Mark W. Steele

1.8k total citations
66 papers, 1.2k citations indexed

About

Mark W. Steele is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mark W. Steele has authored 66 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 24 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mark W. Steele's work include Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Mark W. Steele is often cited by papers focused on Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Mark W. Steele collaborates with scholars based in United States and Italy. Mark W. Steele's co-authors include Sharon L. Wenger, William J. Young, Barton Childs, Jennifer A. Scott, Aravinda Chakravarti, Sylvia F. Pan, Wendy L. Golden, James H. Cummins, W. Roy Breg and James F. Reynolds and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Academy of Child & Adolescent Psychiatry.

In The Last Decade

Mark W. Steele

65 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mark W. Steele United States 24 846 498 323 229 131 66 1.2k
A Kleczkowska Belgium 22 1.1k 1.3× 490 1.0× 439 1.4× 346 1.5× 122 0.9× 80 1.3k
M O Rethoré France 21 754 0.9× 599 1.2× 395 1.2× 259 1.1× 47 0.4× 62 1.5k
R H Lindenbaum United Kingdom 20 960 1.1× 715 1.4× 529 1.6× 192 0.8× 157 1.2× 39 1.7k
P.A. Jacobs United Kingdom 19 1.1k 1.3× 723 1.5× 336 1.0× 360 1.6× 148 1.1× 28 1.8k
J. O. Van Hemel Netherlands 21 809 1.0× 457 0.9× 356 1.1× 193 0.8× 164 1.3× 38 1.1k
Gholamali Tariverdian Germany 18 812 1.0× 721 1.4× 212 0.7× 76 0.3× 77 0.6× 64 1.3k
Art Daniel Australia 26 1.5k 1.7× 705 1.4× 617 1.9× 457 2.0× 195 1.5× 56 1.9k
Arabella Smith Australia 22 1.2k 1.4× 605 1.2× 591 1.8× 103 0.4× 95 0.7× 119 1.8k
Harriet von Koskull Finland 19 689 0.8× 465 0.9× 272 0.8× 85 0.4× 225 1.7× 52 1.1k
G. Shashidhar Pai United States 25 981 1.2× 796 1.6× 450 1.4× 257 1.1× 78 0.6× 55 1.9k

Countries citing papers authored by Mark W. Steele

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Mark W. Steele

This figure shows the co-authorship network connecting the top 25 collaborators of Mark W. Steele. A scholar is included among the top collaborators of Mark W. Steele based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mark W. Steele. Mark W. Steele is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Tantiwongkosi, Bundhit, Marilyn J. Goske, & Mark W. Steele. (2008). Congenital solid neck mass: a unique presentation of Langerhans cell histiocytosis. Pediatric Radiology. 38(5). 575–578. 7 indexed citations
2.
Rogan, Peter K., James R. Seip, Lisa White, et al.. (1998). Relaxation of imprinting in Prader-Willi syndrome. Human Genetics. 103(6). 694–694. 13 indexed citations
3.
Wenger, Sharon L., Susan L. Sell, Michael J. Painter, & Mark W. Steele. (1997). Inherited unbalanced subtelomeric translocation in a child with 8p‐ and Angelman syndromes. American Journal of Medical Genetics. 70(2). 150–154. 2 indexed citations
4.
Greally, John M., Katherine Neiswanger, James H. Cummins, et al.. (1996). A molecular anatomical analysis of mosaic trisomy 16. Human Genetics. 98(1). 86–90. 25 indexed citations
5.
Steele, Mark W., et al.. (1996). A simplified six item checklist for screening for fragile X syndrome in the pediatric population. The Journal of Pediatrics. 129(4). 611–614. 46 indexed citations
6.
Lubetsky, Martin J., et al.. (1995). Chromosomal abnormalities in a psychiatric population. American Journal of Medical Genetics. 60(1). 53–54. 7 indexed citations
7.
Wenger, Sharon L., et al.. (1995). “Balanced” karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents. American Journal of Medical Genetics. 55(1). 47–52. 25 indexed citations
8.
Kobayashi, Megumi, Bernard S. Kaplan, Richard D. Bellah, et al.. (1995). Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: Clinical observations and genetic analysis. American Journal of Medical Genetics. 59(2). 218–224. 6 indexed citations
9.
Scott, Jennifer A., Sharon L. Wenger, Mark W. Steele, & Aravinda Chakravarti. (1995). Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation. American Journal of Medical Genetics. 56(1). 67–71. 77 indexed citations
10.
Estop, A., et al.. (1994). Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes. American Journal of Medical Genetics. 49(4). 410–413. 3 indexed citations
11.
Donahue, Sean P., Sharon L. Wenger, Mark W. Steele, & Michael B. Gorin. (1993). Broad-Spectrum Möbius Syndrome Associated with a 1;11 Chromosome Translocation. Ophthalmic Paediatrics and Genetics. 14(1). 17–21. 40 indexed citations
12.
Wenger, Sharon L., Mark W. Steele, Eric P. Hoffman, Mamdouha A. Barmada, & Henry B. Wessel. (1992). X inactivation and dystrophin studies in a t(X;12) female: Evidence for biochemical normalization in Duchenne muscular dystrophy carriers. American Journal of Medical Genetics. 43(6). 1012–1015. 15 indexed citations
13.
Greally, John M., et al.. (1992). Acrometageria: A spectrum of “premature aging” syndromes. American Journal of Medical Genetics. 44(3). 334–339. 12 indexed citations
14.
Steele, Mark W., et al.. (1990). Chromosome mosaicism in hypomelanosis of Ito. American Journal of Medical Genetics. 35(1). 14–17. 60 indexed citations
15.
Wenger, Sharon L., Mark W. Steele, & Dorothy J. Becker. (1988). Clinical consequences of deletion 1p35.. Journal of Medical Genetics. 25(4). 263–263. 23 indexed citations
16.
Hoffman, Robert P., et al.. (1988). 46XY Siblings with Inadequate Virilization and CNS Deficiency. Hormone Research. 29(5-6). 207–210. 5 indexed citations
17.
Wenger, Sharon L., Julie Blatt, Mark W. Steele, et al.. (1988). Rhabdomyosarcoma in Roberts syndrome. Cancer Genetics and Cytogenetics. 31(2). 285–289. 16 indexed citations
18.
Lin, Angela E., Kenneth L. Garver, Michele Clemens, et al.. (1988). Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes. American Journal of Medical Genetics. 31(3). 533–548. 87 indexed citations
19.
Wenger, Sharon L., et al.. (1987). Clinical comparison of 59 Prader‐Willi patients with and without the 15(Q12) deletion. American Journal of Medical Genetics. 28(4). 881–887. 25 indexed citations
20.
Steele, Mark W., et al.. (1974). Trisomy for the distal half of the long arm of chromosome No. 18. The Journal of Pediatrics. 85(6). 827–829. 11 indexed citations

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.

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