prof. dr. Martijn Huisman

Search results

• 2023

  Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

  EADB contributors, GR@ACE study group, DEGESCO consortium, IGAP (ADGC, CHARGE, EADI, GERAD) & PGC-ALZ consortia, 9 Feb 2023, In: Nature Communications. 14, 1 p., 716.

  Research output: Contribution to Journal › Erratum / Corrigendum › Academic

  Open Access
• 2022

  Correction to: Multiple domains of functioning in older adults during the pandemic: design and basic characteristics of the Longitudinal Aging Study Amsterdam COVID-19 questionnaire

  Hoogendijk, E. O., van der Horst, M. H. L., Poppelaars, J., van Vliet, M. & Huisman, M., Dec 2022, In: Aging Clinical and Experimental Research. 34, 12, p. 3183-3138 1 p.

  Research output: Contribution to Journal › Erratum / Corrigendum › Academic

  Open Access

  File

  • COVID-19 100%
  • Aging 50%
  • Older Adult 50%
  • Amsterdam 50%
  • Longi-tudinal 50%
  18 Downloads (Pure)
• 2021

  Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes (Nature Communications, (2019), 10, 1, (3669), 10.1038/s41467-019-11558-2)

  Deelen, J., Evans, D. S., Arking, D. E., Tesi, N., Nygaard, M., Liu, X., Wojczynski, M. K., Biggs, M. L., van der Spek, A., Atzmon, G., Ware, E. B., Sarnowski, C., Smith, A. V., Seppälä, I., Cordell, H. J., Dose, J., Amin, N., Arnold, A. M., Ayers, K. L., Barzilai, N., & 64 othersBecker, E. J., Beekman, M., Blanché, H., Christensen, K., Christiansen, L., Collerton, J. C., Cubaynes, S., Cummings, S. R., Davies, K., Debrabant, B., Deleuze, J-F., Duncan, R., Faul, J. D., Franceschi, C., Galan, P., Gudnason, V., Harris, T. B., Huisman, M., Hurme, M. A., Jagger, C., Jansen, I., Jylhä, M., Kähönen, M., Karasik, D., Kardia, S. L. R., Kingston, A., Kirkwood, T. B. L., Launer, L. J., Lehtimäki, T., Lieb, W., Lyytikäinen, L-P., Martin-Ruiz, C., Min, J., Nebel, A., Newman, A. B., Nie, C., Nohr, E. A., Orwoll, E. S., Perls, T. T., Province, M. A., Psaty, B. M., Raitakari, O. T., Reinders, M. J. T., Robine, J-M., Rotter, J. I., Sebastiani, P., Smith, J., Sørensen, T. I. A., Taylor, K. D., Uitterlinden, A. G., van der Flier, W., van der Lee, S. J., van Duijn, C. M., van Heemst, D., Vaupel, J. W., Weir, D., Ye, K., Zeng, Y., Zheng, W., Holstege, H., Kiel, D. P., Lunetta, K. L., Slagboom, P. E. & Murabito, J. M., 1 Dec 2021, In: Nature Communications. 12, 1, 2463.

  Research output: Contribution to Journal › Erratum / Corrigendum › Academic

  Open Access

  • Meta-Analysis 100%
  • Genome Wide Association Study 100%
  • Single Nucleotide Polymorphism 100%
  • Genome-Wide Association Study 100%

• Correction to: Perceived Importance and Enjoyment of Sexuality in Late Midlife: Cohort Differences in the Longitudinal Aging Study Amsterdam (LASA) (Sexuality Research and Social Policy, (2021), 18, 3, (621-635), 10.1007/s13178-020-00486-2)

  Kolodziejczak, K., Drewelies, J., Deeg, D. J. H., Huisman, M. & Gerstorf, D., 1 Sept 2021, In: Sexuality Research and Social Policy. 18, 3, p. 636

  Research output: Contribution to Journal › Erratum / Corrigendum › Academic

  Open Access

  • Perceived Importance 100%
  • Science Policy 100%
• 2020

  Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

  EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group & DESGESCO (Dementia Genetics Spanish Consortium), May 2020, In: Acta Neuropathologica. 139, 5, p. 959-962 4 p.

  Research output: Contribution to Journal › Erratum / Corrigendum › Academic

  Open Access

  • Alzheimer's Disease 100%
  • Frontotemporal Lobar Degeneration 100%
  • Diffuse Lewy Body Disease 100%
  • Parkinson's Disease 50%
  • Complex Genomic Disorder 50%