Bianca Russell
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- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 2
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- Acute Myeloid Leukemia Research 2
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- Epigenetics and DNA Methylation 4
- Renal and related cancers 2
- Congenital heart defects research 2
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- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 2
- Co-authors
- John M. GrahamWen‐Hann TanRachel HarrisonBenjamin M. HelmNancy KramerAvi Z. RosenbergSamantha A. Schrier VerganoLeslie G. Biesecker
- Cited by
- GeneticsHematologyMolecular Biology
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Bianca Russell
14 papers receiving 140 citations
Peers
Comparison fields: 5 of 30
- Genetics 71
- Hematology 18
- Molecular Biology 77
- Pediatrics, Perinatology and Child Health 20
- Genetics 10
Countries citing papers authored by Bianca Russell
This map shows the geographic impact of Bianca Russell'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 Bianca Russell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bianca Russell more than expected).
Fields of papers citing papers by Bianca Russell
This network shows the impact of papers produced by Bianca Russell. 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 Bianca Russell. The network helps show where Bianca Russell may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Bianca Russell, 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 | 2025 | 1 | |
| 2 | 2025 | 0 | |
| 3 | 2024 | 2 | |
| 4 | 2024 | 0 | |
| 5 | 2024 | 0 | |
| 6 | 2024 | 1 | |
| 7 | 2023 | 3 | |
| 8 | 2023 | 7 | |
| 9 | 2023 | 6 | |
| 10 | 2023 | 6 | |
| 11 | 2022 | 14 | |
| 12 | 2021 | 9 | |
| 13 | 2021 | 11 | |
| 14 | 2020 | 6 | |
| 15 | 2019 | 7 | |
| 16 | Bohring-Opitz Syndrome | 2018 | 6 |
| 17 | 2015 | 47 | |
| 18 | 2013 | 16 |
About Bianca Russell
Bianca Russell is a scholar working on Genetics, Genetics and Hematology, having authored 18 papers that have together received 142 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Epigenetics and DNA Methylation (4 papers), Acute Myeloid Leukemia Research (2 papers), Genetic Syndromes and Imprinting (2 papers), Renal and related cancers (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (71 citations), Hematology (18 citations) and Molecular Biology (77 citations). Bianca Russell has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include John M. Graham, Wen‐Hann Tan, Rachel Harrison, Benjamin M. Helm, Nancy Kramer, Avi Z. Rosenberg, Samantha A. Schrier Vergano, Leslie G. Biesecker, Jennifer J. Johnston and William J. Rhead. Their work appears in journals such as PEDIATRICS, Cancer Research and Epilepsia.
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.