Author

Christina M. Volpe

Children's Hospital of PhiladelphiaORCID 0009-0006-2752-9264Unclaimed ORCID profile · follow to get notified of new preprints

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Genetics· 1

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Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

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Alessandra ChesiiD· 1 shared Andrew D. WellsiD· 1 shared Bao Khanh TrangiD· 1 shared James A. PippiniD· 1 shared Jean Ann Maguire· 1 shared Jonathan P. Bradfield· 1 shared Keith D. BoehmiD· 1 shared Kenyaita M. Hodge· 1 shared

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Alessandra ChesiORCID

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1 paper

Recent·Most cited

GeneticsCell GenomicsPeer-reviewedMay 1, 2024

Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2

Sheridan H. Littleton, Bao Khanh Trang, Christina M. Volpe…·Struan F.A. Grant

The paper identifies rs7132908 as a causal variant in the chr12q13 obesity locus, showing it affects FAIM2 expression and neurodevelopment through cis-regulatory mechanisms.

19 citationstop 4%

humanDNA methylation

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