Michael Wright

10.3k total citations
149 papers, 4.8k citations indexed

About

Michael Wright is a scholar working on Applied Mathematics, Aerospace Engineering and Computational Mechanics. According to data from OpenAlex, Michael Wright has authored 149 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 89 papers in Applied Mathematics, 87 papers in Aerospace Engineering and 49 papers in Computational Mechanics. Recurrent topics in Michael Wright's work include Gas Dynamics and Kinetic Theory (89 papers), Computational Fluid Dynamics and Aerodynamics (46 papers) and Rocket and propulsion systems research (40 papers). Michael Wright is often cited by papers focused on Gas Dynamics and Kinetic Theory (89 papers), Computational Fluid Dynamics and Aerodynamics (46 papers) and Rocket and propulsion systems research (40 papers). Michael Wright collaborates with scholars based in United States, United Kingdom and Germany. Michael Wright's co-authors include Deepak Bose, Grant Palmer, Graham V. Candler, Eugene Levin, Karl T. Edquist, Helen Hwang, Joseph Olejniczak, Iain D. Boyd, Dinesh Prabhu and Gary Allen and has published in prestigious journals such as Nature Genetics, Water Resources Research and Chemical Engineering Journal.

In The Last Decade

Michael Wright

146 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael Wright United States 40 2.8k 2.0k 1.8k 920 791 149 4.8k
Jonathan B. Freund United States 40 238 0.1× 2.1k 1.0× 3.3k 1.8× 30 0.0× 237 0.3× 200 5.5k
William W. Wood United States 35 255 0.1× 506 0.3× 456 0.2× 67 0.1× 466 0.6× 110 4.3k
Eric Johnsen United States 31 409 0.1× 474 0.2× 1.5k 0.8× 26 0.0× 50 0.1× 119 3.8k
Luigi Preziosi Italy 40 275 0.1× 58 0.0× 856 0.5× 83 0.1× 831 1.1× 156 6.5k
Robert W. Barber United Kingdom 28 559 0.2× 213 0.1× 752 0.4× 15 0.0× 129 0.2× 115 2.4k
Kazuyoshi Takayama Japan 24 218 0.1× 464 0.2× 553 0.3× 6 0.0× 98 0.1× 231 2.2k
G. T. Gillies United States 32 33 0.0× 264 0.1× 192 0.1× 93 0.1× 321 0.4× 201 4.4k
Yiannis Ventikos United Kingdom 37 36 0.0× 316 0.2× 1.3k 0.7× 194 0.2× 246 0.3× 167 4.2k
Peter Huang United States 19 28 0.0× 243 0.1× 460 0.3× 183 0.2× 244 0.3× 58 1.6k
David Adalsteinsson United States 19 35 0.0× 178 0.1× 1.2k 0.6× 124 0.1× 492 0.6× 37 2.9k

Countries citing papers authored by Michael Wright

Since Specialization
Citations

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

Fields of papers citing papers by Michael Wright

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Wright

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Wright. A scholar is included among the top collaborators of Michael Wright 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 Michael Wright. Michael Wright 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
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Lim, Derek, Dominic McMullan, Michael Wright, et al.. (2023). A case of mosaic deletion of paternally‐inherited PLAGL1 and two cases of upd(6)mat add to evidence for PLAGL1 under‐expression as a cause of growth restriction. American Journal of Medical Genetics Part A. 194(2). 383–388. 1 indexed citations
3.
Savarirayan, Ravi, Wagner Antonio da Rosa Baratela, Thomas Butt, et al.. (2022). Literature review and expert opinion on the impact of achondroplasia on medical complications and health-related quality of life and expectations for long-term impact of vosoritide: a modified Delphi study. Orphanet Journal of Rare Diseases. 17(1). 224–224. 11 indexed citations
4.
Fredwall, Svein O., Moeenaldeen AlSayed, Tawfeg Ben‐Omran, et al.. (2022). Optimising care and follow-up of adults with achondroplasia. Orphanet Journal of Rare Diseases. 17(1). 318–318. 6 indexed citations
5.
6.
Wilson, Brian T., et al.. (2012). Interstitial microduplication 12q13.2–q13.3 in a patient with dysmorphism, developmental delay, atypical seizures and hypospadias. Clinical Dysmorphology. 21(4). 196–199. 1 indexed citations
7.
Wright, Michael & Melita Irving. (2011). Clinical management of achondroplasia. Archives of Disease in Childhood. 97(2). 129–134. 64 indexed citations
8.
Morán, Patricia, et al.. (2011). Rhizomelic chondrodysplasia punctata: a classic ‘spot’ diagnosis. BMJ Case Reports. 2011. bcr0120113747–bcr0120113747. 2 indexed citations
9.
Wright, Michael, et al.. (2009). Data Parallel Line Relaxation (DPLR) Code User Manual: Acadia - Version 4.01.1. Nutrients. 15(6). 109 indexed citations
10.
Cole, Ben, et al.. (2006). Severe hypodontia in a set of triplets. BDJ. 201(2). 93–96. 4 indexed citations
11.
Heuertz, S., Martine Le Merrer, Bernhard Zabel, et al.. (2006). Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia. European Journal of Human Genetics. 14(12). 1240–1247. 65 indexed citations
12.
Hellemans, Jan, Philippe Debeer, Michael Wright, et al.. (2006). GermlineLEMD3 mutations are rare in sporadic patients with isolated melorheostosis. Human Mutation. 27(3). 290–290. 53 indexed citations
13.
Tompson, Stuart W., Víctor L. Ruiz‐Pérez, Helen J. Blair, et al.. (2006). Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients. Human Genetics. 120(5). 663–670. 83 indexed citations
14.
Evans, Julie, Hayley Archer, James Colley, et al.. (2005). Early onset seizures and Rett-like features associated with mutations in CDKL5. European Journal of Human Genetics. 13(10). 1113–1120. 135 indexed citations
15.
Kennedy, Jason, Gail C. Jackson, Simon Ramsden, et al.. (2005). COMP mutation screening as an aid for the clinical diagnosis and counselling of patients with a suspected diagnosis of pseudoachondroplasia or multiple epiphyseal dysplasia. European Journal of Human Genetics. 13(5). 547–555. 47 indexed citations
16.
17.
Zankl, Andreas, Luitgard M. Neumann, Peter G. J. Nikkels, et al.. (2005). Dominant negative mutations in the C-propeptide of COL2A1 cause platyspondylic lethal skeletal dysplasia, torrance type, and define a novel subfamily within the type 2 collagenopathies. American Journal of Medical Genetics Part A. 133A(1). 61–67. 39 indexed citations
18.
Wright, Michael, et al.. (2003). Motion analysis of stereotyped hand movements in Rett syndrome. Journal of Intellectual Disability Research. 47(2). 85–89. 11 indexed citations
19.
Ruiz‐Pérez, Víctor L., Susan Ide, Tim M. Strom, et al.. (2000). Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis. Nature Genetics. 24(3). 283–286. 224 indexed citations
20.
Rutherfurd, Ian, et al.. (1995). Vegetation and Stream Stability: A Scale Analysis. Water resources engineering. 1. 800–804. 1 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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