S Malcolm

3.1k total citations
71 papers, 2.3k citations indexed

About

S Malcolm is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, S Malcolm has authored 71 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 30 papers in Genetics and 9 papers in Genetics. Recurrent topics in S Malcolm's work include Genomic variations and chromosomal abnormalities (11 papers), Craniofacial Disorders and Treatments (10 papers) and Genetic Syndromes and Imprinting (9 papers). S Malcolm is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Craniofacial Disorders and Treatments (10 papers) and Genetic Syndromes and Imprinting (9 papers). S Malcolm collaborates with scholars based in United Kingdom, India and Greece. S Malcolm's co-authors include Marcus Pembrey, William Reardon, Paul Rutland, R M Winter, Jess Tyson, R J Levinsky, Maria Bitner‐Glindzicz, Louise J. Pulleyn, Helen Middleton‐Price and Jill Clayton‐Smith and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

S Malcolm

69 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S Malcolm United Kingdom 31 1.2k 1.1k 258 248 247 71 2.3k
Mohnish Suri United Kingdom 24 1.2k 1.0× 736 0.6× 222 0.9× 180 0.7× 131 0.5× 82 2.2k
Hans G. Dauwerse Netherlands 25 2.1k 1.8× 1.2k 1.1× 520 2.0× 147 0.6× 161 0.7× 43 3.5k
Brith Otterud United States 23 865 0.7× 421 0.4× 519 2.0× 61 0.2× 231 0.9× 41 2.1k
Renaud Touraine France 25 1.1k 1.0× 633 0.6× 108 0.4× 120 0.5× 97 0.4× 93 2.0k
Jaakko Leisti Finland 27 1.1k 1.0× 873 0.8× 338 1.3× 267 1.1× 51 0.2× 82 2.1k
Tatsuya Kishino Japan 27 2.4k 2.0× 1.9k 1.7× 164 0.6× 572 2.3× 318 1.3× 64 3.3k
Arnold Munnich France 25 1.9k 1.7× 724 0.6× 254 1.0× 109 0.4× 272 1.1× 54 3.2k
Valérie Delague France 28 1.7k 1.5× 647 0.6× 435 1.7× 72 0.3× 344 1.4× 91 2.6k
Giorgio Bernardi France 11 1.3k 1.1× 767 0.7× 130 0.5× 81 0.3× 103 0.4× 11 2.1k
Jeff Mann United States 20 1.5k 1.3× 917 0.8× 268 1.0× 433 1.7× 227 0.9× 28 2.2k

Countries citing papers authored by S Malcolm

Since Specialization
Citations

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

Fields of papers citing papers by S Malcolm

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S Malcolm

This figure shows the co-authorship network connecting the top 25 collaborators of S Malcolm. A scholar is included among the top collaborators of S Malcolm 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 S Malcolm. S Malcolm 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.
Jenkins, Dagan, Maria Bitner‐Glindzicz, S Malcolm, et al.. (2006). Mutation analyses of Uroplakin II in children with renal tract malformations. Nephrology Dialysis Transplantation. 21(12). 3415–3421. 21 indexed citations
2.
Blaydon, Diana C., et al.. (2003). The contribution of USH1C mutations to syndromic and non‐syndromic deafness in the UK. Clinical Genetics. 63(4). 303–307. 14 indexed citations
3.
Kelberman, Daniel, et al.. (2000). Mapping of a locus for autosomal dominant Hemifacial Microsomia. UCL Discovery (University College London). 1 indexed citations
4.
Tyson, Jess, Lisbeth Tranebjærg, S. Bellman, et al.. (1997). IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome. Human Molecular Genetics. 6(12). 2179–2185. 233 indexed citations
5.
Chan, Christopher T., Tristan R. McKay, S Cottrell, et al.. (1997). Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.. Journal of Medical Genetics. 34(8). 651–655. 5 indexed citations
6.
Wilkes, David, Paul Rutland, Louise J. Pulleyn, et al.. (1996). A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.. Journal of Medical Genetics. 33(9). 744–748. 72 indexed citations
7.
Merkx, Gerard, Silvère M. van der Maarel, I Huber, et al.. (1995). A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene. Human Molecular Genetics. 4(11). 2145–2150. 60 indexed citations
8.
Harding, Brian, David Ellis, & S Malcolm. (1995). A case of PelizaeusMerzbacher disease showing increased dosage of the proteolipid protein gene. Neuropathology and Applied Neurobiology. 21(2). 111–115. 31 indexed citations
9.
Herwerden, Lynne van, C S Rose, William Reardon, et al.. (1994). Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q.. PubMed. 54(4). 669–74. 29 indexed citations
10.
Chan, Christopher T., Jill Clayton‐Smith, Xingbo Cheng, et al.. (1993). Molecular mechanisms in Angelman syndrome: a survey of 93 patients.. Journal of Medical Genetics. 30(11). 895–902. 66 indexed citations
11.
Gregory, Robert A., P. K. Thomas, R. H. M. King, et al.. (1993). Coexistence of hereditary motor and sensory neuropathy type IA and IGM paraproteinemic neuropathy. Annals of Neurology. 33(6). 649–652. 24 indexed citations
12.
Robinson, Wendy P., Fosco Bernasconi, Apiwat Mutirangura, et al.. (1993). Nondisjunction of chromosome 15: origin and recombination. PubMed. 53(3). 740–51. 92 indexed citations
13.
Reardon, William, et al.. (1992). Carrier detection for X-linked agammaglobulinaemia (Bruton type) in an Irish family using linked DNA probes.. PubMed. 84(4). 116–8. 1 indexed citations
14.
Strautnieks, Sandra, Paul Rutland, R M Winter, M Baraitser, & S Malcolm. (1992). Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosis.. PubMed. 51(4). 871–8. 34 indexed citations
15.
Feighery, Conleth, Adam Finn, C. McKeown, et al.. (1992). Mapping of the x-linked form of hyper-IgM syndrome (HIGM1) to Xq26 by close linkage to HPRT. Genomics. 14(2). 551–553. 47 indexed citations
16.
Malcolm, S. (1992). Charcot-Marie-Tooth disease type 1.. Journal of Medical Genetics. 29(1). 3–4. 4 indexed citations
17.
Middleton‐Price, Helen, et al.. (1988). Regional chromosomal localisation of APOA2 to 1q21–1q23. Human Genetics. 79(3). 283–285. 20 indexed citations
18.
Hodgson, SV, M. E. Robertson, Claudine Fear, et al.. (1987). Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion. Human Genetics. 75(3). 286–290. 45 indexed citations
19.
Malcolm, S, Meryl A. Davis, & Terence H. Rabbitts. (1985). Breakage on chromosome 2 brings the Ck gene to a region 3’ of <i>c-myc</i> in a Burkitt’s lymphoma line carrying a (2;8) translocation. Cytogenetic and Genome Research. 39(3). 168–172. 5 indexed citations
20.
Malcolm, S, et al.. (1979). Use of chromosomal translocations with in situ DNA hybridisation to confirm localisation of human 5S ribosomal RNA genes.. Journal of Medical Genetics. 16(4). 246–253. 8 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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