M Town

1.0k total citations
15 papers, 806 citations indexed

About

M Town is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, M Town has authored 15 papers receiving a total of 806 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 5 papers in Molecular Biology and 4 papers in Biomedical Engineering. Recurrent topics in M Town's work include Neonatal Health and Biochemistry (9 papers), Erythrocyte Function and Pathophysiology (3 papers) and Blood groups and transfusion (3 papers). M Town is often cited by papers focused on Neonatal Health and Biochemistry (9 papers), Erythrocyte Function and Pathophysiology (3 papers) and Blood groups and transfusion (3 papers). M Town collaborates with scholars based in United Kingdom, Belgium and Italy. M Town's co-authors include Lucio Luzzatto, Tom Vulliamy, Valeria Poggi, Nicholas S. Foulkes, Viola Calabrò, Julia F. Markusen, Michele D’Urso, Mario Pablo Estrada, G. Battistuzzi and Roberta Giordano and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Biochemical Journal.

In The Last Decade

M Town

15 papers receiving 766 citations

Peers

Countries citing papers authored by M Town

Since Specialization

Citations

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

Fields of papers citing papers by M Town

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Town

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Creating Spaces for Decolonization and Indigenization Among Mental Health Professionals in Higher Education 2023 ·Smith College Studies in Social Work ·Laurie D. McCubbin, M Town, (unknown), (unknown)	3
2	Impact of aeration strategies on fed-batch cell culture kinetics in a single-use 24-well miniature bioreactor 2013 ·Biochemical Engineering Journal ·(unknown), (unknown), (unknown), (unknown), M Town, Joachim Janda, Frank Baganz, Gary J. Lye	27
3	Behavior of Adult Human Mesenchymal Stem Cells Entrapped in Alginate-GRGDY Beads 2006 ·Tissue Engineering ·Julia F. Markusen, Christopher Mason, (unknown), M Town, Alethea B. Tabor, Mark O. Clements, C. Boshoff, (unknown)	68
4	The potential of optical coherence tomography in the engineering of living tissue 2004 ·Physics in Medicine and Biology ·Chris Mason, Julia F. Markusen, M Town, P. Dunnill, Ruikang K. Wang	51
5	Doppler optical coherence tomography for measuring flow in engineered tissue 2004 ·Biosensors and Bioelectronics ·Christopher E. Mason, Julia F. Markusen, M Town, P. Dunnill, Ruikang K. Wang	30
6	Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin 1999 ·Human Molecular Genetics ·Marlene Attard, G Jean, Lionel Forestier, Stéphanie Cherqui, William van’t Hoff, M. Broyer, Corinne Antignac, M Town	100
7	Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu archipelago (southwestern Pacific). 1995 ·Europe PMC (PubMed Central) ·Mary Ganczakowski, M Town, D. K. Bowden, Tom Vulliamy, Akira Kaneko, J. B. Clegg, D. J. Weatherall, Lucio Luzzatto	72
8	New glucose-6-phosphate dehydrogenase mutations associated with chronic anemia 1995 ·Blood ·(unknown), (unknown), D. Macdonald, Cristiano Lanza, (unknown), M Town, (unknown), (unknown), (unknown), Saad Al‐Ismail	36
9	Molecular heterogeneity underlying the G6PD Mediterranean phenotype 1992 ·Human Genetics ·(unknown), Viola Calabrò, (unknown), M Town, (unknown), Tom Vulliamy, Philip J. Mason, Lucio Luzzatto	38
10	Linkage disequilibrium of polymorphic sites in the G6PD gene in African populations and the origin of G6PD A-. 1992 ·PubMed ·(unknown), Ahmad Sofiman Othman, M Town, Amit Nathwani, (unknown), Lucio Luzzatto	5
11	Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-. 1991 ·Proceedings of the National Academy of Sciences ·Tom Vulliamy, (unknown), M Town, Amit Nathwani, Adeyinka G. Falusi, Philip J. Mason, Lucio Luzzatto	67
12	Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-). 1990 ·BMJ ·S. Galiano, Gian Franco Gaetani, (unknown), (unknown), (unknown), M Town, Lucio Luzzatto	26
13	Intragenic interspecific complementation of glucose 6-phosphate dehydrogenase in human-hamster cell hybrids 1990 ·Somatic Cell and Molecular Genetics ·M Town, (unknown), Lucio Luzzatto	6
14	Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA 1990 ·Biochemical Journal ·Valeria Poggi, M Town, Nicholas S. Foulkes, Lucio Luzzatto	76
15	Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia. 1988 ·Proceedings of the National Academy of Sciences ·Tom Vulliamy, Michele D’Urso, G. Battistuzzi, Mario Pablo Estrada, Nicholas S. Foulkes, G. Martini, Viola Calabrò, Valeria Poggi, Roberta Giordano, M Town	201

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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