Raymond Dalgleish

5.9k total citations · 1 hit paper
99 papers, 3.5k citations indexed

About

Raymond Dalgleish is a scholar working on Genetics, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Raymond Dalgleish has authored 99 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Genetics, 32 papers in Molecular Biology and 14 papers in Immunology and Allergy. Recurrent topics in Raymond Dalgleish's work include Connective tissue disorders research (29 papers), Genomics and Rare Diseases (16 papers) and Cell Adhesion Molecules Research (14 papers). Raymond Dalgleish is often cited by papers focused on Connective tissue disorders research (29 papers), Genomics and Rare Diseases (16 papers) and Cell Adhesion Molecules Research (14 papers). Raymond Dalgleish collaborates with scholars based in United Kingdom, United States and Netherlands. Raymond Dalgleish's co-authors include Johan T. den Dunnen, Reece K. Hart, Peter E.M. Taschner, Donna Maglott, Marc S. Greenblatt, Anne‐Françoise Roux, Jean McGowan‐Jordan, Stylianos E. Antonarakis, Tim D. Smith and Judith Lee Smith and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Raymond Dalgleish

93 papers receiving 3.4k 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.

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

2016 1.0k citations Johan T. den Dunnen, Raymond Dalgleish et al. Human Mutation profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Raymond Dalgleish United Kingdom	28	1.7k	1.4k	457	449	292	99	3.5k
Tobias Gedde‐Dahl Norway	39	1.0k 0.6×	1.8k 1.4×	288 0.6×	245 0.5×	316 1.1×	225	5.3k
W. Scott Argraves United States	37	1.0k 0.6×	1.6k 1.2×	642 1.4×	212 0.5×	170 0.6×	66	3.7k
Laure Coulombel France	43	777 0.5×	1.9k 1.4×	200 0.4×	156 0.3×	199 0.7×	127	5.3k
Daniel Graf Canada	34	839 0.5×	2.4k 1.8×	597 1.3×	360 0.8×	272 0.9×	97	5.3k
David Vetrie United Kingdom	32	1.1k 0.7×	3.1k 2.3×	1.4k 3.0×	158 0.4×	283 1.0×	59	5.7k
Shukti Chakravarti United States	40	992 0.6×	1.9k 1.4×	982 2.1×	379 0.8×	362 1.2×	94	6.2k
Stephen G. Emerson United States	46	632 0.4×	2.1k 1.5×	430 0.9×	460 1.0×	316 1.1×	117	8.2k
Peter Lonai Israel	35	1.3k 0.8×	4.6k 3.4×	413 0.9×	149 0.3×	251 0.9×	89	6.4k
Joseph J. Catanese United States	34	1.3k 0.8×	1.3k 1.0×	329 0.7×	456 1.0×	486 1.7×	64	4.7k
S. Hadj‐Rabia France	33	769 0.5×	1.6k 1.2×	146 0.3×	380 0.8×	317 1.1×	148	3.7k

Countries citing papers authored by Raymond Dalgleish

Since Specialization

Citations

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

Fields of papers citing papers by Raymond Dalgleish

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raymond Dalgleish

This figure shows the co-authorship network connecting the top 25 collaborators of Raymond Dalgleish. A scholar is included among the top collaborators of Raymond Dalgleish 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 Raymond Dalgleish. Raymond Dalgleish 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

Freeman, Peter, Ivo F.A.C. Fokkema, Garry R. Cutting, et al.. (2024). Standardizing variant naming in literature with VariantValidator to increase diagnostic rates. Nature Genetics. 56(11). 2284–2286. 2 indexed citations

Besio, Roberta, Raymond Dalgleish, Simona Villani, et al.. (2022). Dissecting the phenotypic variability of osteogenesis imperfecta. Disease Models & Mechanisms. 15(5). 31 indexed citations

Bruford, Elspeth A., Cristina R. Antonescu, Andrew J. Carroll, et al.. (2021). HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions. Leukemia. 35(11). 3040–3043. 47 indexed citations

Leske, Henning, Raymond Dalgleish, Alexander J. Lazar, Guido Reifenberger, & Ian A. Cree. (2021). A common classification framework for histone sequence alterations in tumours: an expert consensus proposal. The Journal of Pathology. 254(2). 109–120. 8 indexed citations

Fratter, Carl, Raymond Dalgleish, Stephanie Allen, et al.. (2020). EMQN best practice guidelines for genetic testing in dystrophinopathies. European Journal of Human Genetics. 28(9). 1141–1159. 39 indexed citations

Wang, Meng, Keith M. Callenberg, Raymond Dalgleish, et al.. (2018). hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update. Human Mutation. 39(12). 1803–1813. 16 indexed citations

Freeman, Peter, et al.. (2017). VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions. Human Mutation. 39(1). 61–68. 99 indexed citations

Zhao, Shidou, Guangyu Li, Raymond Dalgleish, et al.. (2014). Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency. Fertility and Sterility. 103(2). 548–553.e5. 27 indexed citations

MacArthur, Jacqueline A. L., Joannella Morales, Alex Astashyn, et al.. (2013). Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants. Nucleic Acids Research. 42(D1). D873–D878. 45 indexed citations

10.

Dijk, Fleur S van, Raymond Dalgleish, Fransiska Malfait, et al.. (2012). Clinical utility gene card for: osteogenesis imperfecta. European Journal of Human Genetics. 21(6). 1–4. 13 indexed citations

11.

Dalgleish, Raymond, et al.. (2012). Solving bottlenecks in data sharing in the life sciences. Human Mutation. 33(10). 1494–1496. 7 indexed citations

12.

Dalgleish, Raymond, et al.. (2007). Linking DNA structure and sequencing using model based learning. Figshare.

13.

Dalgleish, Raymond. (1997). The human type I collagen mutation database. Nucleic Acids Research. 25(1). 181–187. 256 indexed citations

14.

Raghunath, Michael, Katrina Mackay, Raymond Dalgleish, & Beat Steinmann. (1995). Genetic counselling on brittle grounds: Recurring osteogenesis imperfecta due to parental mosaicism for a dominant mutation. European Journal of Pediatrics. 154(2). 123–129. 26 indexed citations

15.

Molyneux, Karen, B J Starman, Peter H. Byers, & Raymond Dalgleish. (1993). A single amino acid deletion in the ?2(I) chain of type I collagen produces osteogenesis imperfecta type III. Human Genetics. 90(6). 621–8. 12 indexed citations

16.

Armour, J., et al.. (1988). Clinical nematodiriasis in calves due to Nematodirus battus infection. Veterinary Record. 123(9). 230–231. 14 indexed citations

17.

Ogilvie, Donald, B P Wordsworth, L. Priestley, et al.. (1987). Segregation of all four major fibrillar collagen genes in the Marfan syndrome.. Europe PMC (PubMed Central). 41(6). 1071–82. 34 indexed citations

18.

Solomon, E., Lynne R. Hiorns, Raymond Dalgleish, et al.. (1983). Regional localization of the human Rα2(I) collagen gene on chromosome 7 by molecular hybridization. Cytogenetic and Genome Research. 35(1). 64–66. 48 indexed citations

19.

Dalgleish, Raymond. (1965). Idiopathic acquired canaliculus obstruction.. PubMed. 85. 191–5. 1 indexed citations

20.

Dalgleish, Raymond. (1964). To-day's Drugs: Agents for Lowering Serum Cholesterol. BMJ. 2(5418). 1181–1183. 2 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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