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Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations. Conceição Isabel et al. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2019 Feb 1-7 Similar articles in PubMed
Draft Recommendation Statement and Draft Evidence Review: Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer
Consensus guidelines for genetic testing for hereditary breast and ovarian cancer American Society for Breast Surgeons, February 14, 2019
Draft Recommendation Statement BRCA-Related Cancer: Risk Assessment, Genetic Counseling, and Genetic Testing USPSTF, February 2019
Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2D6 genotype and use of ondansetron and tropisetron. Bell G C et al. Clinical pharmacology and therapeutics 2017 102(2) 213-218 Similar articles in PubMed
Recommendations for the clinical interpretation of genetic variants and presentation of results to patients with inherited bleeding disorders. A UK Haemophilia Centre Doctors' Organisation Good Practice Paper. Gomez Keith et al. Haemophilia : the official journal of the World Federation of Hemophilia 2019 Jan 25(1) 116-126 Similar articles in PubMed
Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG). David Karen L et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Dec Similar articles in PubMed
Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer-an European consensus statement and expert recommendations. Singer Christian F et al. European journal of cancer (Oxford, England : 1990) 2018 Nov 10654-60 Similar articles in PubMed
Evaluating Susceptibility to Pancreatic Cancer: ASCO Provisional Clinical Opinion. Stoffel Elena M et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 Nov JCO1801489 Similar articles in PubMed
Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia. Newson Ainsley J et al. Twin research and human genetics : the official journal of the International Society for Twin Studies 2018 Nov 1-5 Similar articles in PubMed
Development of Criteria for Epilepsy Genetic Testing in Ontario, Canada. Jain Puneet et al. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2018 Nov 1-7 Similar articles in PubMed
Updated Canadian Expert Consensus on Assessing Risk of Disease Progression and Pharmacological Management of Autosomal Dominant Polycystic Kidney Disease. Soroka Steven et al. Canadian journal of kidney health and disease 2018 52054358118801589 Similar articles in PubMed
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics. Carrieri Daniele et al. European journal of human genetics : EJHG 2018 Oct Similar articles in PubMed
Venous thromboembolism laboratory testing (factor V Leiden and factor II c.*97G>A), 2018 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Zhang Shulin et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Oct Similar articles in PubMed
Disclosure of sex when incidentally revealed as part of preimplantation genetic testing (PGT): an Ethics Committee opinion. et al. Fertility and sterility 2018 Sep 110(4) 625-627 Similar articles in PubMed
Consensus Statement of the Indian Academy of Pediatrics in Diagnosis and Management of Hemophilia. Sachdeva Anupam et al. Indian pediatrics 2018 Jul 55(7) 582-590 Similar articles in PubMed
Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel. Sturm Amy C et al. Journal of the American College of Cardiology 2018 Aug 72(6) 662-680 Similar articles in PubMed
Recommendations for genetic testing and counselling after sudden cardiac death: practical aspects for Swiss practice. Medeiros Domingo Argelia et al. Swiss medical weekly 2018 148w14638 Similar articles in PubMed
Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Stewart Douglas R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jul 20(7) 671-682 Similar articles in PubMed
Expert consensus guidelines for the genetic diagnosis of Alport syndrome. Savige Judy et al. Pediatric nephrology (Berlin, Germany) 2018 Jul Similar articles in PubMed
Use of preimplantation genetic testing for monogenic defects (PGT-M) for adult-onset conditions: an Ethics Committee opinion. et al. Fertility and sterility 2018 Jun 109(6) 989-992 Similar articles in PubMed
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Hershberger Ray E et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jun Similar articles in PubMed
Japanese Society of Medical Oncology Clinical Guidelines: Molecular Testing for Colorectal Cancer Treatment, Third Edition. Yamazaki Kentaro et al. Cancer science 2018 Jun 109(6) 2074-2079 Similar articles in PubMed
