Doherty M - Search Results

1

Mutations in ANKH cause chondrocalcinosis.

Pendleton A, Johnson MD, Hughes A, Gurley KA, Ho AM, Doherty M, Dixey J, Gillet P, Loeuille D, McGrath R, Reginato A, Shiang R, Wright G, Netter P, Williams C, Kingsley DM. Pendleton A, et al. Among authors: doherty m. Am J Hum Genet. 2002 Oct;71(4):933-40. doi: 10.1086/343054. Epub 2002 Sep 20. Am J Hum Genet. 2002. PMID: 12297987 Free PMC article.

2

Autosomal dominant early childhood seizures associated with chondrocalcinosis and a mutation in the ANKH Gene.

McKee S, Pendleton A, Dixey J, Doherty M, Hughes A. McKee S, et al. Among authors: doherty m. Epilepsia. 2004 Oct;45(10):1258-60. doi: 10.1111/j.0013-9580.2004.19504.x. Epilepsia. 2004. PMID: 15461680 Free article.

3

Mutations in the amino terminus of ANKH in two US families with calcium pyrophosphate dihydrate crystal deposition disease.

Williams CJ, Pendleton A, Bonavita G, Reginato AJ, Hughes AE, Peariso S, Doherty M, McCarty DJ, Ryan LM. Williams CJ, et al. Among authors: doherty m. Arthritis Rheum. 2003 Sep;48(9):2627-31. doi: 10.1002/art.11133. Arthritis Rheum. 2003. PMID: 13130483 Free article.

4

Lack of support for the presence of an osteoarthritis susceptibility locus on chromosome 6p.

Meenagh GK, McGibbon D, Nixon J, Wright GD, Doherty M, Hughes AE. Meenagh GK, et al. Among authors: doherty m. Arthritis Rheum. 2005 Jul;52(7):2040-3. doi: 10.1002/art.21120. Arthritis Rheum. 2005. PMID: 15986344 Free article.

5

Pathophysiology of articular chondrocalcinosis--role of ANKH.

Abhishek A, Doherty M. Abhishek A, et al. Among authors: doherty m. Nat Rev Rheumatol. 2011 Feb;7(2):96-104. doi: 10.1038/nrrheum.2010.182. Epub 2010 Nov 23. Nat Rev Rheumatol. 2011. PMID: 21102543 Review.

6

The association between ANKH promoter polymorphism and chondrocalcinosis is independent of age and osteoarthritis: results of a case-control study.

Abhishek A, Doherty S, Maciewicz R, Muir K, Zhang W, Doherty M, Valdes AM. Abhishek A, et al. Among authors: doherty m, doherty s. Arthritis Res Ther. 2014 Jan 27;16(1):R25. doi: 10.1186/ar4453. Arthritis Res Ther. 2014. PMID: 24467728 Free PMC article.

7

Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.

Valdes AM, Loughlin J, Timms KM, van Meurs JJ, Southam L, Wilson SG, Doherty S, Lories RJ, Luyten FP, Gutin A, Abkevich V, Ge D, Hofman A, Uitterlinden AG, Hart DJ, Zhang F, Zhai G, Egli RJ, Doherty M, Lanchbury J, Spector TD. Valdes AM, et al. Among authors: doherty m, doherty s. Am J Hum Genet. 2008 Jun;82(6):1231-40. doi: 10.1016/j.ajhg.2008.04.006. Epub 2008 May 8. Am J Hum Genet. 2008. PMID: 18471798 Free PMC article.

8

An update on the epidemiology of calcium pyrophosphate dihydrate crystal deposition disease.

Richette P, Bardin T, Doherty M. Richette P, et al. Among authors: doherty m. Rheumatology (Oxford). 2009 Jul;48(7):711-5. doi: 10.1093/rheumatology/kep081. Epub 2009 Apr 27. Rheumatology (Oxford). 2009. PMID: 19398486 Review.

9

Genome-wide association scan of neuropathic pain symptoms post total joint replacement highlights a variant in the protein-kinase C gene.

Warner SC, van Meurs JB, Schiphof D, Bierma-Zeinstra SM, Hofman A, Uitterlinden AG, Richardson H, Jenkins W, Doherty M, Valdes AM. Warner SC, et al. Among authors: doherty m. Eur J Hum Genet. 2017 Apr;25(4):446-451. doi: 10.1038/ejhg.2016.196. Epub 2017 Jan 4. Eur J Hum Genet. 2017. PMID: 28051079 Free PMC article.

10

Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis.

Castaño-Betancourt MC, Evans DS, Ramos YF, Boer CG, Metrustry S, Liu Y, den Hollander W, van Rooij J, Kraus VB, Yau MS, Mitchell BD, Muir K, Hofman A, Doherty M, Doherty S, Zhang W, Kraaij R, Rivadeneira F, Barrett-Connor E, Maciewicz RA, Arden N, Nelissen RG, Kloppenburg M, Jordan JM, Nevitt MC, Slagboom EP, Hart DJ, Lafeber F, Styrkarsdottir U, Zeggini E, Evangelou E, Spector TD, Uitterlinden AG, Lane NE, Meulenbelt I, Valdes AM, van Meurs JB. Castaño-Betancourt MC, et al. Among authors: doherty m, doherty s. PLoS Genet. 2016 Oct 4;12(10):e1006260. doi: 10.1371/journal.pgen.1006260. eCollection 2016 Oct. PLoS Genet. 2016. PMID: 27701424 Free PMC article.

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