Alex V. Postma

4.7k total citations
60 papers, 2.4k citations indexed

About

Alex V. Postma is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Epidemiology. According to data from OpenAlex, Alex V. Postma has authored 60 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 28 papers in Cardiology and Cardiovascular Medicine and 17 papers in Epidemiology. Recurrent topics in Alex V. Postma's work include Congenital heart defects research (29 papers), Congenital Heart Disease Studies (16 papers) and Cardiac electrophysiology and arrhythmias (11 papers). Alex V. Postma is often cited by papers focused on Congenital heart defects research (29 papers), Congenital Heart Disease Studies (16 papers) and Cardiac electrophysiology and arrhythmias (11 papers). Alex V. Postma collaborates with scholars based in Netherlands, United States and United Kingdom. Alex V. Postma's 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, Marieke W. Veldkamp and Annemarie H. van der Hout and has published in prestigious journals such as Circulation, Genes & Development and SHILAP Revista de lepidopterología.

In The Last Decade

Alex V. Postma

58 papers receiving 2.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Alex V. Postma Netherlands	25	1.7k	1.6k	404	225	170	60	2.4k
Andreas Perrot Germany	35	1.8k 1.1×	2.1k 1.3×	444 1.1×	197 0.9×	162 1.0×	71	3.1k
Richard D. Bagnall Australia	32	1.6k 0.9×	1.6k 1.0×	344 0.9×	481 2.1×	163 1.0×	79	3.3k
Patrice Bouvagnet France	33	1.6k 0.9×	1.3k 0.8×	345 0.9×	498 2.2×	280 1.6×	80	2.8k
Bastiaan J. Boukens Netherlands	28	1.5k 0.9×	1.5k 0.9×	148 0.4×	108 0.5×	209 1.2×	90	2.4k
Patrick Y. Jay United States	22	1.1k 0.7×	627 0.4×	276 0.7×	210 0.9×	266 1.6×	69	1.8k
Florence Kyndt France	19	1.9k 1.1×	2.3k 1.4×	119 0.3×	141 0.6×	147 0.9×	45	2.7k
Ludwig Thierfelder Germany	28	2.5k 1.5×	5.2k 3.2×	483 1.2×	194 0.9×	268 1.6×	62	5.9k
Roddy Walsh United Kingdom	22	952 0.6×	1.2k 0.8×	156 0.4×	392 1.7×	87 0.5×	50	1.9k
Ana Morales United States	25	1.3k 0.8×	2.1k 1.3×	88 0.2×	460 2.0×	159 0.9×	59	2.9k
Angela deAlmeida United States	11	788 0.5×	646 0.4×	194 0.5×	41 0.2×	166 1.0×	13	1.1k

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-authorship network of co-authors of Alex V. Postma

This figure shows the co-authorship network connecting the top 25 collaborators of Alex V. Postma. A scholar is included among the top collaborators of Alex V. Postma based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Alex V. Postma. Alex V. Postma is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Postma, Alex V., Saskia N. van der Crabben, Leander Beekman, et al.. (2025). Sinus Bradycardia and Long QT Syndrome: Double Heterozygosity for Variants in KCNH2 and HCN4. Pure Amsterdam UMC. 15(4). 31–31.

Postma, Alex V., et al.. (2023). GMDS Intragenic Deletions Associate with Congenital Heart Disease including Ebstein Anomaly. SHILAP Revista de lepidopterología. 13(3). 106–112. 2 indexed citations

Alaamery, Manal, Nour Albesher, Fahad Alhabshan, et al.. (2023). TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy. Journal of Cardiovascular Development and Disease. 10(11). 455–455. 1 indexed citations

Beek, Irma van de, Michael W.T. Tanck, Monique Luijten, et al.. (2023). Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene. Journal of Human Genetics. 68(4). 273–279. 5 indexed citations

Postma, Alex V., Christina Rapp, Katrin Knoflach, et al.. (2023). Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension. SHILAP Revista de lepidopterología. 1(1). 100811–100811. 1 indexed citations

Lahrouchi, Najim, Elisabeth M. Lodder, Rafik Tadros, et al.. (2017). Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. European Journal of Human Genetics. 25(6). 783–787. 20 indexed citations

Jansweijer, Joeri A., Francesco Paolo Russo, Edgar T. Hoorntje, et al.. (2016). Truncating Titin Mutations are Associated with a Mild and Treatable form of Dilated Cardiomyopathy. European Journal of Heart Failure. 19(4). 512–521. 108 indexed citations

Mohan, Rajiv A., Klaartje van Engelen, Sonia Stefanovic, et al.. (2014). A mutation in the Kozak sequence of GATA4 hampers translation in a family with atrial septal defects. American Journal of Medical Genetics Part A. 164(11). 2732–2738. 18 indexed citations

Milano, Annalisa, Alexa M.C. Vermeer, Elisabeth M. Lodder, et al.. (2014). HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy. Journal of the American College of Cardiology. 64(8). 745–756. 126 indexed citations

10.

Baban, Anwar, Alex V. Postma, Monica Marini, et al.. (2014). Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot. American Journal of Medical Genetics Part A. 164(12). 3100–3107. 41 indexed citations

11.

Engelen, Klaartje van, et al.. (2013). The value of the clinical geneticist caring for adults with congenital heart disease: Diagnostic yield and patients' perspective. American Journal of Medical Genetics Part A. 161(7). 1628–1637. 16 indexed citations

12.

Vermeer, Alexa M.C., Klaartje van Engelen, Alex V. Postma, et al.. (2013). 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. 163(3). 178–184. 38 indexed citations

13.

Christiaans, Imke, Phil Barnett, Ronald H. Lekanne Deprez, et al.. (2012). A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1833(4). 833–839. 15 indexed citations

14.

Jensen, Bjarke, Bastiaan J. Boukens, Alex V. Postma, et al.. (2012). Identifying the Evolutionary Building Blocks of the Cardiac Conduction System. PLoS ONE. 7(9). e44231–e44231. 88 indexed citations

15.

Laat, Monique W. M. de, Petronella G. Pieper, Martijn A. Oudijk, et al.. (2012). The Clinical and Molecular Relations Between Idiopathic Preterm Labor and Maternal Congenital Heart Defects. Reproductive Sciences. 20(2). 190–201. 7 indexed citations

16.

Engelen, Klaartje van, Mathilda T.M. Mommersteeg, Marieke J.H. Baars, et al.. (2012). The Ambiguous Role of NKX2-5 Mutations in Thyroid Dysgenesis. PLoS ONE. 7(12). e52685–e52685. 27 indexed citations

17.

Engelen, Klaartje van, Ana Töpf, Bernard Keavney, et al.. (2010). 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia: Table 1. Heart. 96(8). 621–624. 33 indexed citations

18.

Thienpont, Bernard, Litu Zhang, Alex V. Postma, et al.. (2010). Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans. The American Journal of Human Genetics. 86(6). 839–849. 72 indexed citations

19.

Postma, Alex V., Connie R. Bezzina, Jeltje F. de Vries, et al.. (2000). Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3. Human Genetics. 106(6). 614–619. 15 indexed citations

20.

Berg, Maarten P. van den, Alex V. Postma, Martin B. Rook, et al.. (1999). A single sodium channel mutation causing both long QT- and Brugada syndrome. Circulation. 100(18). 494–494. 6 indexed citations

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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