Evidence-based best practices for EGFR T790M testing in lung cancer in Canada. Stockley T et al. Current oncology (Toronto, Ont.) 2018 Apr 25(2) 163-169 Similar articles in PubMed
Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group. Taylor Amy et al. Journal of medical genetics 2018 Apr Similar articles in PubMed
The use of preimplantation genetic testing for aneuploidy (PGT-A): a committee opinion. et al. Fertility and sterility 2018 Mar 109(3) 429-436 Similar articles in PubMed
Genetic Evaluation of Cardiomyopathy - a Heart Failure Society of America Practice Guideline. Hershberger Ray E et al. Journal of cardiac failure 2018 Mar Similar articles in PubMed
Pediatric clinical exome/genome sequencing and the engagement process: encouraging active conversation with the older child and adolescent: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG). Bush Lynn W et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Mar Similar articles in PubMed
ClinGen's RASopathy Expert Panel consensus methods for variant interpretation. Gelb Bruce D et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Mar Similar articles in PubMed
Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives. Verhagen Judith M A et al. International journal of cardiology 2018 Feb Similar articles in PubMed
Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors: Guideline From the College of American Pathologists, the International Association for the Study of Lung Cancer, and the Association for Molecular Pathology. Lindeman Neal I et al. Archives of pathology & laboratory medicine 2018 Jan Similar articles in PubMed
Professional responsibilities regarding the provision, publication, and dissemination of patient phenotypes in the context of clinical genetic and genomic testing: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG). Bush Lynn W et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jan Similar articles in PubMed
All patients with colorectal cancer should be tested for genetic condition, NICE advises. Gulland Anne et al. BMJ (Clinical research ed.) 2017 356j998 Similar articles in PubMed
Clinical implications and considerations for evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines. Bean Lora J H et al. Genome medicine 2017 Dec 9(1) 111 Similar articles in PubMed
Laboratory diagnosis of galactosemia: a technical standard and guideline of the American College of Medical Genetics and Genomics (ACMG). Pasquali Marzia et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Oct Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Don't order APOE genetic testing as a predictive test for Alzheimer disease. American College of Medical Genetics and Genomics, Choosing Wisely Campaign Recommendation, 2016
Recent developments in genetics and medically assisted reproduction: from research to clinical applications. Harper J C et al. European journal of human genetics : EJHG 2017 Dec Similar articles in PubMed
European Respiratory Society statement: diagnosis and treatment of pulmonary disease in ?1-antitrypsin deficiency. Miravitlles Marc et al. The European respiratory journal 2017 Nov 50(5) Similar articles in PubMed
Points to consider for laboratories reporting results from diagnostic genomic sequencing. Vears D F et al. European journal of human genetics : EJHG 2017 Nov Similar articles in PubMed
Genetic testing for exercise prescription and injury prevention: AIS-Athlome consortium-FIMS joint statement. Vlahovich Nicole et al. BMC genomics 2017 Nov 18(Suppl 8) 818 Similar articles in PubMed
Committee Opinion No. 724 Summary: Consumer Testing for Disease Risk. et al. Obstetrics and gynecology 2017 Nov 130(5) 1176-1177 Similar articles in PubMed
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 Similar articles in PubMed
People at risk of familial hypercholesterolaemia should have DNA test, says NICE. et al. BMJ (Clinical research ed.) 2017 Nov 359j5112 Similar articles in PubMed
Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant. Borghesi Alessandro et al. Italian journal of pediatrics 2017 Nov 43(1) 100 Similar articles in PubMed
Committee Opinion No. 724: Consumer Testing for Disease Risk. et al. Obstetrics and gynecology 2017 130(5) e270-e273 Similar articles in PubMed
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 Similar articles in PubMed
What's New in Prenatal Genetics? A Review of Current Recommendations and Guidelines. Post Annalisa L et al. Obstetrical & gynecological survey 2017 Oct 72(10) 610-617 Similar articles in PubMed
Familial Hypercholesterolemia: A Systematic Review of Guidelines on Genetic Testing and Patient Management. Migliara Giuseppe et al. Frontiers in public health 2017 5252 Similar articles in PubMed
