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1. Full Text Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
by Lee, Shermin and Ripke, S and Neale, B.M and Faraone, S.V and Purcell, S.M and Perlis, R.H and Mowry, B.J and Thapar, A and Goddard, M.E and Witte, J.S and Absher, D and Agartz, I and Akil, H and Amin, F and Aneassen, O.A and Anjorin, A and Anney, R and Anttila, V and Arking, D.E and Asherson, P and Azevedo, M.H and Backlund, L and Badner, J.A and Bailey, A.J and Banaschewski, T and Barchas, J.D and Barnes, M.R and Barrett, T.B and Bass, N and Battaglia, A and Bauer, M and Bayes, M and Bellivier, F and Bergen, S.E and Berrettini, W and Betancur, C and Bettecken, T and Biederman, J and Binder, E.B and Black, D.W and Blackwood, D.H and Bloss, C.S and Boehnke, M and Boomsma, D.I and Breen, G and Breuer, R and Bruggeman, R and Cormican, P and Buccola, N.G and Buitelaar, J.K and Bunney, W.E and Buxbaum, J.D and Byerley, W.F and Byrne, E.M and Caesar, S and Cahn, W and Cantor, R.M and Casas, M and Chakravarti, A and Chambert, K and Choudhury, K and Cichon, S and Cloninger, C.R and Collier, D.A and Cook, E.H and Coon, H and Cormand, B and Corvin, A and Coryell, W.H and Craig, D.W and Craig, I.W and Crosbie, J and Cuccaro, M.L and Curtis, D and Czamara, D and Datta, S and Dawson, G and Day, R and Geus, E.J. de and Degenhardt, F and Djurovic, S and Donohoe, G.J and Doyle, A.E and Duan, J and Dudbridge, F and Duketis, E and Ebstein, R.P and Edenberg, H.J and Elia, J and Ennis, S and Etain, B and Fanous, A and Farmer, A.E and Ferrier, I.N and Flickinger, M and Fombonne, E and Foroud, T and Frank, J and Franke, B and et al and Cross-Disorder Grp Psychiat Genomi and Int Inflammatory Bowel Dis Genetic and Cross-Disorder Group of the Psychiatric Genomics Consortium
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 9, pp. 984 - 994
Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across... 
ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | CROHNS-DISEASE | DEFICIT HYPERACTIVITY DISORDER | COMMON SNPS | GENETICS & HEREDITY | SCHIZOPHRENIA | RISK | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | HERITABILITY | Usage | Genetic aspects | Research | Single nucleotide polymorphisms | Psychoses | Genomics | Life Sciences | Biochemistry, Molecular Biology
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2. Full Text Common genetic variants influence human subcortical brain structures
by Hibar, Derrek and Stein, J.L and Rentería, Miguel and Arias-Vásquez, Alejano and Desrivières, Sylvane and Jahanshad, Neda and Toro, Roberto and Wittfeld, Katharina and Abramovic, Lucija and Andersson, Micael and Aribisala, Benjamin and Armstrong, Nicola J and Bernard, Manon and Bohlken, Marc M and Boks, Marco and Bralten, Linda and Brown, Anew and Chakravarty, M. Mallar and Chen, Qiang and Ching, Christopher and Cuellar-Partida, Gabriel and Braber, Anouk and Giddaluru, Sudheer and Goldman, Aaron L and Grimm, Oliver and Guadalupe, Tulio and Hass, Johanna and Woldehawariat, Girma and Holmes, Avram and Hoogman, Martine and Janowitz, Deborah and Jia, Tianye and Kim, Shinseog and Klein, Marieke and Kraemer, Bernd and Lee, Phil H and Olde Loohuis, Loes M and Luciano, Michelle and MacAre, Christine and Mather, R and Mattheisen, Manuel and Milaneschi, Yuri and Nho, Kwangsik and Papmeyer, Martina and Ramasamy, Adaikalavan and Risacher, Shannon and Roiz-Santiañez, Roberto and Rose, Emma and Salami, Alireza and Sämann, Philipp and Schmaal, Lianne and Schork, Nicholas and Shin, Jean and Strike, Lachlan and Teumer, Alexander and Van Donkelaar, Marjolein M. J and Eijk, Kristel and Walters, Raymond and Westlye, Lars and Whelan, Christopher and Winkler, Anderson and Zwiers, Marcel and Alhusaini, Saud and Athanasiu, Lavinia and Ehrlich, Stefan and Hakobjan, Marina and Hartberg, Cecilie B and Haukvik, Unn and Heister, Angelien J. G. A. M and Hoehn, David and Kasperaviciute, Dalia and Liewald, David C and Lopez, Lorna and Makkinje, Remco R. R and Matarin, Mar and Naber, Marlies A. M and McKay, Reese and Needham, Margaret and Nugent, Allison and Pütz, Benno and Royle, Natalie and Shen, Li and Sprooten, Roy and Trabzuni, Danyah and Van Der Marel, Saskia S. L and Van Hulzen, Kimm J. E and Walton, Esther and Björnsson, Asgeir and Almasy, Laura and Ames, David and Arepalli, Sampath and Assareh, A.A and Bastin, Mark and Brodaty, Henry and Bulayeva, Kazima and Carless, Melanie and Cichon, Sven and Corvin, Aiden and Curran, Joanne and Czisch, Michael and ... and EPIGEN and SYS and Alzheimers Dis Neuroimaging and CHARGE Consortium and IMAGEN and Alzheimer’s Disease Neuroimaging Initiative and The Alzheimer’s Disease Neuroimaging Initiative and The CHARGE Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 04/2015, Volume 520, Issue 7546, pp. 224 - 229
textabstractThe highly complex structure of the human brain is strongly shaped by genetic influences. Subcortical brain regions form circuits with cortical... 
