Mark Stephan
Impact in
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
- Developmental Neuroscience top 10%
Papers in
- Genetics 3
- Neurogenetic and Muscular Disorders Research 2
- Genetics and Neurodevelopmental Disorders 2
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- Autism Spectrum Disorder Research 2
- Co-authors
- John O King (2 shared papers)Michael L. Cunningham (2 shared papers)Gail Williams (2 shared papers)Joseph H. Hersh (2 shared papers)Bronwyn A. Kerr (2 shared papers)Shahenaz Najjar (1 shared paper)Barbara C. McGillivray (1 shared paper)Ann B. Moser (1 shared paper)
- Journals
- Developmental Medicine & Child Neurology (2 papers)European Archives of Oto-Rhino-Laryngology (1 paper)Archives of Disease in Childhood (1 paper)Acta Haematologica (1 paper)Clinical Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Mark Stephan
10 papers receiving 765 citations
Peers
Comparison fields: 5 of 73
- Cognitive Neuroscience 351
- Developmental Neuroscience 44
- Genetics 308
- Pediatrics, Perinatology and Child Health 152
- Psychiatry and Mental health 90
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 | 302 | |
| 2 | 2001 | 241 | |
| 3 | 2016 | 137 | |
| 4 | 1990 | 45 | |
| 5 | 2000 | 36 | |
| 6 | 1969 | 29 | |
| 7 | 2019 | 8 | |
| 8 | 1981 | 6 | |
| 9 | 2011 | 1 | |
| 10 | [Hereditary conduction defect in the His system: a dominant autosome disease]. | 1979 | 1 |
| 11 | 2009 | 0 |
About Mark Stephan
Mark Stephan is a scholar working on Genetics, Cognitive Neuroscience, Speech and Hearing, Clinical Biochemistry and Nephrology, having authored 11 papers that have together received 806 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (2 papers), Autism Spectrum Disorder Research (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Viral gastroenteritis research and epidemiology (1 paper), Polyamine Metabolism and Applications (1 paper), Vascular Malformations and Hemangiomas (1 paper), Histiocytic Disorders and Treatments (1 paper) and Gout, Hyperuricemia, Uric Acid (1 paper). The work is most often cited by research in Cognitive Neuroscience (351 citations), Developmental Neuroscience (44 citations), Genetics (308 citations), Pediatrics, Perinatology and Child Health (152 citations) and Psychiatry and Mental health (90 citations). Mark Stephan has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include John O King, Michael L. Cunningham, Gail Williams, Joseph H. Hersh, Bronwyn A. Kerr, Shahenaz Najjar, Barbara C. McGillivray, Ann B. Moser, Roberta A Pagon and J. Zonana. Their work appears in journals such as Developmental Medicine & Child Neurology, European Archives of Oto-Rhino-Laryngology, Archives of Disease in Childhood, Acta Haematologica 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.