Practice Bulletin No. 182 Summary: Hereditary Breast and Ovarian Cancer Syndrome. et al. Obstetrics and gynecology 2017 Sep 130(3) 657-659 Similar articles in PubMed
Practice Bulletin No 182: Hereditary Breast and Ovarian Cancer Syndrome. et al. Obstetrics and gynecology 2017 130(3) e110-e126 Similar articles in PubMed
Brazilian consensus on Duchenne muscular dystrophy. Part 1: diagnosis, steroid therapy and perspectives. Araujo Alexandra P Q C et al. Arquivos de neuro-psiquiatria 2017 Aug 75(8) 104-113 Similar articles in PubMed
Don't order HFE genetic testing for a patient without iron overload or a family history of HFE-associated hereditary hemochromatosis. American College of Medical Genetics, 2015
Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics. Strovel Erin T et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jul Similar articles in PubMed
Position Statement on the Diagnosis and Management of Familial Dilated Cardiomyopathy. Fatkin Diane et al. Heart, lung & circulation 2017 Jun Similar articles in PubMed
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 Similar articles in PubMed
Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria. Nykamp Keith et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 May Similar articles in PubMed
Investigation of the utility of various diagnostic guidelines for Wilson's disease. Nakai Masato et al. Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology 2017 114(5) 839-845 Similar articles in PubMed
Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiency. McGovern Margaret M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Apr Similar articles in PubMed
Guidelines for Validation of Next-Generation Sequencing-Based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists. Jennings Lawrence J et al. The Journal of molecular diagnostics : JMD 2017 Mar Similar articles in PubMed
What do the new American College of Medical Genetics and Genomics (ACMG) guidelines mean for the provision of non-invasive prenatal genetic screening? Allyse Megan et al. Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology 2017 Apr 1-4 Similar articles in PubMed
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 Similar articles in PubMed
Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel. Wirrell Elaine C et al. Pediatric neurology 2017 Mar 6818-34.e3 Similar articles in PubMed
Clinical use of biomarkers in breast cancer: Updated guidelines from the European Group on Tumor Markers (EGTM). Duffy M J et al. European journal of cancer (Oxford, England : 1990) 2017 Feb 75284-298 Similar articles in PubMed
Genomic newborn screening: public health policy considerations and recommendations. Friedman Jan M et al. BMC medical genomics 2017 Feb 10(1) 9 Similar articles in PubMed
Committee Opinion No. 691 Summary: Carrier Screening for Genetic Conditions. et al. Obstetrics and gynecology 2017 Mar 129(3) 597-599 Similar articles in PubMed
Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine. et al. Obstetrics and gynecology 2017 Mar 129(3) 595-596 Similar articles in PubMed
Initial Diagnostic Workup of Acute Leukemia: Guideline From the College of American Pathologists and the American Society of Hematology. Arber Daniel A et al. Archives of pathology & laboratory medicine 2017 Feb Similar articles in PubMed
Pharmacogenetics in cardiovascular diseases: State of the art and implementation-recommendations of the French National Network of Pharmacogenetics (RNPGx). Lamoureux Fabien et al. Therapie 2017 Jan Similar articles in PubMed
HER2 Testing and Clinical Decision Making in Gastroesophageal Adenocarcinoma: Guideline From the College of American Pathologists, American Society for Clinical Pathology, and American Society of Clinical Oncology. Bartley Angela N et al. American journal of clinical pathology 2016 Dec 146(6) 647-669 Similar articles in PubMed
American college of medical genetics and genomics updates secondary findings guidelines: Revision adds new genes to testing list, outlines standardized process for including variants on list. et al. American journal of medical genetics. Part A 2017 Mar 173(3) 576-577 Similar articles in PubMed
Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and American Society of Clinical Oncology. Sepulveda Antonia R et al. Archives of pathology & laboratory medicine 2017 Feb Similar articles in PubMed
Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation. Farrell Philip M et al. The Journal of pediatrics 2017 Feb 181SS4-S15.e1 Similar articles in PubMed
Diagnosis of Cystic Fibrosis in Screened Populations. Farrell Philip M et al. The Journal of pediatrics 2017 Feb 181SS33-S44.e2 Similar articles in PubMed
