J. J. Pointon - Concepedia

Author

J. J. Pointon

Also Known As

C. J. Cohen, J J Pointon, J Pointon, J. J. Pointon, J. POINTON, J. Pointon, J.J. Pointon, JJ Pointon, Jennifer Pointon, S. Brophy

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Nuffield Orthopaedic Centre John Radcliffe Hospital University of Oxford Institute of Molecular Medicine The University of Queensland

About

J. J. Pointon is an author at Nuffield Orthopaedic Centre specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	1.7K
2	Education	1	1	32
3	Health Sciences	1	1	23
4	Public Health	1	1	27
5	Biochemistry	1	1	16

J. J. Pointon

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Global prevalence of putative haemochromatosis mutations. Alison T. Merryweather‐Clarke, J. J. Pointon, Jeremy D. Shearman, Journal of Medical Genetics BiologyAmino Acid 282Haplotype DeterminationHeme HomeostasisGenetic Disorder	1997	791
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation Samantha J.L. Knight, A Flannery, Mark C. Hirst, Cell Cpg IslandGenetic DisorderGeneticsMolecular BiologyMolecular Genetics	1993	520
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility David M. Evans, Chris C. A. Spencer, J. J. Pointon, UWA Profiles and Research Repository (University of Western Australia)	2011	253
Multicentric Origin of Hemochromatosis Gene (HFE) Mutations Jacques Rochette, J. J. Pointon, Christopher A. Fisher, The American Journal of Human Genetics Genetic DisorderGeneticsMolecular GeneticsMulticentric OriginHeme Homeostasis	1999	150
Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene J. J. Pointon, David Harvey, Tugce Karaderi, Genes and Immunity CytogeneticsGeneticsHuman PolymorphismChromosome BiologyMolecular Genetics	2010	71
Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients Pille Harrison, J. J. Pointon, C. Farrar, Lara D. Veeken	2006	64
The Frequency of Hemochromatosis–Associated Alleles Is Increased in British Patients With Sporadic Porphyria Cutanea Tarda Andrew Roberts, Sharon D. Whatley, Stuart A. Nicklin, Hepatology	1997	50
The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis Philip C. Robinson, Paul Leo, J. J. Pointon, Genes and Immunity Genetic AssociationsRheumatologyAutoimmune DiseaseSpondyloarthritisGenetics	2015	43
DNA testing for fragile X syndrome in schools for learning difficulties. Sarah F. Slaney, Andrew O.M. Wilkie, Mark C. Hirst, Archives of Disease in Childhood Fragile X SyndromeGenetic TestingMendelian DisorderGenetic DisorderGenetics	1995	32
The HLA A1‐B8 haplotype extends 6 Mb beyond HLA‐A: associations between HLA‐A, B, F and 15 microsatellite markers Mark Worwood, RN Chowdhury, Kathryn Robson, Tissue Antigens HlaImmunohematologyGeneticsHla ImmunogeneticsHuman Polymorphism	1997	27

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