Amsterdam Cardiovascular Sciences

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

German Competence Network for Congenital Heart Defects, Oct 2021, In: Genetics in medicine. 23, 10, p. 1952-1960 9 p.

Research output: Contribution to journal › Article* › Academic › peer-review

Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (Nature Genetics, (2020), 52, 12, (1314-1332), 10.1038/s41588-020-00713-x)

LifeLines Cohort Study, EPIC-CVD, EPIC-InterAct, Million Veteran Program & Understanding Society Scientific Group, May 2021, In: Nature genetics. 53, 5, p. 762 1 p.

Research output: Contribution to journal › Comment/Letter to the editor* › Academic

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 others, Robinson, 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