J. J. Pointon

2.4k total citations · 1 hit paper
27 papers, 1.6k citations indexed

About

J. J. Pointon is a scholar working on Rheumatology, Hematology and Immunology. According to data from OpenAlex, J. J. Pointon has authored 27 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Rheumatology, 9 papers in Hematology and 9 papers in Immunology. Recurrent topics in J. J. Pointon's work include Spondyloarthritis Studies and Treatments (7 papers), Iron Metabolism and Disorders (7 papers) and Hemoglobinopathies and Related Disorders (5 papers). J. J. Pointon is often cited by papers focused on Spondyloarthritis Studies and Treatments (7 papers), Iron Metabolism and Disorders (7 papers) and Hemoglobinopathies and Related Disorders (5 papers). J. J. Pointon collaborates with scholars based in United Kingdom, Australia and India. J. J. Pointon's co-authors include Kathryn Robson, Alison T. Merryweather‐Clarke, Jeremy D. Shearman, Mark C. Hirst, Zóe Christodoulou, Kay E. Davies, Martin Bobrow, Helen Middleton‐Price, Angela Barnicoat and Samantha J.L. Knight and has published in prestigious journals such as Cell, Hepatology and The American Journal of Human Genetics.

In The Last Decade

J. J. Pointon

26 papers receiving 1.5k 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.

Global prevalence of putative haemochromatosis mutations.

1997 612 citations Alison T. Merryweather‐Clarke, J. J. Pointon et al. Journal of Medical Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. J. Pointon United Kingdom	15	758	606	537	525	437	27	1.6k
Odile Raguénès France	21	479 0.6×	447 0.7×	345 0.6×	194 0.4×	168 0.4×	36	1.5k
Adrian Wiestner Switzerland	10	539 0.7×	425 0.7×	395 0.7×	368 0.7×	54 0.1×	12	1.5k
Cécile Cazeneuve France	24	112 0.1×	330 0.5×	44 0.1×	975 1.9×	115 0.3×	44	1.9k
Veronique Duke United Kingdom	14	209 0.3×	156 0.3×	45 0.1×	384 0.7×	202 0.5×	22	923
Virginia K. Proud United States	17	59 0.1×	67 0.1×	184 0.3×	549 1.0×	320 0.7×	32	1.1k
Maria Antonietta Melis Italy	17	319 0.4×	385 0.6×	110 0.2×	576 1.1×	118 0.3×	41	1.1k
Anju Shukla India	18	63 0.1×	121 0.2×	36 0.1×	610 1.2×	496 1.1×	112	1.2k
Séverine Drunat France	21	72 0.1×	77 0.1×	21 0.0×	581 1.1×	443 1.0×	57	1.1k
Christine Wittevrongel Belgium	18	397 0.5×	68 0.1×	9 0.0×	241 0.5×	175 0.4×	36	882

Countries citing papers authored by J. J. Pointon

Since Specialization

Citations

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

Fields of papers citing papers by J. J. Pointon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. J. Pointon

This figure shows the co-authorship network connecting the top 25 collaborators of J. J. Pointon. A scholar is included among the top collaborators of J. J. Pointon 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 J. J. Pointon. J. J. Pointon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Karaderi, Tugce, J. J. Pointon, Louise Appleton, et al.. (2014). Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). QUT ePrints (Queensland University of Technology). 1 indexed citations

Karaderi, Tugce, J. J. Pointon, Louise Appleton, et al.. (2014). Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). Annals of the Rheumatic Diseases. 73(11). 2054–2058. 16 indexed citations

Karaderi, Tugce, J. J. Pointon, David Harvey, et al.. (2012). Evidence of genetic association between TNFRSF1A encoding the p55 tumour necrosis factor receptor, and ankylosing spondylitis in UK Caucasians. QUT ePrints (Queensland University of Technology). 10 indexed citations

