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Maria Knol

 https://orcid.org/0000-0002-3597-1531

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  • Developing a Core Outcome Set for Netherton Syndrome: An International Multi-Stakeholder e-Delphi Consensus Study

    Nouwen, A. E. M., Ragamin, A., Knol, M. J., Ott, H., Weibel, L., Has, C., Hovnanian, A., Paller, A. S., Bodemer, C., Dalm, V. A. S. H., Pasmans, S. G. M. A. & Schappin, R., Feb 2025, In: Dermatology. 241, 1, p. 35-48 14 p.

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

    Open Access
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    8 Downloads (Pure)

  • Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

    García-Marín, L. M., Campos, A. I., Diaz-Torres, S., Rabinowitz, J. A., Ceja, Z., Mitchell, B. L., Grasby, K. L., Thorp, J. G., Agartz, I., Alhusaini, S., Ames, D., Amouyel, P., Andreassen, O. A., Arfanakis, K., Arias-Vasquez, A., Armstrong, N. J., Athanasiu, L., Bastin, M. E., Beiser, A. S. & Bennett, D. A. & 170 others, Bis, J. C., Boks, M. P. M., Boomsma, D. I., Brodaty, H., Brouwer, R. M., Buitelaar, J. K., Burkhardt, R., Cahn, W., Calhoun, V. D., Carmichael, O. T., Chakravarty, M., Chen, Q., Ching, C. R. K., Cichon, S., Crespo-Facorro, B., Crivello, F., Dale, A. M., Smith, G. D., de Geus, E. J. C., De Jager, P. L., de Zubicaray, G. I., Debette, S., DeCarli, C., Depondt, C., Desrivières, S., Djurovic, S., Ehrlich, S., Erk, S., Espeseth, T., Fernández, G., Filippi, I., Fisher, S. E., Fleischman, D. A., Fletcher, E., Fornage, M., Forstner, A. J., Francks, C., Franke, B., Ge, T., Goldman, A. L., Grabe, H. J., Green, R. C., Grimm, O., Groenewold, N. A., Gruber, O., Gudnason, V., Håberg, A. K., Haukvik, U. K., Heinz, A., Hibar, D. P., Hilal, S., Himali, J. J., Ho, B. C., Hoehn, D. F., Hoekstra, P. J., Hofer, E., Hoffmann, W., Holmes, A. J., Homuth, G., Hosten, N., Ikram, M. K., Ipser, J. C., Jack, C. R., Jahanshad, N., Jönsson, E. G., Kahn, R. S., Kanai, R., Klein, M., Knol, M. J., Launer, L. J., Lawrie, S. M., Hellard, S. L., Lee, P. H., Lemaître, H., Li, S., Liewald, D. C. M., Lin, H., Longstreth, W. T., Lopez, O. L., Luciano, M., Maillard, P., Marquand, A. F., Martin, N. G., Martinot, J. L., Mather, K. A., Mattay, V. S., McMahon, K. L., Mecocci, P., Melle, I., Meyer-Lindenberg, A., Mirza-Schreiber, N., Milaneschi, Y., Mosley, T. H., Mühleisen, T. W., Müller-Myhsok, B., Maniega, S. M., Nauck, M., Nho, K., Niessen, W. J., Nöthen, M. M., Nyquist, P. A., Oosterlaan, J., Pandolfo, M., Paus, T., Pausova, Z., Penninx, B. W. J. H., Pike, G. B., Psaty, B. M., Pütz, B., Reppermund, S., Rietschel, M. D., Risacher, S. L., Romanczuk-Seiferth, N., Romero-Garcia, R., Roshchupkin, G. V., Rotter, J. I., Sachdev, P. S., Sämann, P. G., Saremi, A., Sargurupremraj, M., Saykin, A. J., Schmaal, L., Schmidt, H., Schmidt, R., Schofield, P. R., Scholz, M., Schumann, G., Schwarz, E., Shen, L., Shin, J., Sisodiya, S. M., Smith, A. V., Smoller, J. W., Soininen, H. S., Steen, V. M., Stein, D. J., Stein, J. L., Thomopoulos, S. I., Toga, A. W., Tordesillas-Gutiérrez, D., Trollor, J. N., Valdes-Hernandez, M. C., van ′t Ent, D., van Bokhoven, H., van der Meer, D., van der Wee, N. J. A., Vázquez-Bourgon, J., Veltman, D. J., Vernooij, M. W., Villringer, A., Vinke, L. N., Völzke, H., Walter, H., Wardlaw, J. M., Weinberger, D. R., Weiner, M. W., Wen, W., Westlye, L. T., Westman, E., White, T., Witte, A. V., Wolf, C., Yang, J., Zwiers, M. P., Ikram, M. A., Seshadri, S., Thompson, P. M., Satizabal, C. L., Medland, S. E. & Rentería, M. E., Nov 2024, In: Nature Genetics. 56, 11, p. 2333-2344 12 p.

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

    Open Access
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    4 Citations (Scopus)

  • A genome-wide association meta-analysis of all-cause and vascular dementia

    The MEGAVCID consortium, Hilal, S., Knol, M. J., Roshchupkin, G. V., Ikram, M. A. & Ghanbari, M., Sept 2024, In: Alzheimer's and Dementia. 20, 9, p. 5973-5995 23 p.

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

    Open Access
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    5 Citations (Scopus)
    27 Downloads (Pure)

  • Association of common genetic variants with chronic axonal polyneuropathy in the general population: a genome-wide association study

    Taams, N. E., Knol, M. J., Hanewinckel, R., Drenthen, J., Reilly, M. M., van Doorn, P. A., Adams, H. H. H. & Ikram, M. A., 3 Jul 2024, In: Frontiers in Neurology. 15, 1422824.

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

    Open Access
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    9 Downloads (Pure)

  • Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

    Sargurupremraj, M., Soumaré, A., Bis, J. C., Surakka, I., Jürgenson, T., Joly, P., Knol, M. J., Wang, R., Yang, Q., Satizabal, C. L., Gudjonsson, A., Mishra, A., Bouteloup, V., Phuah, C. L., van Duijn, C. M., Cruchaga, C., Dufouil, C., Chêne, G., Lopez, O. L. & Psaty, B. M. & 14 others, Tzourio, C., Amouyel, P., Adams, H. H., Jacqmin-Gadda, H., Ikram, M. A., Gudnason, V., Milani, L., Winsvold, B. S., Hveem, K., Matthews, P. M., Longstreth, W. T., Seshadri, S., Launer, L. J. & Debette, S., 22 May 2024, In: JAMA network open. 7, 5, e2412824.

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

    Open Access
    File
    6 Citations (Scopus)
    8 Downloads (Pure)
View all 33 research outputs