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Genomics and Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB
Last data update: Jan 15, 2021. (Total: 38226 Documents since 2012)
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Records 1-30 (of 40 Record(s))
Query Trace: Education[original query]>>Tools/Methods[Product Type]
Publication
Guideline No. 410: Prevention, Screening, Diagnosis, and Pregnancy Management for Fetal Neural Tube Defects.
Wilson R Douglas et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2020 Nov
Human Genetics Society of Australasia Position Statement: Online DNA Testing.
Savard Jacqueline et al. Twin research and human genetics : the official journal of the International Society for Twin Studies 2020 Aug 1-3
Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Position statement on multigene panel testing for patients with colorectal cancer and/or polyposis.
Heald Brandie et al. Familial cancer 2020 Mar
Hereditary Cancer Syndromes and Risk Assessment: ACOG COMMITTEE OPINION SUMMARY, Number 793.
et al. Obstetrics and gynecology 2019 Dec 134(6) 1366-1367
Local Coverage Determination (LCD): Genetic Testing for Lynch Syndrome (L34912)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): BRCA1 and BRCA2 Genetic Testing (L36715)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Flow Cytometry (L33661)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): BRCA1 and BRCA2 Genetic Testing (L36499)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Biomarkers Overview (L35062)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Genomic Sequence Analysis Panels in the Treatment of Hematolymphoid Diseases (L37606)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Foodborne Gastrointestinal Panels Identified by Multiplex Nucleic Acid Amplification (NAATs) (L37709)
The U.S. Centers for Medicare & Medicaid Services
Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes.
Beygo Jasmin et al. European journal of human genetics : EJHG 2019 Jun
Pathophysiology, diagnosis and management of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Study Group on peripartum cardiomyopathy.
Bauersachs Johann et al. European journal of heart failure 2019 Jun
Fifteen-minute consultation: Efficient investigation of the child with early developmental impairment in the era of genomic sequencing.
Coysh Thomas et al. Archives of disease in childhood. Education and practice edition 2019 May
ACOG Committee Opinion No. 778: Newborn Screening and the Role of the Obstetrician-Gynecologist.
et al. Obstetrics and gynecology 2019 May 133(5) e357-e361
ACOG Committee Opinion No. 778 Summary: Newborn Screening and the Role of the Obstetrician-Gynecologist.
et al. Obstetrics and gynecology 2019 May 133(5) 1073-1074
ACOG Committee Opinion No. 768: Genetic Syndromes and Gynecologic Implications in Adolescents.
et al. Obstetrics and gynecology 2019 Mar 133(3) e226-e234
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
Systemic sclerosis: state of the art on clinical practice guidelines.
Smith Vanessa et al. RMD open 2018 4(Suppl 1) e000782
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
Improving Emergency Department-Based Care of Sickle Cell Pain.
Glassberg Jeffrey A et al. Hematology. American Society of Hematology. Education Program 2017 Dec 2017(1) 412-417
Expanded Newborn Screening: Information and Resources for the Family Physician.
Weismiller David Glenn et al. American family physician 2017 Jun 95(11) 703-709
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
Improving molecular testing and personalized medicine in non-small-cell lung cancer in Ontario.
Lim C et al. Current oncology (Toronto, Ont.) 2017 Apr 24(2) 103-110
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
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
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
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
American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility.
Robson Mark E, et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2015 11 0. (31) 3660-7
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