M A Patton

2.9k total citations
61 papers, 1.9k citations indexed

About

M A Patton is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, M A Patton has authored 61 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 18 papers in Genetics and 13 papers in Surgery. Recurrent topics in M A Patton's work include Protein Tyrosine Phosphatases (9 papers), RNA modifications and cancer (7 papers) and Genetic Syndromes and Imprinting (5 papers). M A Patton is often cited by papers focused on Protein Tyrosine Phosphatases (9 papers), RNA modifications and cancer (7 papers) and Genetic Syndromes and Imprinting (5 papers). M A Patton collaborates with scholars based in United Kingdom, Oman and United States. M A Patton's co-authors include Andrew H. Crosby, M Baraitser, A. Harden, Stewart Boyd, Kamini Kalidas, Adam Shaw, Steven Jeffery, Mike Sharland, William J. McKenna and Michael A. Simpson and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

M A Patton

60 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M A Patton United Kingdom 26 1.0k 751 316 234 231 61 1.9k
S Malcolm United Kingdom 31 1.2k 1.1× 1.1k 1.5× 247 0.8× 156 0.7× 248 1.1× 71 2.3k
Bruno Leheup France 29 1.1k 1.1× 758 1.0× 238 0.8× 239 1.0× 149 0.6× 97 2.2k
Jean‐Pierre Fryns Belgium 21 1.2k 1.2× 909 1.2× 127 0.4× 206 0.9× 202 0.9× 25 2.0k
Mirja Somer Finland 25 1.5k 1.4× 816 1.1× 128 0.4× 117 0.5× 240 1.0× 49 2.4k
Louise Brueton United Kingdom 24 908 0.9× 604 0.8× 91 0.3× 154 0.7× 205 0.9× 34 1.5k
Renaud Touraine France 25 1.1k 1.1× 633 0.8× 97 0.3× 354 1.5× 120 0.5× 93 2.0k
Charles I. Scott United States 33 1.2k 1.2× 1.7k 2.3× 157 0.5× 606 2.6× 328 1.4× 99 3.2k
Peter Wieacker Germany 35 2.4k 2.3× 1.6k 2.2× 194 0.6× 191 0.8× 397 1.7× 141 3.8k
Yoshio Makita Japan 24 916 0.9× 797 1.1× 143 0.5× 213 0.9× 129 0.6× 77 1.8k
Daniel Kelberman United Kingdom 28 1.1k 1.1× 967 1.3× 179 0.6× 269 1.1× 124 0.5× 43 2.2k

Countries citing papers authored by M A Patton

Since Specialization
Citations

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

Fields of papers citing papers by M A Patton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M A Patton. 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 M A Patton. The network helps show where M A Patton may publish in the future.

Co-authorship network of co-authors of M A Patton

This figure shows the co-authorship network connecting the top 25 collaborators of M A Patton. A scholar is included among the top collaborators of M A Patton 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 M A Patton. M A Patton 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.
2.
Zahka, Kenneth, Kamini Kalidas, Michael A. Simpson, et al.. (2008). Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish. Heart. 94(10). 1326–1330. 47 indexed citations
3.
Shaw, Adam, Kamini Kalidas, Andrew H. Crosby, Steven Jeffery, & M A Patton. (2006). The natural history of Noonan syndrome: a long-term follow-up study. Archives of Disease in Childhood. 92(2). 128–132. 184 indexed citations
4.
Proukakis, Christos, Michaela Auer‐Grumbach, Klaus Wagner, et al.. (2003). Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in theSPG4 (Spastin) gene. Human Mutation. 21(2). 170–170. 25 indexed citations
5.
Patton, M A, et al.. (2002). Robinow syndrome. Journal of Medical Genetics. 39(5). 305–310. 87 indexed citations
6.
Brown, Donald C., William J. McKenna, M A Patton, et al.. (2002). Growth Hormone Therapy in Noonan's Syndrome: Non-Cardiomyopathic Congenital Heart Disease Does Not Adversely Affect Growth Improvement. Journal of Pediatric Endocrinology and Metabolism. 15(6). 851–2. 14 indexed citations
7.
Patel, Harshad B., Paul Hart, Thomas T. Warner, et al.. (2001). Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci. American Journal of Medical Genetics. 102(1). 68–72. 7 indexed citations
8.
Rajab, Anna, M A Patton, & B Modell. (2000). Study of hemoglobinopathies in Oman through a national register.. PubMed. 21(12). 1168–72. 27 indexed citations
9.
Afzal, Ali R., Anna Rajab, Christiane Fenske, et al.. (2000). Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2. Journal of Medical Genetics. 37. 2 indexed citations
10.
Afzal, Ali R., Anna Rajab, Christiane Fenske, et al.. (2000). Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22. Human Genetics. 106(3). 351–354. 16 indexed citations
11.
Romey, Marie‐Catherine, Caroline Guittard, J. P. Chazalette, et al.. (1999). Complex allele [-102T>A+S549R(T>G)] is associated with milder forms of cystic fibrosis than allele S549R(T>G) alone. Human Genetics. 105(1-2). 145–150. 23 indexed citations
12.
Rajab, Ahmad Mamoun, N.V. Freeman, & M A Patton. (1997). Hirschsprung's disease in Oman. Journal of Pediatric Surgery. 32(5). 724–727. 23 indexed citations
13.
Freeman, N.V., et al.. (1996). The frequency of posterior urethral valves in Oman. British Journal of Urology. 77(6). 900–904. 14 indexed citations
14.
Lacombe, Didier, et al.. (1995). Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritance. European Journal of Pediatrics. 154(8). 658–661. 33 indexed citations
15.
George, Christopher D., et al.. (1993). Abdominal ultrasound in Noonan syndrome: A study of 44 patients. Pediatric Radiology. 23(4). 316–318. 22 indexed citations
16.
Burch, M., Jessica M. Mann, Mike Sharland, et al.. (1992). Myocardial disarray in Noonan syndrome. Heart. 68(12). 586–588. 48 indexed citations
17.
Evans, D. Gareth, Ray Lonsdale, & M A Patton. (1991). Cutaneous lymphangioma and amegakaryocytic thrombocytopenia in Noonan syndrome. Clinical Genetics. 39(3). 228–232. 17 indexed citations
18.
Patton, M A. (1988). Russell-Silver syndrome.. Journal of Medical Genetics. 25(8). 557–560. 41 indexed citations
19.
Boyd, Stewart, A. Harden, & M A Patton. (1988). The EEG in early diagnosis of the Angelman (Happy Puppet) syndrome. European Journal of Pediatrics. 147(5). 508–513. 176 indexed citations
20.
Patton, M A, et al.. (1987). Congenital cutis laxa with retardation of growth and development.. Journal of Medical Genetics. 24(9). 556–561. 29 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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