M. Boxer

650 total citations
18 papers, 493 citations indexed

About

M. Boxer is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Pulmonary and Respiratory Medicine. According to data from OpenAlex, M. Boxer has authored 18 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Cardiology and Cardiovascular Medicine and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in M. Boxer's work include Connective tissue disorders research (10 papers), Cardiac Valve Diseases and Treatments (5 papers) and Skin and Cellular Biology Research (3 papers). M. Boxer is often cited by papers focused on Connective tissue disorders research (10 papers), Cardiac Valve Diseases and Treatments (5 papers) and Skin and Cellular Biology Research (3 papers). M. Boxer collaborates with scholars based in United Kingdom, United States and Israel. M. Boxer's co-authors include J. Gray, John Dean, M.J.W. Faed, E. Birgitte Lane, E.L. Rugg, P S Baines, Frances J.D. Smith, Irene M. Leigh, S. Morley and Michael J. Tidman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

M. Boxer

18 papers receiving 475 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Boxer United Kingdom	14	277	146	137	131	120	18	493
Elena Gallo MacFarlane United States	11	242 0.9×	218 1.5×	114 0.8×	177 1.4×	45 0.4×	22	560
Kristine D. Estrada United States	8	94 0.3×	45 0.3×	82 0.6×	269 2.1×	37 0.3×	10	441
Christine F. Poliks United States	6	58 0.2×	122 0.8×	29 0.2×	210 1.6×	37 0.3×	7	453
E. Futo Switzerland	10	139 0.5×	44 0.3×	101 0.7×	400 3.1×	75 0.6×	11	807
Lisa M. Vincent United States	10	318 1.1×	37 0.3×	60 0.4×	239 1.8×	33 0.3×	19	659
Sanae Soma Japan	7	55 0.2×	118 0.8×	62 0.5×	136 1.0×	21 0.2×	8	376
Cathy J. Hatcher United States	13	97 0.4×	142 1.0×	221 1.6×	481 3.7×	33 0.3×	22	710
Tyler J. Creamer United States	10	97 0.4×	142 1.0×	56 0.4×	306 2.3×	21 0.2×	13	496
Toichiro Takizawa Japan	5	41 0.1×	280 1.9×	88 0.6×	349 2.7×	44 0.4×	8	625
T Arai United States	8	58 0.2×	38 0.3×	48 0.4×	221 1.7×	80 0.7×	13	502

Countries citing papers authored by M. Boxer

Since Specialization

Citations

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

Fields of papers citing papers by M. Boxer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Boxer

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

18 of 18 papers shown

Lang, Julie, M. Boxer, & R.M. MACKIE. (2005). CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families. British Journal of Dermatology. 153(6). 1121–1125. 11 indexed citations

Rugg, E.L., Carrie S. Shemanko, Tamar Kadar, et al.. (2000). DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplex. Prenatal Diagnosis. 20(5). 371–377. 2 indexed citations

Rugg, E.L., David Baty, Carrie S. Shemanko, et al.. (2000). DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplex. Prenatal Diagnosis. 20(5). 371–377. 23 indexed citations

Black, Colin, et al.. (1999). Neonatal Marfan syndrome: A case report. Journal of Paediatrics and Child Health. 35(3). 321–323. 18 indexed citations

D’Arrigo, Corrado, et al.. (1998). TGF-β₁Binding Protein-Like Modules of Fibrillin-1 and -2 Mediate Integrin-Dependent Cell Adhesion. Connective Tissue Research. 37(1-2). 29–51. 37 indexed citations

Stuart, Graham, et al.. (1998). Life expectancy in British Marfan syndrome populations. Clinical Genetics. 54(2). 124–128. 51 indexed citations

Collod‐Béroud, Gwenaëlle, Christophe Béroud, Lesley C. Adès, et al.. (1997). Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene. Nucleic Acids Research. 25(1). 147–150. 25 indexed citations

Boxer, M., M. Scot Roberts, & Leslie C. Grammer. (1997). Cumin anaphylaxis: A case report. Journal of Allergy and Clinical Immunology. 99(5). 722–723. 15 indexed citations

Gray, J., et al.. (1994). Ascertainment and severity of Marfan syndrome in a Scottish population.. Journal of Medical Genetics. 31(1). 51–54. 81 indexed citations

10.

Rugg, E.L., S. Morley, Frances J.D. Smith, et al.. (1993). Missing links: Weber–Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton function. Nature Genetics. 5(3). 294–300. 84 indexed citations

11.

Gray, J., et al.. (1993). Osteoporosis and the Marfan syndrome. Postgraduate Medical Journal. 69(811). 373–375. 22 indexed citations

12.

Moghrabi, Nabil, L. Sutherland, Richard Wooster, et al.. (1992). Chromosomal assignment of human phenol and bilirubin UDP‐glucuronosyltransferase genes (UGT1A‐subfamily). Annals of Human Genetics. 56(2). 81–91. 26 indexed citations

13.

Faed, M.J.W., et al.. (1992). Marfan syndrome in a large family: response of family members to a screening programme.. Journal of Medical Genetics. 29(2). 81–85. 9 indexed citations

14.

Sarfarazi, M., Petros Tsipouras, M W Kilpatrick, et al.. (1992). A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study.. Journal of Medical Genetics. 29(2). 75–80. 21 indexed citations

15.

Faed, M.J.W., et al.. (1991). Marfan syndrome affecting four generations of a family without ocular involvement. Postgraduate Medical Journal. 67(788). 538–542. 3 indexed citations

16.

Tsipouras, Petros, et al.. (1991). Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1.. Proceedings of the National Academy of Sciences. 88(10). 4486–4488. 32 indexed citations

17.

Curtis, Ann, Moira Mennie, S Holloway, et al.. (1989). Prenatal exclusion testing for Huntington's disease: a problem of too much information.. Journal of Medical Genetics. 26(2). 83–85. 15 indexed citations

18.

Sano, Terunori, M. Boxer, Laurence A. Boxer, & Masaru Yokoyama. (1971). Platelet sensitivity to aggregation in normal and diseased groups. A method for assessment of platelet aggregability.. PubMed. 25(3). 524–31. 18 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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