Christopher Hartl
Impact in
- Genetics top 0.1%
- Genomics and Rare Diseases
- Genetic diversity and population structure
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 8
- Genetic Associations and Epidemiology 5
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Stacey GabrielDavid AltshulerKiran GarimellaEric BanksRyan PoplinGuillermo del AngelMark A. DePristoAndrey Sivachenko
- Journals
- Cell (2 papers)Nature Genetics (1 paper)Nature Communications (1 paper)Bioinformatics (1 paper)Nature Neuroscience (1 paper)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Christopher Hartl
14 papers receiving 12.6k citations
Hit Papers
Peers
Comparison fields: 5 of 167
- Genetics 5.5k
- Cancer Research 2.0k
- Molecular Biology 6.6k
- Plant Science 1.6k
- Aging 72
Countries citing papers authored by Christopher Hartl
This map shows the geographic impact of Christopher Hartl's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christopher Hartl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Hartl more than expected).
Fields of papers citing papers by Christopher Hartl
This network shows the impact of papers produced by Christopher Hartl. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christopher Hartl. The network helps show where Christopher Hartl may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Christopher Hartl, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 1 | |
| 2 | 2021 | 38 | |
| 3 | 2021 | 41 | |
| 4 | 2019 | 146 | |
| 5 | 2019 | 87 | |
| 6 | Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks Hit paper breakdown → | 2019 | 257 |
| 7 | 2019 | 113 | |
| 8 | 2019 | 2 | |
| 9 | Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism Hit paper breakdown → | 2016 | 445 |
| 10 | 2014 | 29 | |
| 11 | SMASH: A Benchmarking Toolkit for Variant Calling | 2013 | 2 |
| 12 | From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline Hit paper breakdown → | 2013 | 4252 |
| 13 | ADAM: Genomics Formats and Processing Patterns for Cloud Scale Computing | 2013 | 58 |
| 14 | A framework for variation discovery and genotyping using next-generation DNA sequencing data Hit paper breakdown → | 2011 | 7268 |
About Christopher Hartl
Christopher Hartl is a scholar working on Genetics, Cognitive Neuroscience, Information Systems and Management, Molecular Biology and Cancer Research, having authored 14 papers that have together received 12.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Phylogenetic Studies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Epigenetics and DNA Methylation (2 papers), Bioinformatics and Genomic Networks (2 papers) and Gene expression and cancer classification (2 papers). The work is most often cited by research in Genetics (5.5k citations), Cancer Research (2.0k citations), Molecular Biology (6.6k citations), Plant Science (1.6k citations) and Aging (72 citations). Christopher Hartl has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Stacey Gabriel, David Altshuler, Kiran Garimella, Eric Banks, Ryan Poplin, Guillermo del Angel, Mark A. DePristo, Andrey Sivachenko, Anthony Philippakis and Andrew Kernytsky. Their work appears in journals such as Cell, Nature Genetics, Nature Communications, Bioinformatics and Nature Neuroscience.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.