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% Source: https://alzhub.org/research?author=Gijselinck+I
% 6 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{cruts2006-16862115,
  author  = {Cruts, M. and Gijselinck, I. and van der Zee, J. and Engelborghs, S. and Wils, H. and Pirici, D. and Rademakers, R. and others},
  title   = {{Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21}},
  journal = {Nature},
  year    = {2006},
  doi     = {10.1038/nature05017},
  pmid    = {16862115},
  url     = {https://doi.org/10.1038/nature05017}
}

@article{cuyvers2014-24119542,
  author  = {Cuyvers, E. and Bettens, K. and Philtjens, S. and Van Langenhove, T. and Gijselinck, I. and van der Zee, J. and Engelborghs, S. and Vandenbulcke, M. and others},
  title   = {{Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia}},
  journal = {Neurobiology of aging},
  year    = {2014},
  doi     = {10.1016/j.neurobiolaging.2013.09.009},
  pmid    = {24119542},
  url     = {https://doi.org/10.1016/j.neurobiolaging.2013.09.009}
}

@article{gijselinck2012-22154785,
  author  = {Gijselinck, I. and Van Langenhove, T. and van der Zee, J. and Sleegers, K. and Philtjens, S. and Kleinberger, G. and Janssens, J. and Bettens, K. and others},
  title   = {{A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study}},
  journal = {The Lancet. Neurology},
  year    = {2012},
  doi     = {10.1016/s1474-4422(11)70261-7},
  pmid    = {22154785},
  url     = {https://doi.org/10.1016/s1474-4422(11)70261-7}
}

@article{mori2013-24132570,
  author  = {Mori, K. and Arzberger, T. and Grässer, F. A. and Gijselinck, I. and May, S. and Rentzsch, K. and Weng, S. M. and Schludi, M. H. and others},
  title   = {{Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins}},
  journal = {Acta neuropathologica},
  year    = {2013},
  doi     = {10.1007/s00401-013-1189-3},
  pmid    = {24132570},
  url     = {https://doi.org/10.1007/s00401-013-1189-3}
}

@article{sleegers2006-16921174,
  author  = {Sleegers, K. and Brouwers, N. and Gijselinck, I. and Theuns, J. and Goossens, D. and Wauters, J. and Del-Favero, J. and Cruts, M. and others},
  title   = {{APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy}},
  journal = {Brain : a journal of neurology},
  year    = {2006},
  doi     = {10.1093/brain/awl203},
  pmid    = {16921174},
  url     = {https://doi.org/10.1093/brain/awl203}
}

@article{cruts2005-15888485,
  author  = {Cruts, M. and Rademakers, R. and Gijselinck, I. and van der Zee, J. and Dermaut, B. and de Pooter, T. and de Rijk, P. and Del-Favero, J. and others},
  title   = {{Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region}},
  journal = {Human molecular genetics},
  year    = {2005},
  doi     = {10.1093/hmg/ddi182},
  pmid    = {15888485},
  url     = {https://doi.org/10.1093/hmg/ddi182}
}