Amsterdam Neuroscience - Complex Trait Genetics

Research output

Research output per year 1995 2021 2022 2023 2024

• 1430 Article
• 100 Review article
• 84 Comment/Letter to the editor
• 40 Meeting Abstract
• 98 More
  • 23 Erratum/Corrigendum
  • 22 Phd-Thesis - Research and graduation internal
  • 20 Letter
  • 15 Chapter
  • 14 Editorial
  • 1 Book
  • 1 Software
  • 1 Other contribution
  • 1 Phd-Thesis - Research internal and graduation external

Research output per year

Research output per year

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

• Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

  23andMe Research Team & Quantitative Trait Working Group of the GenLang Consortium, Mar 2023, In: Nature Genetics. 55, 3, p. 520-520 1 p.

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

  Open Access
• 2022

  Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

  23andMe Research Team, Jul 2022, In: Nature Genetics. 54, 7, 1 p., 1062.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic
  2 Citations (Scopus)

• Correction: Early-life stress exposure and large-scale covariance brain networks in extremely preterm-born infants

  Lammertink, F., van den Heuvel, M. P., Hermans, E. J., Dudink, J., Tataranno, M. L., Benders, M. J. N. L. & Vinkers, C. H., 8 Jul 2022, In: Translational Psychiatry. 12, 1 p., 269.

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

  Open Access

• Corrigendum: Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: A polygenic risk score analysis(Front. Psychiatry, (2021), 12, (734077), 10.3389/fpsyt.2021.734077)

  Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 4 Aug 2022, In: Frontiers in psychiatry. 13, 893816.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  1 Citation (Scopus)
• 2021

  Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

  23andMe Research Team, Dec 2021, In: Nature Genetics. 53, 12, p. 1722-1722 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic
  2 Citations (Scopus)

• Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (Molecular Psychiatry, (2020), 10.1038/s41380-019-0546-6)

  on the behalf of Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 2021, In: Molecular psychiatry. 26, p. 5465 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  1 Citation (Scopus)

• Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

  on the behalf of Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Sept 2021, In: Molecular psychiatry. 26, 9, p. 5465-5465 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic
  1 Citation (Scopus)

• Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

  Jia, X., Goes, F. S., Locke, A. E., Palmer, D., Wang, W., Cohen-Woods, S., Genovese, G., Jackson, A. U., Jiang, C., Kvale, M., Mullins, N., Nguyen, H., Pirooznia, M., Rivera, M., Ruderfer, D. M., Shen, L., Thai, K., Zawistowski, M., Zhuang, Y., Abecasis, G., & 56 othersAkil, H., Bergen, S., Burmeister, M., Chapman, S., DelaBastide, M., Juréus, A., Kang, H. M., Kwok, P. Y., Li, J. Z., Levy, S. E., Monson, E. T., Moran, J., Sobell, J., Watson, S., Willour, V., Zöllner, S., Adolfsson, R., Blackwood, D., Boehnke, M., Breen, G., Corvin, A., Craddock, N., DiFlorio, A., Hultman, C. M., Landen, M., Lewis, C., McCarroll, S. A., Richard McCombie, W., McGuffin, P., McIntosh, A., McQuillin, A., Morris, D., Myers, R. M., O’Donovan, M., Ophoff, R., Boks, M., Kahn, R., Ouwehand, W., Owen, M., Pato, C., Pato, M., Posthuma, D., Potash, J. B., Reif, A., Sklar, P., Smoller, J., Sullivan, P. F., Vincent, J., Walters, J., Neale, B., Purcell, S., Risch, N., Schaefer, C., Stahl, E. A., Zandi, P. P. & Scott, L. J., Sept 2021, In: Molecular psychiatry. 26, 9, p. 5251-5251 1 p.

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

• Corrigendum to “Evaluating a dimensional approach to treatment resistance in anxiety disorders: A two-year follow-up study” [Journal of Affective Disorders Reports 4 (2021) 1–8](S2666915321000664)(10.1016/j.jadr.2021.100139)

  Bokma, W. A., Batelaan, N. M., Penninx, B. W. J. H. & van Balkom, A. J. L. M., 1 Jul 2021, In: Journal of Affective Disorders Reports. 5, 100160.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

• Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (Nature Communications, (2021), 12, 1, (24), 10.1038/s41467-020-19366-9): Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (Nature Communications, (2021), 12, 1, (24), 10.1038/s41467-020-19366-9)

  Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC), 1 Dec 2021, In: Nature communications. 12, 1, 995.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  4 Citations (Scopus)
• 2020

  Author Correction: A global overview of pleiotropy and genetic architecture in complex traits (Nature Genetics, (2019), 51, 9, (1339-1348), 10.1038/s41588-019-0481-0)

