Shelin Adam
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 1%
- Neurological disorders and treatments
Papers in
- Genetics 23
- Genomics and Rare Diseases 16
- BRCA gene mutations in cancer 14
-
- Genetic Neurodegenerative Diseases 19
- Co-authors
- Michael R. Hayden (15 shared papers)Susan E. Andrew (4 shared papers)Jane Theilmann (10 shared papers)Håkan Telenius (3 shared papers)Maurice Bloch (11 shared papers)Ferdinando Squitieri (4 shared papers)Jan M. Friedman (26 shared papers)Marlene J. Huggins (7 shared papers)
- Journals
- Genetics in Medicine (6 papers)Nature Genetics (3 papers)Journal of Medical Genetics (2 papers)European Journal of Medical Genetics (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- CanadaUnited StatesNetherlands
In The Last Decade
Shelin Adam
50 papers receiving 3.3k citations
Shelin Adam's Hit Papers
Peers
Comparison fields: 5 of 111
- Cellular and Molecular Neuroscience 1.8k
- Neurology 729
- Genetics 1.2k
- Molecular Biology 1.5k
- Pediatrics, Perinatology and Child Health 237
Countries citing papers authored by Shelin Adam
This map shows the geographic impact of Shelin Adam'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 Shelin Adam with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shelin Adam more than expected).
Fields of papers citing papers by Shelin Adam
This network shows the impact of papers produced by Shelin Adam. 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 Shelin Adam. The network helps show where Shelin Adam may publish in the future.
Co-authors
The 25 scholars most cited alongside Shelin Adam, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease Hit paper breakdown → | 1993 | 818 |
| 2 | 1992 | 338 | |
| 3 | 1994 | 336 | |
| 4 | 1993 | 183 | |
| 5 | 1992 | 180 | |
| 6 | 2014 | 137 | |
| 7 | 2012 | 132 | |
| 8 | 1992 | 126 | |
| 9 | 2020 | 88 | |
| 10 | Proceed with care: direct predictive testing for Huntington disease. | 1994 | 82 |
| 11 | Huntington disease without CAG expansion: phenocopies or errors in assignment? | 1994 | 82 |
| 12 | 1993 | 67 | |
| 13 | 2013 | 66 | |
| 14 | 2018 | 63 | |
| 15 | Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease. | 1993 | 55 |
| 16 | 2013 | 49 | |
| 17 | 1996 | 48 | |
| 18 | 1989 | 38 | |
| 19 | 2013 | 38 | |
| 20 | 2016 | 35 |
About Shelin Adam
Shelin Adam is a scholar working on Genetics, Cellular and Molecular Neuroscience, Molecular Biology, Neurology and Public Health, Environmental and Occupational Health, having authored 51 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (19 papers), Genomics and Rare Diseases (16 papers), BRCA gene mutations in cancer (14 papers), Mitochondrial Function and Pathology (6 papers), DNA Repair Mechanisms (5 papers), Neurological disorders and treatments (5 papers), Ethics in Clinical Research (4 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.8k citations), Neurology (729 citations), Genetics (1.2k citations), Molecular Biology (1.5k citations) and Pediatrics, Perinatology and Child Health (237 citations). Shelin Adam has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include Michael R. Hayden, Susan E. Andrew, Jane Theilmann, Håkan Telenius, Maurice Bloch, Ferdinando Squitieri, Jan M. Friedman, Marlene J. Huggins, Elizabeth Starr and Rona K. Graham. Their work appears in journals such as Genetics in Medicine, Nature Genetics, Journal of Medical Genetics, European Journal of Medical Genetics and Prenatal Diagnosis.
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.