Andrew Farrell

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Mark Chaisson, Ashley D. Sanders, Xuefang Zhao et al. · Nature Communications · 2019 · 983 citations · Full text

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Donna M. Werling, Harrison Brand, Joon‐Yong An et al. · Nature Genetics · 2018 · 335 citations · Full text

Genome-wide Association Study, Syndromic Autism, Genetics +8

Genomic analyses implicate noncoding de novo variants in congenital heart disease

Felix Richter, Sarah U. Morton, Seong Won Kim et al. · Nature Genetics · 2020 · 167 citations · Full text

Variant Interpretation, Genetics, Congenital Heart Defect +7

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Mark Chaisson, Ashley D. Sanders, Xuefang Zhao et al. · 2017 · 157 citations · Full text

Genetics, Genomics, Multi-platform Discovery +19

Human-specific tandem repeat expansion and differential gene expression during primate evolution

Arvis Sulovari, Ruiyang Li, Peter A. Audano et al. · Proceedings of the National Academy of Sciences · 2019 · 153 citations · Full text