Similar articles for PMID: 22608500

Year	Number of Results
1989	1
1993	1
1999	1
2000	1
2001	2
2002	2
2003	3
2004	4
2005	1
2006	2
2007	3
2008	9
2009	11
2010	8
2011	5
2012	8
2013	2
2014	3
2015	9
2016	2
2017	2
2018	2
2019	4
2020	1
2021	3
2022	2
2023	1
2024	0

1

Evolutionary history of copy-number-variable locus for the low-affinity Fcγ receptor: mutation rate, autoimmune disease, and the legacy of helminth infection.

Machado LR, Hardwick RJ, Bowdrey J, Bogle H, Knowles TJ, Sironi M, Hollox EJ. Machado LR, et al. Am J Hum Genet. 2012 Jun 8;90(6):973-85. doi: 10.1016/j.ajhg.2012.04.018. Epub 2012 May 17. Am J Hum Genet. 2012. PMID: 22608500 Free PMC article.

2

Understanding the Genomic Structure of Copy-Number Variation of the Low-Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid Arthritis.

Rahbari R, Zuccherato LW, Tischler G, Chihota B, Ozturk H, Saleem S, Tarazona-Santos E, Machado LR, Hollox EJ. Rahbari R, et al. Hum Mutat. 2017 Apr;38(4):390-399. doi: 10.1002/humu.23159. Epub 2017 Feb 15. Hum Mutat. 2017. PMID: 27995740 Free PMC article.

3

Allelic and copy-number variations of FcγRs affect granulocyte function and susceptibility for autoimmune blistering diseases.

Recke A, Vidarsson G, Ludwig RJ, Freitag M, Möller S, Vonthein R, Schellenberger J, Haase O, Görg S, Nebel A, Flachsbart F, Schreiber S, Lieb W, Gläser R, Benoit S, Sárdy M, Eming R, Hertl M, Zillikens D, König IR, Schmidt E, Ibrahim S; German AIBD Genetic Study Group. Recke A, et al. J Autoimmun. 2015 Jul;61:36-44. doi: 10.1016/j.jaut.2015.05.004. Epub 2015 May 29. J Autoimmun. 2015. PMID: 26032265

4

Nonallelic homologous recombination of the FCGR2/3 locus results in copy number variation and novel chimeric FCGR2 genes with aberrant functional expression.

Nagelkerke SQ, Tacke CE, Breunis WB, Geissler J, Sins JW, Appelhof B, van den Berg TK, de Boer M, Kuijpers TW. Nagelkerke SQ, et al. Genes Immun. 2015 Sep;16(6):422-9. doi: 10.1038/gene.2015.25. Epub 2015 Jul 2. Genes Immun. 2015. PMID: 26133275

5

Genetic Variation in Low-To-Medium-Affinity Fcγ Receptors: Functional Consequences, Disease Associations, and Opportunities for Personalized Medicine.

Nagelkerke SQ, Schmidt DE, de Haas M, Kuijpers TW. Nagelkerke SQ, et al. Front Immunol. 2019 Oct 3;10:2237. doi: 10.3389/fimmu.2019.02237. eCollection 2019. Front Immunol. 2019. PMID: 31632391 Free PMC article. Review.

6

Evidence for both copy number and allelic (NA1/NA2) risk at the FCGR3B locus in systemic lupus erythematosus.

Morris DL, Roberts AL, Witherden AS, Tarzi R, Barros P, Whittaker JC, Cook TH, Aitman TJ, Vyse TJ. Morris DL, et al. Eur J Hum Genet. 2010 Sep;18(9):1027-31. doi: 10.1038/ejhg.2010.56. Epub 2010 May 5. Eur J Hum Genet. 2010. PMID: 20442749 Free PMC article.

7

FCGR Genetic Variation in Two Populations From Ecuador Highlands-Extensive Copy-Number Variation, Distinctive Distribution of Functional Polymorphisms, and a Novel, Locally Common, Chimeric FCGR3B/A (CD16B/A) Gene.

Moraru M, Perez-Portilla A, Al-Akioui Sanz K, Blazquez-Moreno A, Arnaiz-Villena A, Reyburn HT, Vilches C. Moraru M, et al. Front Immunol. 2021 May 24;12:615645. doi: 10.3389/fimmu.2021.615645. eCollection 2021. Front Immunol. 2021. PMID: 34108956 Free PMC article.

8

Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases.

Mamtani M, Anaya JM, He W, Ahuja SK. Mamtani M, et al. Genes Immun. 2010 Mar;11(2):155-60. doi: 10.1038/gene.2009.71. Epub 2009 Sep 10. Genes Immun. 2010. PMID: 19741716

9

Meta-analysis confirms a role for deletion in FCGR3B in autoimmune phenotypes.

McKinney C, Merriman TR. McKinney C, et al. Hum Mol Genet. 2012 May 15;21(10):2370-6. doi: 10.1093/hmg/dds039. Epub 2012 Feb 14. Hum Mol Genet. 2012. PMID: 22337955

10

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans.

Aitman TJ, Dong R, Vyse TJ, Norsworthy PJ, Johnson MD, Smith J, Mangion J, Roberton-Lowe C, Marshall AJ, Petretto E, Hodges MD, Bhangal G, Patel SG, Sheehan-Rooney K, Duda M, Cook PR, Evans DJ, Domin J, Flint J, Boyle JJ, Pusey CD, Cook HT. Aitman TJ, et al. Nature. 2006 Feb 16;439(7078):851-5. doi: 10.1038/nature04489. Nature. 2006. PMID: 16482158

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