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Author Details

Megan E Grove
Stanford Medicine Clinical Genomics Program
2011
22
13
PMIDPaper TitleJournal TitlePublished Year
35020984Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting.N Engl J Med2022
35347328Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing.Nat Biotechnol2022
35394429PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families.Genet Med2022
35133172Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock.Circ Genom Precis Med2022
34400813PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families.Genet Med2021
31570382Informed Consent in the Genomics Era.Cold Spring Harb Perspect Med2020
33319814Clinical utility of genomic sequencing: a measurement toolkit.NPJ Genom Med2020
30964584A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.J Genet Couns2019
30920161Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.Am J Med Genet A2019
30706981Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.J Genet Couns2019
28640241Long-read genome sequencing identifies causal structural variation in a Mendelian disease.Genet Med2018
29478781Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.Am J Hum Genet2018
29234989Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.J Genet Couns2018
29240077Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience.Genet Med2018
28798026Navigating Genetic and Phenotypic Uncertainty in Left Ventricular Noncompaction.Circ Cardiovasc Genet2017
26932475Medical implications of technical accuracy in genome sequencing.Genome Med2016
27681629Early somatic mosaicism is a rare cause of long-QT syndrome.Proc Natl Acad Sci U S A2016
26448358Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data.PLoS Genet2015
23728783Views of genetics health professionals on the return of genomic results.J Genet Couns2014
24973560Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing.Heart Rhythm2014
24618965Clinical interpretation and implications of whole-genome sequencing.JAMA2014
21292329Faster REM sleep EEG and worse restedness in older insomniacs with HLA DQB1*0602.Psychiatry Res2011
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Collaborators

Euan A Ashley
Stanford University
Co-authored papers 14
Dianna G Fisk
Stanford Medicine Clinical Genomics Program
Co-authored papers 8
Jonathan A Bernstein
Stanford University
Co-authored papers 8
Matthew T Wheeler
Stanford University School of Medicine
Co-authored papers 6
Daryl Waggott
Ontario Institute for Cancer Research
Co-authored papers 5
Jason D Merker
UNC School of Medicine, The University of North Carolina at Chapel Hill
Co-authored papers 5
Jennefer N Kohler
Stanford Center for Undiagnosed Diseases
Co-authored papers 4
James R Priest
Stanford University School of Medicine
Co-authored papers 4
Frederick E Dewey
Co-authored papers 4
Kelly E Ormond
Stanford University School of Medicine
Co-authored papers 4
Marco V Perez
Co-authored papers 3
Jean Monlong
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Robert McFarland
Newcastle University
Co-authored papers 3
Robert W Taylor
Newcastle upon Tyne Hospitals NHS Foundation Trust
Co-authored papers 3
Michael Snyder
Stanford University
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Johannes A Mayr
University Children's Hospital, Paracelsus Medical University
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Miten Jain
Northeastern University
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Andrew Carroll
Google LLC
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Paul G Fisher
Stanford University
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Thomas Quertermous
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Fritz J Sedlazeck
Baylor College of Medicine
Co-authored papers 3
Benedict Paten
UC Santa Cruz Genomics Institute, University of California
Co-authored papers 3
Laure Fr??sard
Invitae Corporation
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Liliana Fernandez
Stanford Center for Undiagnosed Diseases
Co-authored papers 2
Matthew T Wheeler
Center for Undiagnosed Diseases, Stanford University
Co-authored papers 2
Peter M George
University of Otago
Co-authored papers 2
Zachary Zappala
Vertex Pharmaceuticals
Co-authored papers 2
Mildred K Cho
Center for Biomedical Ethics, Stanford University School of Medicine
Co-authored papers 2
Teri E Klein
Stanford University
Co-authored papers 2
Yaping Yang
Baylor College of Medicine
Co-authored papers 2
Release 1.2