Corrigendum to Using genome-wide complex trait analysis to quantify 'missing heritability' in parkinson's disease [Human Molecular Genetics, 21

22 (2012) 4996-5009] doi: 10.1093/hmg/dds335]

Margaux F. Keller, Mohamad Saad, Jose Bras, Francesco Bettella, Nayia Nicolaou, Javier Siḿn-śnchez, Florian Mittag, Finja B̈chel, 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 Stef́nsson & 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

1 Citation (Scopus)
Original languageEnglish
Article numberddt030
Number of pages1
JournalHuman Molecular Genetics
Volume22
Issue number8
DOIs
Publication statusPublished - 1 Apr 2013
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Corrigendum to Using genome-wide complex trait analysis to quantify 'missing heritability' in parkinson's disease [Human Molecular Genetics, 21 : 22 (2012) 4996-5009] doi: 10.1093/hmg/dds335]. / Keller, Margaux F.; Saad, Mohamad; Bras, Jose; Bettella, Francesco; Nicolaou, Nayia; Siḿn-śnchez, Javier; Mittag, Florian; B̈chel, 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; Stef́nsson, 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. 8, ddt030, 01.04.2013.

Research output: Contribution to journalComment/debate

Keller, MF, Saad, M, Bras, J, Bettella, F, Nicolaou, N, Siḿn-śnchez, J, Mittag, F, B̈chel, F, Sharma, M, Gibbs, JR, Schulte, C, Moskvina, V, Durr, A, Holmans, P, Kilarski, LL, Guerreiro, R, Hernandez, DG, Brice, A, Ylikotila, P, Stef́nsson, H, Majamaa, K, Morris, HR, Williams, N, Gasser, T, Heutink, P, Wood, NW, Hardy, J, Martinez, M, Singleton, AB & Nalls, MA 2013, 'Corrigendum to Using genome-wide complex trait analysis to quantify 'missing heritability' in parkinson's disease [Human Molecular Genetics, 21: 22 (2012) 4996-5009] doi: 10.1093/hmg/dds335]', Human Molecular Genetics, vol. 22, no. 8, ddt030. https://doi.org/10.1093/hmg/ddt030
Keller, Margaux F. ; Saad, Mohamad ; Bras, Jose ; Bettella, Francesco ; Nicolaou, Nayia ; Siḿn-śnchez, Javier ; Mittag, Florian ; B̈chel, 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 ; Stef́nsson, 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. / Corrigendum to Using genome-wide complex trait analysis to quantify 'missing heritability' in parkinson's disease [Human Molecular Genetics, 21 : 22 (2012) 4996-5009] doi: 10.1093/hmg/dds335]. In: Human Molecular Genetics. 2013 ; Vol. 22, No. 8.
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AU - Keller, Margaux F.

AU - Saad, Mohamad

AU - Bras, Jose

AU - Bettella, Francesco

AU - Nicolaou, Nayia

AU - Siḿn-śnchez, Javier

AU - Mittag, Florian

AU - B̈chel, Finja

AU - Sharma, Manu

AU - Gibbs, J. Raphael

AU - Schulte, Claudia

AU - Moskvina, Valentina

AU - Durr, Alexandra

AU - Holmans, Peter

AU - Kilarski, Laura L.

AU - Guerreiro, Rita

AU - Hernandez, Dena G.

AU - Brice, Alexis

AU - Ylikotila, Pauli

AU - Stef́nsson, 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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