M. Parton

1.0k total citations
26 papers, 588 citations indexed

About

M. Parton is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, M. Parton has authored 26 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 10 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in M. Parton's work include Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Muscle Physiology and Disorders (5 papers). M. Parton is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Muscle Physiology and Disorders (5 papers). M. Parton collaborates with scholars based in United Kingdom, United States and Sweden. M. Parton's co-authors include Ammar Al‐Chalabi, Michael G. Hanna, Christopher E. Shaw, P. Nigel Leigh, David Hilton‐Jones, John Powell, Peter M. Andersen, Janice L. Holton, P. Nigel Leigh and Martin R. Turner and has published in prestigious journals such as Neurology, Annals of Neurology and Cochrane Database of Systematic Reviews.

In The Last Decade

M. Parton

26 papers receiving 568 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Parton United Kingdom	13	320	198	193	164	101	26	588
Maria Rita Murru Italy	16	220 0.7×	72 0.4×	140 0.7×	54 0.3×	83 0.8×	38	686
Keiji Chida Japan	9	170 0.5×	59 0.3×	203 1.1×	167 1.0×	92 0.9×	23	468
Jana Zschüntzsch Germany	12	109 0.3×	46 0.2×	144 0.7×	119 0.7×	67 0.7×	38	384
Deborah Ruddy United Kingdom	8	338 1.1×	149 0.8×	237 1.2×	48 0.3×	44 0.4×	11	594
Paulo Victor Sgobbi de Souza Brazil	14	277 0.9×	179 0.9×	250 1.3×	24 0.1×	240 2.4×	82	707
Robin Howard United Kingdom	7	443 1.4×	105 0.5×	69 0.4×	29 0.2×	44 0.4×	9	557
Mulder Dw	8	596 1.9×	291 1.5×	146 0.8×	93 0.6×	130 1.3×	20	830
Magali Periquet United States	9	416 1.3×	75 0.4×	115 0.6×	47 0.3×	161 1.6×	21	742
Yuzhou Guan China	14	307 1.0×	141 0.7×	101 0.5×	26 0.2×	71 0.7×	42	461
Susana Alvarez Denmark	12	100 0.3×	36 0.2×	105 0.5×	61 0.4×	166 1.6×	21	417

Countries citing papers authored by M. Parton

Since Specialization

Citations

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

Fields of papers citing papers by M. Parton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of M. Parton. A scholar is included among the top collaborators of M. Parton 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. Parton. M. Parton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Vivekanandam, Vinojini, Enrico Bugiardini, Ashirwad Merve, et al.. (2020). Differential Diagnoses of Inclusion Body Myositis. Neurologic Clinics. 38(3). 697–710. 2 indexed citations

Horga, Alejandro, Isabel Pareés, Iain P. Hargreaves, et al.. (2019). Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair. Human Genetics. 138(11-12). 1313–1322. 9 indexed citations

Schütz, Peter W., R. Scalco, Rita Barresi, et al.. (2017). Calpainopathy with macrophage-rich, regional inflammatory infiltrates. Neuromuscular Disorders. 27(8). 738–741. 8 indexed citations

Machado, Pedro, Mhoriam Ahmed, Stefen Brady, et al.. (2014). Ongoing Developments in Sporadic Inclusion Body Myositis. Current Rheumatology Reports. 16(12). 477–477. 20 indexed citations

Dewar, L., et al.. (2013). Frequency and circumstances of falls in people with inclusion body myositis: a questionnaire survey to explore falls management and physiotherapy provision. Physiotherapy. 100(1). 61–65. 15 indexed citations

Jaffer, Fatima, Mary M. Reilly, Rosaline C. M. Quinlivan, et al.. (2013). EMERGENCY NEUROMUSCULAR ADMISSIONS ARE AVOIDABLE: A REGIONAL AUDIT OF UNPLANNED HOSPITAL ADMISSIONS OF NEUROMUSCULAR PATIENTS 2009–2011: FINAL RESULTS AND RECOMMENDATIONS. Journal of Neurology Neurosurgery & Psychiatry. 84(11). e2.189–e2. 3 indexed citations

Cortese, Andrea, Pedro Machado, Jasper M. Morrow, et al.. (2013). Longitudinal observational study of sporadic inclusion body myositis: Implications for clinical trials. Neuromuscular Disorders. 23(5). 404–412. 54 indexed citations

Hilton‐Jones, David, et al.. (2010). Inclusion body myositis. Neuromuscular Disorders. 20(2). 142–147. 80 indexed citations

Parton, M., Hiroshi Mitsumoto, & P. Nigel Leigh. (2008). Amino acids for amyotrophic lateral sclerosis / motor neuron disease. Cochrane Database of Systematic Reviews. CD003457–CD003457. 2 indexed citations

10.

Al‐Chalabi, Ammar, Margaret Scheffler, Bradley Smith, et al.. (2003). Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosis. Annals of Neurology. 54(1). 130–134. 27 indexed citations

11.

Ruddy, Deborah, M. Parton, Ammar Al‐Chalabi, et al.. (2003). Two Families with Familial Amyotrophic Lateral Sclerosis Are Linked to a Novel Locus on Chromosome 16q. The American Journal of Human Genetics. 73(2). 390–396. 56 indexed citations

12.

Parton, M., Wendy Broom, Peter M. Andersen, et al.. (2002). D90A-SOD1 mediated amyotrophic lateral sclerosis: A single founder for all cases with evidence for aCis-acting disease modifier in the recessive haplotype. Human Mutation. 20(6). 473–473. 80 indexed citations

13.

Jonsson, P. Andreas, Peter M. Andersen, Johan Jacobsson, et al.. (2002). CuZn-Superoxide Dismutase in D90A Heterozygotes from Recessive and Dominant ALS Pedigrees. Neurobiology of Disease. 10(3). 327–333. 22 indexed citations

14.

Berg‐Vos, Renske M. van den, Leonard H. van den Berg, Gerard H. Jansen, et al.. (2001). Hereditary pure lower motor neuron disease with adult onset and rapid progression. Journal of Neurology. 248(4). 290–296. 8 indexed citations

15.

Winkler, Andrea Sylvia, Joanne Marsden, M. Parton, Peter Watkins, & К. Ray Chaudhuri. (2001). Erythropoietin deficiency and anaemia in multiple system atrophy. Movement Disorders. 16(2). 233–239. 24 indexed citations

16.

Turner, Martin R., M. Parton, & P. Nigel Leigh. (2001). Clinical Trials in ALS: An Overview. Seminars in Neurology. 21(2). 167–176. 37 indexed citations

17.

Andrews, William D., P. W. Tuke, Ammar Al‐Chalabi, et al.. (2000). Detection of reverse transcriptase activity in the serum of patients with motor neurone disease. Journal of Medical Virology. 61(4). 527–532. 54 indexed citations

18.

Parton, M.. (1999). Amyotrophic Lateral Sclerosis: A Synthesis of Research and Clinical Practice. Journal of Neurology Neurosurgery & Psychiatry. 66(4). 554a–554a. 6 indexed citations

19.

Parton, M., Daisy Walter, D. A. Ritchie, & Louis Luke. (1998). Case report: Fracture of an ossified achilles tendon—MR appearances. Clinical Radiology. 53(7). 538–540. 12 indexed citations

20.

Parton, M., et al.. (1997). Four cases of aggressive MRSA wound infection following head and neck surgery. The Journal of Laryngology & Otology. 111(9). 874–876. 16 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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