Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

O.M.E. Albagha; M. Visconti; N. Alonso; A.L. Langston; T. Cundy; R. Dargie; M.G. Dunlop; W.D. Fraser; M.J. Hooper; G. Isaia; G.C. Micholson; J. Del Pino Montes; R. Gonzalez-Sarmiento; M. Di Stefano; John Walsh; S.H. Ralston

doi:10.1038/ng.562

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

O.M.E. Albagha, M. Visconti, N. Alonso, A.L. Langston, T. Cundy, R. Dargie, M.G. Dunlop, W.D. Fraser, M.J. Hooper, G. Isaia, G.C. Micholson, J. Del Pino Montes, R. Gonzalez-Sarmiento, M. Di Stefano, John Walsh, S.H. Ralston

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242 Citations (Scopus)

Original language	English
Pages (from-to)	520-525
Journal	Nature Genetics
Volume	42
Issue number	6
DOIs	https://doi.org/10.1038/ng.562
Publication status	Published - 2010

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10.1038/ng.562

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Albagha, O. M. E., Visconti, M., Alonso, N., Langston, A. L., Cundy, T., Dargie, R., Dunlop, M. G., Fraser, W. D., Hooper, M. J., Isaia, G., Micholson, G. C., Del Pino Montes, J., Gonzalez-Sarmiento, R., Di Stefano, M., Walsh, J., & Ralston, S. H. (2010). Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. Nature Genetics, 42(6), 520-525. https://doi.org/10.1038/ng.562

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title = "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone",

author = "O.M.E. Albagha and M. Visconti and N. Alonso and A.L. Langston and T. Cundy and R. Dargie and M.G. Dunlop and W.D. Fraser and M.J. Hooper and G. Isaia and G.C. Micholson and {Del Pino Montes}, J. and R. Gonzalez-Sarmiento and {Di Stefano}, M. and John Walsh and S.H. Ralston",

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Albagha, OME, Visconti, M, Alonso, N, Langston, AL, Cundy, T, Dargie, R, Dunlop, MG, Fraser, WD, Hooper, MJ, Isaia, G, Micholson, GC, Del Pino Montes, J, Gonzalez-Sarmiento, R, Di Stefano, M, Walsh, J & Ralston, SH 2010, 'Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone', Nature Genetics, vol. 42, no. 6, pp. 520-525. https://doi.org/10.1038/ng.562

TY - JOUR

T1 - Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

AU - Albagha, O.M.E.

AU - Visconti, M.

AU - Alonso, N.

AU - Langston, A.L.

AU - Cundy, T.

AU - Dargie, R.

AU - Dunlop, M.G.

AU - Fraser, W.D.

AU - Hooper, M.J.

AU - Isaia, G.

AU - Micholson, G.C.

AU - Del Pino Montes, J.

AU - Gonzalez-Sarmiento, R.

AU - Di Stefano, M.

AU - Walsh, John

AU - Ralston, S.H.

PY - 2010

Y1 - 2010

U2 - 10.1038/ng.562

DO - 10.1038/ng.562

M3 - Article

C2 - 20436471

SN - 1061-4036

VL - 42

SP - 520

EP - 525

JO - Nature Genetics

JF - Nature Genetics

IS - 6

ER -