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; Kari Majamaa; Huw R. Morris; Nigel Williams; Thomas Gasser; Peter Heutink; Nicholas W. Wood; John Hardy; Maria Martinez; Andrew B. Singleton; Michael A. Nalls

doi:10.1093/hmg/ddt030

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

Kari Majamaa, Huw R. Morris, Nigel Williams, Thomas Gasser, Peter Heutink, Nicholas W. Wood, John Hardy, Maria Martinez, Andrew B. Singleton, Michael A. Nalls

^*Corresponding author for this work

Qatar Computing Research Institute

Research output: Contribution to journal › Comment/debate

1 Citation (Scopus)

Original language	English
Article number	ddt030
Pages (from-to)	1696
Number of pages	1
Journal	Human Molecular Genetics
Volume	22
Issue number	8
DOIs	https://doi.org/10.1093/hmg/ddt030
Publication status	Published - Apr 2013

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10.1093/hmg/ddt030

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Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Siḿn-śnchez, J., Mittag, F., B̈chel, F., Sharma, M., Gibbs, J. R., Schulte, C., Moskvina, V., Durr, A., Holmans, P., Kilarski, L. L., Guerreiro, R., Hernandez, D. G., Brice, A., Ylikotila, P., ... Nalls, M. A. (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, 22(8), 1696. Article ddt030. https://doi.org/10.1093/hmg/ddt030

@article{caa6efb6db6545698076b4cfc89e5af4,

title = "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]",

author = "Keller, \{Margaux F.\} and Mohamad Saad and Jose Bras and Francesco Bettella and Nayia Nicolaou and Javier Siḿn-{\'s}nchez and Florian Mittag and Finja {\"B}chel and Manu Sharma and Gibbs, \{J. Raphael\} and Claudia Schulte and Valentina Moskvina and Alexandra Durr and Peter Holmans and Kilarski, \{Laura L.\} and Rita Guerreiro and Hernandez, \{Dena G.\} and Alexis Brice and Pauli Ylikotila and Hreinn Ste{\'f}nsson and Kari Majamaa and Morris, \{Huw R.\} and Nigel Williams and Thomas Gasser and Peter Heutink and Wood, \{Nicholas W.\} and John Hardy and Maria Martinez and Singleton, \{Andrew B.\} and Nalls, \{Michael A.\}",

year = "2013",

month = apr,

doi = "10.1093/hmg/ddt030",

language = "English",

volume = "22",

pages = "1696",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "8",

}

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, pp. 1696. https://doi.org/10.1093/hmg/ddt030

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 et al.
In: Human Molecular Genetics, Vol. 22, No. 8, ddt030, 04.2013, p. 1696.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - 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

T2 - 10.1093/hmg/dds335]

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.

PY - 2013/4

Y1 - 2013/4

UR - https://www.scopus.com/pages/publications/84890714469

U2 - 10.1093/hmg/ddt030

DO - 10.1093/hmg/ddt030

M3 - Comment/debate

AN - SCOPUS:84890714469

SN - 0964-6906

VL - 22

SP - 1696

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 8

M1 - ddt030

ER -

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]

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