Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

Margaux F. Keller, Mohamad Saad, Jose Bras, Francesco Bettella, Nayia Nicolaou, Javier Simón-Sánchez, Florian Mittag, Finja Büchel, Manu Sharma, J. Raphael Gibbs, Claudia Schulte, Valentina Moskvina, Alexandra Durr, Peter Holmans, Laura L. Kilarski, Rita Guerreiro, Dena G. Hernandez, Alexis Brice, Pauli Ylikotila, Hreinn Stefánsson & 10 others Kari Majamaa, Huw R. Morris, Nigel Williams, Thomas Gasser, Peter Heutink, Nicholas W. Wood, John Hardy, Maria Martinez, Andrew B. Singleton, Michael A. Nalls

Research output: Contribution to journalComment/debate

Original languageEnglish
Article numberddt199
Number of pages1
JournalHuman Molecular Genetics
Volume22
Issue number14
DOIs
Publication statusPublished - 1 Jul 2013
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simón-Sánchez, J., ... Nalls, M. A. (2013). Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics, 22(14), [ddt199]. https://doi.org/10.1093/hmg/ddt199

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. / Keller, Margaux F.; Saad, Mohamad; Bras, Jose; Bettella, Francesco; Nicolaou, Nayia; Simón-Sánchez, Javier; Mittag, Florian; Büchel, Finja; Sharma, Manu; Gibbs, J. Raphael; Schulte, Claudia; Moskvina, Valentina; Durr, Alexandra; Holmans, Peter; Kilarski, Laura L.; Guerreiro, Rita; Hernandez, Dena G.; Brice, Alexis; Ylikotila, Pauli; Stefánsson, Hreinn; Majamaa, Kari; Morris, Huw R.; Williams, Nigel; Gasser, Thomas; Heutink, Peter; Wood, Nicholas W.; Hardy, John; Martinez, Maria; Singleton, Andrew B.; Nalls, Michael A.

In: Human Molecular Genetics, Vol. 22, No. 14, ddt199, 01.07.2013.

Research output: Contribution to journalComment/debate

Keller, MF, Saad, M, Bras, J, Bettella, F, Nicolaou, N, Simón-Sánchez, J, Mittag, F, Büchel, F, Sharma, M, Gibbs, JR, Schulte, C, Moskvina, V, Durr, A, Holmans, P, Kilarski, LL, Guerreiro, R, Hernandez, DG, Brice, A, Ylikotila, P, Stefánsson, H, Majamaa, K, Morris, HR, Williams, N, Gasser, T, Heutink, P, Wood, NW, Hardy, J, Martinez, M, Singleton, AB & Nalls, MA 2013, 'Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease', Human Molecular Genetics, vol. 22, no. 14, ddt199. https://doi.org/10.1093/hmg/ddt199
Keller, Margaux F. ; Saad, Mohamad ; Bras, Jose ; Bettella, Francesco ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Mittag, Florian ; Büchel, Finja ; Sharma, Manu ; Gibbs, J. Raphael ; Schulte, Claudia ; Moskvina, Valentina ; Durr, Alexandra ; Holmans, Peter ; Kilarski, Laura L. ; Guerreiro, Rita ; Hernandez, Dena G. ; Brice, Alexis ; Ylikotila, Pauli ; Stefánsson, Hreinn ; Majamaa, Kari ; Morris, Huw R. ; Williams, Nigel ; Gasser, Thomas ; Heutink, Peter ; Wood, Nicholas W. ; Hardy, John ; Martinez, Maria ; Singleton, Andrew B. ; Nalls, Michael A. / Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. In: Human Molecular Genetics. 2013 ; Vol. 22, No. 14.
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AU - Bras, Jose

AU - Bettella, Francesco

AU - Nicolaou, Nayia

AU - Simón-Sánchez, Javier

AU - Mittag, Florian

AU - Büchel, Finja

AU - Sharma, Manu

AU - Gibbs, J. Raphael

AU - Schulte, Claudia

AU - Moskvina, Valentina

AU - Durr, Alexandra

AU - Holmans, Peter

AU - Kilarski, Laura L.

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AU - Hernandez, Dena G.

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AU - Ylikotila, Pauli

AU - Stefánsson, Hreinn

AU - Majamaa, Kari

AU - Morris, Huw R.

AU - Williams, Nigel

AU - Gasser, Thomas

AU - Heutink, Peter

AU - Wood, Nicholas W.

AU - Hardy, John

AU - Martinez, Maria

AU - Singleton, Andrew B.

AU - Nalls, Michael A.

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