S Malcolm
Impact in
- Genetics top 0.5%
- 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
-
- dental development and anomalies 4
- Glycosylation and Glycoproteins Research 3
- Genetics 24
- Cleft Lip and Palate Research 9
- Genomic variations and chromosomal abnormalities 7
- Craniofacial Disorders and Treatments 6
- Genetic Syndromes and Imprinting 5
- 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)Richard Hayward (1 shared paper)William Reardon (2 shared papers)Michael Oldridge (1 shared paper)Michael D. Poole (1 shared paper)
- Journals
- Human Molecular Genetics (4 papers)Journal of Medical Genetics (4 papers)Human Genetics (2 papers)Blood (2 papers)Annals of Human Genetics (2 papers)
- Partner nations
- United KingdomIndiaUnited States
In The Last Decade
S Malcolm
47 papers receiving 2.8k citations
S Malcolm's Hit Papers
Peers
Comparison fields: 5 of 107
- Genetics 1.7k
- Sensory Systems 282
- Genetics 275
- Molecular Biology 1.6k
- Pediatrics, Perinatology and Child Health 363
Countries citing papers authored by S Malcolm
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
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.
All Works
Showing the 20 most-cited of 49 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 Hit paper breakdown → | 1995 | 671 |
| 2 | 1995 | 327 | |
| 3 | 1991 | 251 | |
| 4 | 1982 | 181 | |
| 5 | 1996 | 146 | |
| 6 | 1985 | 139 | |
| 7 | 2000 | 112 | |
| 8 | Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. | 1995 | 87 |
| 9 | 1984 | 76 | |
| 10 | 1992 | 76 | |
| 11 | 1995 | 58 | |
| 12 | 1988 | 56 | |
| 13 | 1992 | 50 | |
| 14 | 2001 | 49 | |
| 15 | 2000 | 48 | |
| 16 | 2001 | 47 | |
| 17 | 1992 | 44 | |
| 18 | Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate. | 1994 | 43 |
| 19 | 1993 | 42 | |
| 20 | 1983 | 36 |
About S Malcolm
S Malcolm is a scholar working on Molecular Biology, Genetics, Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 49 papers that have together received 2.9k 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), Glycosylation and Glycoproteins Research (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Chronic Myeloid Leukemia Treatments (3 papers). The work is most often cited by research in Genetics (1.7k citations), Sensory Systems (282 citations), Genetics (275 citations), Molecular Biology (1.6k citations) and Pediatrics, Perinatology and Child Health (363 citations). S Malcolm has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include R M Winter, Natalie J. Prescott, Robin M. Winter, Terence H. Rabbitts, Richard Hayward, William Reardon, Michael Oldridge, Michael D. Poole, Anthony D. Hockley and Sarah F. Slaney. Their work appears in journals such as Human Molecular Genetics, Journal of Medical Genetics, Human Genetics, Blood and Annals of Human Genetics.
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.