Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

C.C.A. Spencer; V. Plagnol; A. Strange; M. Gardner; C. Paisan-Ruiz; G. Band; R.A. Barker; C. Bellenguez; K. Bhatia; H. Blackburn; J.M. Blackwell; E. Bramon; M.A. Brown; D. Burn; J.-P. Casas; P.F. Chinnery; C.E. Clarke; A. Corvin; N. Craddock; P. Deloukas; S. Edkins; J. Evans; C. Freeman; E. Gray; J. Hardy; G. Hudson; S. Hunt; J. Jankowski; C. Langford; A.J. Lees; H.S. Markus; C.G. Mathew; M.I. McCarthy; K.E. Morrison; C.N.A. Palmer; J.P. Pearson; L. Peltonen; M. Pirinen; R. Plomin; S. Potter; A. Rautanen; S.J. Sawcer; Z. Su; R.C. Trembath; A.C. Viswanathan; N.W. Williams; H.R. Morris; P. Donnelly; N.W. Wood

doi:10.1093/hmg/ddq469

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

C.C.A. Spencer, V. Plagnol, A. Strange, M. Gardner, C. Paisan-Ruiz, G. Band, R.A. Barker, C. Bellenguez, K. Bhatia, H. Blackburn, J.M. Blackwell, E. Bramon, M.A. Brown, D. Burn, J.-P. Casas, P.F. Chinnery, C.E. Clarke, A. Corvin, N. Craddock, P. DeloukasS. Edkins, J. Evans, C. Freeman, E. Gray, J. Hardy, G. Hudson, S. Hunt, J. Jankowski, C. Langford, A.J. Lees, H.S. Markus, C.G. Mathew, M.I. McCarthy, K.E. Morrison, C.N.A. Palmer, J.P. Pearson, L. Peltonen, M. Pirinen, R. Plomin, S. Potter, A. Rautanen, S.J. Sawcer, Z. Su, R.C. Trembath, A.C. Viswanathan, N.W. Williams, H.R. Morris, P. Donnelly, N.W. Wood

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

166 Citations (Scopus)

Original language	English
Pages (from-to)	345-353
Number of pages	9
Journal	Human Molecular Genetics
Volume	20
Issue number	2
DOIs	https://doi.org/10.1093/hmg/ddq469
Publication status	Published - 15 Jan 2011

Access to Document

10.1093/hmg/ddq469

Cite this

Spencer, C. C. A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., Barker, R. A., Bellenguez, C., Bhatia, K., Blackburn, H., Blackwell, J. M., Bramon, E., Brown, M. A., Burn, D., Casas, J-P., Chinnery, P. F., Clarke, C. E., Corvin, A., Craddock, N., ... Wood, N. W. (2011). Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Human Molecular Genetics, 20(2), 345-353. https://doi.org/10.1093/hmg/ddq469

Spencer, C.C.A. ; Plagnol, V. ; Strange, A. ; Gardner, M. ; Paisan-Ruiz, C. ; Band, G. ; Barker, R.A. ; Bellenguez, C. ; Bhatia, K. ; Blackburn, H. ; Blackwell, J.M. ; Bramon, E. ; Brown, M.A. ; Burn, D. ; Casas, J.-P. ; Chinnery, P.F. ; Clarke, C.E. ; Corvin, A. ; Craddock, N. ; Deloukas, P. ; Edkins, S. ; Evans, J. ; Freeman, C. ; Gray, E. ; Hardy, J. ; Hudson, G. ; Hunt, S. ; Jankowski, J. ; Langford, C. ; Lees, A.J. ; Markus, H.S. ; Mathew, C.G. ; McCarthy, M.I. ; Morrison, K.E. ; Palmer, C.N.A. ; Pearson, J.P. ; Peltonen, L. ; Pirinen, M. ; Plomin, R. ; Potter, S. ; Rautanen, A. ; Sawcer, S.J. ; Su, Z. ; Trembath, R.C. ; Viswanathan, A.C. ; Williams, N.W. ; Morris, H.R. ; Donnelly, P. ; Wood, N.W. / Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. In: Human Molecular Genetics. 2011 ; Vol. 20, No. 2. pp. 345-353.

