Christopher Hartl
Epigenomics (Germany)(DE)
Publications by Year
Research Areas
Bioinformatics and Genomic Networks, Genetic Associations and Epidemiology, Genomics and Rare Diseases, Gene expression and cancer classification, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → A framework for variation discovery and genotyping using next-generation DNA sequencing data(2011)12,242 cited
- → From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline(2013)7,118 cited
- → Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap(2018)1,119 cited
- → The genetic architecture of type 2 diabetes(2016)1,100 cited
- → Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism(2016)726 cited
- → Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks(2019)487 cited
- → Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms(2019)300 cited
- → Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD(2022)275 cited
- → The functional spectrum of low-frequency coding variation(2011)198 cited