Mark W. Steele
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 41
- Genomic variations and chromosomal abnormalities 26
- Genetics and Neurodevelopmental Disorders 10
- Genetic Syndromes and Imprinting 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Biochemical and Molecular Research 4
- Co-authors
- Sharon L. Wenger (31 shared papers)William J. Young (2 shared papers)Barton Childs (2 shared papers)Aravinda Chakravarti (1 shared paper)Jennifer A. Scott (1 shared paper)James H. Cummins (3 shared papers)Sylvia F. Pan (3 shared papers)Wendy L. Golden (4 shared papers)
- Journals
- Clinical Genetics (11 papers)The Journal of Pediatrics (6 papers)Biochemical Genetics (5 papers)Journal of the American Academy of Child & Adolescent Psychiatry (2 papers)Human Genetics (2 papers)
- Partner nations
- United StatesItaly
In The Last Decade
Mark W. Steele
65 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 96
- Genetics 913
- Pediatrics, Perinatology and Child Health 345
- Developmental Biology 41
- Molecular Biology 511
- Cognitive Neuroscience 127
Countries citing papers authored by Mark W. Steele
This map shows the geographic impact of Mark W. Steele'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 W. Steele with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark W. Steele more than expected).
Fields of papers citing papers by Mark W. Steele
This network shows the impact of papers produced by Mark W. Steele. 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 W. Steele. The network helps show where Mark W. Steele may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark W. Steele, 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 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 94 | |
| 2 | 1988 | 89 | |
| 3 | 1970 | 71 | |
| 4 | 1990 | 66 | |
| 5 | 1991 | 57 | |
| 6 | 1996 | 48 | |
| 7 | 1968 | 45 | |
| 8 | 1977 | 43 | |
| 9 | 1990 | 43 | |
| 10 | 1993 | 43 | |
| 11 | 1995 | 41 | |
| 12 | 1996 | 41 | |
| 13 | 1989 | 37 | |
| 14 | 1976 | 36 | |
| 15 | 1969 | 36 | |
| 16 | 1988 | 34 | |
| 17 | 1973 | 29 | |
| 18 | 1962 | 28 | |
| 19 | 1984 | 27 | |
| 20 | 1966 | 27 |
About Mark W. Steele
Mark W. Steele is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 66 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (12 papers), Genetics and Neurodevelopmental Disorders (10 papers), Chromosomal and Genetic Variations (7 papers), Genetic Syndromes and Imprinting (6 papers), Neonatal Health and Biochemistry (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Biochemical and Molecular Research (4 papers). The work is most often cited by research in Genetics (913 citations), Pediatrics, Perinatology and Child Health (345 citations), Developmental Biology (41 citations), Molecular Biology (511 citations) and Cognitive Neuroscience (127 citations). Mark W. Steele has collaborated with scholars based in United States and Italy. Frequent co-authors include Sharon L. Wenger, William J. Young, Barton Childs, Aravinda Chakravarti, Jennifer A. Scott, James H. Cummins, Sylvia F. Pan, Wendy L. Golden, W. Roy Breg and Bernard A. Cohen. Their work appears in journals such as Clinical Genetics, The Journal of Pediatrics, Biochemical Genetics, Journal of the American Academy of Child & Adolescent Psychiatry 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.