Literature DB >> 33951936

Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network.

Sadiya S Khan1,2, Christin Hoell3, Lisa M Castillo3, John J Connolly4, David R Crosslin5, Wendy K Chung6, Adam S Gordon3, Margaret Harr4, Gail P Jarvik7, Iftikhar Kullo8, Eric B Larson9, Kathleen A Leppig9, Teri Manolio10, Jennifer A Pacheco3, James D Ralston9, Megan J Puckelwartz3, Maureen E Smith3, Quinn Wells11, Elizabeth M McNally1,3, Laura J Rasmussen-Torvik2.   

Abstract

Entities:  

Keywords:  cardiomyopathies; diagnosis; genetics; medical records; population

Mesh:

Year:  2021        PMID: 33951936      PMCID: PMC8488964          DOI: 10.1161/CIRCHEARTFAILURE.120.008155

Source DB:  PubMed          Journal:  Circ Heart Fail        ISSN: 1941-3289            Impact factor:   8.790


× No keyword cloud information.
  5 in total

1.  Heart Disease and Stroke Statistics-2020 Update: A Report From the American Heart Association.

Authors:  Salim S Virani; Alvaro Alonso; Emelia J Benjamin; Marcio S Bittencourt; Clifton W Callaway; April P Carson; Alanna M Chamberlain; Alexander R Chang; Susan Cheng; Francesca N Delling; Luc Djousse; Mitchell S V Elkind; Jane F Ferguson; Myriam Fornage; Sadiya S Khan; Brett M Kissela; Kristen L Knutson; Tak W Kwan; Daniel T Lackland; Tené T Lewis; Judith H Lichtman; Chris T Longenecker; Matthew Shane Loop; Pamela L Lutsey; Seth S Martin; Kunihiro Matsushita; Andrew E Moran; Michael E Mussolino; Amanda Marma Perak; Wayne D Rosamond; Gregory A Roth; Uchechukwu K A Sampson; Gary M Satou; Emily B Schroeder; Svati H Shah; Christina M Shay; Nicole L Spartano; Andrew Stokes; David L Tirschwell; Lisa B VanWagner; Connie W Tsao
Journal:  Circulation       Date:  2020-01-29       Impact factor: 29.690

2.  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.

Authors:  Sarah S Kalia; Kathy Adelman; Sherri J Bale; Wendy K Chung; Christine Eng; James P Evans; Gail E Herman; Sophia B Hufnagel; Teri E Klein; Bruce R Korf; Kent D McKelvey; Kelly E Ormond; C Sue Richards; Christopher N Vlangos; Michael Watson; Christa L Martin; David T Miller
Journal:  Genet Med       Date:  2016-11-17       Impact factor: 8.822

3.  Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.

Authors:  Georgia L Wiesner; Alanna Kulchak Rahm; Paul Appelbaum; Sharon Aufox; Sarah T Bland; Carrie L Blout; Kurt D Christensen; Wendy K Chung; Ellen Wright Clayton; Robert C Green; Margaret H Harr; Nora Henrikson; Christin Hoell; Ingrid A Holm; Gail P Jarvik; Iftikhar J Kullo; Philip E Lammers; Eric B Larson; Noralane M Lindor; Maddalena Marasa; Melanie F Myers; Josh F Peterson; Cynthia A Prows; James D Ralston; Hila Milo Rasouly; Richard R Sharp; Maureen E Smith; Sara L Van Driest; Janet L Williams; Marc S Williams; Julia Wynn; Kathleen A Leppig
Journal:  J Pers Med       Date:  2020-04-27

4.  Primary Care Physicians' Knowledge, Attitudes, and Experience with Personal Genetic Testing.

Authors:  Susanne B Haga; Esther Kim; Rachel A Myers; Geoffrey S Ginsburg
Journal:  J Pers Med       Date:  2019-05-24

5.  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

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.