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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1978 1
1979 1
1994 1
1995 1
1996 1
1997 5
1998 4
1999 3
2000 3
2002 2
2003 3
2004 3
2005 1
2006 3
2007 4
2008 6
2009 6
2010 3
2011 3
2012 3
2013 1
2014 1
2015 3
2016 2
2022 0
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Search Results

57 results
Results by year
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Page 1
Hemochromatosis-related mutation detection.
Merryweather-Clarke AT, Shearman JD, Robson KJ, Pointon JJ, Liu YT, Bomford A, Dooley J, Walker AP, Worwood M. Merryweather-Clarke AT, et al. Among authors: pointon jj. Blood. 1998 Apr 1;91(7):2620-1. Blood. 1998. PMID: 9516166 Free article. No abstract available.
Recent advances in understanding haemochromatosis: a transition state.
Robson KJ, Merryweather-Clarke AT, Cadet E, Viprakasit V, Zaahl MG, Pointon JJ, Weatherall DJ, Rochette J. Robson KJ, et al. Among authors: pointon jj. J Med Genet. 2004 Oct;41(10):721-30. doi: 10.1136/jmg.2004.020644. J Med Genet. 2004. PMID: 15466004 Free PMC article. Review.
Detection of C282Y and H63D in the HFE gene.
Pointon JJ, Merryweather-Clarke AT, Carella M, Robson KJ. Pointon JJ, et al. Genet Test. 2000;4(2):115-20. doi: 10.1089/10906570050114803. Genet Test. 2000. PMID: 10953949 Review.
Haemochromatosis: a gene at last?
Robson KJ, Shearman JD, Merryweather-Clarke AT, Pointon JJ, Rosenberg WM, Walker AP, Dooley JS, Bomford A, Raha-Chowdhury R, Worwood M. Robson KJ, et al. Among authors: pointon jj. J Med Genet. 1997 Feb;34(2):148-51. doi: 10.1136/jmg.34.2.148. J Med Genet. 1997. PMID: 9039993 Free PMC article. No abstract available.
Global prevalence of putative haemochromatosis mutations.
Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ. Merryweather-Clarke AT, et al. Among authors: pointon jj. J Med Genet. 1997 Apr;34(4):275-8. doi: 10.1136/jmg.34.4.275. J Med Genet. 1997. PMID: 9138148 Free PMC article.
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease.
Robinson PC, Leo PJ, Pointon JJ, Harris J, Cremin K, Bradbury LA, Stebbings S, Harrison AA; Australian Osteoporosis Genetics Consortium; Wellcome Trust Case Control Consortium; Management Committee; Data and Analysis Group; DNA, Genotyping, Data QC and Informatics Group; Publications Committee, Duncan EL, Evans DM, Wordsworth PB, Brown MA. Robinson PC, et al. Among authors: pointon jj. NPJ Genom Med. 2016 May 4;1:16008. doi: 10.1038/npjgenmed.2016.8. eCollection 2016. NPJ Genom Med. 2016. PMID: 29263810 Free PMC article.
Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1.
Cortes A, Pulit SL, Leo PJ, Pointon JJ, Robinson PC, Weisman MH, Ward M, Gensler LS, Zhou X, Garchon HJ, Chiocchia G, Nossent J, Lie BA, Førre Ø, Tuomilehto J, Laiho K, Bradbury LA, Elewaut D, Burgos-Vargas R, Stebbings S, Appleton L, Farrah C, Lau J, Haroon N, Mulero J, Blanco FJ, Gonzalez-Gay MA, Lopez-Larrea C, Bowness P, Gaffney K, Gaston H, Gladman DD, Rahman P, Maksymowych WP, Crusius JB, van der Horst-Bruinsma IE, Valle-Oñate R, Romero-Sánchez C, Hansen IM, Pimentel-Santos FM, Inman RD, Martin J, Breban M, Wordsworth BP, Reveille JD, Evans DM, de Bakker PI, Brown MA. Cortes A, et al. Among authors: pointon jj. Nat Commun. 2015 May 21;6:7146. doi: 10.1038/ncomms8146. Nat Commun. 2015. PMID: 25994336 Free PMC article.
57 results