Alex V. Postma

4.7k citations

60 papers · 2.4k · h-index 25

Impact in

Cardiology and Cardiovascular Medicine top 1%
- Cardiac electrophysiology and arrhythmias
- Cardiomyopathy and Myosin Studies
- Cardiac Arrhythmias and Treatments
- Cardiovascular Effects of Exercise
- Cardiac pacing and defibrillation studies
Molecular Biology top 5%
- Ion channel regulation and function
- Congenital heart defects research

Papers in

Molecular Biology 48
- Congenital heart defects research 29
- Ion channel regulation and function 8
Cardiology and Cardiovascular Medicine 28
- Cardiomyopathy and Myosin Studies 11
- Cardiac electrophysiology and arrhythmias 11
- Cardiovascular Effects of Exercise 6

Co-authors: Arthur A.M. Wilde (12 shared papers)Marcel M. A. M. Mannens (13 shared papers)Connie R. Bezzina (10 shared papers)Irene M. van Langen (4 shared papers)Maarten P. van den Berg (4 shared papers)Vincent M. Christoffels (11 shared papers)Margreet Th.E. Bink‐Boelkens (2 shared papers)Martin B. Rook (2 shared papers)
Journals: Circulation Research (3 papers)Cardiovascular Research (3 papers)Trends in Cardiovascular Medicine (3 papers)Journal of Molecular and Cellular Cardiology (2 papers)European Journal of Human Genetics (2 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Alex V. Postma

58 papers receiving 2.4k citations

Peers

Countries citing papers authored by Alex V. Postma

Since Specialization

Citations

This map shows the geographic impact of Alex V. Postma's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Alex V. Postma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alex V. Postma more than expected).

Fields of papers citing papers by Alex V. Postma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alex V. Postma. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Alex V. Postma. The network helps show where Alex V. Postma may publish in the future.

