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Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case-control study.

Tzuyao LoItaru KushimaHiroki KimuraBranko AleksicTakashi OkadaHidekazu KatoToshiya InadaYoshihiro NawaYouta ToriiMaeri YamamotoRyo KimuraYasuko FunabikiHirotaka KosakaShusuke NumataKiyoto KasaiTsukasa SasakiShigeru YokoyamaToshio MunesueRyota HashimotoYuka YasudaMichiko FujimotoMasahide UsamiMasanari ItokawaMakoto AraiKazutaka OhiToshiyuki SomeyaYuichiro WatanabeJun EgawaTsutomu TakahashiMichio SuzukiHidenori YamasueNakao IwataMasashi IkedaNorio Ozaki
Published in: Neuropsychopharmacology reports (2023)
The present findings suggest that monoallelic CNVs in PRKN do not confer a significant risk for SCZ or ASD. However, further studies to investigate the association between biallelic CNVs in PRKN and SCZ and ASD are warranted.
Keyphrases
  • autism spectrum disorder
  • copy number
  • intellectual disability
  • mitochondrial dna
  • attention deficit hyperactivity disorder
  • genome wide
  • bipolar disorder
  • dna methylation
  • case control