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Public Health Genomics and Precision Health Knowledge Base (v8.2)
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Last data update: Jan 27, 2023
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all[original query]>>Original Studies[Product Type]
Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark.
Charlotte Glinge et al. JAMA network open 2023 6(1) e2252724
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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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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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Incorporating family history of disease improves polygenic risk scores in diverse populations
MLA Hujeol et al, Cell Genomics, July 13, 2022
Prevalence of Hemoglobin-S and Baseline Level of Knowledge on Sickle Cell Disease Among Pregnant Women Attending Antenatal Clinics in Dar-Es-Salaam, Tanzania.
Tutuba Hilda J et al. Frontiers in genetics 2022 13805709
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Prevalence of Clinically Relevant Germline BRCA Variants in a Large Unselected South African Breast and Ovarian Cancer Cohort: A Public Sector Experience.
Van der Merwe Nerina C et al. Frontiers in genetics 2022 13834265
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An Exploratory Study Using Electronic Medical Records to Assess the Feasibility of Establishing Cohorts of Patients with Genetic Causes of Parkinson's Disease.
Lee Susan J et al. Journal of Parkinson's disease 2022
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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
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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
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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
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Association of Lipoprotein (a) in Coronary Artery Disease in Young Individuals.
Patted Aishwarya et al. The Journal of the Association of Physicians of India 2022 70(4) 11-12
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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
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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)
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Pancreatic Ductal Carcinoma Risk Associated with Hereditary Cancer-Risk Genes.
Gardiner Anna et al. Journal of the National Cancer Institute 2022
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Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
Kowalczyk Katarzyna et al. Genes 2022 13(4)
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Age determines the risk of familial inflammatory bowel disease-A nationwide study.
Halfvarson Jonas F et al. Alimentary pharmacology & therapeutics 2022
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Cost-effectiveness of artificial intelligence for screening colonoscopy: a modelling study.
Areia Miguel et al. The Lancet. Digital health 2022
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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)
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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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Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome.
Guan Bao et al. Frontiers in oncology 2022 12774202
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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
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Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive-aged women in Flanders (Belgium).
Van Steijvoort Eva et al. Journal of genetic counseling 2022
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Diagnostic yield of massively parallel sequencing in patients with chronic kidney disease of unknown etiology: rationale and design of a national prospective cohort study.
de Haan Amber et al. BMJ open 2022 12(4) e057829
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Phenotypic and genotypic characterization of familial hypercholesterolemia in French adult and pediatric populations.
Fourgeaud Mélanie et al. Journal of clinical lipidology 2022
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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
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Awareness and Availability of Routine Germline BRCA1/2 Mutation Testing in Patients with Advanced Breast Cancer in Germany.
Lux Michael P et al. Breast care (Basel, Switzerland) 2022 17(1) 40-46
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Special issue "The advance of solid tumor research in China": Participants with a family history of cancer have a higher participation rate in low-dose computed tomography for lung cancer screening.
Guo Lan-Wei et al. International journal of cancer 2022
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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
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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
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Hereditary evaluation and genetic counselling in young individuals with colorectal cancer in a population-based cohort.
Lundqvist Erik et al. Surgical oncology 2022 41101741
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Page last reviewed:
Jul 25, 2022
Page last updated:
Jan 27, 2023
Content source:
Office of Genomics and Precision Public Health
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