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  1. 2019

  2. Flotillins in the intercalated disc are potential modulators of cardiac excitability

    Kessler, E. L., van Stuijvenberg, L., van Bavel, J. J. A., van Bennekom, J., Zwartsen, A., Rivaud, M. R., Vink, A., Efimov, I. R., Postma, A. V., van Tintelen, J. P., Remme, C. A., Vos, M. A., Banning, A., de Boer, T. P., Tikkanen, R. & van Veen, T. A. B., 2019, In: Journal of molecular and cellular cardiology. 126, p. 86-95

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

  3. GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum

    Škorić-Milosavljević, D., Tjong, F. V. Y., Barc, J., Backx, A. P. C. M., Clur, S-A. B., van Spaendonck-Zwarts, K., Oostra, R-J., Lahrouchi, N., Beekman, L., Bökenkamp, R., Barge-Schaapveld, D. Q. C. M., Mulder, B. J., Lodder, E. M., Bezzina, C. R. & Postma, A. V., 2019, In: American journal of medical genetics. Part A. 179, 9, p. 1836-1845

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

  4. Identifying pathogenic variants in the Follistatin-like 1 gene (FSTL1) in patients with skeletal and atrioventricular valve disorders

    Prakash, S., Mattiotti, A., Sylva, M., Mulder, B. J. M., Postma, A. V. & van den Hoff, M. J. B., 2019, In: Molecular genetics and genomic medicine. 7, 4, e00567.

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

  5. Loss-of-function variants in myocardin cause congenital megabladder in humans and mice

    Houweling, A. C., Beaman, G. M., Postma, A. V., Blair Gainous, T., Lichtenbelt, K. D., Brancati, F., Lopes, F. M., van der Made, I., Polstra, A. M., Robinson, M. L., Wright, K. D., Ellingford, J. M., Jackson, A. R., Overwater, E., Genesio, R., Romano, S., Camerota, L., D'Angelo, E., Meijers-Heijboer, E. J., Christoffels, V. M., & 5 othersMcHugh, K. M., Black, B. L., Newman, W. G., Woolf, A. S. & Creemers, E. E., 2019, In: Journal of clinical investigation. 129, 12, p. 5374-5380

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

  6. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

    Page, D. J., Miossec, M. J., Williams, S. G., Monaghan, R. M., Fotiou, E., Cordell, H. J., Sutcliffe, L., Topf, A., Bourgey, M., Bourque, G., Eveleigh, R., Dunwoodie, S. L., Winlaw, D. S., Bhattacharya, S., Breckpot, J., Devriendt, K., Gewillig, M., Brook, J. D., Setchfield, K. J., Bu'Lock, F. A., & 14 othersO'Sullivan, J., Stuart, G., Bezzina, C. R., Mulder, B. J. M., Postma, A. V., Bentham, J. R., Baron, M., Bhaskar, S. S., Black, G. C., Newman, W. G., Hentges, K. E., Lathrop, G. M., Santibanez-Koref, M. & Keavney, B. D., 2019, In: Circulation research. 124, 4, p. 553-563

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

  7. 2018

  8. An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality

    Ferrer, C. M., Alders, M., Postma, A. V., Park, S., Klein, M. A., Cetinbas, M., Pajkrt, E., Glas, A., van Koningsbruggen, S., Christoffels, V. M., Mannens, M. M. A. M., Knegt, L., Etchegaray, J-P., Sadreyev, R. I., Denu, J. M., Mostoslavsky, G., van Maarle, M. C. & Mostoslavsky, R., 2018, In: Genes & development. 32, 5-6, p. 373-388

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

  9. Familial co-occurrence of congenital heart defects follows distinct patterns

    Ellesøe, S. G., Workman, C. T., Bouvagnet, P., Loffredo, C. A., McBride, K. L., Hinton, R. B., van Engelen, K., Gertsen, E. C., Mulder, B. J. M., Postma, A. V., Anderson, R. H., Hjortdal, V. E., Brunak, S. & Larsen, L. A., 2018, In: European heart journal. 39, 12, p. 1015-1022

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

  10. Specialized impulse conduction pathway in the alligator heart

    Jensen, B., Boukens, B. J., Crossley, D. A., Conner, J., Mohan, R. A., van Duijvenboden, K., Postma, A. V., Gloschat, C. R., Elsey, R. M., Sedmera, D., Efimov, I. R. & Christoffels, V. M., 2018, In: eLife. 7, e32120.

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

  11. Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy

    de Bortoli, M., Postma, A. V., Poloni, G., Calore, M., Minervini, G., Mazzotti, E., Rigato, I., Ebert, M., Lorenzon, A., Vazza, G., Cipriani, A., Bariani, R., Perazzolo Marra, M., Husser, D., Thiene, G., Daliento, L., Corrado, D., Basso, C., Tosatto, S. C. E., Bauce, B., & 2 othersvan Tintelen, J. P. & Rampazzo, A., 2018, In: Circulation. Genomic and precision medicine. 11, 10, p. e002123

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

  12. 2017

  13. Editorial Commentary: Keeping the congenitally malformed heart in shape

    van den Berg, G., Krasemann, T. & Postma, A. V., 2017, In: Trends in cardiovascular medicine. 27, 8, p. 532-533

    Research output: Contribution to journal › Editorial › Academic › peer-review

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ID: 79221