Mark Stephan

1.0k total citations
10 papers, 617 citations indexed

About

Mark Stephan is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Mark Stephan has authored 10 papers receiving a total of 617 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Mark Stephan's work include Genetics and Neurodevelopmental Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Autism Spectrum Disorder Research (2 papers). Mark Stephan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Autism Spectrum Disorder Research (2 papers). Mark Stephan collaborates with scholars based in United States, United Kingdom and Canada. Mark Stephan's co-authors include Joseph H. Hersh, Gail Williams, John King, Michael L. Cunningham, Bronwyn Kerr, Shahenaz Najjar, Roberta A Pagon, Berkley R. Powell, J. Zonana and Ann B. Moser and has published in prestigious journals such as Archives of Disease in Childhood, Developmental Medicine & Child Neurology and European Journal of Human Genetics.

In The Last Decade

Mark Stephan

9 papers receiving 588 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark Stephan United States	6	357	263	168	150	105	10	617
Diane C. Lanham United States	11	425 1.2×	349 1.3×	181 1.1×	107 0.7×	88 0.8×	16	717
David S. Hong United States	19	385 1.1×	649 2.5×	317 1.9×	73 0.5×	121 1.2×	51	1.1k
William J. Cutter United Kingdom	12	276 0.8×	305 1.2×	212 1.3×	31 0.2×	86 0.8×	16	659
Natalia V. Malkova United States	11	250 0.7×	155 0.6×	284 1.7×	95 0.6×	100 1.0×	20	991
Luke S. Heuer United States	12	360 1.0×	200 0.8×	96 0.6×	86 0.6×	122 1.2×	21	745
Paula Goines United States	9	857 2.4×	465 1.8×	217 1.3×	144 1.0×	282 2.7×	9	1.4k
Tomoyuki Takano Japan	17	156 0.4×	100 0.4×	150 0.9×	209 1.4×	253 2.4×	74	825
Mari Wakahiro United States	15	385 1.1×	211 0.8×	129 0.8×	446 3.0×	63 0.6×	18	1.0k
Nicholas R. Dennis United Kingdom	16	206 0.6×	640 2.4×	368 2.2×	353 2.4×	101 1.0×	23	1.0k
Laura B. K. Herzing United States	12	182 0.5×	482 1.8×	442 2.6×	102 0.7×	34 0.3×	13	793

Countries citing papers authored by Mark Stephan

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Mark Stephan

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Stephan. A scholar is included among the top collaborators of Mark 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 Stephan. Mark 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:

10 of 10 papers shown

1.

Stephan, Mark, et al.. (2019). NRAS associated RASopathy and embryonal rhabdomyosarcoma. American Journal of Medical Genetics Part A. 182(1). 195–200. 6 indexed citations

2.

Deterding, Robin R., Megan K. Dishop, Derek A. Uchida, et al.. (2010). Thyroid Transcription Factor 1 Gene Abnormalities: An under Recognized Cause Of Children’s Interstitial Lung Disease. A6725–A6725. 2 indexed citations

3.

Williams, Gail, John King, Michael L. Cunningham, et al.. (2001). Fetal valproate syndrome and autism: additional evidence of an association. Developmental Medicine & Child Neurology. 43(3). 202–206. 226 indexed citations

4.

Williams, Gail, John King, Michael L. Cunningham, et al.. (2001). Fetal valproate syndrome and autism: additional evidence of an association. Developmental Medicine & Child Neurology. 43(3). 202–202. 284 indexed citations

5.

Kibar, Zoha, Marie‐Pierre Dubé, Julie Powell, et al.. (2000). Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping. European Journal of Human Genetics. 8(5). 372–380. 31 indexed citations

6.

Pagon, Roberta A, Berkley R. Powell, Barbara McGillivray, et al.. (1990). Rhizomelic chondrodysplasia punctata and survival beyond one year: a review of the literature and five case reports. Clinical Genetics. 38(2). 84–93. 36 indexed citations

7.

Oertel, Joachim, Mark Stephan, & Michael Kästner. (1982). Localization and Characteristics of Ferritin in Human Bone Marrow. Acta Haematologica. 67(2). 73–79. 1 indexed citations

8.

Pesch, H.-J., et al.. (1981). Zum Ossifikationsprinzip des Schildknorpels. European Archives of Oto-Rhino-Laryngology. 231(2-3). 829–831. 3 indexed citations

9.

Stephan, Mark. (1979). [Hereditary conduction defect in the His system: a dominant autosome disease].. PubMed. 72(1). 62–71. 1 indexed citations

10.

Najjar, Shahenaz, et al.. (1969). Serum levels of immunoglobulins in marasmic infants.. Archives of Disease in Childhood. 44(233). 120–123. 27 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.

Explore authors with similar magnitude of impact