Berivan Baskin
Impact in
- Genetics top 1%
- Glioma Diagnosis and Treatment
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Immunology top 5%
- Immunodeficiency and Autoimmune Disorders
Papers in
- Genetics 23
- Genetics and Neurodevelopmental Disorders 10
- Glioma Diagnosis and Treatment 7
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
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- T-cell and B-cell Immunology 5
- Immunodeficiency and Autoimmune Disorders 5
- Co-authors
- Peter N. Ray (21 shared papers)Tony J. Pawson (2 shared papers)Lennart L G Hammarström (7 shared papers)David M. Malkin (6 shared papers)Frank Sicheri (1 shared paper)Siew Hwa Ong (1 shared paper)Leanne E. Wybenga-Groot (1 shared paper)Jiefei Tong (1 shared paper)
- Journals
- The American Journal of Human Genetics (7 papers)Clinical Genetics (4 papers)Neuromuscular Disorders (3 papers)Clinical & Experimental Immunology (3 papers)Human Genetics (3 papers)
- Partner nations
- CanadaSwedenUnited States
In The Last Decade
Berivan Baskin
59 papers receiving 3.4k citations
Peers
Comparison fields: 5 of 91
- Genetics 733
- Genetics 664
- Immunology 353
- Molecular Biology 946
- Cellular and Molecular Neuroscience 216
Countries citing papers authored by Berivan Baskin
This map shows the geographic impact of Berivan Baskin'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 Berivan Baskin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Berivan Baskin more than expected).
Fields of papers citing papers by Berivan Baskin
This network shows the impact of papers produced by Berivan Baskin. 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 Berivan Baskin. The network helps show where Berivan Baskin may publish in the future.
Co-authors
The 25 scholars most cited alongside Berivan Baskin, 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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 381 | |
| 2 | 2001 | 270 | |
| 3 | 1994 | 264 | |
| 4 | 2003 | 248 | |
| 5 | 2010 | 162 | |
| 6 | 2018 | 155 | |
| 7 | 2010 | 136 | |
| 8 | 2015 | 136 | |
| 9 | 2010 | 120 | |
| 10 | 2018 | 100 | |
| 11 | 1994 | 95 | |
| 12 | 2016 | 85 | |
| 13 | 2016 | 85 | |
| 14 | 2016 | 83 | |
| 15 | 1994 | 74 | |
| 16 | 2013 | 65 | |
| 17 | 2016 | 63 | |
| 18 | 1998 | 60 | |
| 19 | 2008 | 57 | |
| 20 | 2011 | 53 |
About Berivan Baskin
Berivan Baskin is a scholar working on Genetics, Genetics, Immunology, Cellular and Molecular Neuroscience and Molecular Biology, having authored 59 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Glioma Diagnosis and Treatment (7 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Muscle Physiology and Disorders (6 papers), T-cell and B-cell Immunology (5 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Hereditary Neurological Disorders (4 papers). The work is most often cited by research in Genetics (733 citations), Genetics (664 citations), Immunology (353 citations), Molecular Biology (946 citations) and Cellular and Molecular Neuroscience (216 citations). Berivan Baskin has collaborated with scholars based in Canada, Sweden and United States. Frequent co-authors include Peter N. Ray, Tony J. Pawson, Lennart L G Hammarström, David M. Malkin, Frank Sicheri, Siew Hwa Ong, Leanne E. Wybenga-Groot, Jiefei Tong, Khalid B. Islam and Igor Vořechovský. Their work appears in journals such as The American Journal of Human Genetics, Clinical Genetics, Neuromuscular Disorders, Clinical & Experimental Immunology and Human Genetics.
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.