Rik Westland

DR.

20112019

Research output per year

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  • Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract (Nature Genetics, (2019), 51, 1, (117-127), 10.1038/s41588-018-0281-y)

    Verbitsky, M., Westland, R., Perez, A., Kiryluk, K., Liu, Q., Krithivasan, P., Mitrotti, A., Fasel, D. A., Batourina, E., Sampson, M. G., Bodria, M., Werth, M., Kao, C., Martino, J., Capone, V. P., Vivante, A., Shril, S., Kil, B. H., Marasa, M., Zhang, J. Y. & 70 others, Na, Y-J., Lim, T. Y., Ahram, D., Weng, P. L., Heinzen, E. L., Carrea, A., Piaggio, G., Gesualdo, L., Manca, V., Masnata, G., Gigante, M., Cusi, D., Izzi, C., Scolari, F., van Wijk, J. A. E., Saraga, M., Santoro, D., Conti, G., Zamboli, P., White, H., Drozdz, D., Zachwieja, K., Miklaszewska, M., Tkaczyk, M., Tomczyk, D., Krakowska, A., Sikora, P., Jarmoliński, T., Borszewska-Kornacka, M. K., Pawluch, R., Szczepanska, M., Adamczyk, P., Mizerska-Wasiak, M., Krzemien, G., Szmigielska, A., Zaniew, M., Dobson, M. G., Darlow, J. M., Puri, P., Barton, D. E., Furth, S. L., Warady, B. A., Gucev, Z., Lozanovski, V. J., Tasic, V., Pisani, I., Allegri, L., Rodas, L. M., Campistol, J. M., Jeanpierre, C. C., Alam, S., Casale, P., Wong, C. S., Lin, F., Miranda, D. B. M., Oliveira, E. A., Simoes-e-Silva, A. C., Barasch, J. M., Levy, B., Wu, N., Hildebrandt, F., Ghiggeri, G. M., Latos-Bielenska, A., Materna-Kiryluk, A., Zhang, F., Hakonarson, H., Papaioannou, V. E., Mendelsohn, C. L., Gharavi, A. G. & Sanna-Cherchi, S., 1 Apr 2019, In : Nature Genetics. 51, 4, p. 764 1 p.

    Research output: Contribution to journalErratumAcademicpeer-review

  • The burden of Candidate pathogenic variants for kidney and genitourinary disorders emerging from exome sequencing

    Rasouly, H. M., Groopman, E. E., Heyman-Kantor, R., Fasel, D. A., Mitrotti, A., Westland, R., Bier, L., Weng, C., Ren, Z., Copeland, B., Krithivasan, P., Chung, W. K., Sanna-Cherchi, S., Goldstein, D. B. & Gharavi, A. G., 1 Jan 2019, In : Annals of Internal Medicine. 170, 1, p. 11-21

    Research output: Contribution to journalArticleAcademicpeer-review

  • The copy number variation landscape of congenital anomalies of the kidney and urinary tract

    Verbitsky, M., Westland, R., Perez, A., Kiryluk, K., Liu, Q., Krithivasan, P., Mitrotti, A., Fasel, D. A., Batourina, E., Sampson, M. G., Bodria, M., Werth, M., Kao, C., Martino, J., Capone, V. P., Vivante, A., Shril, S., Kil, B. H., Marasà, M., Zhang, J. Y. & 70 others, Na, Y-J., Lim, T. Y., Ahram, D., Weng, P. L., Heinzen, E. L., Carrea, A., Piaggio, G., Gesualdo, L., Manca, V., Masnata, G., Gigante, M., Cusi, D., Izzi, C., Scolari, F., van Wijk, J. A. E., Saraga, M., Santoro, D., Conti, G., Zamboli, P., White, H., Drozdz, D., Zachwieja, K., Miklaszewska, M., Tkaczyk, M., Tomczyk, D., Krakowska, A., Sikora, P., Jarmoliński, T., Borszewska-Kornacka, M. K., Pawluch, R., Szczepanska, M., Adamczyk, P., Mizerska-Wasiak, M., Krzemien, G., Szmigielska, A., Zaniew, M., Dobson, M. G., Darlow, J. M., Puri, P., Barton, D. E., Furth, S. L., Warady, B. A., Gucev, Z., Lozanovski, V. J., Tasic, V., Pisani, I., Allegri, L., Rodas, L. M., Campistol, J. M., Jeanpierre, C. C., Alam, S., Casale, P., Wong, C. S., Lin, F., Miranda, D. B. M., Oliveira, E. A., Simões-e-Silva, A. C., Barasch, J. M., Levy, B., Wu, N., Hildebrandt, F., Ghiggeri, G. M., Latos-Bielenska, A., Materna-Kiryluk, A., Zhang, F., Hakonarson, H., Papaioannou, V. E., Mendelsohn, C. L., Gharavi, A. G. & Sanna-Cherchi, S., 1 Jan 2019, In : Nature Genetics. 51, 1, p. 117-127

    Research output: Contribution to journalArticleAcademicpeer-review

  • Genetic basis of human congenital anomalies of the kidney and urinary tract

    Sanna-Cherchi, S., Westland, R., Ghiggeri, G. M. & Gharavi, A. G., 2018, In : Journal of Clinical Investigation. 128, 1, p. 4-15

    Research output: Contribution to journalReview articleAcademicpeer-review

    Open Access
  • Erratum: Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))

    Sanna-Cherchi, S., Khan, K., Westland, R., Krithivasan, P., Fievet, L., Rasouly, H. M., Ionita-Laza, I., Capone, V. P., Fasel, D. A., Kiryluk, K., Kamalakaran, S., Bodria, M., Otto, E. A., Sampson, M. G., Gillies, C. E., Vega-Warner, V., Vukojevic, K., Pediaditakis, I., Makar, G. S., Mitrotti, A. & 29 others, Verbitsky, M., Martino, J., Liu, Q., Na, Y. J., Goj, V., Ardissino, G., Gigante, M., Gesualdo, L., Janezcko, M., Zaniew, M., Mendelsohn, C. L., Shril, S., Hildebrandt, F., van Wijk, J. A. E., Arapovic, A., Saraga, M., Allegri, L., Izzi, C., Scolari, F., Tasic, V., Ghiggeri, G. M., Latos-Bielenska, A., Materna-Kiryluk, A., Mane, S., Goldstein, D. B., Lifton, R. P., Katsanis, N., Davis, E. E. & Gharavi, A. G., 7 Dec 2017, In : American journal of human genetics. 101, 6, p. 1034 1 p.

    Research output: Contribution to journalComment/Letter to the editorAcademic

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