Pointon, J. J., David Harvey, Tugce Karaderi, et al.. (2010). Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene. Genes and Immunity. 11(6). 490–496. 55 indexed citations

Danoy, Patrick, Karena Pryce, Johanna Hadler, et al.. (2010). Association of Variants at 1q32 and STAT3 with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease. PLoS Genetics. 6(12). e1001195–e1001195. 14 indexed citations

Harvey, David, J. J. Pointon, C. Sleator, et al.. (2009). Analysis of killer immunoglobulin-like receptor genes in ankylosing spondylitis. Queensland's institutional digital repository (The University of Queensland). 3 indexed citations

Gregson, Celia L., K. Addison, Marieke Brugmans, et al.. (2009). Mutations in LRP5 and SOST are a rare cause of high bone mass in the general population. Bone. 44. S340–S341. 6 indexed citations

Harrison, Pille, J. J. Pointon, K Chapman, Andrew Roddam, & B P Wordsworth. (2008). Interleukin-1 promoter region polymorphism role in rheumatoid arthritis: a meta-analysis of IL-1B-511A/G variant reveals association with rheumatoid arthritis. Lara D. Veeken. 47(12). 1768–1770. 63 indexed citations

Harrison, Pille, J. J. Pointon, C. Farrar, Matthew A. Brown, & B. P. Wordsworth. (2006). Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients. Lara D. Veeken. 45(8). 1009–1011. 46 indexed citations

10.

Jaakkola, E., Alison M. Crane, J. J. Pointon, et al.. (2004). A novel human leucocyte antigen‐DRB1 genotyping method based on multiplex primer extension reactions. Tissue Antigens. 64(1). 88–95. 6 indexed citations

11.

Capron, Dominique, Sabrina Crépin, S Arlot, et al.. (2003). A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis. Journal of Internal Medicine. 253(2). 217–224. 19 indexed citations

12.

Rochette, Jacques, J. J. Pointon, Christopher A. Fisher, et al.. (1999). Multicentric Origin of Hemochromatosis Gene (HFE) Mutations. The American Journal of Human Genetics. 64(4). 1056–1062. 113 indexed citations

13.

Pointon, J. J., et al.. (1998). Caring for the mentally ill.. PubMed. 4(1). 14–14. 2 indexed citations

14.

Worwood, Mark, Jeremy D. Shearman, Daniel F. Wallace, et al.. (1997). A simple genetic test identifies 90% of UK patients with haemochromatosis. QUT ePrints (Queensland University of Technology). 6 indexed citations

15.

Pointon, J. J., et al.. (1997). Measurement of liver fat by MRI and its reduction by dexfenfluramine in NIDDM. International Journal of Obesity. 21(4). 274–279. 18 indexed citations

16.

Roberts, Andrew, Sharon D. Whatley, Stuart A. Nicklin, et al.. (1997). The Frequency of Hemochromatosis–Associated Alleles Is Increased in British Patients With Sporadic Porphyria Cutanea Tarda. Hepatology. 25(1). 159–161. 34 indexed citations

17.

Robson, Kathryn, Jeremy D. Shearman, Alison T. Merryweather‐Clarke, et al.. (1997). Haemochromatosis: a gene at last?. Journal of Medical Genetics. 34(2). 148–151. 4 indexed citations

18.

Worwood, Mark, M. Tevfik Dorak, Stuart A. Nicklin, et al.. (1996). The frequency of the haemochromatosis‐associated genotype D6S265‐1:D6S105‐8 in blood donors. British Journal of Haematology. 93(4). 838–840. 8 indexed citations

19.

Slaney, Sarah F., Andrew O.M. Wilkie, Mark C. Hirst, et al.. (1995). DNA testing for fragile X syndrome in schools for learning difficulties.. Archives of Disease in Childhood. 72(1). 33–37. 22 indexed citations

20.

Knight, Samantha J.L., A Flannery, Mark C. Hirst, et al.. (1993). Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell. 74(1). 127–134. 436 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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