Mark J. Stephan

1.4k total citations
23 papers, 762 citations indexed

About

Mark J. Stephan is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Mark J. Stephan has authored 23 papers receiving a total of 762 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Surgery and 6 papers in Genetics. Recurrent topics in Mark J. Stephan's work include Fetal and Pediatric Neurological Disorders (4 papers), Congenital limb and hand anomalies (2 papers) and Mitochondrial Function and Pathology (2 papers). Mark J. Stephan is often cited by papers focused on Fetal and Pediatric Neurological Disorders (4 papers), Congenital limb and hand anomalies (2 papers) and Mitochondrial Function and Pathology (2 papers). Mark J. Stephan collaborates with scholars based in United States, Canada and Switzerland. Mark J. Stephan's co-authors include John M. Graham, David W. Smith, Marvin E. Miller, Bryan D. Hall, David W. Smith, Roberta A Pagon, David W. Smith, Errol R. Alden, Richard I. Kelley and William O. Walker and has published in prestigious journals such as CHEST Journal, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Mark J. Stephan

23 papers receiving 728 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark J. Stephan United States	15	279	263	230	142	131	23	762
Brad Angle United States	18	444 1.6×	527 2.0×	191 0.8×	107 0.8×	117 0.9×	33	1000
B. Le Marec France	19	506 1.8×	474 1.8×	115 0.5×	88 0.6×	150 1.1×	67	1.0k
James V. Higgins United States	18	332 1.2×	414 1.6×	241 1.0×	52 0.4×	182 1.4×	39	927
Yolande van Bever Netherlands	18	297 1.1×	441 1.7×	218 0.9×	134 0.9×	191 1.5×	46	871
E Tarantino Italy	13	217 0.8×	198 0.8×	101 0.4×	68 0.5×	50 0.4×	28	460
Reuven Sharony Israel	20	215 0.8×	254 1.0×	184 0.8×	78 0.5×	474 3.6×	79	1.0k
Lakshmi Mehta United States	16	403 1.4×	348 1.3×	96 0.4×	44 0.3×	86 0.7×	46	754
Rocio Moran United States	16	324 1.2×	378 1.4×	128 0.6×	307 2.2×	48 0.4×	27	854
Marga Schepens Netherlands	14	539 1.9×	336 1.3×	83 0.4×	120 0.8×	185 1.4×	20	779
Louise C. Wilson United Kingdom	20	629 2.3×	638 2.4×	178 0.8×	88 0.6×	104 0.8×	46	1.2k

Countries citing papers authored by Mark J. Stephan

Since Specialization

Citations

This map shows the geographic impact of Mark J. 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 J. 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 J. Stephan more than expected).

Fields of papers citing papers by Mark J. Stephan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark J. 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 J. Stephan. The network helps show where Mark J. Stephan may publish in the future.

Co-authorship network of co-authors of Mark J. Stephan

This figure shows the co-authorship network connecting the top 25 collaborators of Mark J. Stephan. A scholar is included among the top collaborators of Mark J. Stephan 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 J. Stephan. Mark J. Stephan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Aldinger, Kimberly A., Martine Tétreault, Jennifer C. Dempsey, et al.. (2014). Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy. The American Journal of Human Genetics. 95(2). 227–234. 78 indexed citations

2.

Aldinger, Kimberly A., Martine Tétreault, Jennifer C. Dempsey, et al.. (2014). Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy. The American Journal of Human Genetics. 95(4). 472–472. 2 indexed citations

3.

Hamvas, Aaron, Robin R. Deterding, Susan E. Wert, et al.. (2013). Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1. CHEST Journal. 144(3). 794–804. 113 indexed citations

4.

Below, Jennifer E., Dawn Earl, Kathryn M. Shively, et al.. (2012). Whole-Genome Analysis Reveals that Mutations in Inositol Polyphosphate Phosphatase-like 1 Cause Opsismodysplasia. The American Journal of Human Genetics. 92(1). 137–143. 44 indexed citations

5.

Gripp, Karen W., et al.. (2007). Selective IgM deficiency and 22q11.2 deletion syndrome. Annals of Allergy Asthma & Immunology. 99(1). 87–92. 23 indexed citations

6.

Tsao, Jack W., Jason Neal, Kira Apse, et al.. (2006). Cerebellar Ataxia With Progressive Improvement. Archives of Neurology. 63(4). 594–594. 5 indexed citations

7.

Stephan, Mark J., et al.. (2005). Endovascular treatment of spinal arteriovenous fistula in a young child with hereditary hemorrhagic telangiectasia. Journal of Neurosurgery Pediatrics. 103(5). 462–465. 13 indexed citations

8.

Stephan, Mark J.. (2005). A tribute to our teacher, Dr. Judith Hall: A child with the trait of the Earl of Shrewsbury. American Journal of Medical Genetics Part A. 140A(2). 156–159. 2 indexed citations

9.

Stephan, Mark J., et al.. (1999). Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation. Journal of Medical Genetics. 36(3). 237–241. 12 indexed citations

10.

Stephan, Mark J., et al.. (1998). Variant RSH/Smith-Lemli-Opitz syndrome with atypical sterol metabolism. American Journal of Medical Genetics. 78(5). 413–418. 44 indexed citations

11.

Vanderhooft, Sheryll L., Mark J. Stephan, & Virginia P. Sybert. (1993). Severe Skin Erosions and Scalp Infections in AEC Syndrome. Pediatric Dermatology. 10(4). 334–340. 27 indexed citations

12.

Stephan, Mark J.. (1989). Mucopolysaccharidosis I Presenting With Endocardial Fibroelastosis of Infancy. Archives of Pediatrics and Adolescent Medicine. 143(7). 782–782. 20 indexed citations

13.

Mader, Thomas H., et al.. (1988). Enlarged Pupillary Membranes. Journal of Pediatric Ophthalmology & Strabismus. 25(2). 73–74. 9 indexed citations

14.

Reynolds, James F., Art Daniel, Thaddeus E. Kelly, et al.. (1987). Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister‐Killian syndrome): Report of 11 cases. American Journal of Medical Genetics. 27(2). 257–274. 107 indexed citations

15.

Stephan, Mark J., et al.. (1985). SEPTO-OPTIC DYSPLASIA WITH DIGITAL ANOMALIES. Journal of Pediatric Orthopaedics. 5(5). 623–623. 1 indexed citations

16.

Mueller, Rebecca, Roberta A Pagon, Melanie Pepin, et al.. (1984). Arteriohepatic dysplasia: phenotypic features and family studies. Clinical Genetics. 25(4). 323–331. 29 indexed citations

17.

Pagon, Roberta A & Mark J. Stephan. (1984). Septo-optic dysplasia with digital anomalies. The Journal of Pediatrics. 105(6). 966–968. 20 indexed citations

18.

Carroll, David, Mark J. Stephan, & Granvil L. Hays. (1983). Epidermolysis Bullosa—Review and Report of Case. The Journal of the American Dental Association. 107(5). 749–751. 17 indexed citations

19.

Graham, John M., Marvin E. Miller, Mark J. Stephan, & David W. Smith. (1980). Limb reduction anomalies and early in utero limb compression. The Journal of Pediatrics. 96(6). 1052–1056. 62 indexed citations

20.

Stephan, Mark J., et al.. (1975). Macrocephaly in association with unusual cutaneous angiomatosis. The Journal of Pediatrics. 87(3). 353–359. 59 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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