Rik Westland

DR.

20112019

Research output per year

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Research Output

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