Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases

Yuan, Kai, Longchamps, Ryan, Pardiñas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Yu, Mingrui, Chen, Tzu-Ting, Lin, Shu-Chin, Chen, Yu, Lam, Max, Daly, Mark, Neale, Benjamine, Yen-Feng, Lin, Chen, Chia-Yen, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Ge, Tian and Huang, Hailiang 2023. Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. European Neuropsychopharmacology 75 (Supp 1) , S6-S7. 10.1016/j.euroneuro.2023.08.021 Item availability restricted.

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Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Medicine MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Publisher:	Elsevier
ISSN:	0924-977X
Date of First Compliant Deposit:	30 January 2024
Date of Acceptance:	24 January 2024
Last Modified:	20 Feb 2024 06:57
URI:	https://orca.cardiff.ac.uk/id/eprint/165908

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