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

Human Molecular Genetics

Volumn 21, Issue 22, 2012, Pages 4996-5009

  Keller, Margaux F ^a,b   Saad, Mohamad ^c,d   Bras, Jose ^e   Bettella, Francesco ^g   Nicolaou, Nayia ^h   Simón Sánchez, Javier ^h   Mittag, Florian ^c   Büchel, Finja ^c   Sharma, Manu ^i,j   Gibbs, J Raphael ^a,e   Schulte, Claudia ^i,j   Moskvina, Valentina ^k   Durr, Alexandra ^c,l,m,n   Holmans, Peter ^k   Kilarski, Laura L ^k   Guerreiro, Rita ^e   Hernandez, Dena G ^a,e   Brice, Alexis ^c,l,m,n,q,ag   Ylikotila, Pauli ^o   Stefánsson, Hreinn ^g   Majamaa, Kari ^p   Morris, Huw R ^k   Williams, Nigel ^k   Gasser, Thomas ^d,e,i,j   Heutink, Peter ^g,h   Wood, Nicholas W ^e,f   Hardy, John ^e   Martinez, Maria ^c,d,f,g   Singleton, Andrew B ^a   Nalls, Michael A ^a   Plagnol, Vincent ^f   Sheerin, Una Marie ^e   Lesage, Suzanne ^l,n,q   Sveinbjörnsdóttir, Sigurlaug ^r,s,t   Arepalli, Sampath ^a   Barker, Roger ^u   Ben Shlomo, Yoav ^v   Berendse, Henk W ^h   Berg, Daniela ⁱ   Bhatia, Kailash ^e   de Bie, Rob M A ^w   Biffi, Alessandro ^x,y   Bloem, Bas ^z   Bochdanovits, Zoltan ^h   Bonin, Michael ^aa   Brockmann, Kathrin ⁱ   Brooks, Janet ^a   Burn, David J ^ab   Charlesworth, Gavin ^e   Chen, Honglei ^ac   Chinnery, Patrick F ^ad   Chong, Sean ^a   Clarke, Carl E ^ae,af   Cookson, Mark R ^a   Cooper, J Mark ^e   Corvol, Jean Christophe ^l,n,q,ag   Counsell, Carl ^ah   Damier, Philippe ^ai   Dartigues, Jean François ^c   Deloukas, Panos ^aj   Deuschl, Günther ^ak   Dexter, David T ^al   van Dijk, Karin D ^h   Dillman, Allissa ^a   Durif, Frank ^am   Dürr, Alexandra ^l,n,q,ag   Edkins, Sarah ^aj   Evans, Jonathan R ^an   Foltynie, Thomas ^e   Gao, Jianjun ^ac   Gardner, Michelle ^e   Goate, Alison ^ao   Gray, Emma ^aj   Gústafsson, Ómar ^g,ap   Harris, Clare ^ah   van Hilten, Jacobus J ^aq   Hofman, Albert ^ar   Hollenbeck, Albert ^as   Holton, Janice ^e   Hu, Michele ^at   Huang, Xuemei ^au   Huber, Heiko ^d   Hudson, Gavin ^ad   Hunt, Sarah E ^aj   Huttenlocher, Johanna ^g   Illig, Thomas ^av   Jónsson, Pálmi V ^r   Lambert, Jean Charles ^c,aw   Langford, Cordelia ^aj,an   Lees, Andrew ^e   Lichtner, Peter ^av   Limousin, Patricia ^e   Lopez, Grisel ^ax   Lorenz, Delia ^ak   McNeill, Alisdair ^e   Moorby, Catriona ^ae   Moore, Matthew ^a   Morrison, Karen E ^ae,ay   Mudanohwo, Ese ^az   O'Sullivan, Sean S ^e   Pearson, Justin ^k   Perlmutter, Joel S ^ao   Pétursson, Hjörvar ^g,aa   Pollak, Pierre ^ba   Post, Bart ^z   Potter, Simon C ^aj   Ravina, Bernard ^bb   Revesz, Tamas ^e   Riess, Olaf ^aa   Rivadeneira, Fernando ^ar   Rizzu, Patrizia ^h   Ryten, Mina ^e   Sawcer, Stephen J ^bc   Schapira, Anthony ^e   Scheffer, Hans ^z   Shaw, Karen ^e   Shoulson, Ira ^bd   Sidransky, Ellen ^ax   Smith, Colin ^be   Spencer, Chris C A ^bf   Steinberg, Stacy ^g   Stockton, Joanna D ^ae   Strange, Amy ^bf   Talbot, Kevin ^bg   Tanner, Carlie M ^bh   Tashakkori Ghanbaria, Avazeh ^aj   Tison, François ^bi   Trabzuni, Daniah ^e   Traynor, Bryan J ^a   Uitterlinden, André G ^bb   Velseboer, Daan ^w   Vidailhet, Marie ^l,q   Walker, Robert ^bd   van de Warrenburg, Bart ^z   Wickremaratchi, Mirdhu ^bj   Williams Gray, Caroline H ^u   Winder Rhodes, Sophie ^aj   Stefánsson, Kári ^g   Donnelly, Peter ^bf,bg   Barroso, Ines ^aj   Blackwell, Jenefer M ^bk,bl   Bramon, Elvira ^bm   Brown, Matthew A ^bn   Casas, Juan P ^f,bo   Corvin, Aiden ^bp   Duncanson, Audrey ^aj   Jankowski, Janusz ^t,bg,bq   Markus, Hugh S ^br   Mathew, Christopher G ^bs   Palmer, Colin N A ^bt   Plomin, Robert ^bm   Rautanen, Anna ^bf   Trembath, Richard C ^br   Viswanathan, Ananth C ^bu   Band, Gavin ^bf   Bellenguez, Céline ^bf   Freeman, Colin ^bf   Hellenthal, Garrett ^bf   Giannoulatou, Eleni ^bf   Pirinen, Matti ^bf   Pearson, Richard ^bf   Su, Zhan ^bf   Vukcevic, Damjan ^bf   Gwilliam, Rhian ^aj   Blackburn, Hannah ^aj   Bumpstead, Suzannah J ^aj   Dronov, Serge ^aj   Gillman, Matthew ^aj   Hammond, Naomi ^aj   Jayakumar, Alagurevathi ^aj   McCann, Owen T ^aj   Liddle, Jennifer ^aj   Ravindrarajah, Radhi ^aj   Ricketts, Michelle ^aj   Waller, Matthew ^aj   Weston, Paul ^aj   Widaa, Sara ^aj   Whittaker, Pamela ^aj   McCarthy, Mark I ^bv   more..

