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Recent advance in the genomic study for osteoarthritis

Clinical calcium, June 2011, Vol.21(6), pp.826-30

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Statin treatment rescues FGFR3 skeletal dysplasia phenotypes

Nature, 2014 [Peer Reviewed Journal]

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Statin treatment rescues FGFR3 skeletal dysplasia phenotypes.

Nature, September 25, 2014, Vol.513(7519), pp.507-511 [Peer Reviewed Journal]

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Genetics of ossification of the posterior longitudinal ligament of the spine: a mini review

Journal of bone metabolism, May 2014, Vol.21(2), pp.127-32 [Peer Reviewed Journal]

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The genetics of common degenerative skeletal disorders: osteoarthritis and degenerative disc disease

Annual review of genomics and human genetics, 2013, Vol.14, pp.245-56 [Peer Reviewed Journal]

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A Short History of the Genome-Wide Association Study: Where We Were and Where We Are Going

Genomics & Informatics, 01 December 2012, Vol.10(4), pp.220-225 [Peer Reviewed Journal]

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Genomic study of adolescent idiopathic scoliosis in Japan

Scoliosis and Spinal Disorders, 2016, Vol.11 [Peer Reviewed Journal]

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Genomic study of ossification of the posterior longitudinal ligament of the spine

Proceedings of the Japan Academy, Dec 2014, Vol.90(10), pp.405-412 [Peer Reviewed Journal]

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Identification and Functional Characterization of RSPO2 as a Susceptibility Gene for Ossification of the Posterior Longitudinal Ligament of the Spine

The American Journal of Human Genetics, 07 July 2016, Vol.99(1), pp.202-207 [Peer Reviewed Journal]

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Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I Deficiency

American Journal of Human Genetics, Jul 7, 2016, Vol.99(1), p.208 [Peer Reviewed Journal]

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by this Author/Contributor:

  1. Ikegawa, Shiro
  2. Ikegawa, S.
  3. Nishimura, Gen
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  5. Nakajima, Masahiro

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