Duane Superneau

1.8k total citations
22 papers, 868 citations indexed

About

Duane Superneau is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Duane Superneau has authored 22 papers receiving a total of 868 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Duane Superneau's work include Genomic variations and chromosomal abnormalities (4 papers), Craniofacial Disorders and Treatments (4 papers) and Neurofibromatosis and Schwannoma Cases (4 papers). Duane Superneau is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Craniofacial Disorders and Treatments (4 papers) and Neurofibromatosis and Schwannoma Cases (4 papers). Duane Superneau collaborates with scholars based in United States, Germany and Netherlands. Duane Superneau's co-authors include Wladimir Wertelecki, James F. Gusella, Jonathan L. Haines, Guy A. Rouleau, Bernd R. Seizinger, Robert L. Martuza, Wendy Hobbs, James A. Trofatter, P. Michael Conneally and John M. Opitz and has published in prestigious journals such as Nature, New England Journal of Medicine and American Journal of Medical Genetics.

In The Last Decade

Duane Superneau

22 papers receiving 827 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Duane Superneau United States 13 420 297 259 202 115 22 868
E Wright United Kingdom 9 431 1.0× 184 0.6× 253 1.0× 172 0.9× 138 1.2× 15 824
Michael L. Nordlund United States 20 663 1.6× 318 1.1× 391 1.5× 93 0.5× 113 1.0× 30 1.5k
Fei‐Yu Han Sweden 8 362 0.9× 241 0.8× 263 1.0× 47 0.2× 120 1.0× 11 654
Raimund Fahsold Germany 14 397 0.9× 90 0.3× 344 1.3× 159 0.8× 128 1.1× 27 777
Donna C. Rich United States 7 241 0.6× 89 0.3× 260 1.0× 176 0.9× 75 0.7× 8 580
Fotios D. Vrionis United States 12 172 0.4× 240 0.8× 213 0.8× 120 0.6× 28 0.2× 15 541
Victor‐F. Mautner Germany 14 693 1.6× 252 0.8× 122 0.5× 64 0.3× 176 1.5× 20 794
A. Al Saadi United States 12 104 0.2× 203 0.7× 201 0.8× 160 0.8× 37 0.3× 16 726
P H Cogen United States 10 276 0.7× 129 0.4× 285 1.1× 62 0.3× 43 0.4× 12 824
David Bourn United Kingdom 13 179 0.4× 130 0.4× 132 0.5× 60 0.3× 64 0.6× 33 604

Countries citing papers authored by Duane Superneau

Since Specialization
Citations

This map shows the geographic impact of Duane Superneau'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 Duane Superneau with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Duane Superneau more than expected).

Fields of papers citing papers by Duane Superneau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Duane Superneau. 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 Duane Superneau. The network helps show where Duane Superneau may publish in the future.

Co-authorship network of co-authors of Duane Superneau

This figure shows the co-authorship network connecting the top 25 collaborators of Duane Superneau. A scholar is included among the top collaborators of Duane Superneau 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 Duane Superneau. Duane Superneau 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.
Superneau, Duane, et al.. (2011). Ventricular Fibrillation in a Patient with Pompe Disease: A Cautionary Tale. Congenital Heart Disease. 6(4). 397–401. 5 indexed citations
2.
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4.
Bongers, Ernie M.H.F., John M. Opitz, Alan Fryer, et al.. (2001). Meier-Gorlin syndrome: Report of eight additional cases and review. American Journal of Medical Genetics. 102(2). 115–124. 47 indexed citations
5.
Bohring, Axel, Margherita Silengo, Margherita Lerone, et al.. (1999). Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?. American Journal of Medical Genetics. 85(5). 438–446. 43 indexed citations
6.
Graham, John M., Duane Superneau, R. Curtis Rogers, et al.. (1999). Clinical and behavioral characteristics in FG syndrome. American Journal of Medical Genetics. 85(5). 470–475. 1 indexed citations
7.
Graham, John M., Duane Superneau, R. Curtis Rogers, et al.. (1999). Clinical and behavioral characteristics in FG syndrome. American Journal of Medical Genetics. 85(5). 470–475. 21 indexed citations
8.
Graham, John M., et al.. (1998). FG syndrome: Report of three new families with linkage to xq12-q22.1. American Journal of Medical Genetics. 80(2). 145–156. 27 indexed citations
9.
Graham, John M., et al.. (1998). FG syndrome: Report of three new families with linkage to xq12‐q22.1. American Journal of Medical Genetics. 80(2). 145–156. 2 indexed citations
10.
Eustis, H. Sprague, Thomas J. Curry, & Duane Superneau. (1995). Peroxisomal Bifunctional Enzyme Complex Deficiency With Associated Retinal Findings. Journal of Pediatric Ophthalmology & Strabismus. 32(2). 125–127. 5 indexed citations
11.
Braddock, Stephen R., Kenneth Lyons Jones, Duane Superneau, & Marilyn C. Jones. (1993). Sagittal craniosynostosis, Dandy‐Walker malformation, and hydrocephalus: A unique multiple malformation syndrome. American Journal of Medical Genetics. 47(5). 640–643. 8 indexed citations
12.
Martínez, José E., Cathy M. Tuck‐Müller, Duane Superneau, & Wladimir Wertelecki. (1993). Fertility and the cri du chat syndrome. Clinical Genetics. 43(4). 212–214. 21 indexed citations
13.
Rouleau, Guy A., Bernd R. Seizinger, Wladimir Wertelecki, et al.. (1990). Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.. PubMed. 46(2). 323–8. 75 indexed citations
14.
Zellweger, H, Paul Maertens, Duane Superneau, & Wladimir Wertelecki. (1988). History of the Cerebrohepatorenal Syndrome of Zellweger and Other Peroxisomal Disorders. Southern Medical Journal. 81(3). 357–364. 16 indexed citations
15.
Wertelecki, Wladimir, et al.. (1988). Neurofibromatosis 2: Clinical and DNA Linkage Studies of a Large Kindred. New England Journal of Medicine. 319(5). 278–283. 123 indexed citations
16.
Wertelecki, Wladimir, et al.. (1988). Angiomas and von Recklinghausen neurofibromatosis.. PubMed. 1(3). 137–45. 7 indexed citations
17.
Wertelecki, Wladimir, et al.. (1987). Effects of education, distance and satellite clinics on the growth of genetic services. Journal of Biosocial Science. 19(4). 487–493. 1 indexed citations
18.
Superneau, Duane, Wladimir Wertelecki, H Zellweger, & Frank O. Bastian. (1987). Myopathy in Marinesco-Sjogren Syndrome. European Neurology. 26(1). 8–16. 38 indexed citations
19.
Superneau, Duane, Wladimir Wertelecki, John M. Opitz, & James F. Reynolds. (1985). Similarity of effects—experimental hyperthermia as a teratogen and maternal febrile illness associated with oromandibular and limb defects. American Journal of Medical Genetics. 21(3). 575–580. 20 indexed citations
20.
Pelias, Mary Z., Duane Superneau, Theodore F. Thurmon, & John M. Opitz. (1981). A sixth report (eighth case) of craniosynostosis‐radial aplasia (Baller–Gerold) syndrome. American Journal of Medical Genetics. 10(2). 133–139. 23 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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