M. Leversha

3.6k total citations
23 papers, 732 citations indexed

About

M. Leversha is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, M. Leversha has authored 23 papers receiving a total of 732 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in M. Leversha's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). M. Leversha is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). M. Leversha collaborates with scholars based in United Kingdom, Australia and United States. M. Leversha's co-authors include M.A. Ferguson‐Smith, Lucille Voullaire, Alistair Reid, Anthony J. Bench, Nick Telford, Juan Chang, Elisabeth P. Nacheva, Anthony R. Green, Kim Champion and Brian J.P. Huntly and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Blood.

In The Last Decade

M. Leversha

22 papers receiving 718 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. Leversha United Kingdom 11 330 330 201 192 164 23 732
Elisena Morizio Italy 20 410 1.2× 396 1.2× 140 0.7× 116 0.6× 96 0.6× 53 907
G.C. Beverstock Netherlands 14 318 1.0× 259 0.8× 198 1.0× 96 0.5× 67 0.4× 30 634
Marie‐France Portnoï France 19 446 1.4× 574 1.7× 105 0.5× 100 0.5× 119 0.7× 29 908
M. C. Hors‐Cayla France 21 603 1.8× 645 2.0× 88 0.4× 67 0.3× 73 0.4× 43 1.1k
James Tepperberg United States 15 362 1.1× 532 1.6× 86 0.4× 67 0.3× 149 0.9× 28 889
Barbara K. Hecht United States 14 334 1.0× 323 1.0× 68 0.3× 61 0.3× 67 0.4× 23 693
T. W. J. Hustinx Netherlands 14 328 1.0× 209 0.6× 169 0.8× 64 0.3× 56 0.3× 21 615
R. A. Pfeiffer Germany 20 467 1.4× 569 1.7× 53 0.3× 70 0.4× 212 1.3× 62 1.0k
Marie Trková Czechia 13 272 0.8× 145 0.4× 97 0.5× 110 0.6× 23 0.1× 33 589
Kevin Clark United Kingdom 11 913 2.8× 781 2.4× 96 0.5× 145 0.8× 128 0.8× 16 1.3k

Countries citing papers authored by M. Leversha

Since Specialization
Citations

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

Fields of papers citing papers by M. Leversha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of M. Leversha. A scholar is included among the top collaborators of M. Leversha 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. Leversha. M. Leversha 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.
Danila, Daniel C., Aseem Anand, Clifford C. Sung, et al.. (2010). Molecular profiling of circulating tumor cells (CTC) in patients with castrate metastatic prostate cancer (CMPC) receiving abiraterone acetate (AA) after failure of docetaxel-based chemotherapy.. Journal of Clinical Oncology. 28(15_suppl). 4635–4635. 2 indexed citations
2.
Fleisher, Martin, Daniel C. Danila, M. Leversha, et al.. (2009). Circulating tumor cells (CTC) in patients with metastatic castration-resistant prostate cancer (CRPC) receiving abiraterone acetate (AA) after failure of docetaxel-based chemotherapy. Journal of Clinical Oncology. 27(15_suppl). 5049–5049. 2 indexed citations
3.
Shaw‐Smith, Charles, Alison J. Coffey, M. Leversha, et al.. (2000). Characterisation of a novel murine intestinal serine protease, DISP. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1490(1-2). 131–136. 9 indexed citations
4.
Sinclair, Paul, Elisabeth P. Nacheva, M. Leversha, et al.. (2000). Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia. Blood. 95(3). 738–743. 215 indexed citations
5.
Goedert, Michel, Junichi Hasegawa, Molly Craxton, M. Leversha, & S. Clegg. (1997). Assignment of the Human Stress-Activated Protein Kinase-3 Gene (SAPK3) to Chromosome 22q13.3 by Fluorescencein SituHybridization. Genomics. 41(3). 501–502. 8 indexed citations
6.
Collins, John, Charlotte G. Cole, Luc J Smink, et al.. (1995). A high-density YAC contig map of human chromosome 22.. PubMed. 377(6547 Suppl). 367–79. 77 indexed citations
7.
Woods, C. Geoffrey, M. Leversha, & John Rogers. (1995). Severe intrauterine growth retardation with increased mitomycin C sensitivity: a further chromosome breakage syndrome.. Journal of Medical Genetics. 32(4). 301–305. 14 indexed citations
8.
Sargent, Carole A., et al.. (1994). A rearrangement on Chromosome 5 of an expressed human ?-glucuronidase pseudogene. Mammalian Genome. 5(12). 791–796. 21 indexed citations
9.
Phipps, Maude E., Eamonn R. Maher, Nabeel A. Affara, et al.. (1993). Physical mapping of chromosome 3p25-p26 by flourescence in situ hybridisation (FISH). Human Genetics. 92(1). 18–22. 9 indexed citations
10.
Tzimagiorgis, Georgios, et al.. (1993). Structure and expression analysis of a member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10p11.2. Human Genetics. 91(5). 433–8. 7 indexed citations
11.
Bailey, David M., et al.. (1993). Coincidence painting: a rapid method for cloning region specific DNA sequences. Nucleic Acids Research. 21(22). 5117–5123. 3 indexed citations
12.
Furlong, R. A., Martin Yuille, David Goudie, et al.. (1992). A dinucleotide repeat polymorphism at the D9S127 locus. Nucleic Acids Research. 20(4). 925–925. 20 indexed citations
13.
Furlong, R. A., et al.. (1992). A dinucleotide repeat polymorphism at the D9S109 locus. Nucleic Acids Research. 20(4). 925–925. 14 indexed citations
14.
Ferguson‐Smith, M.A., et al.. (1992). Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.. Journal of Medical Genetics. 29(5). 299–307. 166 indexed citations
15.
Yuille, Martin, M. Leversha, David Goudie, Nabeel A. Affara, & M.A. Ferguson‐Smith. (1991). Microsatellite polymorphism at the D9S12 locus. Nucleic Acids Research. 19(18). 5097–5097. 6 indexed citations
16.
Earle, E. D., Miriam G. Wilson, Vida Petrovic, et al.. (1991). The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]. Human Genetics. 87(2). 173–176. 3 indexed citations
17.
Colley, Andrew, M. Leversha, Lucille Voullaire, & John Rogers. (1990). Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p 11.2 p 11.2) (Smith‐Magenis syndrome). Journal of Paediatrics and Child Health. 26(1). 17–21. 47 indexed citations
18.
Voullaire, Lucille, Graham C. Webb, & M. Leversha. (1989). Fragile X testing in a diagnostic cytogenetics laboratory.. Journal of Medical Genetics. 26(7). 439–442. 8 indexed citations
19.
Voullaire, Lucille, Graham C. Webb, & M. Leversha. (1987). Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23. Human Genetics. 76(2). 202–204. 24 indexed citations
20.
Pitt, David, et al.. (1981). Tetraploidy in a liveborn infant with spina bifida and other anomalies.. Journal of Medical Genetics. 18(4). 309–311. 45 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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