Ian Carr

7.3k total citations
111 papers, 3.5k citations indexed

About

Ian Carr is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Ian Carr has authored 111 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 36 papers in Genetics and 15 papers in Pathology and Forensic Medicine. Recurrent topics in Ian Carr's work include Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genomics and Phylogenetic Studies (9 papers). Ian Carr is often cited by papers focused on Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genomics and Phylogenetic Studies (9 papers). Ian Carr collaborates with scholars based in United Kingdom, United States and Australia. Ian Carr's co-authors include David T. Bonthron, Alexander F. Markham, Agne Antanaviciute, Christine P. Diggle, Graham R. Taylor, Eamonn Sheridan, Bruce E. Hayward, Adrian Whitehouse, Christopher M. Watson and Ann W Morgan and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Nature Communications.

In The Last Decade

Ian Carr

108 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ian Carr United Kingdom 32 1.7k 908 470 423 384 111 3.5k
Alexandre Montpetit Canada 33 1.4k 0.8× 897 1.0× 621 1.3× 243 0.6× 286 0.7× 66 3.5k
Roberto Ravazzolo Italy 39 3.6k 2.1× 936 1.0× 505 1.1× 533 1.3× 265 0.7× 206 6.5k
Jing Zhou China 35 2.2k 1.2× 1.1k 1.3× 705 1.5× 172 0.4× 203 0.5× 132 4.7k
Domenico Lazzaro Italy 24 2.1k 1.2× 862 0.9× 797 1.7× 239 0.6× 307 0.8× 37 4.3k
Alexander G. Bassuk United States 37 2.4k 1.4× 1.0k 1.1× 505 1.1× 452 1.1× 189 0.5× 153 4.4k
Naomi Nakagata Japan 46 3.6k 2.1× 1.7k 1.9× 578 1.2× 215 0.5× 277 0.7× 236 7.4k
Björn Rozell Sweden 39 2.4k 1.4× 601 0.7× 743 1.6× 153 0.4× 321 0.8× 88 4.4k
Aleksandar Rajkovic United States 39 2.1k 1.2× 2.2k 2.4× 293 0.6× 361 0.9× 154 0.4× 117 5.6k
Patrick Nitschké France 33 1.9k 1.1× 1.0k 1.1× 1.1k 2.4× 159 0.4× 242 0.6× 78 3.7k
Moshe Frydman Israel 37 2.4k 1.4× 1.4k 1.5× 363 0.8× 201 0.5× 351 0.9× 132 4.6k

Countries citing papers authored by Ian Carr

Since Specialization
Citations

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

Fields of papers citing papers by Ian Carr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ian Carr

