S Malcolm

4.1k citations

51 papers · 3.0k indexed · 1 hit paper · h-index 29

Impact in

Genetics top 1%
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in ⓘ

Genetics 25
- Cleft Lip and Palate Research 9
- Genomic variations and chromosomal abnormalities 7
- Craniofacial Disorders and Treatments 6
- Genetic Syndromes and Imprinting 5
Sensory Systems 3

Co-authors: R M Winter (8 shared papers)Natalie J. Prescott (3 shared papers)Robin M. Winter (2 shared papers)Terence H. Rabbitts (2 shared papers)William Reardon (2 shared papers)Paul Rutland (1 shared paper)Andrew O.M. Wilkie (1 shared paper)Louise J. Pulleyn (1 shared paper)
Journals: Human Molecular Genetics (4 papers)Journal of Medical Genetics (4 papers)Cytogenetic and Genome Research (3 papers)Annals of Human Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)
Partner nations: United Kingdom United States India

In The Last Decade

S Malcolm

51 papers receiving 2.8k citations

Hit Papers

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome 1995 · 666 citations

Peers

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-authors

The 25 scholars most cited alongside S Malcolm, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with S Malcolm Line = papers co-authored together S Malcolm links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome Nature Genetics ·Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge, Michael D. Poole, Geraldine J. Ashworth, Anthony D. Hockley, Richard Hayward, David J. David, Louise J. Pulleyn, Paul Rutland, S Malcolm, Robin M. Winter, William Reardon Hit paper breakdown →	1995	666
2	Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4 Science ·Yvette J.M. de Kok, Silvère M. van der Maarel, Maria Bitner‐Glindzicz, I Huber, Anthony P. Monaco, S Malcolm, Marcus Pembrey, Hans‐Hilger Ropers, Frans P.M. Cremers	1995	326
3	Uniparental paternal disomy in Angelman's syndrome The Lancet ·S Malcolm, Jill Clayton‐Smith, M. Nichols, M.E. Pembrey, John A.L. Armour, A.J. Jeffreys, S. Robb, T. Webb	1991	252
4	Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization. Proceedings of the National Academy of Sciences ·S Malcolm, Paul J.R. Barton, Clifton N. Murphy, M.A. Ferguson‐Smith, David L. Bentley, Terence H. Rabbitts	1982	181
5	Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. Proceedings of the National Academy of Sciences ·Shinji Saitoh, Karin Buiting, Peter K. Rogan, Jessica L. Buxton, Daniel J. Driscoll, J Arnemann, Rainer König, S Malcolm, B. Horsthemke, Robert D. Nicholls	1996	146
6	Resistance to hygromycin B Plant Molecular Biology ·Clive Waldron, E. Murphy, Jean L. Roberts, Gary Gustafson, Susan Armour, S Malcolm	1985	139
7	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 ·Natalie J. Prescott, Melissa Lees, R M Winter, S Malcolm	2000	112
8	Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. PubMed ·Jürgen M. Stein, John B. Mulliken, Samuel Stal, David L. Gasser, S Malcolm, Robin Winter, Susan H. Blanton, Christopher I. Amos, E Seemanová, Jacqueline T. Hecht	1995	87
9	Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate. Journal of Medical Genetics ·Susan Holder, G M Vintiner, Bernadette Farren, S Malcolm, R M Winter	1992	76
10	Chromosome translocation can occur on either side of the c-myc oncogene in Burkitt lymphoma cells Nature ·Mary B. Davis, S Malcolm, Terence H. Rabbitts	1984	76
11	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3 Human Molecular Genetics ·Maria Bitner‐Glindzicz, Peter D. Turnpenny, Pia Höglund, Helena Kääriäinen, Eeva‐Marja Sankila, Silvère M. van der Maarel, Yvette J.M. de Kok, Hans‐Hilger Ropers, Frans P.M. Cremers, Marcus Pembrey, S Malcolm	1995	58
12	Cellular and molecular studies on infant null acute lymphoblastic leukemia Blood ·F Katz, S Malcolm, Barbara Gibbons, Rita Tilly, Grace Lam, Robertson Me, Barbara Czepulkowski, Judith M. Chessells	1988	55
13	No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate. Journal of Medical Genetics ·G M Vintiner, Susan Holder, R M Winter, S Malcolm	1992	50
14	Nonsyndromic cleft lip and palate: complex genetics and environmental effects. PubMed ·Natalie J. Prescott, R M Winter, S Malcolm	2001	49
15	Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15 Clinical Genetics ·Wendy P. Robinson, Susan L. Christian, Brian D. Kuchinka, Maria S. Peñaherrera, Soma Das, Simone Schuffenhauer, S Malcolm, Albert Schinzel, Terry Hassold, David H. Ledbetter	2000	48
16	Nonsyndromic cleft lip and palate: Complex genetics and environmental effects Annals of Human Genetics ·Natalie J. Prescott, R M Winter, S Malcolm	2001	47
17	Female twin with hunter disease due to nonrandom inactivation of the X‐chromosome: A consequence of twinning American Journal of Medical Genetics ·Bryan Winchester, Elisabeth Young, Stella Geddes, Sally Genet, Jane A. Hurst, Helen Middelton‐Price, Nicola Williams, Michael R. Webb, Alex Habel, S Malcolm	1992	44
18	Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate. PubMed ·Hongshu Feng, Russell Sassani, Scott P. Bartlett, Alice Lee, Jacqueline T. Hecht, S Malcolm, Robin M. Winter, G M Vintiner, Kenneth H. Buetow, David L. Gasser	1994	43
19	Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies. Journal of Medical Genetics ·G M Vintiner, K.K. Lo, Susan Holder, R M Winter, S Malcolm	1993	42
20	Localization of the human α-globin gene cluster to the short arm of chromosome 16 (16p12–16pter) by hybridization in situ Journal of Molecular Biology ·Paul J.R. Barton, S Malcolm, Clifton N. Murphy, M.A. Ferguson‐Smith	1982	36

About S Malcolm

S Malcolm is a scholar working on Genetics, Sensory Systems, Genetics, Molecular Biology and Transplantation, having authored 51 papers that have together received 3.0k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (9 papers), Genomic variations and chromosomal abnormalities (7 papers), Craniofacial Disorders and Treatments (6 papers), Genetic Syndromes and Imprinting (5 papers), dental development and anomalies (4 papers), DNA Repair Mechanisms (3 papers), RNA modifications and cancer (3 papers) and Cancer-related gene regulation (3 papers). The work is most often cited by research in Genetics (1.8k citations), Sensory Systems (290 citations), Genetics (290 citations), Molecular Biology (1.7k citations) and Pediatrics, Perinatology and Child Health (394 citations). S Malcolm has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include R M Winter, Natalie J. Prescott, Robin M. Winter, Terence H. Rabbitts, William Reardon, Paul Rutland, Andrew O.M. Wilkie, Louise J. Pulleyn, Michael D. Poole and Michael Oldridge. Their work appears in journals such as Human Molecular Genetics, Journal of Medical Genetics, Cytogenetic and Genome Research, Annals of Human Genetics and Proceedings of the National Academy of Sciences.

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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