Christopher Hartl

A framework for variation discovery and genotyping using next-generation DNA sequencing data

Mark A. DePristo, Eric Banks, Ryan Poplin et al. · Nature Genetics · 2011 · 12.4K citations · Full text

Life Sciences, Bioinformatics, Genetics +14

From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline

Géraldine Van der Auwera, Mauricio O. Carneiro, Christopher Hartl et al. · Current Protocols in Bioinformatics · 2013 · 7.2K citations

Life Sciences, Bioinformatics, Genetics +14

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

Michael J. Gandal, Jillian R. Haney, Neelroop Parikshak et al. · Science · 2018 · 1.2K citations · Full text

Medicine, Genetics, Molecular Genetics +17

The genetic architecture of type 2 diabetes

Christian Fuchsberger, Jason Flannick, Tanya M. Teslovich et al. · Nature · 2016 · 1.1K citations · Full text

Medicine, Genetics, Molecular Genetics +14

Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism

Neelroop Parikshak, Vivek Swarup, T. Grant Belgard et al. · Nature · 2016 · 740 citations

Life Sciences, Genetics, Molecular Genetics +14