M. P. Champion

1.1k total citations
17 papers, 728 citations indexed

About

M. P. Champion is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, M. P. Champion has authored 17 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 6 papers in Rheumatology. Recurrent topics in M. P. Champion's work include Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). M. P. Champion is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). M. P. Champion collaborates with scholars based in United Kingdom, Germany and Netherlands. M. P. Champion's co-authors include Georg F. Hoffmann, Johannes Zschocke, Anil Dhawan, Peter Scambler, Philippa B. Mills, Irene Scheimberg, Robert Surtees, Clare Beesley, Neil Dalton and A. Briddon and has published in prestigious journals such as Human Molecular Genetics, American Journal of Transplantation and British Journal of Anaesthesia.

In The Last Decade

M. P. Champion

17 papers receiving 711 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. P. Champion United Kingdom 14 317 299 132 109 107 17 728
Ann Bowron United Kingdom 13 303 1.0× 424 1.4× 219 1.7× 255 2.3× 69 0.6× 29 997
Arianna Maiorana Italy 17 130 0.4× 226 0.8× 123 0.9× 89 0.8× 51 0.5× 52 839
Karine Mention France 18 280 0.9× 263 0.9× 200 1.5× 154 1.4× 76 0.7× 43 885
Leyla Tümer Türkiye 15 149 0.5× 218 0.7× 74 0.6× 121 1.1× 35 0.3× 84 663
Hiroki‎ Yoshimatsu Japan 13 151 0.5× 143 0.5× 136 1.0× 119 1.1× 66 0.6× 31 549
Mohamed A. Nada United States 11 409 1.3× 424 1.4× 74 0.6× 31 0.3× 47 0.4× 30 636
Catrina Colomé Spain 13 206 0.6× 265 0.9× 54 0.4× 188 1.7× 62 0.6× 19 564
Lance H. Rodan United States 17 144 0.5× 285 1.0× 32 0.2× 64 0.6× 58 0.5× 48 763
F. A. M. Baumeister Germany 11 225 0.7× 203 0.7× 54 0.4× 45 0.4× 76 0.7× 27 528
José Antonio Arranz Spain 13 206 0.6× 208 0.7× 94 0.7× 44 0.4× 66 0.6× 29 578

Countries citing papers authored by M. P. Champion

Since Specialization
Citations

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

Fields of papers citing papers by M. P. Champion

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. P. Champion

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

All Works

17 of 17 papers shown
1.
Bhattacharya, Kaustuv, Helen Mundy, M. Lilburn, et al.. (2015). A pilot longitudinal study of the use of waxy maize heat modified starch in the treatment of adults with glycogen storage disease type I: a randomized double-blind cross-over study. Orphanet Journal of Rare Diseases. 10(1). 18–18. 18 indexed citations
2.
Wortmann, Saskia B., M. P. Champion, Lambert van den Heuvel, et al.. (2012). Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?. European Journal of Medical Genetics. 55(10). 552–556. 25 indexed citations
3.
Lashkari, Harsha Prasada, Donna Lancaster, Ayad Atra, M. P. Champion, & Mary Taj. (2011). Symptomatic severe hypertriglyceridaemia with asparaginase therapy in acute lymphoblastic leukaemia (ALL) and lymphoblastic lymphoma: is rechallenging safe?. International Journal of Hematology. 94(6). 571–575. 9 indexed citations
4.
Jungbluth, Heinz, Keith Pohl, Ata Siddiqui, et al.. (2010). Adenylosuccinate Lyase Deficiency in the United Kingdom Pediatric Population: First Three Cases. Pediatric Neurology. 43(5). 351–354. 19 indexed citations
5.
Hernández, Mónica, Reiner Schulz, Tracy Chaplin, et al.. (2010). The diagnosis of inherited metabolic diseases by microarray gene expression profiling. Orphanet Journal of Rare Diseases. 5(1). 34–34. 3 indexed citations
6.
Sinha, Manish D., et al.. (2009). Congenital disorders of glycosylation: a rare cause of nephrotic syndrome. Nephrology Dialysis Transplantation. 24(8). 2591–2594. 6 indexed citations
7.
Footitt, Emma, et al.. (2008). Mitochondrial disorders and general anaesthesia: a case series and review. British Journal of Anaesthesia. 100(4). 436–441. 64 indexed citations
8.
Puppi, Juliana, Ragai R. Mitry, Robin D. Hughes, et al.. (2008). Hepatocyte Transplantation Followed by Auxiliary Liver Transplantation—a Novel Treatment for Ornithine Transcarbamylase Deficiency. American Journal of Transplantation. 8(2). 452–457. 77 indexed citations
9.
Dlamini, Nomazulu, Wajanat Jan, Fiona Norwood, et al.. (2008). Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease). Neuromuscular Disorders. 18(5). 408–409. 21 indexed citations
10.
Hardelid, Pia, Mario Cortina‐Borja, Alastair Munro, et al.. (2007). The Birth Prevalence of PKU in Populations of European, South Asian and Sub‐Saharan African Ancestry Living in South East England. Annals of Human Genetics. 72(1). 65–71. 40 indexed citations
11.
Beauchamp, Nicholas, Joanna Taybert, M. P. Champion, et al.. (2007). High frequency of missense mutations in glycogen storage disease type VI. Journal of Inherited Metabolic Disease. 30(5). 722–734. 31 indexed citations
12.
Salomons, Gajja S., C. Jakobs, Lorna Pope, et al.. (2006). Clinical, enzymatic and molecular characterization of nine new patients with malonyl‐coenzyme A decarboxylase deficiency. Journal of Inherited Metabolic Disease. 30(1). 23–28. 34 indexed citations
13.
Mills, Philippa B., Robert Surtees, M. P. Champion, et al.. (2005). Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5′-phosphate oxidase. Human Molecular Genetics. 14(8). 1077–1086. 211 indexed citations
14.
Grünewald, Susanne, M. P. Champion, J V Leonard, Jutta Schaper, & A. A. M. Morris. (2004). Biotinidase Deficiency: a Treatable Leukoencephalopathy. Neuropediatrics. 35(4). 211–216. 26 indexed citations
15.
Grünewald, Susanne, Lynette D. Fairbanks, Treena Cranston, et al.. (2004). How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?. Journal of Inherited Metabolic Disease. 27(2). 179–186. 15 indexed citations
16.
Hatherill, Mark, Tina Sajjanhar, SM Tibby, et al.. (1997). Serum lactate as a predictor of mortality after paediatric cardiac surgery. Archives of Disease in Childhood. 77(3). 235–238. 95 indexed citations
17.
Cook, David I., Margot L. Day, M. P. Champion, & J. A. Young. (1988). Ca2+ not cyclic AMP mediates the fluid secretory response to isoproterenol in the rat mandibular salivary gland: Whole-cell patch-clamp studies. Pflügers Archiv - European Journal of Physiology. 413(1). 67–76. 34 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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