James S. Ware

Citirano

	Sve	Od 2019.
Citati	35014	29735
H-indeks	62	60
i10-indeks	121	116

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Suautori

Nicola WhiffinUniversity of OxfordPotvrđena adresa e-pošte na well.ox.ac.uk
Paul J BartonImperial College LondonPotvrđena adresa e-pošte na imperial.ac.uk
Stuart CookImperial College, Duke-NUS, MRC-LMSPotvrđena adresa e-pošte na imperial.ac.uk
Roddy WalshCity St George's University of LondonPotvrđena adresa e-pošte na sgul.ac.uk
Carolyn HoProfessor of Medicine, Harvard Medical School and Cardiology Division, Brigham and Women's HospitalPotvrđena adresa e-pošte na bwh.harvard.edu
iacopo olivottoCardiomyopathy Unit, Careggi University Hospital, FlorencePotvrđena adresa e-pošte na aou-careggi.toscana.it
Sharlene DayUniversity of PennsylvaniaPotvrđena adresa e-pošte na pennmedicine.upenn.edu
Euan A. AshleyChair, Department of Medicine, Stanford UniversityPotvrđena adresa e-pošte na stanford.edu
Daniel JacobyYale School of MedicinePotvrđena adresa e-pošte na yale.edu
Declan O'ReganBHF Chair of Cardiovascular AI, MRC Laboratory of Medical Sciences, Imperial College LondonPotvrđena adresa e-pošte na imperial.ac.uk
Daniel G MacArthurGarvan Institute of Medical Research, Murdoch Children's Research InstitutePotvrđena adresa e-pošte na atgu.mgh.harvard.edu
Shibu JohnStaff Bioinformatics Scientist, Illumina Cambridge LtdPotvrđena adresa e-pošte na illumina.com
Anne O'Donnell-LuriaCo-Director for the Broad Center for Mendelian Genomics, Broad Institute of MIT and HarvardPotvrđena adresa e-pošte na broadinstitute.org
Xiaolei Zhang (张小蕾)European Bioinformatics InstitutePotvrđena adresa e-pošte na ebi.ac.uk
Eric Vallabh MinikelPrion Scientist, Broad Institute of MIT and HarvardPotvrđena adresa e-pošte na broadinstitute.org
Konrad KarczewskiAssistant Professor, Massachusetts General Hospital; Computational Biologist, Broad InstitutePotvrđena adresa e-pošte na broadinstitute.org
Amy Curry SturmProfessor, Licensed Genetic Counselor, GeisingerPotvrđena adresa e-pošte na sturmie.com
Elijah BehrProfessor of Cardiovascular Medicine, St George's University of LondonPotvrđena adresa e-pošte na sgul.ac.uk
Deborah Morris-RosendahlRoyal Brompton and Harefield NHS Foundation Trust and Imperial College LondonPotvrđena adresa e-pošte na imperial.ac.uk
Piers DaubeneyImperial College, LondonPotvrđena adresa e-pošte na rbht.nhs.uk

Prati

James S. Ware

Professor of Cardiovascular and Genomic Medicine, Imperial College London

Potvrđena adresa e-pošte na imperial.ac.uk - Početna stranica

Medicine Biology Genomics


Naslov Poredaj po navodima Poredaj po godini Poredaj po naslovu	Citirano Citirano	Godina
Analysis of protein-coding genetic variation in 60,706 humans M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ... Nature 536 (7616), 285-291, 2016	10609	2016
The mutational constraint spectrum quantified from variation in 141,456 humans KJ Karczewski, LC Francioli, G Tiao, BB Cummings, J Alföldi, Q Wang, ... Nature 581 (7809), 434-443, 2020	8076	2020
Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes KJ Karczewski, LC Francioli, G Tiao, BB Cummings, J Alföldi, Q Wang, ... biorxiv, 531210, 2019	1178	2019
2023 ESC Guidelines for the management of cardiomyopathies: Developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC) E Arbelo, A Protonotarios, JR Gimeno, E Arbustini, R Barriales-Villa, ... European heart journal 44 (37), 3503-3626, 2023	899	2023
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ... Science 350 (6265), 1262-1266, 2015	824	2015
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples R Walsh, KL Thomson, JS Ware, BH Funke, J Woodley, KJ McGuire, ... Genetics in Medicine 19 (2), 192-203, 2017	720	2017
Genotype and lifetime burden of disease in hypertrophic cardiomyopathy: insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe) CY Ho, SM Day, EA Ashley, M Michels, AC Pereira, D Jacoby, AL Cirino, ... Circulation 138 (14), 1387-1398, 2018	662	2018
Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trial BP Halliday, R Wassall, AS Lota, Z Khalique, J Gregson, S Newsome, ... The Lancet 393 (10166), 61-73, 2019	615	2019
Shared genetic predisposition in peripartum and dilated cardiomyopathies JS Ware, J Li, E Mazaika, CM Yasso, T DeSouza, TP Cappola, EJ Tsai, ... New England Journal of Medicine 374 (3), 233-241, 2016	506	2016
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease AM Roberts, JS Ware, DS Herman, S Schafer, J Baksi, AG Bick, ... Science translational medicine 7 (270), 270ra6-270ra6, 2015	495	2015
Using high-resolution variant frequencies to empower clinical genome interpretation N Whiffin, E Minikel, R Walsh, AH O’Donnell-Luria, K Karczewski, AY Ing, ... Genetics in Medicine 19 (10), 1151-1158, 2017	451	2017
Evaluating the clinical validity of hypertrophic cardiomyopathy genes J Ingles, J Goldstein, C Thaxton, C Caleshu, EW Corty, SB Crowley, ... Circulation: Genomic and Precision Medicine 12 (2), e002460, 2019	381	2019
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy … MA Kelly, C Caleshu, A Morales, J Buchan, Z Wolf, SM Harrison, S Cook, ... Genetics in Medicine 20 (3), 351-359, 2018	360	2018
Evidence-based assessment of genes in dilated cardiomyopathy E Jordan, L Peterson, T Ai, B Asatryan, L Bronicki, E Brown, R Celeghin, ... Circulation 144 (1), 7-19, 2021	346	2021
An international, multicentered, evidence-based reappraisal of genes reported to cause congenital long QT syndrome A Adler, V Novelli, AS Amin, E Abiusi, M Care, EA Nannenberg, ... Circulation 141 (6), 418-428, 2020	330	2020
Reappraisal of reported genes for sudden arrhythmic death: evidence-based evaluation of gene validity for Brugada syndrome SM Hosseini, R Kim, S Udupa, G Costain, R Jobling, E Liston, SM Jamal, ... Circulation 138 (12), 1195-1205, 2018	322	2018
Titin-truncating variants affect heart function in disease cohorts and the general population S Schafer, A De Marvao, E Adami, LR Fiedler, B Ng, E Khin, ... Nature genetics 49 (1), 46-53, 2017	316	2017
Genetic variants associated with cancer therapy–induced cardiomyopathy P Garcia-Pavia, Y Kim, MA Restrepo-Cordoba, IG Lunde, H Wakimoto, ... Circulation 140 (1), 31-41, 2019	282	2019
European heart rhythm association (EHRA)/heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus … AAM Wilde, C Semsarian, MF Márquez, AS Shamloo, MJ Ackerman, ... Europace 24 (8), 1307-1367, 2022	280	2022
Utility of post-mortem genetic testing in cases of sudden arrhythmic death syndrome N Lahrouchi, H Raju, EM Lodder, E Papatheodorou, JS Ware, ... Journal of the American College of Cardiology 69 (17), 2134-2145, 2017	274	2017

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