[find our papers on PubMed]
* co-first author; ¶ co-corresponding author

2019 (3)

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations
Fragoza R, Das J, Wierbowski S, Liang J, Tran T, Liang S, Beltran J, Rivera-Erick C, Ye K, Wang T, Yao L, Mort M, Stenson P, Cooper D, Wei X, Keinan A, Schimenti J, Clark A and Yu H. Nature Communications 2019 10(1):4141.
GRAM: A generalized model to predict the molecular effect of a non-coding variant in a cell-type specific manner
Lou S, Kellie C, Li T, Liang J, Mohsen H, Liu J, Zhang J, Cohen S, Xu J, Yu H, Rubin M, and Gerstein M. PLOS Genetics 2019 15(8):e1007860.
MaXLinker: proteome-wide cross-link identifications with high specificity and sensitivity
Kumar Y, Wang T, Leung A, Lanz M, Motorykin I, Liang J, Shayhidin E, Smolka M, Zhang S, and Yu H. Molecular & Cellular Proteomics 2019.
First published on bioRxiv 2019 (DOI:10.1101/526897)

2018 (1)

Interactome INSIDER: a structural interactome browser for genomic studies
Meyer M, Beltrán J, Liang S, Fragoza R, Rumack A, Liang J, Wei X, and Yu H. Nature Methods 2018 February 15(2):107-114.

2014 (2)

A Massively Parallel Pipeline to Clone DNA Variants and Examine Molecular Phenotypes of Human Disease Mutations
Wei X, Das J, Fragoza R, Liang J, Bastos de Oliviera FM, Lee HR, Wang X, Mort M, Stenson PD, Cooper DN, Lipkin SM, Smolka MB, Yu H. PLoS Genetics 2014 Dec 11 10(12): e1004819.
Elucidating common structural features of human pathogenic variations using large-scale atomic-resolution protein networks
Das J, Lee HR, Sagar A, Fragoza R, Liang J, Wei X, Wang X, Mort M, Stenson PD, Cooper DN and Yu H. Human Mutation 2014 May 35(5):585-593.
Featured as a video highlight in Human Mutation