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Family-based association study of DYX1C1 variants in autism

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Year: 2004
Type: article
Study design: Observational Study
Source: European Journal of Human Genetics
DOI: 10.1038/sj.ejhg.5201272
Authors: Tero Ylisaukko-oja, Myriam Peyrard-Janvid, Cecilia M Lindgren, Karola Rehnström, Raija Vanhala, Leena Peltonen, Irma Järvelä, Juha Kere
Institutions: Karolinska Institutet, University of Helsinki, Helsinki Children's Hospital
Language: English

Topic: Autism Spectrum Disorder Research
Subfield: Cognitive Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: Pfizer, Wellcome Trust, Academy of Finland, Biomedicum Helsinki-säätiö, Vetenskapsrådet, Medical Research Council
Award: Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics.
OpenAlex ID: W2012468328
FWCI: 1.119
Cites: 35
Cited by: 17
Related to: 10
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