Duncan J. Shaw

7.5k total citations · 1 hit paper
78 papers, 3.7k citations indexed

About

Duncan J. Shaw is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Duncan J. Shaw has authored 78 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 22 papers in Cellular and Molecular Neuroscience and 19 papers in Genetics. Recurrent topics in Duncan J. Shaw's work include Genetic Neurodegenerative Diseases (22 papers), Antifungal resistance and susceptibility (10 papers) and Mitochondrial Function and Pathology (8 papers). Duncan J. Shaw is often cited by papers focused on Genetic Neurodegenerative Diseases (22 papers), Antifungal resistance and susceptibility (10 papers) and Mitochondrial Function and Pathology (8 papers). Duncan J. Shaw collaborates with scholars based in United Kingdom, United States and Netherlands. Duncan J. Shaw's co-authors include Peter S. Harper, John R. Guest, J. David Brook, H G Harley, Iain Fenton, Neil A. R. Gow, William Reardon, Frank C. Odds, Russell G. Snell and Martin Maiden and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Duncan J. Shaw

75 papers receiving 3.5k 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.

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1993 558 citations Russell G. Snell, John MacMillan et al. Nature Genetics profile →

Peers

Duncan J. Shaw

CMN

GENET

NEURO

Michael A. Innis United States

Sylvia Krobitsch Germany

Ayako Nakamura Japan

Do Hee Lee South Korea

Penelope J. Duerksen-Hughes United States

Ayako Yamamoto Japan

Rory A. Fisher United States

Haiying Li China

Rakesh K. Mishra India

Germán Soler Spain

Michael A. Innis United States

Duncan J. Shaw

3.6k ×1.6

244 ×0.2

CMN

605 ×0.8

GENET

490 ×0.7

NEURO

112 ×0.2

Citations per year, relative to Duncan J. Shaw Duncan J. Shaw (= 1×) peers Michael A. Innis

Countries citing papers authored by Duncan J. Shaw

Since Specialization

Citations

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

Fields of papers citing papers by Duncan J. Shaw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Duncan J. Shaw

This figure shows the co-authorship network connecting the top 25 collaborators of Duncan J. Shaw. A scholar is included among the top collaborators of Duncan J. Shaw 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 Duncan J. Shaw. Duncan J. Shaw 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

Mathur, Aditi, et al.. (2009). No association between the PPARG gene and schizophrenia in a British population. Prostaglandins Leukotrienes and Essential Fatty Acids. 81(4). 273–277. 7 indexed citations

Jacobsen, Mette D., Amanda D. Davidson, Shuying Li, et al.. (2008). Molecular phylogenetic analysis of Candida tropicalis isolates by multi-locus sequence typing. Fungal Genetics and Biology. 45(6). 1040–1042. 18 indexed citations

Jacobsen, Mette D., et al.. (2008). Mitochondrial haplotypes and recombination in Candida albicans. Medical Mycology. 46(7). 647–654. 14 indexed citations

Takakura, Shunji, Satoshi Ichiyama, Judith M. Bain, et al.. (2008). Comparison of Candida albicans strain types among isolates from three countries. International Journal of Medical Microbiology. 298(7-8). 663–668. 21 indexed citations

Jacobsen, Mette D., Judith M. Bain, Elizabeth M. Johnson, et al.. (2008). MixedCandida albicansstrain populations in colonized and infected mucosal tissues. FEMS Yeast Research. 8(8). 1334–1338. 27 indexed citations

Lange, Robert P.J. de, Karen Burr, James S. Clark, et al.. (2001). Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of stroke. Neurogenetics. 3(2). 99–106. 3 indexed citations

Li, Tao, Gerome Breen, Janine L. Brown, et al.. (1999). No evidence of linkage disequilibrium between a CAG repeat in the SCA1 gene and schizophrenia in Caucasian and Chinese schizophrenic subjects. Psychiatric Genetics. 9(3). 123–128. 2 indexed citations

Price, Stacey, Henrik Fox, David St Clair, & Duncan J. Shaw. (1997). Lack of association between schizophrenia and a polymorphism close to the cytosolic phospholipase A2 gene. Psychiatric Genetics. 7(3). 111–114. 27 indexed citations

Shaw, Duncan J.. (1995). Molecular genetics of human inherited disease. 1 indexed citations

10.

Upadhyaya, Meena, Duncan J. Shaw, & Peter S. Harper. (1994). Molecular basis of neurofibromatosis type 1 (NF1): Mutation analysis and polymorphisms in the NF1 gene. Human Mutation. 4(2). 83–101. 60 indexed citations

11.

Snell, Russell G., John MacMillan, Jeremy P. Cheadle, et al.. (1993). Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nature Genetics. 4(4). 393–397. 558 indexed citations breakdown →

12.

Crow, Steve, H G Harley, J. David Brook, S.A. Rundle, & Duncan J. Shaw. (1992). Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat. Human Molecular Genetics. 1(6). 451–451. 8 indexed citations

13.

Jansen, Gert, Pieter J. de Jong, Chris T. Amemiya, et al.. (1992). Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q. Genomics. 13(3). 509–517. 30 indexed citations

14.

Brook, J. David, Boris V. Zemelman, Michael J. Siciliano, et al.. (1992). Radiation-reduced hybrids for the myotonic dystrophy locus. Genomics. 13(2). 243–250. 16 indexed citations

15.

Harley, H G, K.V. Walsh, S.A. Rundle, et al.. (1991). Localisation of the myotonic dystrophy locus to 19q13.2?19q13.3 and its relationship to twelve polymorphic loci on 19q. Human Genetics. 87(1). 73–80. 26 indexed citations

16.

Snell, Russell G. & Duncan J. Shaw. (1991). A simple vacuum blotter design. Nucleic Acids Research. 19(21). 6054–6054. 1 indexed citations

17.

Brook, J. David, K.V. Walsh, H G Harley, S.A. Rundle, & Duncan J. Shaw. (1990). A polymorphic DNA clone which maps to 19q13.2 - 19qter (D19S62). Nucleic Acids Research. 18(4). 1086–1086. 5 indexed citations

18.

Upadhyaya, Meena, Alan Fryer, Duncan J. Shaw, et al.. (1990). A 90 kb DNA deletion associated with neurofibromatosis type 1.. Journal of Medical Genetics. 27(12). 738–741. 26 indexed citations

19.

Brook, J. David & Duncan J. Shaw. (1988). A polymorphic DNA clone which maps to 19p13.2 → 19q12 (D19S27). Nucleic Acids Research. 16(15). 7751–7751. 1 indexed citations

20.

Brook, J. David, Duncan J. Shaw, N S Thomas, et al.. (1986). Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids. Cytogenetic and Genome Research. 41(1). 30–37. 26 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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