The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes

Pui Yan Jenny Chung; Greet Beyens; Steven Boonen; Socrates Papapoulos; Piet Geusens; Marcel Karperien; Filip Vanhoenacker; Leon Verbruggen; Erik Fransen; Jan Van Offel; Stefan Goemaere; Hans-Georg Zmierczak; Rene Westhovens; Jean-Pierre Devogelaer; Wim Van Hul

doi:10.1007/s00439-010-0888-2

The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes

Pui Yan Jenny Chung, Greet Beyens, Steven Boonen, Socrates Papapoulos, Piet Geusens, Marcel Karperien, Filip Vanhoenacker, Leon Verbruggen, Erik Fransen, Jan Van Offel, Stefan Goemaere, Hans-Georg Zmierczak, Rene Westhovens, Jean-Pierre Devogelaer, Wim Van Hul^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	615-626
Journal	Human Genetics
Volume	128
Issue number	6
DOIs	https://doi.org/10.1007/s00439-010-0888-2
Publication status	Published - Dec 2010

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10.1007/s00439-010-0888-2

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Chung, P. Y. J., Beyens, G., Boonen, S., Papapoulos, S., Geusens, P., Karperien, M., Vanhoenacker, F., Verbruggen, L., Fransen, E., Van Offel, J., Goemaere, S., Zmierczak, H-G., Westhovens, R., Devogelaer, J-P., & Van Hul, W. (2010). The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes. Human Genetics, 128(6), 615-626. https://doi.org/10.1007/s00439-010-0888-2

Chung, Pui Yan Jenny ; Beyens, Greet ; Boonen, Steven ; Papapoulos, Socrates ; Geusens, Piet ; Karperien, Marcel ; Vanhoenacker, Filip ; Verbruggen, Leon ; Fransen, Erik ; Van Offel, Jan ; Goemaere, Stefan ; Zmierczak, Hans-Georg ; Westhovens, Rene ; Devogelaer, Jean-Pierre ; Van Hul, Wim. / The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes. In: Human Genetics. 2010 ; Vol. 128, No. 6. pp. 615-626.

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Chung, PYJ, Beyens, G, Boonen, S, Papapoulos, S, Geusens, P, Karperien, M, Vanhoenacker, F, Verbruggen, L, Fransen, E, Van Offel, J, Goemaere, S, Zmierczak, H-G, Westhovens, R, Devogelaer, J-P & Van Hul, W 2010, 'The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes', Human Genetics, vol. 128, no. 6, pp. 615-626. https://doi.org/10.1007/s00439-010-0888-2

The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes. / Chung, Pui Yan Jenny; Beyens, Greet; Boonen, Steven; Papapoulos, Socrates; Geusens, Piet; Karperien, Marcel; Vanhoenacker, Filip; Verbruggen, Leon; Fransen, Erik; Van Offel, Jan; Goemaere, Stefan; Zmierczak, Hans-Georg; Westhovens, Rene; Devogelaer, Jean-Pierre; Van Hul, Wim.

In: Human Genetics, Vol. 128, No. 6, 12.2010, p. 615-626.

Research output: Contribution to journal › Article › Academic › peer-review

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AU - Chung, Pui Yan Jenny

AU - Beyens, Greet

AU - Boonen, Steven

AU - Papapoulos, Socrates

AU - Geusens, Piet

AU - Karperien, Marcel

AU - Vanhoenacker, Filip

AU - Verbruggen, Leon

AU - Fransen, Erik

AU - Van Offel, Jan

AU - Goemaere, Stefan

AU - Zmierczak, Hans-Georg

AU - Westhovens, Rene

AU - Devogelaer, Jean-Pierre

AU - Van Hul, Wim

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DO - 10.1007/s00439-010-0888-2

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VL - 128

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