^a NATIONAL INSTITUTE ON AGING   (United States)

^b TEMPLE UNIVERSITY   (United States)

^c INSERM   (France)

^d UNIVERSITÉ DE TOULOUSE   (France)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

^f UNIVERSITY COLLEGE LONDON   (United Kingdom)

^g DECODE GENETICS   (Iceland)

^h VU UNIVERSITY MEDICAL CENTER   (Netherlands)

ⁱ UNIVERSITY OF TÜBINGEN   (Germany)

^j GERMAN CENTER FOR NEURODEGENERATIVE DISEASES DZNE   (Germany)

^k CARDIFF UNIVERSITY SCHOOL OF MEDICINE   (United Kingdom)

^l SORBONNE UNIVERSITÉ   (France)

^m ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

ⁿ CNRS   (France)

^o TURKU UNIVERSITY HOSPITAL   (Finland)

^p UNIVERSITY OF OULU   (Finland)

^q INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE   (France)

^r LANDSPITALI UNIVERSITY HOSPITAL   (Iceland)

^s BROOMFIELD HOSPITAL   (United Kingdom)

^t QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^u UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^v UNIVERSITY OF BRISTOL   (United Kingdom)

^w UNIVERSITY OF AMSTERDAM   (Netherlands)

^x MASSACHUSETTS GENERAL HOSPITAL   (United States)

^y BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^z RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^aa UNIVERSITY OF TÜBINGEN   (Germany)

^ab NEWCASTLE UNIVERSITY   (United Kingdom)

^ac NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES   (United States)

^ad NEWCASTLE UNIVERSITY   (United Kingdom)

^ae UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^af CITY HOSPITAL   (United Kingdom)

^ag PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^ah UNIVERSITY OF ABERDEEN   (United Kingdom)

^ai NANTES UNIVERSITY HOSPITAL   (France)

^aj WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^ak UNIVERSITY OF KIEL   (Germany)

^al IMPERIAL COLLEGE LONDON   (United Kingdom)

^am SERVICE DE RHUMATOLOGIE   (France)

^an UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^ao WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^ap OSLO UNIVERSITY HOSPITAL   (Norway)

^aq LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^ar ERASMUS MEDICAL CENTER   (Netherlands)

^as AARP   (United States)

^at JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^au PENN STATE MILTON S HERSHEY MEDICAL CENTER   (United States)

^av INSTITUTE OF EPIDEMIOLOGY   (Germany)

^aw UNIV LILLE   (France)

^ax NATIONAL INSTITUTES OF HEALTH   (United States)

^ay QUEEN ELIZABETH HOSPITAL   (United Kingdom)

^az NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^ba GRENOBLE UNIVERSITY HOSPITAL   (France)

^bb BIOGEN   (United States)

^bc UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^bd UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^be UNIVERSITY OF EDINBURGH   (United Kingdom)

^bf UNIVERSITY OF OXFORD   (United Kingdom)

^bg UNIVERSITY OF OXFORD   (United Kingdom)

^bh PARKINSON S INSTITUTE   (United States)

^bi HAUT LÉVÊQUE HOSPITAL   (France)

^bj CARDIFF UNIVERSITY   (United Kingdom)

^bk UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^bl UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^bm KING'S COLLEGE LONDON   (United Kingdom)

^bn UNIVERSITY OF QUEENSLAND   (Australia)

^bo LONDON SCHOOL OF HYGIENE AND TROPICAL MEDICINE   (United Kingdom)

^bp TRINITY COLLEGE DUBLIN   (Ireland)

^bq LEICESTER ROYAL INFIRMARY   (United Kingdom)

^br ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^bs GUY S HOSPITAL   (United Kingdom)

^bt UNIVERSITY OF DUNDEE   (United Kingdom)

^bu MOORFIELDS EYE HOSPITAL   (United Kingdom)

^bv CHURCHILL HOSPITAL   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE CONTROL STUDY; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE COURSE; EUROPEAN AMERICAN; GENE LOCUS; GENETIC ASSOCIATION; GENETIC TRAIT; GENOME ANALYSIS; GENOME WIDE COMPLEX TRAIT ANALYSIS; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MATHEMATICAL MODEL; META ANALYSIS (TOPIC); PARKINSON DISEASE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS;

EID: 84868134823     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt030     Document Type: Erratum

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