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Family Health History

Last data update: Oct 04, 2022. (Total: 49850 Documents since 2012)
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Query Trace: all[original query]>>Original Studies[Product Type]
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
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
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
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
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
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
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
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
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)
Pancreatic Ductal Carcinoma Risk Associated with Hereditary Cancer-Risk Genes.
Gardiner Anna et al. Journal of the National Cancer Institute 2022
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)
Age determines the risk of familial inflammatory bowel disease-A nationwide study.
Halfvarson Jonas F et al. Alimentary pharmacology & therapeutics 2022
Cost-effectiveness of artificial intelligence for screening colonoscopy: a modelling study.
Areia Miguel et al. The Lancet. Digital health 2022
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)
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)
Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome.
Guan Bao et al. Frontiers in oncology 2022 12774202
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
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
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
Phenotypic and genotypic characterization of familial hypercholesterolemia in French adult and pediatric populations.
Fourgeaud Mélanie et al. Journal of clinical lipidology 2022
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
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
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
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
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
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
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
Prostate cancer incidence and survival in relation to prostate cancer as second cancer in relatives.
Zheng Guoqiao et al. Cancer medicine 2022
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