This figure shows the co-authorship network connecting the top 25 collaborators of Ian Carr. A scholar is included among the top collaborators of Ian Carr 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 Ian Carr. Ian Carr 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.
Gratton, Paolo, Emiliano Trucchi, Ian Carr, et al.. (2025). Genomic insights into the biogeography and evolution of Galápagos iguanas. Molecular Phylogenetics and Evolution. 204. 108294–108294.
2.
Chau, Chalmers, Georgette Tanner, Morag Taylor, et al.. (2024). Single-cell nanobiopsy enables multigenerational longitudinal transcriptomics of cancer cells. Science Advances. 10(10). eadl0515–eadl0515. 17 indexed citations
3.
Watson, Christopher M., Ian Carr, Martin McKibbin, et al.. (2023). Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells. Molecular Diagnosis & Therapy. 27(4). 525–535. 4 indexed citations
4.
Harris, Erica, Vincent Roy, Martin Montagne, et al.. (2023). A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes. The American Journal of Human Genetics. 111(1). 119–132. 4 indexed citations
5.
Wijetunga, Imeshi, Agne Antanaviciute, Ian Carr, et al.. (2020). Translating Biomarkers of Cholangiocarcinoma for Theranosis: A Systematic Review. Cancers. 12(10). 2817–2817. 4 indexed citations
6.
Watson, Christopher M., Laura A. Crinnion, Helen Lindsay, et al.. (2020). Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertions. Laboratory Investigation. 101(4). 442–449. 12 indexed citations
7.
Romano, Marco, Satveer K. Mahil, Siew Eng Choon, et al.. (2019). IL-36 Promotes Systemic IFN-I Responses in Severe Forms of Psoriasis. Journal of Investigative Dermatology. 140(4). 816–826.e3. 65 indexed citations
8.
Diggle, Christine P., Isabel Martínez‐Garay, Zoltán Molnár, et al.. (2017). A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development. PLoS ONE. 12(4). e0174264–e0174264. 23 indexed citations
9.
Karamendin, Kobey, et al.. (2017). Novel avian paramyxovirus isolated from gulls in Caspian seashore in Kazakhstan. PLoS ONE. 12(12). e0190339–e0190339. 11 indexed citations
10.
Watson, Christopher M., Laura A. Crinnion, Ian Berry, et al.. (2016). Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping. BMC Medical Genetics. 17(1). 1–1. 59 indexed citations
11.
Antanaviciute, Agne, Christopher M. Watson, Sally M. Harrison, et al.. (2015). OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization. Bioinformatics. 31(23). 3822–3829. 19 indexed citations
12.
Robinson, James, Ian Carr, Stephen G. Martin, et al.. (2012). Confirmation of association ofFCGR3Bbut notFCGR3Acopy number with susceptibility to autoantibody positive rheumatoid arthritis. Human Mutation. 33(4). 741–749. 32 indexed citations
13.
Parry, David, Clare V. Logan, Bruce E. Hayward, et al.. (2011). Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte. The American Journal of Human Genetics. 89(3). 451–458. 174 indexed citations
14.
Carr, Ian, Joanne Morgan, Christine P. Diggle, et al.. (2011). Illuminator, a desktop program for mutation detection using short-read clonal sequencing. Genomics. 98(4). 302–309. 3 indexed citations
15.
Carr, Ian, Colin A. Johnson, Alex Markham, et al.. (2011). DominantMapper: Rule-based analysis of SNP data for rapid mapping of dominant diseases in related nuclear families. Human Mutation. 32(12). 1359–1366. 4 indexed citations
16.
Diggle, Christine P., Ian Carr, Emanuel Zitt, et al.. (2010). Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy. Lara D. Veeken. 49(6). 1056–1062. 40 indexed citations
17.
Valleley, Elizabeth M. A., Sarah F. Cordery, Ian Carr, Kenneth MacLennan, & David T. Bonthron. (2010). Loss of expression of ZAC/PLAGL1 in diffuse large B‐cell lymphoma is independent of promoter hypermethylation. Genes Chromosomes and Cancer. 49(5). 480–486. 9 indexed citations
18.
Carr, Ian, Katarzyna Szymańska, Eamonn Sheridan, et al.. (2009). Shadow autozygosity mapping by linkage exclusion (SAMPLE): a simple strategy to identify the genetic basis of lethal autosomal recessive disorders. Human Mutation. 30(12). 1642–1649. 5 indexed citations
19.
Abdollahi, Mohammad Reza, Ewan E. Morrison, Tamara Sirey, et al.. (2009). Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia. The American Journal of Human Genetics. 85(5). 737–744. 122 indexed citations
20.
Robinson, Philip A., J.P. Leek, Ian Carr, et al.. (1996). Yeast artificial chromosome cloning and chromosomal localization of the abundant odontogenic keratocyst protein elafin. Archives of Oral Biology. 41(5). 445–452. 3 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Alexandre Montpetit Breakdown of academic impact, for papers by Roberto Ravazzolo Breakdown of academic impact, for papers by Jing Zhou Breakdown of academic impact, for papers by Domenico Lazzaro Breakdown of academic impact, for papers by Alexander G. Bassuk Breakdown of academic impact, for papers by Naomi Nakagata Breakdown of academic impact, for papers by Björn Rozell Breakdown of academic impact, for papers by Aleksandar Rajkovic Breakdown of academic impact, for papers by Patrick Nitschké Breakdown of academic impact, for papers by Moshe Frydman
Rankless by CCL
2026