Megan E Grove

Megan E Grove

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Megan E Grove

Megan E Grove

Publications by authors named "Megan E Grove"

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14Publications

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Informed Consent in the Genomics Era.

Cold Spring Harb Perspect Med 2019 Sep 30. Epub 2019 Sep 30.

Stanford Center for Biomedical Ethics, Stanford, California 94305, USA.

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http://dx.doi.org/10.1101/cshperspect.a036582DOI Listing
September 2019

Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.

J Genet Couns 2018 08 12;27(4):751-760. Epub 2017 Dec 12.

Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, CA, USA.

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http://dx.doi.org/10.1007/s10897-017-0175-7DOI Listing
August 2018

Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience.

Genet Med 2018 Mar 14;20(3):369-373. Epub 2017 Dec 14.

Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, USA.

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http://dx.doi.org/10.1038/gim.2017.212DOI Listing
March 2018

Navigating Genetic and Phenotypic Uncertainty in Left Ventricular Noncompaction.

Circ Cardiovasc Genet 2017 08;10(4)

From the Department of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, CA (J.-W.R., E.A.A.); Clinical Genomics Program, Stanford Health Care, CA (M.E.G., E.A.A.); and Department of Genetics (E.A.A.) and Center for Inherited Cardiovascular Disease (E.A.A.), Stanford University, CA.

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http://dx.doi.org/10.1161/CIRCGENETICS.117.001857DOI Listing
August 2017

Medical implications of technical accuracy in genome sequencing.

Genome Med 2016 Mar 2;8(1):24. Epub 2016 Mar 2.

Department of Medicine, Stanford University, Stanford, CA, 94305, USA.

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http://dx.doi.org/10.1186/s13073-016-0269-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774017PMC
March 2016

Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data.

PLoS Genet 2015 Oct 8;11(10):e1005496. Epub 2015 Oct 8.

Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Cardiovascular Medicine, Stanford University, Stanford, California, United States of America; Department of Genetics, Stanford University, Stanford, California, United States of America.

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http://dx.plos.org/10.1371/journal.pgen.1005496
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http://dx.doi.org/10.1371/journal.pgen.1005496DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598191PMC
October 2015

Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing.

Heart Rhythm 2014 Oct 25;11(10):1707-13. Epub 2014 Jun 25.

Division of Cardiovascular Medicine; Child Health Research Institute; Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California. Electronic address:

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http://dx.doi.org/10.1016/j.hrthm.2014.06.030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379486PMC
October 2014

Views of genetics health professionals on the return of genomic results.

J Genet Couns 2014 Aug 2;23(4):531-8. Epub 2013 Jun 2.

Department of Genetics, Stanford University, Stanford, CA, USA.

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http://dx.doi.org/10.1007/s10897-013-9611-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809025PMC
August 2014