Genetic Evaluation of Cardiomyopathy - a Heart Failure Society of America Practice Guideline

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Genetic Evaluation of Cardiomyopathy - a Heart Failure Society of America Practice Guideline.   Hershberger Ray E et al. Journal of cardiac failure 2018 Mar
Diagnosis and Management of Gaucher Disease in India - Consensus Guidelines of the Gaucher Disease Task Force of the Society for Indian Academy of Medical Genetics and the Indian Academy of Pediatrics.   et al. Indian pediatrics 2018 Feb 55(2) 143-153
ACOG Committee Opinion No. 727: Cascade Testing: Testing Women for Known Hereditary Genetic Mutations Associated With Cancer.   et al. Obstetrics and gynecology 2018 Jan 131(1) e31-e34
ACOG Committee Opinion No. 727 Summary: Cascade Testing: Testing Women For Known Hereditary Genetic Mutations Associated With Cancer.   et al. Obstetrics and gynecology 2018 Jan 131(1) 194-195
Role of Genetic Testing for Inherited Prostate Cancer Risk: Philadelphia Prostate Cancer Consensus Conference 2017.   Giri Veda N et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2017 Dec JCO2017741173
Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.   Ripperger Tim et al. American journal of medical genetics. Part A 2017 Apr 173(4) 1017-1037
Screening Children at Risk for Retinoblastoma: Consensus Report from the American Association of Ophthalmic Oncologists and Pathologists.   Skalet Alison H et al. Ophthalmology 2017 Oct
Practice Bulletin No. 182 Summary: Hereditary Breast and Ovarian Cancer Syndrome.   et al. Obstetrics and gynecology 2017 Sep 130(3) 657-659
Committee Opinion No. 716 Summary: The Role of the Obstetrician-Gynecologist in the Early Detection of Epithelial Ovarian Cancer in Women at Average Risk.   et al. Obstetrics and gynecology 2017 Sep 130(3) 664-665
Practice Bulletin No 182: Hereditary Breast and Ovarian Cancer Syndrome.   et al. Obstetrics and gynecology 2017 130(3) e110-e126
Multi-disciplinary summit on genetics services for women with gynecologic cancers: A Society of Gynecologic Oncology White Paper.   Randall Leslie M et al. Gynecologic oncology 2017 Jun
Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.   Durno Carol et al. Gastroenterology 2017 Mar
Committee Opinion No. 693: Counseling About Genetic Testing and Communication of Genetic Test Results.   et al. Obstetrics and gynecology 2017 Apr 129(4) e96-e101
The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors.   Middleton Anna et al. European journal of human genetics : EJHG 2017 Mar
Standards for the Reporting of Genetic Counseling Interventions in Research and Other Studies (GCIRS): an NSGC Task Force Report.   Hooker Gillian W et al. Journal of genetic counseling 2017 Feb
Committee Opinion No. 691 Summary: Carrier Screening for Genetic Conditions.   et al. Obstetrics and gynecology 2017 Mar 129(3) 597-599
Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine.   et al. Obstetrics and gynecology 2017 Mar 129(3) 595-596
NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.   Daly Mary B et al. Journal of the National Comprehensive Cancer Network : JNCCN 2017 Jan 15(1) 9-20
Guidelines for the diagnosis, treatment and clinical monitoring of patients with juvenile and adult Pompe disease.   Llerena Junior Juan Clinton et al. Arquivos de neuro-psiquiatria 2016 Feb 74(2) 166-76
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Psychosocial Care.   Tong Allison et al. Seminars in nephrology 2015 Nov 35(6) 590-594.e5
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Screening for Polycystic Kidney Disease.   Rangan Gopala K et al. Seminars in nephrology 2015 Nov 35(6) 557-564.e6
Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot Project.   Hart Sarah J et al. Journal of genetic counseling 2016 Feb 25(1) 6-17
Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing.   Wilson R Douglas et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obste´trique et gyne´cologie du Canada : JOGC 2016 Aug 38(8) 742-762.e3
Prenatal Testing for Adult-Onset Conditions: the Position of the National Society of Genetic Counselors.   Hercher Laura et al. Journal of genetic counseling 2016 Jul
Presymptomatic ALS genetic counseling and testing: Experience and recommendations.   Benatar Michael et al. Neurology 2016 May
Recommendations for the integration of genomics into clinical practice.   Bowdin Sarah et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 May
ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent.   ACOG Committee on Genetics. Obstet Gynecol 2009 Oct (4) 950-3
Responsible implementation of expanded carrier screening.   Henneman Lidewij et al. European journal of human genetics : EJHG 2016 Mar
Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers.   van der Post Rachel S et al. Journal of medical genetics 2015 Jun 52(6) 361-74
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.   Bocchetta Martina et al. Journal of Alzheimer's disease : JAD 2016 Jan
Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.   Daly Mary B et al. Journal of the National Comprehensive Cancer Network : JNCCN 2016 Feb 14(2) 153-62
Singapore Cancer Network (SCAN) Guidelines for Referral for Genetic Evaluation of Common Hereditary Cancer Syndromes.   et al. Annals of the Academy of Medicine, Singapore 2015 Oct 44(10) 492-510
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetics and Genetic Counseling.   Patel Chirag et al. Seminars in nephrology 2015 Nov 35(6) 550-556.e1
Statement of principles on the return of research results and incidental findings in paediatric research: a multi-site consultative process.   Sénécal Karine et al. Genome / National Research Council Canada = Genome / Conseil national de recherches Canada 2015 Nov 1-8
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.   Syngal Sapna et al. The American journal of gastroenterology 2015 Feb 110(2) 223-62; quiz 263
Prenatal Diagnosis Procedures and Techniques to Obtain a Diagnostic Fetal Specimen or Tissue: Maternal and Fetal Risks and Benefits.   Wilson R Douglas et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obste´trique et gyne´cologie du Canada : JOGC 2015 Jul 37(7) 656-70
Committee Opinion No. 640: Cell-free DNA Screening for Fetal Aneuploidy.   Obstet Gynecol 2015 Jun 29.
The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus.   Girardet Anne et al. Eur. J. Hum. Genet. 2015 May 27.
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the U.S. Multi-Society Task Force on Colorectal Cancer.   Giardiello Francis M et al. Gastrointest. Endosc. 2014 Aug 80(2) 197-220
Society of Gynecologic Oncology recommendations for the prevention of ovarian cancer.   Walker Joan L et al. Cancer 2015 Mar 27.
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.   Dondorp Wybo et al. Eur. J. Hum. Genet. 2015 Mar 18.
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.   Stoffel Elena M et al. J. Clin. Oncol. 2015 Jan 10. 33(2) 209-17
Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the american college of medical genetics and genomics, american college of obstetricians and gynecologists, national society of genetic counselors, perinatal quality foundation, and society for maternal-fetal medicine.
Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
Summaries for patients. Assessing the genetic risk for BRCA-related breast or ovarian cancer in women: recommendations from the U.S. Preventive Services Task Force.
EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.
Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation.
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss.
Fabry disease practice guidelines: recommendations of the National Society of Genetic Counselors.
Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors.
ACMG statement on noninvasive prenatal screening for fetal aneuploidy.
The establishment of core competencies for canadian genetic counsellors: validation of practice based competencies.
Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].
Molecular testing for cystic fibrosis carrier status practice guidelines: recommendations of the National Society of Genetic Counselors.
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic).
Newborn screening: education, consent, and the residual blood spot. The position of the national society of genetic counselors.
NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy.
NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer.
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy. European Society of Human Genetics and European Society of Human Reproduction and Embryology.
Recommendations for genetic testing of inherited eye diseases: report of the American Academy of Ophthalmology task force on genetic testing.
Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions.
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors.
ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening.