Work

25. Dissecting the Contribution of Common Variants to Risk of Rare Neurodevelopmental Conditions

Year: 2024

Type: article

Study design: Observational Study

Source: European Neuropsychopharmacology

DOI: 10.1016/j.euroneuro.2024.08.139

Authors: Qinqin Huang, Emilie Wigdor, Patrick Campbell, Daniel Malawsky, Kaitlin Samocha, Kartik Chundru, Petr Danecek, Elizabeth Radford, Jeffrey Barrett, Caroline Wright, Helen Firth, Varun Warrier, Alexander Young, Matt Hurles, Hilary Martin

Institutions: Wellcome Sanger Institute, Massachusetts General Hospital, University of Exeter, University of Cambridge, University of California, Los Angeles

Language: English

Topic: Genetic Associations and Epidemiology

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4403450350

FWCI:

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Related to: 10