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1. Full Text The Routledge Companion to African American Theatre and Performance
by Perkins, Kathy A and Richards, Sandra L and Craft, Renee Alexander and DeFrantz, Thomas F
12/2018, 1, ISBN 1138726710, Volume 1, 450
The Routledge Companion to African American Theatre and Performance is an outstanding collection of specially written essays that charts the emergence,... 
African American theater | Performance Genres | American Performance | Performance Theory | African-American history | 20th Century Performance
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2. Full Text Biological insights from 108 schizophrenia-associated genetic loci
by Ripke, Stephan and Neale, Benjamin M and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Lee, Phil and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberly D and Chan, Raymond C. K and Chen, Ronald Y. L and Chen, Eric Y. H and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Durmishi, Naser and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Friedman, Joseph I and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Golimbet, Vera and Gopal, Srihari and Gratten, Jacob and de Haan, Lieuwe and Hammer, Christian and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Hollegaard, Mads V and Hougaard, David M and Ikeda, Masashi and Joa, Inge and ... and Psychiat Genomics Consortium and Wellcome Trust Case-Control Consor and Psychosis Endophenotypes Int Conso and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature, ISSN 0028-0836, 2014, Volume 511, Issue 7510, pp. 421 - 427
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be... 
COMMON VARIANTS | MUTATIONS | MULTIDISCIPLINARY SCIENCES | CONFERRING RISK | GENOME-WIDE ASSOCIATION | Schizophrenia | Genetic research | Research | Health aspects | Analysis | Studies | Confidence intervals | Hypotheses | Genealogy | Sample size | Genomics | Genetics | Trends | Clinical Medicine | Psykiatri | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Psychiatry
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3. Full Text Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
by Marshall, Christian R and Howrigan, Daniel P and Merico, Daniele and Thiruvahinapuram, Bhooma and Wu, Wenting and Greer, Douglas S and Antaki, Danny and Shetty, Aniket and Holmans, Peter A and Pinto, Dalila and Gujral, Madhusudan and Brandler, William M and Malhotra, Dheeraj and Wang, Zhouzhi and Fajarado, Karin V Fuentes and Maile, Michelle S and Ripke, Stephan and Agartz, Ingrid and Albus, Margot and Alexander, Madeline and Amin, Farooq and Atkins, Joshua and Bacanu, Silviu A and Belliveau, Richard A and Bergen, Sarah E and Bertalan, Marcelo and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Bulik-Sullivan, Brendan and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Cairns, Murray J and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberley D and Cheng, Wei and Cloninger, C Robert and Cohen, David and Cormican, Paul and Craddock, Nick and Crespo-Facorro, Benedicto and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and Del Favero, Jurgen and DeLisi, Lynn E and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farh, Kai-How and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedman, Joseph I and Forstner, Aneas J and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Gershon, Elliot S and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Gratten, Jacob and de Haan, Lieuwe and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Huang, Hailiang and Ikeda, Masashi and Joa, Inge and Kähler, Anna K and ... and Schizophrenia Working Grp and Psychosis Endophenotypes and CNV and Psychosis Endophenotypes International Consortium and CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature Genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 27 - 35
Copy number variants (CNVs) have been strongly implicated in the genetic etiology of schizophrenia (SCZ). However, genome-wide investigation of the... 
