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
- Genetic and rare skin diseases.
- Genomics and Rare Diseases
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 47
- Genomic variations and chromosomal abnormalities 26
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 12
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 5
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- Neonatal Health and Biochemistry 6
- Prenatal Screening and Diagnostics 6
- Co-authors
- Sharon L. Wenger (34 shared papers)Barton Childs (2 shared papers)William John Young (2 shared papers)Aravinda Chakravarti (1 shared paper)James H. Cummins (3 shared papers)Bernard Cohen (1 shared paper)James F. Reynolds (4 shared papers)Wendy L. Golden (4 shared papers)
- Journals
- Clinical Genetics (13 papers)The Journal of Pediatrics (6 papers)Biochemical Genetics (5 papers)Nature (2 papers)Pediatric Research (2 papers)
- Partner nations
- United States
In The Last Decade
Mark W. Steele
69 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 75
- Genetics 922
- Pediatrics, Perinatology and Child Health 239
- Developmental Biology 39
- Aging 11
- Reproductive Medicine 29
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 71 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 99 | |
| 2 | 1988 | 92 | |
| 3 | 1990 | 79 | |
| 4 | 1970 | 71 | |
| 5 | 1991 | 62 | |
| 6 | 1996 | 49 | |
| 7 | 1990 | 44 | |
| 8 | 1968 | 43 | |
| 9 | 1977 | 43 | |
| 10 | 1993 | 43 | |
| 11 | 1995 | 41 | |
| 12 | 1996 | 41 | |
| 13 | 1989 | 38 | |
| 14 | 1976 | 36 | |
| 15 | 1988 | 35 | |
| 16 | 1969 | 34 | |
| 17 | 1973 | 30 | |
| 18 | 1962 | 28 | |
| 19 | 1984 | 28 | |
| 20 | 1987 | 28 |
About Mark W. Steele
Mark W. Steele is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Developmental Biology and Clinical Biochemistry, having authored 71 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Down syndrome and intellectual disability research (6 papers), Neonatal Health and Biochemistry (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (5 papers), Biochemical and Molecular Research (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (922 citations), Pediatrics, Perinatology and Child Health (239 citations), Developmental Biology (39 citations), Aging (11 citations) and Reproductive Medicine (29 citations). Mark W. Steele has collaborated with scholars based in United States. Frequent co-authors include Sharon L. Wenger, Barton Childs, William John Young, Aravinda Chakravarti, James H. Cummins, Bernard Cohen, James F. Reynolds, Wendy L. Golden, Sylvia F. Pan and W. Roy Breg. Their work appears in journals such as Clinical Genetics, The Journal of Pediatrics, Biochemical Genetics, Nature and Pediatric Research.
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.