Ledia Brunga
Impact in
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
Papers in
-
- Cancer Genomics and Diagnostics 6
- Genetics 6
- BRCA gene mutations in cancer 3
- Genomics and Rare Diseases 3
- Co-authors
- Cyrus G. Boelman (2 shared papers)Adam Shlien (3 shared papers)Giovanna Pellecchia (1 shared paper)James M. Drake (1 shared paper)Lesley Ann Turner (1 shared paper)Mary B. Connolly (1 shared paper)Kelly Hancock (1 shared paper)David M. Malkin (2 shared papers)
- Journals
- Nature Communications (2 papers)Cancer Discovery (2 papers)Nature Medicine (1 paper)npj Genomic Medicine (1 paper)Nature Cancer (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Ledia Brunga
17 papers receiving 982 citations
Ledia Brunga's Hit Papers
Peers
Comparison fields: 5 of 61
- Psychiatry and Mental health 234
- Genetics 305
- Cancer Research 99
- Oncology 96
- Pathology and Forensic Medicine 71
Countries citing papers authored by Ledia Brunga
This map shows the geographic impact of Ledia Brunga'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 Ledia Brunga with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ledia Brunga more than expected).
Fields of papers citing papers by Ledia Brunga
This network shows the impact of papers produced by Ledia Brunga. 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 Ledia Brunga. The network helps show where Ledia Brunga may publish in the future.
Co-authors
The 25 scholars most cited alongside Ledia Brunga, 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 | High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies Hit paper breakdown → | 2017 | 364 |
| 2 | 2018 | 125 | |
| 3 | 2022 | 78 | |
| 4 | 2020 | 69 | |
| 5 | 2020 | 65 | |
| 6 | 2018 | 49 | |
| 7 | 2023 | 43 | |
| 8 | 2017 | 42 | |
| 9 | 2021 | 40 | |
| 10 | 2018 | 29 | |
| 11 | 2022 | 28 | |
| 12 | 2023 | 28 | |
| 13 | 2022 | 15 | |
| 14 | 2023 | 11 | |
| 15 | 2017 | 6 | |
| 16 | 2023 | 5 | |
| 17 | 2023 | 1 | |
| 18 | 2024 | 0 | |
| 19 | 2025 | 0 | |
| 20 | 2026 | 0 |
About Ledia Brunga
Ledia Brunga is a scholar working on Cancer Research, Genetics, Pathology and Forensic Medicine, Psychiatry and Mental health and Oncology, having authored 20 papers that have together received 998 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (6 papers), Genetic factors in colorectal cancer (4 papers), Epilepsy research and treatment (3 papers), Cancer-related Molecular Pathways (3 papers), BRCA gene mutations in cancer (3 papers), Genomics and Rare Diseases (3 papers), Chronic Myeloid Leukemia Treatments (1 paper) and Gastrointestinal Tumor Research and Treatment (1 paper). The work is most often cited by research in Psychiatry and Mental health (234 citations), Genetics (305 citations), Cancer Research (99 citations), Oncology (96 citations) and Pathology and Forensic Medicine (71 citations). Ledia Brunga has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Cyrus G. Boelman, Adam Shlien, Giovanna Pellecchia, James M. Drake, Lesley Ann Turner, Mary B. Connolly, Kelly Hancock, David M. Malkin, Berge Arakel Minassian and Anita Villani. Their work appears in journals such as Nature Communications, Cancer Discovery, Nature Medicine, npj Genomic Medicine and Nature Cancer.
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.