Skip to Main Content

Author Details

James R Priest
Stanford University School of Medicine
2004
56
26
PMIDPaper TitleJournal TitlePublished Year
36601961Relationship Between Ascending Thoracic Aortic Diameter and Blood Pressure: A Mendelian Randomization Study.Arterioscler Thromb Vasc Biol2023
37663545Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndrome.HGG Adv2023
37017090Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.Circ Genom Precis Med2023
36546574Maternal first trimester metabolic profile in pregnancies with transposition of the great arteries.Birth Defects Res2023
34714385Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic Conditions.Pediatr Cardiol2022
35902172Leveraging Machine Learning for Translational Genetics of Cardiovascular Imaging.J Am Coll Cardiol2022
35896539Maternal and perinatal obesity induce bronchial obstruction and pulmonary hypertension via IL-6-FoxO1-axis in later life.Nat Commun2022
35132965Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.JCI Insight2022
33201861Congenital heart disease risk loci identified by genome-wide association study in European patients.J Clin Invest2021
34569705Single-cell transcriptomic landscape of cardiac neural crest cell derivatives during development.EMBO Rep2021
32541024Clonally expanding smooth muscle cells promote atherosclerosis by escaping efferocytosis and activating the complement cascade.Proc Natl Acad Sci U S A2020
32078439Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries.Circ Res2020
31891211Pediatric waitlist and heart transplant outcomes in patients with syndromic anomalies.Pediatr Transplant2020
33226994A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population.PLoS Genet2020
33191768Inherited Extremes of Aortic Diameter Confer Risk for a Specific Class of Congenital Heart Disease.Circ Genom Precis Med2020
33125279Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes.Circ Genom Precis Med2020
32981450Adults With Mild-to-Moderate Congenital Heart Disease Demonstrate Measurable Neurocognitive Deficits.J Am Heart Assoc2020
32308111Maternal Obesity and Diabetes Mellitus as Risk Factors for Congenital Heart Disease in the Offspring.J Am Heart Assoc2020
32327713Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank.Eur J Hum Genet2020
30476213Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.Nucleic Acids Res2019
31712678Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank.Sci Rep2019
31353025Phenome-wide Burden of Copy-Number Variation in the UK Biobank.Am J Hum Genet2019
31308376Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequences.Nat Commun2019
31365875Single-Cell RNA-Seq of the Developing Cardiac Outflow Tract Reveals Convergent Development of the Vascular Smooth Muscle Cells.Cell Rep2019
30813762Substantial Cardiovascular Morbidity in Adults With Lower-Complexity Congenital Heart Disease.Circulation2019
30920163Risk factors associated with the development of double-inlet ventricle congenital heart disease.Birth Defects Res2019
30511478Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts.Genet Epidemiol2019
29254757First Trimester Plasma Glucose Values in Women without Diabetes are Associated with Risk for Congenital Heart Disease in Offspring.J Pediatr2018
29875125Birthweight, Type 2 Diabetes Mellitus, and Cardiovascular Disease: Addressing the Barker Hypothesis With Mendelian Randomization.Circ Genom Precis Med2018
30571578Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.Circulation2018
29555674Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease.Circ Genom Precis Med2018
28786837A primer to clinical genome sequencing.Curr Opin Pediatr2017
27058611De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.PLoS Genet2016
27840109Transcriptomic Profiling Maps Anatomically Patterned Subpopulations among Single Embryonic Cardiac Cells.Dev Cell2016
27681629Early somatic mosaicism is a rare cause of long-QT syndrome.Proc Natl Acad Sci U S A2016
27166384Prepregnancy Diabetes and Offspring Risk of Congenital Heart Disease: A Nationwide Cohort Study.Circulation2016
27466618Standards of Evidence and Mechanistic Inference in Autosomal Recessive Hypercholesterolemia.Arterioscler Thromb Vasc Biol2016
26932475Medical implications of technical accuracy in genome sequencing.Genome Med2016
26173643Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome.Hum Mutat2015
26457543Maternal Midpregnancy Glucose Levels and Risk of Congenital Heart Disease in Offspring.JAMA Pediatr2015
26448358Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data.PLoS Genet2015
24701093Ebstein anomaly and Trisomy 21: A rare association.Ann Pediatr Cardiol2014
25063760Genomics in clinical practice.Heart2014
24973560Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing.Heart Rhythm2014
24558458Self-reported history of childhood smoking is associated with an increased risk for peripheral arterial disease independent of lifetime smoking burden.PLoS One2014
22529060Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects.Am J Med Genet A2012
22743177Triiodothyronine supplementation and cytokines during cardiopulmonary bypass in infants and children.J Thorac Cardiovasc Surg2012
20574534Relationships of the location and content of rounds to specialty, institution, patient-census, and team size.PLoS One2010
17959182A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease.Atherosclerosis2008
18343865Brucellosis and sacroiliitis: a common presentation of an uncommon pathogen.J Am Board Fam Med2008
  • 1 - 50 of 56

