The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis

Edna Gruenblatt*, Zsofia Nemoda, Anna Maria Werling, Alexander Roth, Nora Angyal, Zsanett Tarnok, Hauke Thomsen, Triinu Peters, Anke Hinney, Johannes Hebebrand, Klaus-Peter Lesch, Marcel Romanos, Susanne Walitza

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)365-376
Number of pages12
JournalAmerican Journal of Medical Genetics Part B-neuropsychiatric Genetics
Volume180
Issue number6
DOIs
Publication statusPublished - Sep 2019

Keywords

  • attention-deficit hyperactivity disorder
  • gender
  • genetics
  • polymorphism
  • SNP
  • GENOME-WIDE ASSOCIATION
  • DEFICIT HYPERACTIVITY DISORDER
  • BONE-MINERAL DENSITY
  • NEURAL-TUBE DEFECTS
  • FUNCTIONAL ANNOTATION
  • BIPOLAR DISORDER
  • OVERLAP
  • RISK
  • LOW-DENSITY-LIPOPROTEIN-RECEPTOR-RELATED-PROTEIN-6
  • DIFFERENTIATION

Cite this

Gruenblatt, E., Nemoda, Z., Werling, A. M., Roth, A., Angyal, N., Tarnok, Z., Thomsen, H., Peters, T., Hinney, A., Hebebrand, J., Lesch, K-P., Romanos, M., & Walitza, S. (2019). The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis. American Journal of Medical Genetics Part B-neuropsychiatric Genetics, 180(6), 365-376. https://doi.org/10.1002/ajmg.b.32695