Mark Stephan
Impact in
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
- Developmental Neuroscience top 10%
- Neurogenesis and neuroplasticity mechanisms
Papers in
-
- Connexins and lens biology 1
- Protein Tyrosine Phosphatases 1
- Genetics 3
- Genetics and Neurodevelopmental Disorders 2
- Neurogenetic and Muscular Disorders Research 2
- Hemoglobinopathies and Related Disorders 1
- Co-authors
- Joseph H. Hersh (2 shared papers)Bronwyn Kerr (2 shared papers)John King (2 shared papers)Gail Williams (2 shared papers)Michael L. Cunningham (2 shared papers)Shahenaz Najjar (1 shared paper)Berkley R. Powell (1 shared paper)Barbara McGillivray (1 shared paper)
- Journals
- Developmental Medicine & Child Neurology (2 papers)Acta Haematologica (1 paper)European Journal of Human Genetics (1 paper)Archives of Disease in Childhood (1 paper)Clinical Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Mark Stephan
9 papers receiving 588 citations
Peers
Comparison fields: 5 of 64
- Cognitive Neuroscience 357
- Developmental Neuroscience 47
- Genetics 263
- Pediatrics, Perinatology and Child Health 150
- Psychiatry and Mental health 105
Countries citing papers authored by Mark Stephan
This map shows the geographic impact of Mark Stephan'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 Mark Stephan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Stephan more than expected).
Fields of papers citing papers by Mark Stephan
This network shows the impact of papers produced by Mark Stephan. 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 Mark Stephan. The network helps show where Mark Stephan may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark Stephan, 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 | 2001 | 284 | |
| 2 | 2001 | 226 | |
| 3 | 1990 | 36 | |
| 4 | 2000 | 31 | |
| 5 | 1969 | 27 | |
| 6 | 2019 | 6 | |
| 7 | 1981 | 3 | |
| 8 | 2010 | 2 | |
| 9 | 1982 | 1 | |
| 10 | [Hereditary conduction defect in the His system: a dominant autosome disease]. | 1979 | 1 |
About Mark Stephan
Mark Stephan is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Genetics and Infectious Diseases, having authored 10 papers that have together received 617 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Autism Spectrum Disorder Research (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Connexins and lens biology (1 paper), Metabolism and Genetic Disorders (1 paper), Cytokine Signaling Pathways and Interactions (1 paper), Hemoglobinopathies and Related Disorders (1 paper) and Protein Tyrosine Phosphatases (1 paper). The work is most often cited by research in Cognitive Neuroscience (357 citations), Developmental Neuroscience (47 citations), Genetics (263 citations), Pediatrics, Perinatology and Child Health (150 citations) and Psychiatry and Mental health (105 citations). Mark Stephan has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Joseph H. Hersh, Bronwyn Kerr, John King, Gail Williams, Michael L. Cunningham, Shahenaz Najjar, Berkley R. Powell, Barbara McGillivray, J. Zonana and Ann B. Moser. Their work appears in journals such as Developmental Medicine & Child Neurology, Acta Haematologica, European Journal of Human Genetics, Archives of Disease in Childhood and Clinical 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.