Literature DB >> 25764213

Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics.

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Abstract

DISCLAIMER: These recommendations are designed primarily as an educational resource for medical geneticists and other health-care providers to help them provide quality medical genetics services. Adherence to these recommendations does not necessarily ensure a successful medical outcome. These recommendations should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, geneticists and other clinicians should apply their own professional judgment to the specific clinical circumstances presented by the individual patient or specimen. It may be prudent, however, to document in the patient's record the rationale for any significant deviation from these recommendations.

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Year:  2015        PMID: 25764213     DOI: 10.1038/gim.2015.41

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  3 in total

Review 1.  American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.

Authors:  Mark E Robson; Courtney D Storm; Jeffrey Weitzel; Dana S Wollins; Kenneth Offit
Journal:  J Clin Oncol       Date:  2010-01-11       Impact factor: 44.544

2.  What is the clinical utility of genetic testing?

Authors:  Scott D Grosse; Muin J Khoury
Journal:  Genet Med       Date:  2006-07       Impact factor: 8.822

3.  ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

Authors:  Robert C Green; Jonathan S Berg; Wayne W Grody; Sarah S Kalia; Bruce R Korf; Christa L Martin; Amy L McGuire; Robert L Nussbaum; Julianne M O'Daniel; Kelly E Ormond; Heidi L Rehm; Michael S Watson; Marc S Williams; Leslie G Biesecker
Journal:  Genet Med       Date:  2013-06-20       Impact factor: 8.822

  3 in total
  58 in total

Review 1.  Ethical considerations in genomic testing for hematologic disorders.

Authors:  Jonathan M Marron; Steven Joffe
Journal:  Blood       Date:  2017-06-09       Impact factor: 22.113

2.  Integrating Genomics into Healthcare: A Global Responsibility.

Authors:  Zornitza Stark; Lena Dolman; Teri A Manolio; Brad Ozenberger; Sue L Hill; Mark J Caulfied; Yves Levy; David Glazer; Julia Wilson; Mark Lawler; Tiffany Boughtwood; Jeffrey Braithwaite; Peter Goodhand; Ewan Birney; Kathryn N North
Journal:  Am J Hum Genet       Date:  2019-01-03       Impact factor: 11.025

3.  Communication of genetic-based risk of disease to influence behavior change.

Authors:  D B Clark
Journal:  Oral Dis       Date:  2016-07-04       Impact factor: 3.511

4.  Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard.

Authors:  Bret S E Heale; Casey Lynnette Overby; Guilherme Del Fiol; Wendy S Rubinstein; Donna R Maglott; Tristan H Nelson; Aleksandar Milosavljevic; Christa L Martin; Scott R Goehringer; Robert Freimuth; Marc S Williams
Journal:  Appl Clin Inform       Date:  2016-08-31       Impact factor: 2.342

5.  Large, Prospective Analysis of the Reasons Patients Do Not Pursue BRCA Genetic Testing Following Genetic Counseling.

Authors:  Sommer Hayden; Sarah Mange; Debra Duquette; Nancie Petrucelli; Victoria M Raymond
Journal:  J Genet Couns       Date:  2017-01-16       Impact factor: 2.537

Review 6.  Family-Specific Variants and the Limits of Human Genetics.

Authors:  Brian H Shirts; Colin C Pritchard; Tom Walsh
Journal:  Trends Mol Med       Date:  2016-10-11       Impact factor: 11.951

7.  Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray.

Authors:  Robin Z Hayeems; Jasmin Bhawra; Kate Tsiplova; M Stephen Meyn; Nasim Monfared; Sarah Bowdin; D James Stavropoulos; Christian R Marshall; Raveen Basran; Cheryl Shuman; Shinya Ito; Iris Cohn; Courtney Hum; Marta Girdea; Michael Brudno; Ronald D Cohn; Stephen W Scherer; Wendy J Ungar
Journal:  Eur J Hum Genet       Date:  2017-11-20       Impact factor: 4.246

8.  Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project.

Authors:  Stacey Pereira; Jill Oliver Robinson; Amanda M Gutierrez; Devan K Petersen; Rebecca L Hsu; Caroline H Lee; Talia S Schwartz; Ingrid A Holm; Alan H Beggs; Robert C Green; Amy L McGuire
Journal:  Pediatrics       Date:  2019-01       Impact factor: 7.124

9.  Development of a Streamlined Work Flow for Handling Patients' Genetic Testing Insurance Authorizations.

Authors:  Wendy R Uhlmann; Katie Schwalm; Victoria M Raymond
Journal:  J Genet Couns       Date:  2017-04-24       Impact factor: 2.537

10.  Cases in Precision Medicine: Should You Participate in a Study Involving Genomic Sequencing of Your Patients?

Authors:  Paul S Appelbaum; Deborah F Stiles; Wendy Chung
Journal:  Ann Intern Med       Date:  2019-10-01       Impact factor: 25.391

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