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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_swepub_ki_se_500933

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

About this item

Full title

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Author / Creator

Merico, Daniele , Antaki, Danny , Shetty, Aniket , Gujral, Madhusudan , Brandler, William M , Malhotra, Dheeraj , Alexander, Madeline , Belliveau, Richard A , Bergen, Sarah E , Bertalan, Marcelo , Bevilacqua, Elizabeth , Cantor, Rita M , Carrera, Noa , Cormican, Paul , Crespo-Facorro, Benedicto , Curtis, David , Davidson, Michael , Degenhardt, Franziska , Del Favero, Jurgen , DeLisi, Lynn E , Dudbridge, Frank , Eichhammer, Peter , Eriksson, Johan , Essioux, Laurent , Farrell, Martilias S , Freedman, Robert , Freimer, Nelson B , Georgieva, Lyudmila , Gershon, Elliot S , Giegling, Ina , Godard, Stephanie , Goldstein, Jacqueline I , Hamshere, Marian L , Hartmann, Annette M , Hofman, Andrea , Kähler, Anna K , Kalaydjieva, Luba , Kelly, Brian J , Lee, S Hong , Legge, Sophie E , Lerer, Bernard , Levy, Deborah L , Maher, Brion S , Mattingsdal, Morten , McDonald, Colm , Metspalu, Andres , Milanova, Vihra , Morris, Derek W , Murray, Robin M , Nestadt, Gerald , Nicodemus, Kristin K , Nordin, Annelie , Oh, Sang-Yun , Olsen, Line , Van Os, Jim , Pantelis, Christos , Pers, Tune H , Powell, John , Price, Alkes , Pulver, Ann E , Purcell, Shaun M , Rasmussen, Henrik B , Richards, Alexander L , Roussos, Panos , Schall, Ulrich , Schwab, Sibylle G , Smoller, Jordan W , Spencer, Chris C A , Stahl, Eli A , Stroup, T Scott , Suvisaari, Jaana , Svrakic, Dragan M , Szatkiewicz, Jin P , Veijola, Juha , Waddington, John , Webb, Bradley T , Williams, Nigel M , Williams, Stephanie , Wolen, Aaron R , Adolfsson, Rolf , Blackwood, Douglas H R , Bramon, Elvira , Buxbaum, Joseph D , Collier, David A , Daly, Mark J , Darvasi, Ariel , Domenici, Enrico , Gill, Michael , Iwata, Nakao , Jablensky, Assen V , Jönsson, Erik G , Kirov, George , Knight, Jo , Levinson, Douglas F , Ophoff, Roel A , Owen, Michael J , Rietschel, Marcella , Rujescu, Dan , O'Donovan, Michael C , Neale, Benjamin M , Psychosis Endophenotypes International Consortium and CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium

Publisher

New York: Nature Publishing Group US

Journal title

Nature genetics, 2017-01, Vol.49 (1), p.27-35

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

The CNV analysis group of the Psychiatric Genomic Consortium analyzes a large schizophrenia cohort to examine genomic copy number variants (CNVs) and disease risk. They find an enrichment of CNV burden in cases versus controls and identify 8 genome-wide significant loci as well as novel suggestive loci conferring either risk or protection to schizo...

Alternative Titles

Full title

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Authors, Artists and Contributors

Author / Creator

Merico, Daniele
Antaki, Danny
Shetty, Aniket
Gujral, Madhusudan
Brandler, William M
Malhotra, Dheeraj
Alexander, Madeline
Belliveau, Richard A
Bergen, Sarah E
Bertalan, Marcelo
Bevilacqua, Elizabeth
Cantor, Rita M
Carrera, Noa
Cormican, Paul
Crespo-Facorro, Benedicto
Curtis, David
Davidson, Michael
Degenhardt, Franziska
Del Favero, Jurgen
DeLisi, Lynn E
Dudbridge, Frank
Eichhammer, Peter
Eriksson, Johan
Essioux, Laurent
Farrell, Martilias S
Freedman, Robert
Freimer, Nelson B
Georgieva, Lyudmila
Gershon, Elliot S
Giegling, Ina
Godard, Stephanie
Goldstein, Jacqueline I
Hamshere, Marian L
Hartmann, Annette M
Hofman, Andrea
Kähler, Anna K
Kalaydjieva, Luba
Kelly, Brian J
Lee, S Hong
Legge, Sophie E
Lerer, Bernard
Levy, Deborah L
Maher, Brion S
Mattingsdal, Morten
McDonald, Colm
Metspalu, Andres
Milanova, Vihra
Morris, Derek W
Murray, Robin M
Nestadt, Gerald
Nicodemus, Kristin K
Nordin, Annelie
Oh, Sang-Yun
Olsen, Line
Van Os, Jim
Pantelis, Christos
Pers, Tune H
Powell, John
Price, Alkes
Pulver, Ann E
Purcell, Shaun M
Rasmussen, Henrik B
Richards, Alexander L
Roussos, Panos
Schall, Ulrich
Schwab, Sibylle G
Smoller, Jordan W
Spencer, Chris C A
Stahl, Eli A
Stroup, T Scott
Suvisaari, Jaana
Svrakic, Dragan M
Szatkiewicz, Jin P
Veijola, Juha
Waddington, John
Webb, Bradley T
Williams, Nigel M
Williams, Stephanie
Wolen, Aaron R
Adolfsson, Rolf
Blackwood, Douglas H R
Bramon, Elvira
Buxbaum, Joseph D
Collier, David A
Daly, Mark J
Darvasi, Ariel
Domenici, Enrico
Gill, Michael
Iwata, Nakao
Jablensky, Assen V
Jönsson, Erik G
Kirov, George
Knight, Jo
Levinson, Douglas F
Ophoff, Roel A
Owen, Michael J
Rietschel, Marcella
Rujescu, Dan
O'Donovan, Michael C
Neale, Benjamin M
Psychosis Endophenotypes International Consortium
CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_swepub_primary_oai_swepub_ki_se_500933

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_swepub_ki_se_500933

Other Identifiers

ISSN

1061-4036,1546-1718

E-ISSN

1546-1718

DOI

10.1038/ng.3725