Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Advances in Family Practice NursingAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Initial sequencing and analysis of the human genome.Nature. 2001; 409: 860-921
- Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis.Gastroenterology. 2004; 127: 444-451
- Recommendations for standardized human pedigree nomenclature. pedigree standardization task force of the national society of genetic counselors.Am J Hum Genet. 1995; 56: 745-752
- Standardized human pedigree nomenclature: update and assessment of the recommendations of the national society of genetic counselors.J Genet Couns. 2008; 17: 424-433
- Family health history: the first genetic test in precision medicine.Med Clin North Am. 2019; 103: 957-966
- Carrier screening for genetic disorders in individuals of Ashkenazi Jewish descent.J Obstet Gynaecol. 2006; 28: 324-332
- A Three-generation pedigree of multifocal heterotopic ossification with bilateral involvement.Orthopedics. 2021; 44: e139-e145
- Monogenic parkinson's disease: genotype, phenotype, pathophysiology, and genetic testing.Genes (Basel). 2022; 13https://doi.org/10.3390/genes13030471
- The complex relationship between genotype, pathology and phenotype in familial dementia.Neurobiol Dis. 2020; 145: 105082
- Collection of pedigree data for genetic analysis in isolate populations.Hum Biol. 2006; 78: 89-101
- Estimating the age at onset distribution of the asymptomatic stage of a genetic disease based on pedigree data.Stat Methods Med Res. 2020; 29: 2344-2359
- The Danish HD Registry-a nationwide family registry of HD families in Denmark.Clin Genet. 2017; 92: 338-341
- Population genetic considerations for using biobanks as international resources in the pandemic era and beyond.BMC Genomics. 2021; 22: 351
- Basic principles of biobanking: from biological samples to precision medicine for patients.Virchows Arch. 2021; 479: 233-246
- Genome-Wide Association Studies Fact Sheet.(Updated 8/17/2020. Accessed August 28, 2022)
- Malignant Hyperthermia Update.Anesthesiol Clin. 2020; 38: 165-181
- Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer.Cancer Med. 2017; 6: 3014-3024
- Melanoma genetics.J Med Genet. 2016; 53: 1-14
- NEK11 as a candidate high-penetrance melanoma susceptibility gene.J Med Genet. 2020; 57: 203-210
- Surveillance for familial melanoma: recommendations from a national centre of expertise.Br J Dermatol. 2019; 181: 594-596
- Role of family history and clinical screening in the identification of families with idiopathic dilated cardiomyopathy in Johannesburg, South Africa.S Afr Med J. 2019; 109: 673-678
- Clinical characteristics and outcomes of familial and idiopathic dilated cardiomyopathy in Cape Town: a comparative study of 120 cases followed up over 14 years.S Afr Med J. 2011; 101: 399-404
- Association of multigenerational family history of depression with lifetime depressive and other psychiatric disorders in children: results from the adolescent brain cognitive development (ABCD) Study.JAMA Psychiatry. 2021; 78: 778-787
- Meaningful associations in the adolescent brain cognitive development study.Neuroimage. 2021; 239: 118262
- Implementation of an electronic genomic and family health history tool in primary prenatal care.Am J Med Genet C Semin Med Genet. 2014; 166c: 34-44
- Family history tools for primary care: A systematic review.Eur J Gen Pract. 2022; 28: 75-86
- Family history tools for primary care are not ready yet to be implemented. A systematic review.Eur J Gen Pract. 2014; 20: 125-133
- SHARE State health alliance for records exchange.Web International, 2022 (Available at:) (Arkansas Department of Health; Arkansas Department of Health Information Technology. Accessed July 4 2022, 2022)
- Development and evaluation of a brief self-completed family history screening tool for common chronic disease prevention in primary care.Br J Gen Pract. 2013; 63: e393-e400
- Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the US Surgeon General's My Family Health Portrait.Genet Med. 2015; 17: 753-756
- The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.Genome Res. 2009; 19: 1665-1674
- Familial colorectal cancer: Patient assessment, surveillance and surgical management.Eur J Surg Oncol. 2017; 43: 294-302
- New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.Gastroenterology. 1999; 116: 1453-1456
- Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.J Natl Cancer Inst. 2004; 96: 261-268
- NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019.J Natl Compr Canc Netw. 2019; 17: 1032-1041
- Utility of a virtual counselor (VICKY) to collect family health histories among vulnerable patient populations: A randomized controlled trial.Patient Educ Couns. 2021; 104: 979-988
- Designing and Evaluating a Digital Family Health History Tool for Spanish Speakers.Int J Environ Res Public Health. 2019; 16: 4979
- Research priorities for evaluating family history in the prevention of common chronic diseases..Am J Of Prev Med. 2003; 24: 128-135
- MMWR Morb Mortal Wkly Rep. 2016; 65: 1305
- APOE and Alzheimer's disease: advances in genetics, pathophysiology, and therapeutic approaches.Lancet Neurol. 2021; 20: 68-80
- Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study.Nat Commun. 2020; 11: 667
- Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.Bull World Health Organ. 2008; 86: 317-319
- Genetic testing for suicide risk assessment: Theoretical premises, research challenges and ethical concerns.Prev Med. 2021; 152: 106685
Article info
Identification
Copyright
© 2022 Elsevier Inc. All rights reserved.