Aniko Sabo
Impact in
- Genetics top 0.02%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Glioma Diagnosis and Treatment
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 40
- Genomics and Rare Diseases 23
- Genomic variations and chromosomal abnormalities 14
- Genetic Associations and Epidemiology 9
- Genetics and Neurodevelopmental Disorders 9
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- Autism Spectrum Disorder Research 9
- Co-authors
- Jian Xu (1 shared paper)Thomas M. Hooton (1 shared paper)Robert S. Fulton (1 shared paper)Chia‐Suei Hung (1 shared paper)Darin Blasiar (1 shared paper)Elaine R. Mardis (1 shared paper)Jeffrey I. Gordon (1 shared paper)Philip Ozersky (1 shared paper)
- Journals
- Nature (9 papers)The American Journal of Human Genetics (5 papers)Proceedings of the National Academy of Sciences (4 papers)Nature Communications (4 papers)Genetics in Medicine (3 papers)
- Partner nations
- United StatesUnited KingdomChina
In The Last Decade
Aniko Sabo
74 papers receiving 44.2k citations
Aniko Sabo's Hit Papers
Peers
Comparison fields: 5 of 208
- Genetics 17.9k
- Cancer Research 5.8k
- Genetics 3.1k
- Molecular Biology 19.7k
- Cognitive Neuroscience 2.6k
Countries citing papers authored by Aniko Sabo
This map shows the geographic impact of Aniko Sabo'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 Aniko Sabo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aniko Sabo more than expected).
Fields of papers citing papers by Aniko Sabo
This network shows the impact of papers produced by Aniko Sabo. 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 Aniko Sabo. The network helps show where Aniko Sabo may publish in the future.
Co-authors
The 25 scholars most cited alongside Aniko Sabo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12574 |
| 2 | Comprehensive genomic characterization defines human glioblastoma genes and core pathways Hit paper breakdown → | 2008 | 6384 |
| 3 | A map of human genome variation from population-scale sequencing Hit paper breakdown → | 2010 | 6317 |
| 4 | An integrated map of genetic variation from 1,092 human genomes Hit paper breakdown → | 2012 | 6211 |
| 5 | Somatic mutations affect key pathways in lung adenocarcinoma Hit paper breakdown → | 2008 | 2237 |
| 6 | Synaptic, transcriptional and chromatin genes disrupted in autism Hit paper breakdown → | 2014 | 2082 |
| 7 | Patterns and rates of exonic de novo mutations in autism spectrum disorders Hit paper breakdown → | 2012 | 1378 |
| 8 | Evolutionary and Biomedical Insights from the Rhesus Macaque Genome Hit paper breakdown → | 2007 | 1081 |
| 9 | The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution Hit paper breakdown → | 2009 | 973 |
| 10 | A framework for the interpretation of de novo mutation in human disease Hit paper breakdown → | 2014 | 704 |
| 11 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 476 |
| 12 | Demographic history and rare allele sharing among human populations Hit paper breakdown → | 2011 | 475 |
| 13 | 2006 | 469 | |
| 14 | 2010 | 416 | |
| 15 | 2004 | 329 | |
| 16 | 2018 | 328 | |
| 17 | 2014 | 321 | |
| 18 | 2013 | 216 | |
| 19 | 2010 | 179 | |
| 20 | 2019 | 174 |
About Aniko Sabo
Aniko Sabo is a scholar working on Genetics, Cognitive Neuroscience, Cancer Research, Molecular Biology and Genetics, having authored 76 papers that have together received 45.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Genomic variations and chromosomal abnormalities (14 papers), Autism Spectrum Disorder Research (9 papers), Genetic Associations and Epidemiology (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Cancer Genomics and Diagnostics (6 papers), Pediatric Hepatobiliary Diseases and Treatments (5 papers) and Genomics and Phylogenetic Studies (4 papers). The work is most often cited by research in Genetics (17.9k citations), Cancer Research (5.8k citations), Genetics (3.1k citations), Molecular Biology (19.7k citations) and Cognitive Neuroscience (2.6k citations). Aniko Sabo has collaborated with scholars based in United States, United Kingdom and China. Frequent co-authors include Jian Xu, Thomas M. Hooton, Robert S. Fulton, Chia‐Suei Hung, Darin Blasiar, Elaine R. Mardis, Jeffrey I. Gordon, Philip Ozersky, John Spieth and Jon R. Armstrong. Their work appears in journals such as Nature, The American Journal of Human Genetics, Proceedings of the National Academy of Sciences, Nature Communications and Genetics in Medicine.
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.