Mark T. Keating - Concepedia

Author

Mark T. Keating

Also Known As

M T Keating, M. T. Keating, M.T. KEATING, M.T. Keating, MARK T. KEATING, Mark T Keating, Mark T. Keating, Mark T. Keating

131

Publications

44K

Citations

H-Index

161

Concepts

All Affiliations

Howard Hughes Medical Institute University of Utah Harvard University Boston Children's Hospital Baylor College of Medicine

About

Mark T. Keating is an author at Howard Hughes Medical Institute specializing in medicine, cell biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	55	61	28.1K
2	Natural Sciences	6	6	681
3	Engineering	4	4	367
4	Health Sciences	3	3	2.4K
5	Arts	1	1	351

Mark T. Keating

100

Publications

42.1K

Citations

H-Index

Page 1

	Year	Citations
A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel Michael C. Sanguinetti, Changan Jiang, Mark Curran, Cell Cardiac MuscleCardiomyopathyMolecular PhysiologyAcquird Cardiac ArrthytmiaPhysiology	1995	2.4K
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome Mark Curran, Igor Splawski, Katherine W. Timothy, Cell Long Qt SyndromeCardiomyopathyGeneticsCardiac ArrhythmiaHerg Mutations	1995	2.3K
Heart Regeneration in Zebrafish Kenneth D. Poss, Lindsay G. Wilson, Mark T. Keating Science RegenerationCardiac MuscleCardiac Progenitor CellsCardiac RegenerationOrgan Regeneration	2002	1.9K
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation Qiuyun Chen, Glenn E. Kirsch, Danmei Zhang, Nature Cardiac MuscleCardiomyopathyHeart FailureGeneticsIdiopathic Ventricular Fibrillation	1998	1.8K
Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel Michael C. Sanguinetti, Mark Curran, Anruo Zou, Nature Cardiac MuscleChannelopathiesCardiomyopathySignal TransductionMolecular Physiology	1996	1.8K
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias Q. Wang, Mark Curran, Igor Splawski, Nature Genetics Cardiac MuscleChannelopathiesKvlqt1 MutationsMolecular PhysiologyGenetics	1996	1.8K
Genotype-Phenotype Correlation in the Long-QT Syndrome Peter J. Schwartz, Silvia G. Priori, Carla Spazzolini, Circulation	2001	1.7K
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome Qing Wang, Jiaxiang Shen, Igor Splawski, Cell Long Qt SyndromeCardiomyopathyGenetic DisorderGeneticsScn5a Mutations	1995	1.7K
CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism Igor Splawski, Katherine W. Timothy, Leah M. Sharpe, Cell ChannelopathiesHyperpolarization (Biology)NeurophysiologyPhysiologyIon Channels	2004	1.6K
MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia Geoffrey W. Abbott, Federico Sesti, Igor Splawski, Cell	1999	1.3K

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