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% Source: https://alzhub.org/research?author=Hulsman+M&access=free
% 4 entries, in the order the page lists them. Built from alzhub.org's own records.
% 0 entries have no readable author in the source record and carry no author field.

@article{holstege2022-36411364,
  author  = {Holstege, H. and Hulsman, M. and Charbonnier, C. and Grenier-Boley, B. and Quenez, O. and Grozeva, D. and van Rooij, J. G. J. and Sims, R. and others},
  title   = {{Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease}},
  journal = {Nature genetics},
  year    = {2022},
  doi     = {10.1038/s41588-022-01208-7},
  pmid    = {36411364},
  url     = {https://doi.org/10.1038/s41588-022-01208-7}
}

@article{quenez2026-42648288,
  author  = {Quenez, O. and Schramm, C. and Cassinari, K. and Nicolas, A. and Groeneveld, J. and Huguet, G. and Grenier-Boley, B. and Hulsman, M. and Walters, G. B. and de Rojas, I. and Rovelet-Lecrux, A. and Feuillette, S. and others},
  title   = {{Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk}},
  journal = {American Journal of Human Genetics},
  year    = {2026},
  doi     = {10.1016/j.ajhg.2026.07.013},
  pmid    = {42648288},
  url     = {https://doi.org/10.1016/j.ajhg.2026.07.013}
}

@article{tesi2019-30258121,
  author  = {Tesi, N. and van der Lee, S. J. and Hulsman, M. and Jansen, I. E. and Stringa, N. and van Schoor, N. and Meijers-Heijboer, H. and Huisman, M. and others},
  title   = {{Centenarian controls increase variant effect sizes by an average twofold in an extreme case-extreme control analysis of Alzheimer's disease}},
  journal = {European journal of human genetics : EJHG},
  year    = {2019},
  doi     = {10.1038/s41431-018-0273-5},
  pmid    = {30258121},
  url     = {https://doi.org/10.1038/s41431-018-0273-5}
}

@article{holstege2017-28537274,
  author  = {Holstege, H. and van der Lee, S. J. and Hulsman, M. and Wong, T. H. and van Rooij, J. G. and Weiss, M. and Louwersheimer, E. and Wolters, F. J. and others},
  title   = {{Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy}},
  journal = {European journal of human genetics : EJHG},
  year    = {2017},
  doi     = {10.1038/ejhg.2017.87},
  pmid    = {28537274},
  url     = {https://doi.org/10.1038/ejhg.2017.87}
}