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Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.
Dickinson RE, Griffin H, Bigley V, Reynard LN, Hussain R, Haniffa M, Lakey JH, Rahman T, Wang XN, McGovern N, Pagan S, Cookson S, McDonald D, Chua I, Wallis J, Cant A, Wright M, Keavney B, Chinnery PF, Loughlin J, Hambleton S, Santibanez-Koref M, Collin M. Dickinson RE, et al. Among authors: loughlin j. Blood. 2011 Sep 8;118(10):2656-8. doi: 10.1182/blood-2011-06-360313. Epub 2011 Jul 15. Blood. 2011. PMID: 21765025 Free PMC article.
Genetics and epigenetics of osteoarthritis.
Reynard LN, Loughlin J. Reynard LN, et al. Among authors: loughlin j. Maturitas. 2012 Mar;71(3):200-4. doi: 10.1016/j.maturitas.2011.12.001. Epub 2011 Dec 29. Maturitas. 2012. PMID: 22209350 Review.
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls.
Hudson G, Panoutsopoulou K, Wilson I, Southam L, Rayner NW, Arden N, Birrell F, Carluke I, Carr A, Chapman K, Deloukas P, Doherty M, McCaskie A, Ollier WE, Ralston SH, Reed MR, Spector TD, Valdes AM, Wallis GA, Wilkinson JM, Zeggini E, Samuels DC, Loughlin J, Chinnery PF; arcOGEN Consortium. Hudson G, et al. Among authors: loughlin j. Ann Rheum Dis. 2013 Jan;72(1):136-9. doi: 10.1136/annrheumdis-2012-201932. Epub 2012 Sep 14. Ann Rheum Dis. 2013. PMID: 22984172 Free PMC article.
246 results