M. J. Dronsfield

1.6k total citations · 1 hit paper
11 papers, 1.2k citations indexed

About

M. J. Dronsfield is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, M. J. Dronsfield has authored 11 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Surgery, 6 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in M. J. Dronsfield's work include Pancreatic function and diabetes (8 papers), Diabetes and associated disorders (3 papers) and Metabolism, Diabetes, and Cancer (3 papers). M. J. Dronsfield is often cited by papers focused on Pancreatic function and diabetes (8 papers), Diabetes and associated disorders (3 papers) and Metabolism, Diabetes, and Cancer (3 papers). M. J. Dronsfield collaborates with scholars based in United Kingdom, France and United States. M. J. Dronsfield's co-authors include Stephen C. Bain, Andrew T. Hattersley, Graeme I. Bell, Stephen Gough, Anthony Barnett, Marilyn E. Merriman, Anne Cambon‐Thomsen, Elizabeth E. Powell, Kjersti S. Rønningen and Jørn Nerup and has published in prestigious journals such as Nature Genetics, Diabetes and Diabetologia.

In The Last Decade

M. J. Dronsfield

11 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1995 583 citations S. T. Bennett, Anneke Lucassen et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. J. Dronsfield United Kingdom	10	865	796	471	434	88	11	1.2k
Annette Møldrup Denmark	18	507 0.6×	834 1.0×	561 1.2×	766 1.8×	69 0.8×	24	1.3k
Manju Surana United States	14	370 0.4×	664 0.8×	521 1.1×	278 0.6×	38 0.4×	16	1.0k
Hirofumi Takino Japan	18	504 0.6×	411 0.5×	201 0.4×	415 1.0×	203 2.3×	46	1000
Lise Bjørkhaug Norway	20	830 1.0×	1.2k 1.5×	708 1.5×	550 1.3×	20 0.2×	37	1.5k
Kerstin Kirchhoff Germany	13	459 0.5×	296 0.4×	369 0.8×	235 0.5×	91 1.0×	14	1.0k
Aurélie Dechaume France	16	614 0.7×	638 0.8×	465 1.0×	382 0.9×	24 0.3×	25	1.1k
Isabelle Avril Switzerland	8	629 0.7×	960 1.2×	444 0.9×	572 1.3×	28 0.3×	11	1.3k
Ong Moua United States	7	845 1.0×	690 0.9×	181 0.4×	581 1.3×	187 2.1×	11	1.2k
Hisako Ohgawara Japan	16	406 0.5×	629 0.8×	280 0.6×	344 0.8×	13 0.1×	54	832
F. Schuit Belgium	12	496 0.6×	737 0.9×	264 0.6×	541 1.2×	92 1.0×	13	939

Countries citing papers authored by M. J. Dronsfield

Since Specialization

Citations

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

Fields of papers citing papers by M. J. Dronsfield

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. J. Dronsfield

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

All Works

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11 of 11 papers shown

Ellard, Sian, M. Bulman, Timothy M. Frayling, et al.. (1999). Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the young.. Diabetes. 48(4). 921–923. 29 indexed citations

Chowdhury, T A, Philip Dyer, Sudhesh Kumar, et al.. (1997). Lack of association of angiotensin II type 1 receptor gene polymorphism with diabetic nephropathy in insulin-dependent diabetes mellitus. Diabetic Medicine. 14(10). 837–840. 24 indexed citations

Smith, Paul, M. J. Dronsfield, C. Mijovic, et al.. (1997). The mitochondrial tRNALeu(UUR) A to G 3243 mutation is associated with insulin-dependent and non-insulin-dependent diabetes in a Chinese population. Diabetic Medicine. 14(12). 1026–1031. 15 indexed citations

Bulman, M., M. J. Dronsfield, Timothy M. Frayling, et al.. (1997). A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young. Diabetologia. 40(7). 859–862. 40 indexed citations

Frayling, Timothy M., et al.. (1997). Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K. Diabetes. 46(4). 720–725. 35 indexed citations

Frayling, Timothy M., Michael Bulman, Sian Ellard, et al.. (1997). Mutations in the Hepatocyte Nuclear Factor–1α Gene Are a Common Cause of Maturity-Onset Diabetes of the Young in the U.K.. Diabetes. 46(4). 720–725. 192 indexed citations

Byrne, M. M., Jeppe Sturis, Stephan Menzel, et al.. (1996). Altered Insulin Secretory Responses to Glucose in Diabetic and Nondiabetic Subjects With Mutations in the Diabetes Susceptibility Gene MODY3 on Chromosome 12. Diabetes. 45(11). 1503–1510. 188 indexed citations

Byrne, M. M., Jeppe Sturis, Stephan Menzel, et al.. (1996). Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12. Diabetes. 45(11). 1503–1510. 58 indexed citations

Bennett, S. T., Anneke Lucassen, Stephen Gough, et al.. (1995). Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus. Nature Genetics. 9(3). 284–292. 583 indexed citations breakdown →

10.

Bennett, Simon T., Anneke Lucassen, Stephen Gough, et al.. (1995). Reply to “Insulin expression: is VNTR allele 698 really anomalous?”. Nature Genetics. 10(4). 379–380. 6 indexed citations

11.

Dronsfield, M. J., et al.. (1991). Experimental allergic encephalomyelitis and corticosterone studies in resistant and susceptible rat strains. Clinical Immunology and Immunopathology. 61(1). 29–40. 25 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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