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Iris Lekkerkerker, MSc

  • Lundlaan 6, Wilhemina Children's Hospital

    3584 EA Utrecht

    Netherlands

20232025

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  • 2 Article
  • 1 Comment/Letter to the editor
  • 1 Review article
  • 1 Preprint

  • Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes

    Milo Rasouly, H., Krishna Murthy, S. B., Vena, N., Povysil, G., Beenken, A., Verbitsky, M., Shril, S., Lekkerkerker, I., Yang, S., Khan, A., Fasel, D., Wongboonsin, J., Martino, J., Ke, J., Elefant, N., Tomar, N., Harnof, O., Kisselev, S., Bheda, S. & Reytan-Miron, S. & 88 others, Lim, T. Y., Jamry-Dziurla, A., Lugani, F., Zhang, J. Y., Marasa, M., Kolupaeva, V., Groopman, E. E., Jin, G., Ghavami, I., Stevens, K. O., Coughlin, A. C., Kil, B. H., Chatterjee, D., Bradbury, D., Zheng, J., Mehl, K., Morban, M., Reingold, R., Piva, S., Mu, X., Mitrotti, A., Szmigielska, A., Gliwińska, A., Ranghino, A., Bomback, A. S., Badenski, A., Latos-Bielenska, A., Capone, V., Materna-Kiryluk, A., Amoroso, A., Izzi, C., La Scola, C., Cohen, D. J., Santoro, D., Drozdz, D., Fiaccadori, E., Lin, F., Scolari, F., Tondolo, F., La Manna, G., Appel, G. B., Ghiggeri, G. M., Zaza, G., Montini, G., Masnata, G., Krzemien, G., Pisani, I., Radhakrishnan, J., Zachwieja, K., Gesualdo, L., Biancone, L., Meneghesso, D., Mizerska-Wasiak, M., Tkaczyk, M., Zaniew, M., Borszewska-Kornacka, M. K., Szczepanska, M., Saraga, M., Rao, M. K., Bodria, M., Miklaszewska, M., Uy, N. S., Baraldi, O., Bjanid, O., Esposito, P., Zamboli, P., Marzuillo, P., Canetta, P. A., Sikora, P., Westland, R., Crew, R. J., Alam, S., Guarino, S., Negrisolo, S., Hays, T., Mane, S., Grandinetti, V., Tasic, V., Lozanovski, V. J., Caliskan, Y., Goldstein, D., Lifton, R. P., Ionita-Laza, I., Kiryluk, K., van Eerde, A. M., Hildebrandt, F., Sanna-Cherchi, S. & Gharavi, A. G., 9 Oct 2025, In: Nature Communications. 16, 1, p. 1-2 2 p., 8980.

    Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

    Open Access
    File
    21 Downloads (Pure)

  • Exome analysis links kidney malformations to developmental disorders and reveals causal genes

    Milo Rasouly, H., Krishna Murthy, S. B., Vena, N., Povysil, G., Beenken, A., Verbitsky, M., Shril, S., Lekkerkerker, I., Yang, S., Khan, A., Fasel, D., Wongboonsin, J., Martino, J., Ke, J., Elefant, N., Tomar, N., Harnof, O., Kisselev, S., Bheda, S. & Reytan-Miron, S. & 88 others, Lim, T. Y., Jamry-Dziurla, A., Lugani, F., Zhang, J. Y., Marasa, M., Kolupaeva, V., Groopman, E. E., Jin, G., Ghavami, I., Stevens, K. O., Coughlin, A. C., Kil, B. H., Chatterjee, D., Bradbury, D., Zheng, J., Mehl, K., Morban, M., Reingold, R., Piva, S., Mu, X., Mittrori, A., Szmigielska, A., Gliwińska, A., Ranghino, A., Bomback, A. S., Badenski, A., Latos-Bielenska, A., Capone, V., Materna-Kiryluk, A., Amoroso, A., Izzi, C., La Scola, C., Cohen, D. J., Santoro, D., Drozdz, D., Fiaccadori, E., Lin, F., Scolari, F., Tondolo, F., La Manna, G., Appel, G. B., Ghiggeri, G. M., Zaza, G., Montini, G., Masnata, G., Krzemien, G., Pisani, I., Radhakrishnan, J., Zachwieja, K., Gesualdo, L., Biancone, L., Meneghesso, D., Mizerska-Wasiak, M., Tkaczyk, M., Zaniew, M., Borszewska-Kornacka, M. K., Szczepanska, M., Saraga, M., Rao, M. K., Bodria, M., Miklaszewska, M., Uy, N. S., Baraldi, O., Bjanid, O., Esposito, P., Zamboli, P., Marzuillo, P., Canetta, P. A., Sikora, P., Westland, R., Crew, R. J., Alam, S., Guarino, S., Negrisolo, S., Hays, T., Mane, S., Grandinetti, V., Tasic, V., Lozanovski, V. J., Caliskan, Y., Goldstein, D., Lifton, R. P., Ionita-Laza, I., Kiryluk, K., van Eerde, A. M., Hildebrandt, F., Sanna-Cherchi, S. & Gharavi, A. G., 7 Aug 2025, In: Nature Communications. 16, 1, 7290.

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

    Open Access
    File
    4 Downloads (Pure)

  • Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract

    on behalf of the ArtDECO consortium, Mar 2025, In: Pediatric Nephrology. 40, 3, p. 685-699 15 p.

    Research output: Contribution to journal › Review article › peer-review

    Open Access
    File
    40 Downloads (Pure)

  • GeNepher data- and biobank for patients with (suspected) genetic kidney disease: Rationale, design and status update

    Claus, L. R., Lekkerkerker, I., van der Zwaag, B., Nguyen, T. Q., Knoers, N. V. A. M., de Borst, M. H., Rookmaker, M. B., Lilien, M. R. & van Eerde, A. M., May 2024, In: Rare. 2, 8 p., 100030.

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

    Open Access
    File
    6 Downloads (Pure)

  • Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

    Cipriani, V., Vestito, L., Magavern, E. F., Jacobsen, J. O., Arno, G., Behr, E. R., Benson, K. A., Bertoli, M., Bockenhauer, D., Bowl, M. R., Burley, K., Chan, L. F., Chinnery, P., Conlon, P., Costa, M., Davidson, A. E., Dawson, S. J., Elhassan, E., Flanagan, S. E. & Futema, M. & 41 others, Gale, D. P., García-Ruiz, S., Corcia, C. G., Griffin, H. R., Hambleton, S., Hicks, A. R., Houlden, H., Houlston, R. S., Howles, S. A., Kleta, R., Lekkerkerker, I., Lin, S., Liskova, P., Mitchison, H., Morsy, H., Mumford, A. D., Newman, W. G., Neatu, R., O'Toole, E. A., Ong, A. C., Pagnamenta, A. T., Rahman, S., Rajan, N., Robinson, P. N., Ryten, M., Sadeghi-Alavijeh, O., Sayer, J. A., Shovlin, C. L., Taylor, J. C., Teltsh, O., Tomlinson, I., Tucci, A., Turnbull, C., van Eerde, A. M., Ware, J. S., Watts, L. M., Webster, A. R., Westbury, S. K., Zheng, S. L., Caulfield, M. & Smedley, D., 21 Dec 2023, medRxiv, 42 p. (medRxiv).

    Research output: Working paper › Preprint › Academic