Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability

Lea Urpa, Mitja I. Kurki, Elisa Rahikkala, Eija Hämäläinen, Veikko Salomaa, Jaana Suvisaari, Riikka Keski-Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen-Ebrahim, H Helander, Päivi Vieira, Johanna Uusimaa, Jukka S. Moilanen, Jarmo Körkkö, Tarjinder Singh, Outi Kuismin, Olli Pietiläinen, Aarno Palotie, Mark J. Daly

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume32
Pages (from-to)576–583
Number of pages8
ISSN1018-4813
DOIs
Publication statusPublished - 2024
MoE publication typeA1 Journal article-refereed

Fields of Science

  • 3111 Biomedicine
  • 1184 Genetics, developmental biology, physiology

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