Recommended Authors

Seung Hoan Choi
Broad Institute of MIT and Harvard
Career Start Year 2009
Number of shared co-authors 7
Megan J Puckelwartz
Center for Genetic Medicine, Northwestern University Feinberg School of Medicine
Career Start Year 2009
Number of shared co-authors 7
Leo-Pekka Lyytik??inen
Tampere University
Career Start Year 2009
Number of shared co-authors 16
Samantha Baxter
Broad Institute of MIT and Harvard
Career Start Year 2009
Number of shared co-authors 11
Quinn S Wells
Vanderbilt University Medical Center
Career Start Year 2008
Number of shared co-authors 9
John D Overton
Regeneron Pharmaceuticals
Career Start Year 2008
Number of shared co-authors 9
Yiran Guo
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Career Start Year 2007
Number of shared co-authors 6
Jennifer E Below
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Career Start Year 2007
Number of shared co-authors 12
Christoph Preuss
Universite de Montreal
Career Start Year 2007
Number of shared co-authors 3
Erin M Miller
College of Medicine, University of Cincinnati
Career Start Year 2006
Number of shared co-authors 2
Sarah U Morton
Boston Children's Hospital
Career Start Year 2006
Number of shared co-authors 6
Sara M Fitzgerald-Butt
Indiana University School of Medicine
Career Start Year 2005
Number of shared co-authors 4
Victoria N Parikh
Stanford University
Career Start Year 2005
Number of shared co-authors 9
Julie Richer
University of Ottawa, Canada Children's Hospital of Eastern Ontario
Career Start Year 2005
Number of shared co-authors 1
Ali Torkamani
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 6
Christian M Shaffer
Vanderbilt University
Career Start Year 2004
Number of shared co-authors 14
Shaine A Morris
Baylor College of Medicine
Career Start Year 2004
Number of shared co-authors 10
Angharad M Roberts
National Heart and Lung Institute, Imperial College London
Career Start Year 2003
Number of shared co-authors 26
Matthew R G Taylor
Cardiovascular Institute, University of Colorado
Career Start Year 2001
Number of shared co-authors 5
Linnea M Baudhuin
Mayo Clinic
Career Start Year 1999
Number of shared co-authors 0
Ulrich Broeckel
Medical College of Wisconsin
Career Start Year 1998
Number of shared co-authors 9
Joshua D Smith
University of Washington
Career Start Year 1998
Number of shared co-authors 14
Neil A Hanchard
Baylor College of Medicine.
Career Start Year 1998
Number of shared co-authors 8
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Career Start Year 1995
Number of shared co-authors 34
Jonathan D Mosley
Vanderbilt University Medical Center
Career Start Year 1995
Number of shared co-authors 7
Birgit Funke
Partners Healthcare Center for Personalized Genetic Medicine
Career Start Year 1994
Number of shared co-authors 14
Gail P Jarvik
University of Washington Medical Center
Career Start Year 1993
Number of shared co-authors 26
Christopher J O'Donnell
Brigham and Women's Hospital, Harvard Medical School
Career Start Year 1983
Number of shared co-authors 27
John W Belmont
Baylor College of Medicine
Career Start Year 1979
Number of shared co-authors 12
Christine E Seidman
Brigham and Women's Hospital (Y.K.
Career Start Year 1975
Number of shared co-authors 22

Collaborators

Euan A Ashley
Stanford University
Co-authored papers 9
Thomas Quertermous
Co-authored papers 8
Priyanka Saha
CSIR-Indian Institute of Chemical Biology
Co-authored papers 7
Catherine Tcheandjieu
Gladstone Institute of Data Science and Biotechnology, Gladstone Institutes
Co-authored papers 7
Erik Ingelsson
Stanford University School of Medicine
Co-authored papers 6
Joshua W Knowles
Co-authored papers 5
Megan E Grove
Stanford Medicine Clinical Genomics Program
Co-authored papers 4
Richard M Myers
HudsonAlpha Institute for Biotechnology
Co-authored papers 4
Praneetha Potiny
Stanford Cardiovascular Institute, Stanford University
Co-authored papers 3
Mark A Hlatky
Co-authored papers 3
Frederick E Dewey
Co-authored papers 3
Carlos Iribarren
Co-authored papers 3
Themistocles L Assimes
Co-authored papers 3
Alan S Go
Kaiser Permanente Northern California
Co-authored papers 3
Seema Mital
Hospital for Sick Children
Co-authored papers 3
Matthew Aguirre
Stanford University School of Medicine.
Co-authored papers 3
Michael A Portman
Seattle Children's Hospital
Co-authored papers 3
Michael J Bamshad
University of Washington
Co-authored papers 3
Bruce D Gelb
Icahn School of Medicine at Mount Sinai
Co-authored papers 3
Manuel A Rivas
Stanford University School of Medicine
Co-authored papers 3
Madalina Fiterau
College of Information & Computer Sciences at University of Massachusetts Amherst
Co-authored papers 3
Holly K Tabor
Stanford Center for Biomedical Ethics (SCBE), Stanford University
Co-authored papers 3
Bernard Keavney
Co-authored papers 3
Daryl Waggott
Ontario Institute for Cancer Research
Co-authored papers 3
Stefan Gustafsson
Uppsala University
Co-authored papers 3
Evan E Eichler
University of Washington
Co-authored papers 3
Len A Pennacchio
Lawrence Berkeley National Laboratory
Co-authored papers 3
Jessica X Chong
Brotman Baty Institute for Precision Medicine, University of Washington
Co-authored papers 2
Melissa A Haendel
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 2
Scott M Damrauer
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 2
Release 1.2