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Comment
. 2022 Mar 16;110(6):905-907.
doi: 10.1016/j.neuron.2022.02.018.

Advancing discovery of risk-altering variants for complex diseases by functionally informed fine-mapping

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Comment

Advancing discovery of risk-altering variants for complex diseases by functionally informed fine-mapping

You Chen et al. Neuron. .
Free article

Abstract

Pinpointing causal variants at risk loci identified by genome-wide association studies (GWAS) has been a great challenge. In this issue of Neuron, Zhang et al. present a fine-mapping approach, RefMap, integrating functional genomics with GWAS summary statistics to prioritize causal variants for amyotrophic lateral sclerosis.

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Conflict of interest statement

Declaration of interests The authors declare no competing interests.

Comment on

  • Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis.
    Zhang S, Cooper-Knock J, Weimer AK, Shi M, Moll T, Marshall JNG, Harvey C, Nezhad HG, Franklin J, Souza CDS, Ning K, Wang C, Li J, Dilliott AA, Farhan S, Elhaik E, Pasniceanu I, Livesey MR, Eitan C, Hornstein E, Kenna KP; Project MinE ALS Sequencing Consortium; Veldink JH, Ferraiuolo L, Shaw PJ, Snyder MP. Zhang S, et al. Neuron. 2022 Mar 16;110(6):992-1008.e11. doi: 10.1016/j.neuron.2021.12.019. Epub 2022 Jan 18. Neuron. 2022. PMID: 35045337 Free PMC article.

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