Neurology & Neurosurgery

Research output

Research output per year 1996 2016 2017 2018 2019 2020 2021 2022 2024

• 210 Article
• 20 Comment/Letter to the editor
• 10 Review article
• 9 Doctoral thesis 1 (Research UU / Graduation UU)
• 22 More
  • 7 Meeting Abstract
  • 7 Letter
  • 4 Editorial
  • 1 Chapter
  • 1 Abstract
  • 1 Short survey
  • 1 Working paper

Research output per year

Research output per year

Search results

• 2024

  Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

  Jul 2024, In: Nature Genetics. 56, 7, p. 1371-1376 6 p.

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

  Open Access

  File
• 2021

  Role of Rare Genetic Variants Found in Families with Intracranial Aneurysms in the General Dutch and UK Population

  Bakker, M. K., Ettema, R. A., Klostermann, M., Rinkel, G. J. E., Veldink, J. H. & Ruigrok, Y. M., Sept 2021, In: Stroke. 52, 9, p. E540-E541

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

  Open Access

  File

  • Intracranial Aneurysm 100%
  • Population 35%
  13 Downloads (Pure)
• 2019

  Unconsented genetic testing in psychiatry: an (almost) no go?

  Luykx, J. J., van der Spek, R., van Veen, S., Lo-A-Foe, W., Giesbertz, N. A. A., Bredenoord, A. L. & Palmboom, G. G., 1 Aug 2019, In: The Lancet Psychiatry. 6, 8, p. 641-642 2 p.

  Research output: Contribution to journal › Letter › Academic › peer-review
• 2016

  A reference panel of 64,976 haplotypes for genotype imputation

  McCarthy, S., Das, S., Kretzschmar, W., Delaneau, O., Wood, A. R., Teumer, A., Kang, H. M., Fuchsberger, C., Danecek, P., Sharp, K., Luo, Y., Sidore, C., Kwong, A., Timpson, N., Koskinen, S., Vrieze, S., Scott, L. J., Zhang, H., Mahajan, A., Veldink, J., & 30 othersPeters, U., Pato, C., van Duijn, C. M., Gillies, C. E., Gandin, I., Mezzavilla, M., Gilly, A., Cocca, M., Traglia, M., Angius, A., Barrett, J. C., Boomsma, D., Branham, K., Breen, G., Brummett, C. M., Busonero, F., Campbell, H., Chan, A., Chen, S., Chew, E., Collins, F. S., Corbin, L. J., Smith, G. D., Dedoussis, G., Dorr, M., Farmaki, A-E., Van den Berg, L. H., Van Rheenen, W., de Bakker, P. I. W. & Dekker, A., 22 Aug 2016, In: Nature Genetics. 48, p. 1279–1283

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

  • Haplotypes 100%
  • Single Nucleotide Polymorphism 89%
  • Genotype 76%
  • Gene Frequency 51%
  • Research Personnel 37%

• Full ablation of C9orf72 in mice causes immune system-related pathology and neoplastic events but no motor neuron defects

  Sudria-Lopez, E., Koppers, M., de Wit, M., van der Meer, C., Westeneng, H. J., Zundel, C. A. C., Youssef, S. A., Harkema, L., de Bruin, A., Veldink, J. H., van Den Berg, L. H. & Pasterkamp, R. J., Jul 2016, In: Acta Neuropathologica. 132, 1, p. 145-147 3 p.

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

  Open Access

  File
  1 Downloads (Pure)

• Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

  van Rheenen, W., Shatunov, A., Dekker, A. M., McLaughlin, R. L., Diekstra, F. P., Pulit, S. L., van der Spek, R. A. A., Võsa, U., de Jong, S., Robinson, M. R., Yang, J., Fogh, I., van Doormaal, P. T., Tazelaar, G. H. P., Koppers, M., Blokhuis, A. M., Sproviero, W., Jones, A. R., Kenna, K. P., van Eijk, K. R., & 30 othersHarschnitz, O., Schellevis, R. D., Brands, W. J., Medic, J., Menelaou, A., Vajda, A., Ticozzi, N., Lin, K., Rogelj, B., Vrabec, K., Ravnik-Glavač, M., Koritnik, B., Zidar, J., Leonardis, L., Grošelj, L. D., Millecamps, S., Salachas, F., Meininger, V., de Carvalho, M., Pinto, S., Mora, J. S., Rojas-García, R., Polak, M., Ophoff, R. A., Blauw, H. M., de Bakker, P. I. W., van Es, M. A., Pasterkamp, R. J., van den Berg, L. H. & Veldink, J. H., Sept 2016, In: Nature Genetics. 48, 9, p. 1043–1048

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

  • Amyotrophic Lateral Sclerosis 100%
  • Genome-Wide Association Study 97%
  • Genome 25%
  • Chromosomes, Human, Pair 21 24%
  • Multifactorial Inheritance 22%
• 2006

  Prenatal ultrasound and MRI predict placental localization in a combined intrauterine and extrauterine twin pregnancy [3]

  Lenglet, J. E., Bekker, M. N., Akkerman, C., Bolte, A. C. & Van Vugt, J. M. G., 1 Apr 2006, In: Prenatal Diagnosis. 26, 4, p. 376-378 3 p.

  Research output: Contribution to journal › Letter › Academic › peer-review
  2 Citations (Scopus)