@article{2fe4282df9ee4057acbea29a9c4adf71,

title = "Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21",

author = "C.C.A. Spencer and V. Plagnol and A. Strange and M. Gardner and C. Paisan-Ruiz and G. Band and R.A. Barker and C. Bellenguez and K. Bhatia and H. Blackburn and J.M. Blackwell and E. Bramon and M.A. Brown and D. Burn and J.-P. Casas and P.F. Chinnery and C.E. Clarke and A. Corvin and N. Craddock and P. Deloukas and S. Edkins and J. Evans and C. Freeman and E. Gray and J. Hardy and G. Hudson and S. Hunt and J. Jankowski and C. Langford and A.J. Lees and H.S. Markus and C.G. Mathew and M.I. McCarthy and K.E. Morrison and C.N.A. Palmer and J.P. Pearson and L. Peltonen and M. Pirinen and R. Plomin and S. Potter and A. Rautanen and S.J. Sawcer and Z. Su and R.C. Trembath and A.C. Viswanathan and N.W. Williams and H.R. Morris and P. Donnelly and N.W. Wood",

year = "2011",

month = jan,

day = "15",

doi = "10.1093/hmg/ddq469",

language = "English",

volume = "20",

pages = "345--353",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "2",

}

Spencer, CCA, Plagnol, V, Strange, A, Gardner, M, Paisan-Ruiz, C, Band, G, Barker, RA, Bellenguez, C, Bhatia, K, Blackburn, H, Blackwell, JM, Bramon, E, Brown, MA, Burn, D, Casas, J-P, Chinnery, PF, Clarke, CE, Corvin, A, Craddock, N, Deloukas, P, Edkins, S, Evans, J, Freeman, C, Gray, E, Hardy, J, Hudson, G, Hunt, S, Jankowski, J, Langford, C, Lees, AJ, Markus, HS, Mathew, CG, McCarthy, MI, Morrison, KE, Palmer, CNA, Pearson, JP, Peltonen, L, Pirinen, M, Plomin, R, Potter, S, Rautanen, A, Sawcer, SJ, Su, Z, Trembath, RC, Viswanathan, AC, Williams, NW, Morris, HR, Donnelly, P & Wood, NW 2011, 'Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21', Human Molecular Genetics, vol. 20, no. 2, pp. 345-353. https://doi.org/10.1093/hmg/ddq469

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. / Spencer, C.C.A.; Plagnol, V.; Strange, A.; Gardner, M.; Paisan-Ruiz, C.; Band, G.; Barker, R.A.; Bellenguez, C.; Bhatia, K.; Blackburn, H.; Blackwell, J.M.; Bramon, E.; Brown, M.A.; Burn, D.; Casas, J.-P.; Chinnery, P.F.; Clarke, C.E.; Corvin, A.; Craddock, N.; Deloukas, P.; Edkins, S.; Evans, J.; Freeman, C.; Gray, E.; Hardy, J.; Hudson, G.; Hunt, S.; Jankowski, J.; Langford, C.; Lees, A.J.; Markus, H.S.; Mathew, C.G.; McCarthy, M.I.; Morrison, K.E.; Palmer, C.N.A.; Pearson, J.P.; Peltonen, L.; Pirinen, M.; Plomin, R.; Potter, S.; Rautanen, A.; Sawcer, S.J.; Su, Z.; Trembath, R.C.; Viswanathan, A.C.; Williams, N.W.; Morris, H.R.; Donnelly, P.; Wood, N.W.

In: Human Molecular Genetics, Vol. 20, No. 2, 15.01.2011, p. 345-353.

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

TY - JOUR

T1 - Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

AU - Spencer, C.C.A.

AU - Plagnol, V.

AU - Strange, A.

AU - Gardner, M.

AU - Paisan-Ruiz, C.

AU - Band, G.

AU - Barker, R.A.

AU - Bellenguez, C.

AU - Bhatia, K.

AU - Blackburn, H.

AU - Blackwell, J.M.

AU - Bramon, E.

AU - Brown, M.A.

AU - Burn, D.

AU - Casas, J.-P.

AU - Chinnery, P.F.

AU - Clarke, C.E.

AU - Corvin, A.

AU - Craddock, N.

AU - Deloukas, P.

AU - Edkins, S.

AU - Evans, J.

AU - Freeman, C.

AU - Gray, E.

AU - Hardy, J.

AU - Hudson, G.

AU - Hunt, S.

AU - Jankowski, J.

AU - Langford, C.

AU - Lees, A.J.

AU - Markus, H.S.

AU - Mathew, C.G.

AU - McCarthy, M.I.

AU - Morrison, K.E.

AU - Palmer, C.N.A.

AU - Pearson, J.P.

AU - Peltonen, L.

AU - Pirinen, M.

AU - Plomin, R.

AU - Potter, S.

AU - Rautanen, A.

AU - Sawcer, S.J.

AU - Su, Z.

AU - Trembath, R.C.

AU - Viswanathan, A.C.

AU - Williams, N.W.

AU - Morris, H.R.

AU - Donnelly, P.

AU - Wood, N.W.

PY - 2011/1/15

Y1 - 2011/1/15

U2 - 10.1093/hmg/ddq469

DO - 10.1093/hmg/ddq469

M3 - Article

VL - 20

SP - 345

EP - 353

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 2

ER -