  Watanabe, K., Stringer, S., Frei, O., Mirkov, M. U., de Leeuw, C., Polderman, T. J. C., van der Sluis, S., Andreassen, O. A., Neale, B. M. & Posthuma, D., 1 Mar 2020, In: Nature Genetics. 52, 3, p. 353 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  6 Citations (Scopus)

• Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular Psychiatry, (2018), 10.1038/s41380-018-0118-1)

  16p11.2 European Consortium, for the ENIGMA-CNV working group, 1 Mar 2020, In: Molecular psychiatry. 25, 3, p. 692-695

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access

• Correction: Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence

  Smeland, O. B., Bahrami, S., Frei, O., Shadrin, A., O’Connell, K., Savage, J., Watanabe, K., Krull, F., Bettella, F., Steen, N. E., Ueland, T., Posthuma, D., Djurovic, S., Dale, A. M. & Andreassen, O. A., Apr 2020, In: Molecular psychiatry. 25, 4, p. 914-914 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic
  5 Citations (Scopus)

• Correction: Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence (Molecular Psychiatry, (2019), 10.1038/s41380-018-0332-x): Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence (Molecular Psychiatry, (2020), 25, 4, (844-853), 10.1038/s41380-018-0332-x)

  Smeland, O. B., Bahrami, S., Frei, O., Shadrin, A., O’Connell, K., Savage, J., Watanabe, K., Krull, F., Bettella, F., Steen, N. E., Ueland, T., Posthuma, D., Djurovic, S., Dale, A. M. & Andreassen, O. A., 1 Apr 2020, In: Molecular psychiatry. 25, 4, p. 914 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  5 Citations (Scopus)

• 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

• Erratum: Identifying underlying medical causes of pediatric obesity: Results of a systematic diagnostic approach in a pediatric obesity center (PLOS ONE (2020) 15:5 (e0232990) DOI: 10.1371/journal.pone.0232990)

  Kleinendorst, L., Abawi, O., van der Voorn, B., Jongejan, M. H. T. M., Brandsma, A. E., Visser, J. A., van Rossum, E. F. C., van der Zwaag, B., Alders, M., Boon, E. M. J., van Haelst, M. M. & van den Akker, E. L. T., 1 Dec 2020, In: PLOS ONE. 15, 12 December, e0244508.

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

  Open Access
• 2019

  Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (Nature Genetics, (2019), 51, 4, (659-674), 10.1038/s41588-019-0364-4)

  CommonMind Consortium, The Schizophrenia Working Group of the Psychiatric Genomics Consortium & iPSYCH-GEMS Schizophrenia Working Group, 1 Jun 2019, In: Nature Genetics. 51, 6, p. 1068 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  3 Citations (Scopus)
• 2018

  Erratum: Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific reports (2017) 7 1 (8899))

  International FTD-Genomics Consortium, 2018, In: Scientific reports. 8, 1, p. 7789

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  1 Citation (Scopus)

• Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x)

  the Million Veteran Program, 1 Oct 2018, In: Nature Genetics. 50, 12, 1 p.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review
  17 Citations (Scopus)

• Erratum to: Majority of human traits do not show evidence for sex-specific genetic and environmental effects (Scientific Reports, (2017), 7, 1, (8688), 10.1038/s41598-017-09249-3)

  Stringer, S., Polderman, T. J. C. & Posthuma, D., 2018, In: Scientific reports. 8, 1, 18060.

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review

  Open Access
  1 Citation (Scopus)
• 2016

  Erratum: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (PLoS Genet (2015) 11:10 (e1005378) DOI: 10.1371/journal.pgen.1005378)

  MAGIC Consortium, 1 Jun 2016, In: PLoS genetics. 12, 6, e1006166.

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

  Open Access
  12 Citations (Scopus)
• 2015

  Erratum: Further delineation of the KBG syndrome caused by ANKRD11 aberrations

  Ockeloen, C. W., Willemsen, M. H., de Munnik, S., van Bon, B. W. M., de Leeuw, N., Verrips, A., Kant, S. G., Jones, E. A., Brunner, H. G., van Loon, R. L. E., Smeets, E. E. J., van Haelst, M. M., van Haaften, G., Nordgren, A., Malmgren, H., Grigelioniene, G., Vermeer, S., Louro, P., Ramos, L., Maal, T. J. J., & 4 othersvan Heumen, C. C., Yntema, H. G., Carels, C. E. L. & Kleefstra, T., Sept 2015, In: European journal of human genetics. 23, 9, p. 1270

  Research output: Contribution to journal › Erratum/Corrigendum › Academic › peer-review