Renee Bend
Impact in
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- Genetics and Neurodevelopmental Disorders
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- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- Protein Tyrosine Phosphatases
- Mitochondrial Function and Pathology
- RNA Research and Splicing
Papers in
- Genetics 2
- Genomic variations and chromosomal abnormalities 1
- Genomics and Rare Diseases 1
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- Folate and B Vitamins Research 1
- Co-authors
- Emil Alexov (1 shared paper)Joy W. Norris (1 shared paper)Michael J. Friez (2 shared papers)Caleb P. Bupp (1 shared paper)Catherine J. Spellicy (2 shared papers)Tracy D. Reynolds (1 shared paper)Charles E. Schwartz (1 shared paper)Jane H. Dean (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)Journal of Medical Genetics (1 paper)Molecular Psychiatry (1 paper)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- United StatesIsraelNorway
In The Last Decade
Renee Bend
5 papers receiving 68 citations
Peers
Comparison fields: 5 of 25
- Genetics 20
- Molecular Biology 39
- Developmental Neuroscience 2
- Rheumatology 6
- Pediatrics, Perinatology and Child Health 7
Countries citing papers authored by Renee Bend
This map shows the geographic impact of Renee Bend'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 Renee Bend with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Renee Bend more than expected).
Fields of papers citing papers by Renee Bend
This network shows the impact of papers produced by Renee Bend. 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 Renee Bend. The network helps show where Renee Bend may publish in the future.
Co-authors
The 25 scholars most cited alongside Renee Bend, 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 | 2018 | 20 | |
| 2 | 2019 | 20 | |
| 3 | 2020 | 12 | |
| 4 | 2022 | 10 | |
| 5 | 2022 | 6 |
About Renee Bend
Renee Bend is a scholar working on Genetics, Rheumatology, Cellular and Molecular Neuroscience, Oncology and Molecular Biology, having authored 5 papers that have together received 68 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (2 papers), Folate and B Vitamins Research (1 paper), RNA modifications and cancer (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Cancer-related Molecular Pathways (1 paper), Genomics and Rare Diseases (1 paper), Enzyme Structure and Function (1 paper) and Neuroscience and Neuropharmacology Research (1 paper). The work is most often cited by research in Genetics (20 citations), Molecular Biology (39 citations), Developmental Neuroscience (2 citations), Rheumatology (6 citations) and Pediatrics, Perinatology and Child Health (7 citations). Renee Bend has collaborated with scholars based in United States, Israel and Norway. Frequent co-authors include Emil Alexov, Joy W. Norris, Michael J. Friez, Caleb P. Bupp, Catherine J. Spellicy, Tracy D. Reynolds, Charles E. Schwartz, Jane H. Dean, Yunhui Peng and Christian Günther. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Molecular Psychiatry and American Journal of Medical Genetics Part A.
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.