Genome editing in clinical genetics: points to consider-a statement of the American College of Medical Genetics and Genomics. Acmg Board Of Directors et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jan Similar articles in PubMed
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 Similar articles in PubMed
Clinical worthlessness of genetic prediction of common forms of diabetes mellitus and related chronic complications.: A position statement of the Italian Society of Diabetology. Buzzetti R et al. Nutrition, metabolism, and cardiovascular diseases : NMCD 2016 Aug Similar articles in PubMed
[Diagnosis and treatment of familial hypercholesterolemia in Spain: consensus document]. Mata Pedro et al. Atencion primaria 2015 Jan 47(1) 56-65 Similar articles in PubMed
Laboratory and clinical genomic data sharing is crucial to improving genetic health care: a position statement of the American College of Medical Genetics and Genomics. Acmg Board Of Directors et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jan Similar articles in PubMed
Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists. Li Marilyn M et al. The Journal of molecular diagnostics : JMD 2017 Jan 19(1) 4-23 Similar articles in PubMed
Ethics of genetic testing and research in sport: a position statement from the Australian Institute of Sport. Vlahovich Nicole et al. British journal of sports medicine 2016 Nov Similar articles in PubMed
Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. Döhner Hartmut et al. Blood 2016 Nov Similar articles in PubMed
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. Kalia Sarah S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Nov Similar articles in PubMed
Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas. et al. Nature reviews. Endocrinology 2016 Nov Similar articles in PubMed
Extended RAS Gene Mutation Testing in Metastatic Colorectal Carcinoma to Predict Response to Anti-Epidermal Growth Factor Receptor Monoclonal Antibody Therapy: American Society of Clinical Oncology Provisional Clinical Opinion Update 2015 Summary. Allegra Carmen J et al. Journal of oncology practice 2016 Feb 12(2) 180-1 Similar articles in PubMed
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient. Liming Bryan J et al. International journal of pediatric otorhinolaryngology 2016 Nov 90251-258 Similar articles in PubMed
Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association. Mital Seema et al. Circulation. Cardiovascular genetics 2016 Sep Similar articles in PubMed
Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening. Paluch-Shimon S et al. Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2016 Sep 27(suppl 5) v103-v110 Similar articles in PubMed
The utility of genetic testing in neuromuscular disease: A Consensus Statement From the AANEM on the Clinical Utility of Genetic Testing in Diagnosis of Neuromuscular Disease. Aanem Aanem et al. Muscle & nerve 2016 Aug Similar articles in PubMed
Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics. Gregg Anthony R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jul Similar articles in PubMed
Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC). Caudle Kelly E et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jul Similar articles in PubMed
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 Similar articles in PubMed
Guide and Position of the International Society of Nutrigenetics/Nutrigenomics on Personalized Nutrition: Part 2 - Ethics, Challenges and Endeavors of Precision Nutrition. Kohlmeier Martin et al. Journal of nutrigenetics and nutrigenomics 2016 Jun 9(1) 28-46 Similar articles in PubMed
Recommendations for the implementation of BRCA testing in the care and treatment pathways of ovarian cancer patients. Pinto Carmine et al. Future oncology (London, England) 2016 May Similar articles in PubMed
Presymptomatic ALS genetic counseling and testing: Experience and recommendations. Benatar Michael et al. Neurology 2016 May Similar articles in PubMed
Recommendations for Genetic Testing to Reduce the Incidence of Anthracycline-induced Cardiotoxicity. Aminkeng Folefac et al. British journal of clinical pharmacology 2016 May Similar articles in PubMed
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome. Eggermann Katja et al. European journal of human genetics : EJHG 2016 May Similar articles in PubMed
AGO Austria recommendations for genetic testing of patients with ovarian cancer. Marth Christian et al. Wiener klinische Wochenschrift 2015 Aug 127(15-16) 652-4 Similar articles in PubMed