Award

U01 NS120241

Funder: National Institute of Neurological Disorders and Stroke

Funded outputs count: 4

Funder award ID: U01 NS120241

OpenAlex ID: G5407203003

Increased frequency of repeat expansion mutations across different populations

2024 · Kristina Ibañez, Bharati Jadhav, et al. · Nature Medicine · 94

A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability

2024 · Bharati Jadhav, Paras Garg, et al. · Nature Genetics · 16

A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits

2022 · Paras Garg, Bharati Jadhav, et al. · The American Journal of Human Genetics · 23

Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression

2021 · Paras Garg, Alejandro Martin-Trujillo, et al. · The American Journal of Human Genetics · 36