A Primer to Clinical Genome Sequencing

por Priest, James R
Publicado en Curr Opin Pediatr (2017)

Maternal Obesity and Diabetes Mellitus as Risk Factors for Congenital Heart Disease in the Offspring

por Helle, Emmi, Priest, James R.
Publicado en J Am Heart Assoc (2020)

Genomics in clinical practice

por Priest, James R, Ashley, Euan A
Publicado en Heart (2014)

Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank

por Córdova-Palomera, Aldo, Priest, James R.
Publicado en Sci Rep (2019)

Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease

por Paige, Sharon L., Saha, Priyanka, Priest, James R.
Publicado en Circ Genom Precis Med (2018)

Relationships of the Location and Content of Rounds to Specialty, Institution, Patient-Census, and Team Size

por Priest, James R., Bereknyei, Sylvia, Hooper, Kambria, Braddock, Clarence H.
Publicado 2010

Ebstein anomaly and Trisomy 21: A rare association

por Siehr, Stephanie L, Punn, Rajesh, Priest, James R, Lowenthal, Alexander
Publicado 2014

Maternal mid-pregnancy glucose levels and risk of congenital heart disease in offspring

por Priest, James R, Yang, Wei, Reaven, Gerald, Knowles, Joshua W., Shaw, Gary M.
Publicado en JAMA Pediatr (2015)

Birthweight, Type 2 Diabetes Mellitus, and Cardiovascular Disease: Addressing the Barker Hypothesis With Mendelian Randomization

por Zanetti, Daniela, Tikkanen, Emmi, Gustafsson, Stefan, Priest, James R., Burgess, Stephen, Ingelsson, Erik
Publicado en Circ Cardiovasc Genet (2018)

Self-Reported History of Childhood Smoking Is Associated with an Increased Risk for Peripheral Arterial Disease Independent of Lifetime Smoking Burden

por Priest, James R., Nead, Kevin T., Wehner, Mackenzie R., Cooke, John P., Leeper, Nicholas J.
Publicado 2014

Triiodothyronine supplementation and cytokines during cardiopulmonary bypass in infants and children

por Priest, James R., Slee, April, Olson, Aaron K., Ledee, Dolena, Morrish, Fionnuala, Portman, Michael A.
Publicado en J Thorac Cardiovasc Surg (2012)

Rare Copy Number Variants in Isolated Sporadic and Syndromic Atrioventricular Septal Defects

por Priest, James R, Girirajan, Santhosh, Vu, Tiffany H, Olson, Aaron, Eichler, Evan E, Portman, Michael A
Publicado 2012

Adults With Mild‐to‐Moderate Congenital Heart Disease Demonstrate Measurable Neurocognitive Deficits

por Perrotta, Melissa L., Saha, Priyanka, Zawadzki, Roy, Beidelman, Mark, Ingelsson, Erik, Lui, George K., Priest, James R.
Publicado en J Am Heart Assoc (2020)

Human-zebrafish non-coding conserved elements act in vivo to regulate transcription

por Shin, Jordan T., Priest, James R., Ovcharenko, Ivan, Ronco, Amy, Moore, Rachel K., Burns, C. Geoffrey, MacRae, Calum A.
Publicado 2005

A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population

por Tcheandjieu, Catherine, Aguirre, Matthew, Gustafsson, Stefan, Saha, Priyanka, Potiny, Praneetha, Haendel, Melissa, Ingelsson, Erik, Rivas, Manuel A., Priest, James R.
Publicado en PLoS Genet (2020)

Medical implications of technical accuracy in genome sequencing

por Goldfeder, Rachel L., Priest, James R., Zook, Justin M., Grove, Megan E., Waggott, Daryl, Wheeler, Matthew T., Salit, Marc, Ashley, Euan A.
Publicado en Genome Med (2016)

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1–BP2) deletion in the UK Biobank

por Williams, Simon G., Nakev, Apostol, Guo, Hui, Frain, Simon, Tenin, Gennadiy, Liakhovitskaia, Anna, Saha, Priyanka, Priest, James R., Hentges, Kathryn E., Keavney, Bernard D.
Publicado en Eur J Hum Genet (2020)

First Trimester Plasma Glucose Values in Non-Diabetic Women are Associated with Risk for Congenital Heart Disease in Offspring

por Helle, Emmi I.T., Biegley, Preston, Knowles, Joshua W., Leader, Joseph B., Pendergrass, Sarah, Yang, Wei, Reaven, Gerald R, Shaw, Gary M., Ritchie, Marylyn, Priest, James R.
Publicado en J Pediatr (2017)

Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts

por Helle, Emmi, Córdova-Palomera, Aldo, Ojala, Tiina, Saha, Priyanka, Potiny, Praneetha, Gustafsson, Stefan, Ingelsson, Erik, Bamshad, Michael, Nickerson, Deborah, Chong, Jessica X., Ashley, Euan, Priest, James R
Publicado en Genet Epidemiol (2018)

Molecular Diagnosis of Long-QT syndrome at 10 Days of Life by Rapid Whole Genome Sequencing

por Priest, James R., Ceresnak, Scott R., Dewey, Frederick E., Malloy-Walton, Lindsey E., Dunn, Kyla, Grove, Megan E., Perez, Marco V., Maeda, Katsuhide, Dubin, Anne M., Ashley, Euan A.
Publicado en Heart Rhythm (2014)