Oracle SOA Suite 11g R1 Developer's Guide

por Reynolds, Antony, Wright, Matt
Publicado 2010

Oracle SOA Suite 11g developer's cookbook

por Reynolds, Antony, Wright, Matt
Publicado 2012

An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease Genetics

por Li, Binglan, Whirl-Carrillo, Michelle, Wright, Matt W., Babb, Larry, Rehm, Heidi L., Klein, Teri E.
Publicado 2022

LitGen: Genetic Literature Recommendation Guided by Human Explanations

por Nie, Allen, Pineda, Arturo L., Wright, Matt W., Wand, Hannah, Wulf, Bryan, Costa, Helio, Patel, Ronak, Bustamante, Carlos D., Zou, James
Publicado 2020

Accessing clinical-grade genomic classification data through the ClinGen Data Platform

por Dalton, Karen P., Rehm, Heidi L., Wright, Matt W., Mandell, Mark E., Krysiak, Kilannin, Babb, Lawrence, Riehle, Kevin, Nelson, Tristan, Wagner, Alex H.
Publicado 2023

Quality of life and healthcare utilisation improvements after atrial fibrillation ablation

por Gupta, Dhiraj, Vijgen, Johan, Potter, Tom De, Scherr, Daniel, Van Herendael, Hugo, Knecht, Sebastien, Kobza, Richard, Berte, Benjamin, Sandgaard, Niels, Albenque, Jean-Paul, Széplaki, Gábor, Stevenhagen, Yorick, Taghji, Philippe, Wright, Matt, Duytschaever, Mattias
Publicado 2021

OpenEP: A Cross-Platform Electroanatomic Mapping Data Format and Analysis Platform for Electrophysiology Research

por Williams, Steven E., Roney, Caroline H., Connolly, Adam, Sim, Iain, Whitaker, John, O’Hare, Daniel, Kotadia, Irum, O’Neill, Louisa, Corrado, Cesare, Bishop, Martin, Niederer, Steven A., Wright, Matt, O’Neill, Mark, Linton, Nick W. F.
Publicado 2021

Time-Averaged Wavefront Analysis Demonstrates Preferential Pathways of Atrial Fibrillation, Predicting Pulmonary Vein Isolation Acute Response

por Roney, Caroline H., Child, Nicholas, Porter, Bradley, Sim, Iain, Whitaker, John, Clayton, Richard H., Laughner, Jacob I., Shuros, Allan, Neuzil, Petr, Williams, Steven E., Razavi, Reza S., O'Neill, Mark, Rinaldi, Christopher A., Taggart, Peter, Wright, Matt, Gill, Jaswinder S., Niederer, Steven A.
Publicado 2021

ClinGen Allele Registry links information about genetic variants

por Pawliczek, Piotr, Patel, Ronak Y., Ashmore, Lillian R., Jackson, Andrew R., Bizon, Chris, Nelson, Tristan, Powell, Bradford, Freimuth, Robert R., Strande, Natasha, Shah, Neethu, Paithankar, Sameer, Wright, Matt W., Dwight, Selina, Zhen, Jimmy, Landrum, Melissa, McGarvey, Peter, Babb, Larry, Plon, Sharon E., Milosavljevic, Aleksandar
Publicado 2018

Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework

por Brnich, Sarah E., Abou Tayoun, Ahmad N., Couch, Fergus J., Cutting, Garry R., Greenblatt, Marc S., Heinen, Christopher D., Kanavy, Dona M., Luo, Xi, McNulty, Shannon M., Starita, Lea M., Tavtigian, Sean V., Wright, Matt W., Harrison, Steven M., Biesecker, Leslie G., Berg, Jonathan S.
Publicado 2019

Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures

por Popejoy, Alice B., Crooks, Kristy R., Fullerton, Stephanie M., Hindorff, Lucia A., Hooker, Gillian W., Koenig, Barbara A., Pino, Natalie, Ramos, Erin M., Ritter, Deborah I., Wand, Hannah, Wright, Matt W., Yudell, Michael, Zou, James Y., Plon, Sharon E., Bustamante, Carlos D., Ormond, Kelly E.
Publicado 2020

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

por Preston, Christine G., Wright, Matt W., Madhavrao, Rao, Harrison, Steven M., Goldstein, Jennifer L., Luo, Xi, Wand, Hannah, Wulf, Bryan, Cheung, Gloria, Mandell, Mark E., Tong, Howard, Cheng, Shaung, Iacocca, Michael A., Pineda, Arturo Lopez, Popejoy, Alice B., Dalton, Karen, Zhen, Jimmy, Dwight, Selina S., Babb, Lawrence, DiStefano, Marina, O’Daniel, Julianne M., Lee, Kristy, Riggs, Erin R., Zastrow, Diane B., Mester, Jessica L., Ritter, Deborah I., Patel, Ronak Y., Subramanian, Sai Lakshmi, Milosavljevic, Aleksander, Berg, Jonathan S., Rehm, Heidi L., Plon, Sharon E., Cherry, J. Michael, Bustamante, Carlos D., Costa, Helio A.
Publicado 2022