Co-authors

The 25 scholars most cited alongside Alex V. Postma, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Alex V. Postma Line = papers co-authored together Alex V. Postma links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 60 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Single Na ⁺ Channel Mutation Causing Both Long-QT and Brugada Syndromes Circulation Research ·Connie R. Bezzina, Marieke W. Veldkamp, Maarten P. van den Berg, Alex V. Postma, Martin B. Rook, Jan-Willem Viersma, Irene M. van Langen, Ghita Tan-Sindhunata, Margreet Th.E. Bink‐Boelkens, Annemarie H. van der Hout, Marcel M. A. M. Mannens, Arthur A.M. Wilde	1999	460
2	Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia Circulation Research ·Alex V. Postma, Isabelle Denjoy, Theo M. Hoorntje, Jean‐Marc Lupoglazoff, Antoine Da Costa, Pascale Sébillon, Marcel M. A. M. Mannens, Arthur A.M. Wilde, Pascale Guicheney	2002	302
3	Expanding Spectrum of Human RYR2 -Related Disease Circulation ·Zahurul A. Bhuiyan, Maarten P. van den Berg, J. Peter van Tintelen, Margreet Th.E. Bink‐Boelkens, Ans C.P. Wiesfeld, Mariëlle Alders, Alex V. Postma, Irene M. van Langen, Marcel M. A. M. Mannens, Arthur A.M. Wilde	2007	170
4	Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly Circulation Cardiovascular Genetics ·Alex V. Postma, Klaartje van Engelen, Judith van de Meerakker, Thahira Rahman, Susanne Probst, Marieke J.H. Baars, Ulrike Bauer, Thomas Pickardt, Silke Sperling, Felix Berger, Antoon F.M. Moorman, Barbara J.M. Mulder, Ludwig Thierfelder, Bernard Keavney, Judith Goodship, Sabine Klaassen	2010	129
5	HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy Journal of the American College of Cardiology ·Annalisa Milano, Alexa M.C. Vermeer, Elisabeth M. Lodder, Julien Barc, Arie O. Verkerk, Alex V. Postma, Ivo A.C. van der Bilt, Marieke J.H. Baars, Paul L. van Haelst, Kadir Çalişkan, Yvonne M. Hoedemaekers, Solena Le Scouarnec, Richard Redon, Yigal M. Pinto, Imke Christiaans, Arthur A.M. Wilde, Connie R. Bezzina	2014	126
6	A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation Circulation Research ·Alex V. Postma, Judith B.A. van de Meerakker, Inge B. Mathijssen, Phil Barnett, Vincent M. Christoffels, Aho Ilgun, Jan Lam, Arthur A.M. Wilde, Ronald H. Lekanne Deprez, Antoon F.M. Moorman	2008	123
7	Truncating Titin Mutations are Associated with a Mild and Treatable form of Dilated Cardiomyopathy European Journal of Heart Failure ·Joeri A. Jansweijer, Karin Nieuwhof, Francesco Paolo Russo, Edgar T. Hoorntje, Jan D.H. Jongbloed, Ronald H. Lekanne Deprez, Alex V. Postma, Marieke Bronk, Ingrid A.W. van Rijsingen, Simone de Haij, Elena Biagini, Paul L. van Haelst, Jan van Wijngaarden, Maarten P. van den Berg, Arthur A.M. Wilde, Marcel M. A. M. Mannens, Rudolf A. de Boer, Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Yigal M. Pinto	2016	108
8	Identifying the Evolutionary Building Blocks of the Cardiac Conduction System PLoS ONE ·Bjarke Jensen, Bastiaan J. Boukens, Alex V. Postma, Quinn D. Gunst, Maurice J.B. van den Hoff, Antoon F.M. Moorman, Tobias Wang, Vincent M. Christoffels	2012	88
9	Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans The American Journal of Human Genetics ·Bernard Thienpont, Litu Zhang, Alex V. Postma, Jeroen Breckpot, Léon-Charles Tranchevent, Peter Van Loo, Kjeld Møllgård, Niels Tommerup, Iben Bache, Zeynep Tümer, Klaartje van Engelen, Björn Menten, Geert Mortier, Darrel Waggoner, Marc Gewillig, Yves Moreau, Koenraad Devriendt, Lars Allan Larsen	2010	72
10	A Novel Early Onset Lethal Form of Catecholaminergic Polymorphic Ventricular Tachycardia Maps to Chromosome 7p14‐p22 Journal of Cardiovascular Electrophysiology ·Zahurul A. Bhuiyan, Mohamed A. Hamdan, EMAN T.A. SHAMSI, Alex V. Postma, Marcel M. A. M. Mannens, ARTHUR A. M. WILDE, Lihadh Al‐Gazali	2007	52
11	Genetics of congenital heart disease: the contribution of the noncoding regulatory genome Journal of Human Genetics ·Alex V. Postma, Connie R. Bezzina, Vincent M. Christoffels	2015	46
12	Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot American Journal of Medical Genetics Part A ·Anwar Baban, Alex V. Postma, Monica Marini, Gianluca Trocchio, Antonella Santilli, Monica Pelegrini, Pietro Sirleto, Margherita Lerone, Sonia Albanese, Phil Barnett, Cornelis J. Boogerd, Bruno Dallapiccola, M. Cristina Digilio, Roberto Ravazzolo, Giacomo Pongiglione	2014	41
13	Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7 American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Alexa M.C. Vermeer, Klaartje van Engelen, Alex V. Postma, Marieke J.H. Baars, Imke Christiaans, Simone de Haij, Sabine Klaassen, Barbara J.M. Mulder, Bernard Keavney	2013	38
14	The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handling Journal of Molecular and Cellular Cardiology ·Uwe Kirchhefer, Diana Wehrmeister, Alex V. Postma, Gottfried Pohlentz, Michael Mormann, Dana Kučerová, Frank Müller, Wilhelm Schmitz, Eric Schulze‐Bahr, Arthur A.M. Wilde, Joachim Neumann	2010	35
15	Specialized impulse conduction pathway in the alligator heart eLife ·Bjarke Jensen, Bastiaan J. Boukens, Dane A. Crossley, Justin Conner, Rajiv A. Mohan, Karel van Duijvenboden, Alex V. Postma, Christopher Gloschat, Ruth M. Elsey, David Sedmera, Igor R. Efimov, Vincent M. Christoffels	2018	35
16	An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality Genes & Development ·Christina M. Ferrer, Mariëlle Alders, Alex V. Postma, Seonmi Park, Mark A. Klein, Murat Çetinbaş, Eva Pajkrt, Astrid Glas, Silvana van Koningsbruggen, Vincent M. Christoffels, Marcel M. A. M. Mannens, Lia Knegt, Jean‐Pierre Etchegaray, Ruslan I. Sadreyev, John M. Denu, Gustavo Mostoslavsky, Merel C. van Maarle, Raúl Mostoslavsky	2018	34
17	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome Cardiovascular Research ·Cornelis J. Boogerd, Dennis Dooijes, Aho Ilgun, Inge B. Mathijssen, Roel Hordijk, Ingrid M.B.H. van de Laar, Patrick Rump, Hermine E. Veenstra‐Knol, Antoon F.M. Moorman, Phil Barnett, Alex V. Postma	2010	34
18	22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia: Table 1 Heart ·Klaartje van Engelen, Ana Töpf, Bernard Keavney, JA Goodship, Enno T. van der Velde, Marieke J.H. Baars, Simone Snijder, Antoon F.M. Moorman, Alex V. Postma, B. J. M. Mulder	2010	33
19	Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal Journal of Medical Genetics ·Alex V. Postma, Mariëlle Alders, Marc Sylva, C. M. Bilardo, Eva Pajkrt, Rick R. van Rijn, S. Schulte-Merker, Saskia Bulk, Sonia Stefanovic, Aho Ilgun, Phil Barnett, Marcel M. A. M. Mannens, Antoon F.M. Moorman, Roelof‐Jan Oostra, Merel C. van Maarle	2013	33
20	A Case of Catecholaminergic Polymorphic Ventricular Tachycardia Caused by Two Calsequestrin 2 Mutations Pacing and Clinical Electrophysiology ·SAM DE LA FUENTE, Irene M. van Langen, Alex V. Postma, HENNI BIKKER, Albert Meijer	2008	32

About Alex V. Postma

Alex V. Postma is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Epidemiology, Pulmonary and Respiratory Medicine and Genetics, having authored 60 papers that have together received 2.4k indexed citations. Recurring topics across this work include Congenital heart defects research (29 papers), Congenital Heart Disease Studies (16 papers), Cardiomyopathy and Myosin Studies (11 papers), Cardiac electrophysiology and arrhythmias (11 papers), Ion channel regulation and function (8 papers), Cardiovascular Effects of Exercise (6 papers), Tracheal and airway disorders (4 papers) and Coronary Artery Anomalies (4 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (1.6k citations), Molecular Biology (1.7k citations), Epidemiology (404 citations), Genetics (225 citations) and Cellular and Molecular Neuroscience (142 citations). Alex V. Postma has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Arthur A.M. Wilde, Marcel M. A. M. Mannens, Connie R. Bezzina, Irene M. van Langen, Maarten P. van den Berg, Vincent M. Christoffels, Margreet Th.E. Bink‐Boelkens, Martin B. Rook, Annemarie H. van der Hout and Marieke W. Veldkamp. Their work appears in journals such as Circulation Research, Cardiovascular Research, Trends in Cardiovascular Medicine, Journal of Molecular and Cellular Cardiology and European Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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