From Genomics & Health Impact Scan Database

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From Genomics & Health Impact Scan Database

This database includes published scientific literature on evidence-based translation of genomic discoveries into improved health care and disease prevention that have a potential impact on population health.

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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
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
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
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
Molecular testing in holoprosencephaly. Kruszka Paul et al. American journal of medical genetics. Part C, Seminars in medical genetics 2018 May 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
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 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
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
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
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
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 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
Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations. Chinsky Jeffrey M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Aug 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
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 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
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 Similar articles in PubMed
Committee Opinion No. 690: Carrier Screening in the Age of Genomic Medicine. et al. Obstetrics and gynecology 2017 Mar 129(3) e35-e40 Similar articles in PubMed
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 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
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
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 Similar articles in PubMed
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Psychosocial Care. Tong Allison et al. Seminars in nephrology 2015 Nov 35(6) 590-594.e5 Similar articles in PubMed
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 Similar articles in PubMed
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 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
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 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
Presymptomatic ALS genetic counseling and testing: Experience and recommendations. Benatar Michael et al. Neurology 2016 May Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Responsible implementation of expanded carrier screening. Henneman Lidewij et al. European journal of human genetics : EJHG 2016 Mar Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Committee Opinion No. 640: Cell-free DNA Screening for Fetal Aneuploidy. Obstet Gynecol 2015 Jun 29. Similar articles in PubMed
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 Similar articles in PubMed
Society of Gynecologic Oncology recommendations for the prevention of ovarian cancer. Walker Joan L et al. Cancer 2015 Mar 27. Similar articles in PubMed
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. Similar articles in PubMed
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 Similar articles in PubMed
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. Similar articles in PubMed
Genetic/familial high-risk assessment: breast and ovarian, version 1.2014. Similar articles in PubMed
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). Similar articles in PubMed
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. Similar articles in PubMed
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. Similar articles in PubMed
EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013. Similar articles in PubMed
Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation. Similar articles in PubMed
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. Similar articles in PubMed
Fabry disease practice guidelines: recommendations of the National Society of Genetic Counselors. Similar articles in PubMed
ACMG statement on noninvasive prenatal screening for fetal aneuploidy. Similar articles in PubMed
The establishment of core competencies for canadian genetic counsellors: validation of practice based competencies. Similar articles in PubMed
Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected]. Similar articles in PubMed
Molecular testing for cystic fibrosis carrier status practice guidelines: recommendations of the National Society of Genetic Counselors. Similar articles in PubMed
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic). Similar articles in PubMed
Newborn screening: education, consent, and the residual blood spot. The position of the national society of genetic counselors. Similar articles in PubMed
NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy. Similar articles in PubMed
NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer. Similar articles in PubMed
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. Similar articles in PubMed
Recommendations for genetic testing of inherited eye diseases: report of the American Academy of Ophthalmology task force on genetic testing. Similar articles in PubMed
Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions. Similar articles in PubMed
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions. Similar articles in PubMed
Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors. Similar articles in PubMed