Alex V. Postma - Concepedia

Author

Alex V. Postma

Amsterdam UMC Location University of Amsterdam ORCID

Also Known As

A Postma, A V Postma, A. Postma, A. V. Postma, A.V. Postma, ALEX V. POSTMA, AV Postma, Alex Postma, Alex V Postma, Alex V. Postma

117

Publications

4.7K

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam University of Amsterdam Amsterdam University Medical Centers Leiden University Medical Center Newcastle University

About

Alex V. Postma is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, genetics, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	2.2K
2	Public Health	4	4	460
3	Natural Sciences	2	2	102
4	Engineering	1	1	184
5	Health Sciences	1	1	124

Alex V. Postma

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
A Single Na <sup>+</sup> Channel Mutation Causing Both Long-QT and Brugada Syndromes Connie R. Bezzina, Marieke W. Veldkamp, Maarten P. van den Berg, Circulation Research Cardiac MuscleFamily MembersGeneticsMolecular GeneticsDisease Gene Identification	1999	637
Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia Alex V. Postma, Isabelle Denjoy, Theo M. Hoorntje, Circulation Research Cardiac MuscleHeart FailureGeneticsCongenital Heart AnomalyCalsequestrin 2	2002	400
Expanding Spectrum of Human <i>RYR2</i> -Related Disease Zahurul A. Bhuiyan, Maarten P. van den Berg, J. Peter van Tintelen, Circulation	2007	243
HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy Annalisa Milano, Alexa M.C. Vermeer, Elisabeth M. Lodder, Journal of the American College of Cardiology Cardiac MuscleCardiomyopathyHeart FailureHcn4 MutationsGenetics	2014	195
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot Donna J. Page, Matthieu J. Miossec, Simon G. Williams, Circulation Research	2019	191
Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly Alex V. Postma, Klaartje van Engelen, Judith van de Meerakker, Circulation Cardiovascular Genetics	2010	186
A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation Alex V. Postma, Judith B.A. van de Meerakker, Inge B. Mathijssen, Circulation Research Systems BiologyEngineeringFamily MembersGenetic DisorderMedicine	2008	184
Truncating Titin Mutations are Associated with a Mild and Treatable form of Dilated Cardiomyopathy Joeri A. Jansweijer, Karin Nieuwhof, Francesco Paolo Russo, European Journal of Heart Failure	2016	170
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 Heather J. Cordell, Jamie Bentham, Ana Töpf, Nature Genetics Atrial Septal DefectGenome-wide Association StudyGenetic DisorderGeneticsGenetic Epidemiology	2013	156
Identifying the Evolutionary Building Blocks of the Cardiac Conduction System Bjarke Jensen, Bastiaan J. Boukens, Alex V. Postma, PLoS ONE Cardiac MuscleHeart FailureMammalian PhysiologyEvolutionary Building BlocksCardiovascular Function	2012	124

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