Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review

Genomics & Health Impact Scan Database|Search|PHGKB

Publication
Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review.   Shah Lisa L et al. Journal of genetic counseling 2018 Feb
A systematic review of genetic mutations in pulmonary arterial hypertension.   Garcia-Rivas Gerardo et al. BMC medical genetics 2017 18(1) 82
A systematic review of perceived risks, psychological and behavioral impacts of genetic testing.   Heshka Jodi T et al. Genetics in medicine : official journal of the American College of Medical Genetics 2008 Jan 10(1) 19-32
Comparing Outcomes of Genetic Counseling Options in Breast and Ovarian Cancer: An Integrative Review?.   Fournier Danielle M et al. Oncology nursing forum 2018 Jan 45(1) 96-105
Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics.   Collet Gaëlle et al. Familial cancer 2017 Oct
Missed therapeutic and prevention opportunities in women with BRCA-mutated epithelial ovarian cancer and their families due to low referral rates for genetic counseling and BRCA testing: A review of the literature.   Hoskins Paul J et al. CA: a cancer journal for clinicians 2017 Sep
A Systematic Review on the Existing Screening Pathways for Lynch Syndrome Identification.   Tognetto Alessia et al. Frontiers in public health 2017 5243
Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: protocol for a systematic review.   Zhong Adrina et al. Systematic reviews 2017 Jul 6(1) 140
Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review.   Young Alison L et al. Journal of genetic counseling 2017 Jun
The Efficacy of Genetic Counseling for Psychiatric Disorders: a Meta-Analysis.   Moldovan Ramona et al. Journal of genetic counseling 2017 Jun
Health risks for ataxia-telangiectasia mutated heterozygotes: a systematic review, meta-analysis and evidence-based guideline.   van Os N J H et al. Clinical genetics 2016 Aug 90(2) 105-17
Personal utility in genomic testing: a systematic literature review.   Kohler Jennefer N et al. European journal of human genetics : EJHG 2017 Mar
A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling.   Athens Barbara A et al. Journal of genetic counseling 2017 Mar
Parents' Attitudes toward Genetic Testing of Children for Health Conditions: A Systematic Review.   Lim Qishan et al. Clinical genetics 2017 Feb
Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counseling for hereditary cancer: a systematic review.   Willis Amanda M et al. Clinical genetics 2016 Sep
Analyzing communication in genetic consultations--a systematic review.   Paul Jean et al. Patient education and counseling 2015 Jan 98(1) 15-33
"Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches".   Butler Merlin G et al. Current pediatric reviews 2015 Nov
Interactive e-counselling for genetics pre-test decisions: where are we now?   Birch P H et al. Clinical genetics 2015 Mar 87(3) 209-17
Components of genetic counsellor education: A systematic review of the peer-reviewed literature.   Ingvoldstad C et al. Journal of community genetics 2015 Oct
Direct-to-Consumer Genetic Testing: A Systematic Review of European Guidelines, Recommendations, and Position Statements.   Rafiq Muhammad et al. Genet Test Mol Biomarkers 2015 Aug 27.
How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence.   Mendes Álvaro et al. Eur. J. Hum. Genet. 2015 Aug 12.
Technical Update: Preimplantation Genetic Diagnosis and Screening.   Dahdouh Elias M et al. J Obstet Gynaecol Can 2015 May 37(5) 451-63
Exploring the Effectiveness of Mandatory Premarital Screening and Genetic Counselling Programmes for ß-Thalassaemia in the Middle East: A Scoping Review.   Saffi Marwa et al. Public Health Genomics 2015 May 29.
Practical guidelines for managing adults with 22q11.2 deletion syndrome.
Medical genetic counseling for breast cancer in primary care: a synthesis of major determinants of physicians' practices in primary care settings.
The role of the genetic counsellor: a systematic review of research evidence.
The Psychological Impact of Predictive Genetic Testing for Huntington's Disease: A Systematic Review of the Literature.
A systematic review of factors that act as barriers to patient referral to genetic services.
Points to consider in the clinical use of NGS panels for mitochondrial disease: an analysis of gene inclusion and consent forms.
Genetic testing in the clinical care of patients with pheochromocytoma and paraganglioma.
Predictors of genetic testing decisions: a systematic review and critique of the literature.
Genetic counselling in ALS: facts, uncertainties and clinical suggestions.
Medical genetics and genetic counseling in Chile.
Incidental findings from clinical genome-wide sequencing: a review.
Development of genetic counseling services in Taiwan.
SCN1A testing for epilepsy: application in clinical practice.
Ethical, legal, and counseling challenges surrounding the return of genetic results in oncology.
Disclosing incidental findings in genetics contexts: a review of the empirical ethical research.
Psychosocial approaches to participation in BRCA1/2 genetic risk assessment among African American women: a systematic review.
Genetic risk assessments in individuals at high risk for inherited breast cancer in the breast oncology care setting.
Hereditary cancer risk assessment: essential tools for a better approach.
A genetic counselor's guide to using next-generation sequencing in clinical practice.
Clinical utility gene card for: Huntington's disease.
Clinical utility gene card for: 16p13.11 microdeletion syndrome.
Leveraging the electronic health record to implement genomic medicine.
Current approaches in hereditary nonpolyposis colorectal cancer.
Management of genetic syndromes predisposing to gynecologic cancers.
Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.