Alex V. Postma

4.8k citations

82 papers · 3.6k · h-index 29

Impact in

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

Papers in

Cardiology and Cardiovascular Medicine 27
- Cardiomyopathy and Myosin Studies 15
- Cardiac electrophysiology and arrhythmias 11
Molecular Biology 54
- Congenital heart defects research 36
- Ion channel regulation and function 6
- RNA modifications and cancer 5

Co-authors: Arthur A.M. Wilde (13 shared papers)Marcel M. A. M. Mannens (12 shared papers)Connie R. Bezzina (10 shared papers)Irene M. van Langen (4 shared papers)Maarten P. van den Berg (4 shared papers)Margreet Th.E. Bink‐Boelkens (2 shared papers)Vincent M. Christoffels (12 shared papers)Martin B. Rook (2 shared papers)
Journals: Circulation Research (5 papers)Genome Medicine (3 papers)Genetics in Medicine (3 papers)Circulation Cardiovascular Genetics (3 papers)Cardiovascular Research (3 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Alex V. Postma

75 papers receiving 3.5k 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 82 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	1999	543
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	2002	337
3	Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients Journal of Medical Genetics ·Alex V. Postma +10 others	2005	241
4	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, Marielle M. Alders, Alex V. Postma, Irene M. van Langen	2007	201
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	2014	158
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	2008	149
7	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 M. M. Bauer, Thomas Pickardt	2010	148
8	Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot Circulation Research ·Donna J. Page, Matthieu J. Miossec, Simon G. Williams, Richard M. Monaghan, Elisavet Fotiou, Heather Jane Cordell, Louise Sutcliffe, Ana Töpf	2019	144
9	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	2016	136
10	Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 Nature Genetics ·Heather Jane Cordell, Jamie Bentham, Ana Töpf, Diana Zélénika, Simon Charles Heath, Chrysovalanto Mamasoula, Catherine Cosgrove, Gillian M. Blue	2013	126
11	Identifying the Evolutionary Building Blocks of the Cardiac Conduction System PLoS ONE ·Bjarke Krogstrup 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	95
12	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	2010	87
13	Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot Human Molecular Genetics ·Heather Jane Cordell, Ana Töpf, Chrysovalanto Mamasoula, Alex V. Postma, Jamie Bentham, Diana Zélénika, Simon Charles Heath, Gillian M. Blue	2013	73
14	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	67
15	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	47
16	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	2014	46
17	Risk of benign meningioma after childhood cancer in the DCOG-LATER cohort: contributions of radiation dose, exposed cranial volume, and age Neuro-Oncology ·Judith L. Kok, Jop C. Teepen, Flora E. van Leeuwen, Wim J. E. Tissing, Sebastian J.C.M.M. Neggers, Helena J. H. van der Pal, Jacqueline J. Loonen, Dorine Bresters	2018	44
18	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	2013	42
19	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 D. Keavney, JA Goodship, Enno Tjeerd van der Velde, Marieke J.H. Baars, Simone Snijder, Antoon F.M. Moorman	2010	40
20	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome Cardiovascular Research ·Cornelis J.J. Boogerd, Dennis Dooijes, Aho Ilgun, Inge B. Mathijssen, Roel Hordijk, Ingrid M.B.H. van de Laar, Patrick Rump, Hermine E. Veenstra‐Knol	2010	39

About Alex V. Postma

Alex V. Postma is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology, Epidemiology, Pulmonary and Respiratory Medicine and Genetics, having authored 82 papers that have together received 3.6k indexed citations. Recurring topics across this work include Congenital heart defects research (36 papers), Congenital Heart Disease Studies (18 papers), Cardiomyopathy and Myosin Studies (15 papers), Cardiac electrophysiology and arrhythmias (11 papers), Ion channel regulation and function (6 papers), Tracheal and airway disorders (5 papers), RNA modifications and cancer (5 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (2.1k citations), Molecular Biology (2.1k citations), Epidemiology (638 citations), Genetics (329 citations) and Cellular and Molecular Neuroscience (158 citations). Alex V. Postma has collaborated with scholars based in Netherlands, United States and Germany. 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, Margreet Th.E. Bink‐Boelkens, Vincent M. Christoffels, Martin B. Rook, Marieke W. Veldkamp and Annemarie H. van der Hout. Their work appears in journals such as Circulation Research, Genome Medicine, Genetics in Medicine, Circulation Cardiovascular Genetics and Cardiovascular Research.

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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