James A. Poulter

4.4k total citations
52 papers, 1.5k citations indexed

About

James A. Poulter is a scholar working on Molecular Biology, Rheumatology and Cell Biology. According to data from OpenAlex, James A. Poulter has authored 52 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 24 papers in Rheumatology and 10 papers in Cell Biology. Recurrent topics in James A. Poulter's work include Bone and Dental Protein Studies (19 papers), dental development and anomalies (17 papers) and Retinal Development and Disorders (6 papers). James A. Poulter is often cited by papers focused on Bone and Dental Protein Studies (19 papers), dental development and anomalies (17 papers) and Retinal Development and Disorders (6 papers). James A. Poulter collaborates with scholars based in United Kingdom, United States and Costa Rica. James A. Poulter's co-authors include Chris F. Inglehearn, Alan J. Mighell, Claire E. L. Smith, Steven J. Brookes, Jennifer Kirkham, Emily A. Caseley, David Parry, Agne Antanaviciute, Michael McDermott and Richard F. Shore and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Journal of Dental Research.

In The Last Decade

James A. Poulter

47 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James A. Poulter United Kingdom 21 1.1k 619 176 160 137 52 1.5k
Jan Procházka Czechia 20 791 0.7× 136 0.2× 38 0.2× 217 1.4× 92 0.7× 92 1.3k
Jessica C. Gardner United Kingdom 18 1.6k 1.5× 213 0.3× 16 0.1× 479 3.0× 122 0.9× 37 2.3k
Sumin Gu United States 30 2.6k 2.4× 103 0.2× 56 0.3× 337 2.1× 375 2.7× 71 3.2k
Sulman Basit Saudi Arabia 21 931 0.9× 76 0.1× 116 0.7× 520 3.3× 277 2.0× 134 1.9k
Turgut Tükel Türkiye 14 510 0.5× 236 0.4× 24 0.1× 211 1.3× 358 2.6× 18 1.5k
Mohnish Suri United Kingdom 24 1.2k 1.1× 171 0.3× 39 0.2× 736 4.6× 260 1.9× 82 2.2k
Wadih M. Zein United States 21 762 0.7× 65 0.1× 20 0.1× 369 2.3× 246 1.8× 86 1.4k
T. Takagi Japan 11 415 0.4× 188 0.3× 55 0.3× 27 0.2× 153 1.1× 21 864
D. M. Juriloff Canada 30 1.6k 1.5× 618 1.0× 87 0.5× 1.1k 6.7× 206 1.5× 79 2.8k
Michael Fietz Australia 24 666 0.6× 221 0.4× 102 0.6× 210 1.3× 302 2.2× 51 1.6k

Countries citing papers authored by James A. Poulter

Since Specialization
Citations

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

Fields of papers citing papers by James A. Poulter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James A. Poulter. 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 James A. Poulter. The network helps show where James A. Poulter may publish in the future.

Co-authorship network of co-authors of James A. Poulter

This figure shows the co-authorship network connecting the top 25 collaborators of James A. Poulter. A scholar is included among the top collaborators of James A. Poulter 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 James A. Poulter. James A. Poulter 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.
Rodríguez, A., Dorota Rowczenio, Alexandra Smith, et al.. (2025). Mapping VEXAS ‐associated and rare UBA1 variants in the United Kingdom : Insights from patient cohorts and the general population. British Journal of Haematology. 208(1). 116–128. 2 indexed citations
2.
Hany, Ummey, Christopher M. Watson, Claire E. L. Smith, et al.. (2025). Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target Loci. Human Mutation. 2025(1). 8942542–8942542.
3.
Rashid, M. H. M., et al.. (2025). Exome sequencing reveals broad genetic heterogeneity for neuromuscular disorders in consanguineous Pakistani Families. European Journal of Human Genetics. 33(10). 1264–1270.
4.
Poulter, James A., Andrew R. Webster, Gavin Arno, et al.. (2025). RP9 revisited; RP9 p.(H137L) remains a likely cause of dominant splicing factor-Retinitis Pigmentosa. European Journal of Human Genetics. 34(2). 227–235.
5.
Topping, Joanne, Samuel Lara‐Reyna, Heledd Jarosz-Griffiths, et al.. (2024). FACS-based detection of extracellular ASC specks from NLRP3 inflammasomes in inflammatory diseases. Clinical & Experimental Immunology. 219(1). 1 indexed citations
6.
Smith, Claire E. L., Virginie Laugel-Haushalter, Ummey Hany, et al.. (2024). Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of Medical Genetics. 61(7). 689–698. 2 indexed citations
7.
King, Aaron A., et al.. (2024). The contradictory role of febuxostat in ABCG2 expression and potentiating hypericin-mediated photodynamic therapy in colorectal cancers. Photochemical & Photobiological Sciences. 23(6). 1067–1075.
8.
Topping, Joanne, James A. Poulter, Samuel Lara‐Reyna, et al.. (2024). Characterization of Genetic Landscape and Novel Inflammatory Biomarkers in Patients With Adult‐Onset Still's Disease. Arthritis & Rheumatology. 77(5). 582–595.
9.
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
10.
Crinnion, Laura A., Martin McKibbin, Rajarshi Mukherjee, et al.. (2023). Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon‐based short‐read sequencing strategies. Molecular Genetics & Genomic Medicine. 11(6). e2164–e2164. 6 indexed citations
11.
Poulter, James A. & Sinisa Savic. (2021). Genetics of somatic auto-inflammatory disorders. Seminars in Hematology. 58(4). 212–217. 25 indexed citations
12.
Lara‐Reyna, Samuel, James A. Poulter, Elton J. R. Vasconcelos, et al.. (2020). Identification of Critical Transcriptomic Signaling Pathways in Patients with H Syndrome and Rosai-Dorfman Disease. Journal of Clinical Immunology. 41(2). 441–457. 4 indexed citations
13.
Caseley, Emily A., James A. Poulter, François Rodrigues, et al.. (2020). Inflammasome inhibition under physiological and pharmacological conditions. Genes and Immunity. 21(4). 211–223. 34 indexed citations
14.
Khan, Kamron N., Anthony G. Robson, Omar A. Mahroo, et al.. (2018). A clinical and molecular characterisation of CRB1-associated maculopathy. European Journal of Human Genetics. 26(5). 687–694. 54 indexed citations
15.
Lord, Emma, James A. Poulter, Andrew R. Webster, et al.. (2017). Mutations in SLC38A8 and FOXD1 in patients with nystagmus and foveal hypoplasia.. Investigative Ophthalmology & Visual Science. 58(8). 2786–2786. 1 indexed citations
16.
Smith, Claire E. L., Jennifer Kirkham, Peter F. Day, et al.. (2017). A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities. Frontiers in Physiology. 8. 333–333. 21 indexed citations
17.
Taylor, Rachel L., Gavin Arno, James A. Poulter, et al.. (2017). Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy. JAMA Ophthalmology. 135(4). 339–339. 32 indexed citations
18.
Khan, Kamron N., Mohammed E. El‐Asrag, Cristy A. Ku, et al.. (2017). Specific Alleles of CLN7 / MFSD8 , a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 58(7). 2906–2906. 38 indexed citations
19.
Smith, Claire E. L., James A. Poulter, Alex V. Levin, et al.. (2016). Spectrum of PEX1 and PEX6 variants in Heimler syndrome. European Journal of Human Genetics. 24(11). 1565–1571. 43 indexed citations
20.
Poulter, James A., Claire E. L. Smith, Sally Feather, et al.. (2015). A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing. Molecular Genetics & Genomic Medicine. 3(6). 543–549. 9 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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