Chris Balak
Impact in
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- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
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- RNA modifications and cancer
- Extracellular vesicles in disease
- RNA Research and Splicing
- Circular RNAs in diseases
Papers in
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- RNA Research and Splicing 2
- RNA regulation and disease 2
- Genetics 5
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Ryan Richholt (6 shared papers)Ashley L. Siniard (6 shared papers)Matthew J. Huentelman (5 shared papers)Kendall Van Keuren‐Jensen (2 shared papers)Elizabeth Carlson (2 shared papers)Elizabeth Hutchins (2 shared papers)Rebecca Reiman (2 shared papers)Ashish Yeri (1 shared paper)
- Journals
- Molecular Case Studies (1 paper)Clinical Genetics (1 paper)Frontiers in Aging Neuroscience (1 paper)Human Genetics (1 paper)Scientific Data (1 paper)
- Partner nations
- United StatesHong KongSpain
In The Last Decade
Chris Balak
10 papers receiving 254 citations
Peers
Comparison fields: 5 of 67
- Cancer Research 91
- Molecular Biology 155
- Neuropsychology and Physiological Psychology 3
- Genetics 45
- Neurology 8
Countries citing papers authored by Chris Balak
This map shows the geographic impact of Chris Balak'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 Chris Balak with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chris Balak more than expected).
Fields of papers citing papers by Chris Balak
This network shows the impact of papers produced by Chris Balak. 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 Chris Balak. The network helps show where Chris Balak may publish in the future.
Co-authors
The 25 scholars most cited alongside Chris Balak, 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 | 2017 | 126 | |
| 2 | 2017 | 30 | |
| 3 | 2018 | 22 | |
| 4 | 2018 | 19 | |
| 5 | 2016 | 16 | |
| 6 | 2021 | 12 | |
| 7 | 2019 | 12 | |
| 8 | 2017 | 9 | |
| 9 | 2022 | 7 | |
| 10 | Novel Genetic Variants in Extreme Phenotypes of Diabetic Retinopathy: DRGen Study | 2018 | 4 |
| 11 | 2021 | 0 |
About Chris Balak
Chris Balak is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cancer Research and Genetics, having authored 11 papers that have together received 257 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), MicroRNA in disease regulation (2 papers), Cancer-related molecular mechanisms research (2 papers), RNA Research and Splicing (2 papers), RNA regulation and disease (2 papers) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Cancer Research (91 citations), Molecular Biology (155 citations), Neuropsychology and Physiological Psychology (3 citations), Genetics (45 citations) and Neurology (8 citations). Chris Balak has collaborated with scholars based in United States, Hong Kong and Spain. Frequent co-authors include Ryan Richholt, Ashley L. Siniard, Matthew J. Huentelman, Kendall Van Keuren‐Jensen, Elizabeth Carlson, Elizabeth Hutchins, Rebecca Reiman, Ashish Yeri, Robert R. Kitchen and Amanda Courtright. Their work appears in journals such as Molecular Case Studies, Clinical Genetics, Frontiers in Aging Neuroscience, Human Genetics and Scientific Data.
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.