S Malcolm

4.1k total citations · 1 hit paper
51 papers, 3.0k citations indexed

About

S Malcolm is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, S Malcolm has authored 51 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 25 papers in Genetics and 6 papers in Genetics. Recurrent topics in S Malcolm's work include Cleft Lip and Palate Research (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Craniofacial Disorders and Treatments (6 papers). S Malcolm is often cited by papers focused on Cleft Lip and Palate Research (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Craniofacial Disorders and Treatments (6 papers). S Malcolm collaborates with scholars based in United Kingdom, United States and India. S Malcolm's co-authors include R M Winter, Natalie J. Prescott, Robin M. Winter, Terence H. Rabbitts, Richard Hayward, David J. David, Paul Rutland, Andrew O.M. Wilkie, Michael Oldridge and William Reardon and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

S Malcolm

51 papers receiving 2.8k citations

Hit Papers

Apert syndrome results from localized mutations of FGFR2 ... 1995 2026 2005 2015 1995 200 400 600
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.

  1. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
    1995 666 citations Andrew O.M. Wilkie, Sarah F. Slaney et al. Nature Genetics profile →

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 29 1.8k 1.7k 394 290 290 51 3.0k
Dvorah Abeliovich Israel 31 1.4k 0.8× 1.5k 0.9× 450 1.1× 158 0.5× 186 0.6× 98 3.0k
S Malcolm United Kingdom 31 1.1k 0.6× 1.2k 0.7× 248 0.6× 210 0.7× 164 0.6× 71 2.3k
Sue Malcolm United Kingdom 33 2.3k 1.3× 2.6k 1.6× 439 1.1× 195 0.7× 416 1.4× 62 4.4k
Keiko Wakui Japan 28 1.4k 0.8× 1.3k 0.8× 283 0.7× 115 0.4× 92 0.3× 89 2.3k
Eva Klopocki Germany 34 1.5k 0.8× 2.3k 1.3× 408 1.0× 157 0.5× 66 0.2× 103 3.7k
E Seemanová Czechia 30 1.1k 0.6× 2.4k 1.4× 202 0.5× 133 0.5× 57 0.2× 92 3.4k
Lingqian Wu China 24 865 0.5× 1.2k 0.7× 619 1.6× 170 0.6× 71 0.2× 186 2.4k
Mohnish Suri United Kingdom 24 736 0.4× 1.2k 0.7× 180 0.5× 94 0.3× 158 0.5× 82 2.2k
Alan Shanske United States 26 931 0.5× 976 0.6× 310 0.8× 100 0.3× 133 0.5× 84 1.9k
Paul Rutland United Kingdom 23 2.1k 1.2× 1.9k 1.1× 139 0.4× 122 0.4× 155 0.5× 40 3.4k

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.
Prescott, Natalie J., R M Winter, & S Malcolm. (2001). Nonsyndromic cleft lip and palate: Complex genetics and environmental effects. Annals of Human Genetics. 65(6). 505–515. 47 indexed citations
2.
Prescott, Natalie J., Melissa Lees, R M Winter, & S Malcolm. (2000). Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs. Human Genetics. 106(3). 345–350. 112 indexed citations
3.
Marques, Wilson, P. K. Thomas, Mary B. Davis, & S Malcolm. (1996). Phenotypic manifestations of chromosome 17 p112 duplication. Journal of Neurology. 243. 20. 1 indexed citations
4.
Bitner‐Glindzicz, Maria, Peter D. Turnpenny, Pia Höglund, et al.. (1995). Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3. Human Molecular Genetics. 4(8). 1467–1469. 58 indexed citations
5.
Armour, John A.L., Moira Crosier, S Malcolm, Juliana C.N. Chan, & A.J. Jeffreys. (1995). Human minisatellite loci composed of interspersed GGA-GGT triplet repeats. Proceedings of the Royal Society B Biological Sciences. 261(1362). 345–349. 4 indexed citations
6.
Malcolm, S, et al.. (1995). Purification of Recombinant Human Rhinovirus 14 3C Protease Expressed in Escherichia coli. Protein Expression and Purification. 6(5). 609–618. 28 indexed citations
7.
Wilkie, Andrew O.M., Sarah F. Slaney, Michael Oldridge, et al.. (1995). Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genetics. 9(2). 165–172. 666 indexed citations breakdown →
8.
Buxton, Jessica L., et al.. (1994). Angelman syndrome associated with a maternal 15q11–13 deletion of less than 200 kb. Human Molecular Genetics. 3(8). 1409–1413. 17 indexed citations
9.
Davies, Joanna P., Helen Christomanou, Bryan Winchester, & S Malcolm. (1994). Detection of 8 new mutations in the α-galactosidase A gene in Fabry disease. Human Molecular Genetics. 3(4). 667–669. 28 indexed citations
10.
Malcolm, S & Tim Donlon. (1994). Report of the, Second International Workshop on Human Chromosome 15 Mapping 1994. Cytogenetic and Genome Research. 67(1). 1–22. 34 indexed citations
11.
Huber, I, Yvette J.M. de Kok, Silvère M. van der Maarel, et al.. (1994). X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions. Human Molecular Genetics. 3(7). 1151–1154. 28 indexed citations
12.
Clayton‐Smith, Jill, T. Webb, S. Robb, et al.. (1992). Further evidence for dominant inheritance at the chromosome 15q11‐13 locus in familial angelman syndrome. American Journal of Medical Genetics. 44(2). 256–260. 29 indexed citations
13.
Winchester, Bryan, Elisabeth Young, Jane A. Hurst, et al.. (1992). Female twin with hunter disease due to nonrandom inactivation of the X‐chromosome: A consequence of twinning. American Journal of Medical Genetics. 44(6). 834–838. 44 indexed citations
14.
Malcolm, S, Jill Clayton‐Smith, M. Nichols, et al.. (1991). Uniparental paternal disomy in Angelman's syndrome. The Lancet. 337(8743). 694–697. 252 indexed citations
15.
Malcolm, S, et al.. (1990). An additional Nsil RFLP at the X-linked chronic granulomatous disease (CYBB) locus. Nucleic Acids Research. 18(23). 7199–7199. 4 indexed citations
16.
17.
18.
Raine, June, M. E. Robertson, S Malcolm, Hilary Hoey, & David Grant. (1989). Absence of Y specific DNA sequences in two siblings with 46XX hermaphroditism.. Archives of Disease in Childhood. 64(8). 1185–1187. 8 indexed citations
19.
Middleton‐Price, Helen, Nigel K. Spurr, A Hall, & S Malcolm. (1988). N‐ras‐like sequences on chromosomes 9, 6 and 22 with a polymorphism at the chromosome 9 locus. Annals of Human Genetics. 52(3). 189–195. 6 indexed citations
20.
Waldron, Clive, E. Murphy, Jean L. Roberts, et al.. (1985). Resistance to hygromycin B. Plant Molecular Biology. 5(2). 103–108. 139 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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