Vineet et al. Indian journal of cancer 2022 59(Supplement) S56-S67
Identification and Management of Pathogenic Variants in BRCA1, BRCA2, and PALB2 in a Tumor-Only Genomic Testing Program.

Bychkovsky Brittany L et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2022
Inherited risk assessment and its clinical utility for predicting prostate cancer from diagnostic prostate biopsies.

Xu Jianfeng et al. Prostate cancer and prostatic diseases 2022
Can Automated Alerts in the Electronic Health Record Encourage Referrals for Genetic Counseling and Testing Among Patients at High Risk for Hereditary Cancer Syndromes?

Zorn Kristin K et al. JCO oncology practice 2022 OP2100641
Do current family history-based genetic testing guidelines contribute to breast cancer health inequities?

Jakuboski Samantha H et al. NPJ breast cancer 2022 8(1) 36
Hereditary evaluation and genetic counselling in young individuals with colorectal cancer in a population-based cohort.

Lundqvist Erik et al. Surgical oncology 2022 41101741
Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access.

Amendola Laura M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
Population-based screening of Uruguayan Ashkenazi Jews for recurrent BRCA1 and BRCA2 pathogenic sequence variants.

Castillo Cecilia et al. Molecular genetics & genomic medicine 2022 e1928
Prostate cancer incidence and survival in relation to prostate cancer as second cancer in relatives.

Zheng Guoqiao et al. Cancer medicine 2022
Time to Diagnosis of Duchenne Muscular Dystrophy Remains Unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet), 2000-2015.

Thomas Shiny et al. Muscle & nerve 2022
Universal Screening for Lynch Syndrome Compared with Pedigree-Based Screening: 10-Year Experience in a Tertiary Hospital.

Kim Min Hyun et al. Cancer research and treatment 2022
Nonlaboratory-based risk assessment model for coronary heart disease screening: Model development and validation.

Zhang Liying et al. International journal of medical informatics 2022 162104746
Familial Risk of Renal Cell Cancer and Interaction with Obesity and Hyperglycemia-A Population-Based Study.

Lee Sung Won et al. The Journal of urology 2022 101097JU0000000000002506
Investigating men's motivations to engage in genetic screening for BRCA1 and BRCA2 mutations.

Annoni Anna Maria et al. PloS one 2022 17(3) e0265387
Referral indications for malignant hyperthermia susceptibility diagnostics in patients without adverse anesthetic events in the era of next-generation sequencing.

van den Bersselaar Luuk R et al. Anesthesiology 2022
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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 (1814)
- 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 (545)
- 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:Oct 1, 2021
- Page last updated:Jun 25, 2022
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