DUPLICATIONS | AUTISM | GENE | CNVS | GENETICS & HEREDITY | RISK | DISORDERS | 16P11.2 | PHENOTYPES | MUTATIONS | REARRANGEMENTS | Genetic Predisposition to Disease | Genome-Wide Association Study | Schizophrenia - genetics | Genetic Markers - genetics | Humans | Risk Factors | Genetic Loci - genetics | Female | Genotype | Male | DNA Copy Number Variations - genetics | Case-Control Studies | Schizophrenia | Genome-wide association studies | Genetic aspects | Copy number variations | Analysis | Studies | Consortia | Datasets | Working groups | Pipelines | Genomics | Quality control | Data processing | Genomes | Meta-analysis | Clinical Medicine | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Cell and Molecular Biology | Psykiatri | Klinisk medicin | Psychiatry | Cell- och molekylärbiologi
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4. Full Text Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
by Gusev, Alexander and Lee, Phil and Lee, S. Hong and Trynka, Gosia and Finucane, Hilary and Vilhjálmsson, Bjarni J and Xu, Han and Zang, Chongzhi and Ripke, Stephan and Bulik-Sullivan, Brendan and Stahl, Eli A and Stahl, Eli and Neale, Benjamin M and Neale, Benjamin M and Corvin, Aiden and Walters, James T.R and Farh, Kai-How and Holmans, Peter A and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Børglum, Anders D and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberly D and Chambert, Kimberly and Chan, Raymond C.K and Chen, Ronald Y.L and Chen, Eric Y.H and Cheng, Wei and Cheung, Eric F.C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and Del Favero, Jurgen and DeLisi, Lynn E and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and Drapeau, Elodie and Duan, Jubao and Dudbridge, Frank and Durmishi, Naser and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Friedman, Joseph I and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Gershon, Elliot S and Giegling, Ina and Giusti-Rodrguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Golimbet, Vera and Gopal, Srihari and Gratten, Jacob and Grove, Jakob and ... and Psychiat Genomics Consortium and SWE-SCZ Consortium and Schizophrenia Working Group of the Psychiatric Genomics Consortium
The American Journal of Human Genetics, ISSN 0002-9297, 11/2014, Volume 95, Issue 5, pp. 535 - 552
Regulatory and coding variants are known to be enriched with associations identified by genome-wide association studies (GWASs) of complex disease, but their... 
PRIOR INFORMATION | GENETIC-VARIATION | GENOTYPE IMPUTATION | GENETICS & HEREDITY | DNA ELEMENTS | SNPS | SCHIZOPHRENIA | LARGE-SCALE | LOCI | EXPRESSION | GENOME-WIDE ASSOCIATION | Computer Simulation | Humans | Genetic Diseases, Inborn - genetics | Inheritance Patterns - genetics | Genetic Variation - genetics | Models, Genetic | Genome-Wide Association Study - methods | Open Reading Frames - genetics | Regulatory Elements, Transcriptional - genetics | Genetic research | Epigenetic inheritance | Research | Genetic regulation
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5. Full Text Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
by Franke, Barbara and Stein, Jason L and Ripke, Stephan and Anttila, Verneri and Hibar, Derrek P and van Hulzen, Kimm J. E and Arias-Vasquez, Alejano and Smoller, Jordan W and Nichols, Thomas E and Neale, Michael C and McIntosh, Anew M and Lee, Phil and McMahon, Francis J and Meyer-Lindenberg, Aneas and Mattheisen, Manuel and Aneassen, Ole A and Gruber, Oliver and Sachdev, Perminder S and Roiz-Santiañez, Roberto and Saykin, Anew J and Ehrlich, Stefan and Mather, Karen A and Turner, Jessica A and Schwarz, Emanuel and Thalamuthu, Anbupalam and Yao, Yin and Ho, Yvonne Y. W and Martin, Nicholas G and Wright, Margaret J and O'Donovan, Michael C and Thompson, Paul M and Neale, Benjamin M and Medland, Sarah E and Sullivan, Patrick F and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William F and Cahn, Wiepke and Cai, Guiqing and Cairns, Murray J and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberley D and Chan, Raymond C. K and Chen, Eric Y. H and Chen, Ronald Y. L and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crespo-Facorro, Benedicto and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and DeLisi, Lynn E and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and ... and ENIGMA Consortium and Psychiat Genomics Consortium and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Enigma Consortium
Nature neuroscience, ISSN 1097-6256, 2016, Volume 19, Issue 3, pp. 420 - +
Schizophrenia is a devastating psychiatric illness with high heritability. Brain structure and function differ, on average, between people with schizophrenia... 
INDIVIDUALS | METAANALYSIS | PERSPECTIVE | RELATIVES | VARIANTS | DISORDERS | PHENOTYPES | NEUROSCIENCES | ENDOPHENOTYPE | DISCOVERY | GENOME-WIDE ASSOCIATION | Neuroimaging | Magnetic Resonance Imaging | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Schizophrenia - genetics | Endophenotypes | Humans | Brain - pathology | Organ Size | Polymorphism, Single Nucleotide - genetics | Schizophrenia - pathology | Linkage Disequilibrium | Genome-wide association studies | Phenotype | Schizophrenia | Disease susceptibility | Genetic aspects | Identification and classification | Health aspects | Methods | Neuroscience | Cognitive science
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