Maria Knol

Polygenic prediction of body mass index and obesity through the life course and across ancestries

23andMe Inc., DiscovEHR (DiscovEHR and MyCode Community Health Initiative), eMERGE (Electronic Medical Records and Genomics Network), GPC-UGR, The PRACTICAL Consortium, Understanding Society Scientific Group & VA Million Veteran Program, Sept 2025, In: Nature Medicine. 31, 9, p. 3151-3168 18 p.

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

Open Access

File

11 Citations (Scopus)

9 Downloads (Pure)

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

File

1 Citation (Scopus)

31 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

File

9 Citations (Scopus)

49 Downloads (Pure)

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

File

31 Citations (Scopus)

61 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

File

45 Downloads (Pure)

Maria Knol

Fingerprint

Collaborations and top research areas from the last five years

Dive into details

Polygenic prediction of body mass index and obesity through the life course and across ancestries

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

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

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

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