Leander Beekman

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1 Active

Bezzina C.R.: Genetics of cardiac arrhythmias
Bezzina, C., Lodder, E., Mengarelli, I., Bakker, D., Beekman, L., Klerk, M., Cocera Ortega, L., Hoekstra, M., Lahrouchi, N., Lieve, K., Skoric - Milosavljevic, D., Podliesna, S., Rivaud, M., Tjong, F. & Veerman, C.
1/01/2007 → …
Project: Research

30 Article
2 Comment/Letter to the editor

Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias
Pham, C., Andrzejczyk, K., Jurgens, S. J., Lekanne Deprez, R., Palm, K. C. A., Vermeer, A. M. C., Nijman, J., Christiaans, I., Barge-Schaapveld, D. Q. C. M., van Dessel, P. F. H. M., Beekman, L., Choi, S. H., Lubitz, S. A., Skoric-Milosavljevic, D., van den Bersselaar, L., Jansen, P. R., Copier, J. S., Ellinor, P. T., Wilde, A. A. M., Bezzina, C. R., & 1 othersLodder, E. M., 1 Aug 2023, In: Circulation. Genomic and precision medicine. 16, 4, p. 328-336 9 p.
Research output: Contribution to journal › Article › Academic › peer-review
Chronically elevated branched chain amino acid levels are pro-arrhythmic
Portero, V., Nicol, T., Podliesna, S., Marchal, G. A., Baartscheer, A., Casini, S., Tadros, R., Treur, J. L., Tanck, M. W. T., Jane Cox, I. J., Probert, F., Hough, T. A., Falcone, S., Beekman, L., Müller-Nurasyid, M., Kastenmüller, G., Gieger, C., Peters, A., Kääb, S., Sinner, M. F., & 5 othersBlease, A., Verkerk, A. O., Bezzina, C. R., Potter, P. K. & Remme, C. A., 1 May 2022, In: Cardiovascular research. 118, 7, p. 1742-1757 16 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

16 Citations (Scopus)
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries
KORA-Study Group, 21 Jan 2022, In: Circulation Research. 130, 2, p. 166-180 15 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

9 Citations (Scopus)
Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy
Lahrouchi, N., Postma, A. V., Salazar, C. M., de Laughter, D. M., Tjong, F., Piherová, L., Bowling, F. Z., Zimmerman, D., Lodder, E. M., Ta-Shma, A., Perles, Z., Beekman, L., Ilgun, A., Gunst, Q., Hababa, M., Škorić-Milosavljević, D., Stránecký, V., Tomek, V., de Knijff, P., de Leeuw, R., & 36 othersRobinson, J. Y., Burn, S. C., Mustafa, H., Ambrose, M., Moss, T., Jacober, J., Niyazov, D. M., Wolf, B., Kim, K. H., Cherny, S., Rousounides, A., Aristidou-Kallika, A., Tanteles, G., Ange-Line, B., Denommé-Pichon, A-S., Francannet, C., Ortiz, D., Haak, M. C., ten Harkel, A. D. J., Manten, G. T. R., Dutman, A. C., Bouman, K., Magliozzi, M., Radio, F. C., Santen, G. W. E., Herkert, J. C., Alex Brown, H., Elpeleg, O., van den Hoff, M. J. B., Mulder, B., Airola, M. V., Kmoch, S., Barnett, J. V., Clur, S-A., Frohman, M. A. & Bezzina, C. R., 1 Mar 2021, In: Journal of clinical investigation. 131, 5, e142148.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

11 Citations (Scopus)
Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)
German Competence Network for Congenital Heart Defects, Oct 2021, In: Genetics in medicine. 23, 10, p. 2013 1 p.
Research output: Contribution to journal › Comment/Letter to the editor › Academic

Open Access

Leander Beekman

Collaborations and top research areas from the last five years

Dive into details

Bezzina C.R.: Genetics of cardiac arrhythmias

Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

Chronically elevated branched chain amino acid levels are pro-arrhythmic

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)

Leander Beekman

Collaborations and top research areas from the last five years

Projects

Bezzina C.R.: Genetics of cardiac arrhythmias

Research output

Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

Chronically elevated branched chain amino acid levels are pro-arrhythmic

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)