EVOLUTION | CHROMATIN | BASAL GANGLIA | MULTIDISCIPLINARY SCIENCES | HIPPOCAMPAL | DYNAMICS | IDENTIFICATION | EXPRESSION | KINECTIN | STRIATUM | GENOME-WIDE ASSOCIATION | Caudate Nucleus - anatomy & histology | Brain - anatomy & histology | Humans | Middle Aged | Genetic Loci - genetics | Gene Expression Regulation, Developmental - genetics | Apoptosis - genetics | Male | Young Adult | Putamen - anatomy & histology | Aging - genetics | Organ Size - genetics | Aged, 80 and over | Adult | Female | Child | Genome-Wide Association Study | Membrane Proteins - genetics | Sex Characteristics | Magnetic Resonance Imaging | Skull - anatomy & histology | Adolescent | Aged | Genetic Variation - genetics | Hippocampus - anatomy & histology | Genetic research | Brain | Genetic aspects | Brain research | Research | Genetic variation | Genomics | Genomes | Epigenetics | Genes | Neuroscience | Cognitive science | Biological Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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3. Full Text Novel genetic loci associated with hippocampal volume
by Hibar, Derrek P and Adams, Hieab H. H and Jahanshad, Neda and Chauhan, Ganesh and Stein, Jason L and Hofer, Edith and Renteria, Miguel E and Bis, Joshua C and Arias-Vasquez, Alejano and Ikram, M. Kamran and Desrivières, Sylvane and Vernooij, Meike W and Abramovic, Lucija and Alhusaini, Saud and Amin, Najaf and Andersson, Micael and Arfanakis, Konstantinos and Aribisala, Benjamin S and Armstrong, Nicola J and Athanasiu, Lavinia and Axelsson, Tomas and Beecham, Ashley H and Beiser, Alexa and Bernard, Manon and Blanton, Susan H and Bohlken, Marc M and Boks, Marco P and Bralten, Janita and Brickman, Adam M and Carmichael, Owen and Chakravarty, M. Mallar and Chen, Qiang and Ching, Christopher R. K and Chouraki, Vincent and Cuellar-Partida, Gabriel and Crivello, Fabrice and den Braber, Anouk and Doan, Nhat Trung and Ehrlich, Stefan and Giddaluru, Sudheer and Goldman, Aaron L and Gottesman, Rebecca F and Grimm, Oliver and Griswold, Michael E and Guadalupe, Tulio and Gutman, Boris A and Hass, Johanna and Haukvik, Unn K and Hoehn, David and Holmes, Avram J and Hoogman, Martine and Janowitz, Deborah and Jia, Tianye and Jørgensen, Kjetil N and Karbalai, Nazanin and Kasperaviciute, Dalia and Kim, Sungeun and Klein, Marieke and Kraemer, Bernd and Lee, Phil H and Liewald, David C. M and Lopez, Lorna M and Luciano, Michelle and Macare, Christine and Marquand, Ane F and Matarin, Mar and Mather, Karen A and Mattheisen, Manuel and McKay, David R and Milaneschi, Yuri and Muñoz Maniega, Susana and Nho, Kwangsik and Nugent, Allison C and Nyquist, Paul and Loohuis, Loes M. Olde and Oosterlaan, Jaap and Papmeyer, Martina and Pirpamer, Lukas and Pütz, Benno and Ramasamy, Adaikalavan and Richards, Jennifer S and Risacher, Shannon L and Roiz-Santiañez, Roberto and Rommelse, Nanda and Ropele, Stefan and Rose, Emma J and Royle, Natalie A and Rundek, Tatjana and Sämann, Philipp G and Saremi, Arvin and Satizabal, Claudia L and Schmaal, Lianne and Schork, Anew J and Shen, Li and Shin, Jean and Shumskaya, Elena and Smith, Albert V and Sprooten, Emma and Strike, Lachlan T and Teumer, Alexander and ... and Medicinska fakulteten and Institutionen för integrativ medicinsk biologi (IMB) and Umeå centrum för funktionell hjärnavbildning (UFBI) and Umeå universitet
Nature communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, p. 13624
The hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness. Structural... 
BRAIN-REGIONS | COMMON VARIANTS | METAANALYSIS | TEMPORAL-LOBE EPILEPSY | MEMORY | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | BIPOLAR DISORDER | SUBFIELDS | GENOME-WIDE ASSOCIATION | Glycoproteins - genetics | Alzheimer Disease - physiopathology | Genetic Predisposition to Disease | Genome-Wide Association Study | Microtubule-Associated Proteins - genetics | Humans | Middle Aged | Protein-Serine-Threonine Kinases - genetics | Organ Size | Dipeptidyl Peptidase 4 - genetics | Male | Genetic Loci | Methionine Sulfoxide Reductases - genetics | Nerve Tissue Proteins - genetics | Young Adult | Adolescent | Aged, 80 and over | Adult | Female | Aged | Alzheimer Disease - genetics | Child | Hippocampus - growth & development | Cohort Studies | Neuroscience | Cognitive science | Basic Medicine | Medical Genetics | Medicinsk genetik | Biological Sciences | Naturvetenskap | Medical and Health Sciences | Medicin och hälsovetenskap | Biologiska vetenskaper | Medicinska och farmaceutiska grundvetenskaper | Natural Sciences | Bioinformatik och systembiologi | Bioinformatics and Systems Biology
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4. Full Text Novel genetic loci underlying human intracranial volume identified through genome-wide association
by Adams, H.H and Hibar, D.P and Chouraki, V and Stein, J.L and Nyquist, P.A and Renteria, M.E and Trompet, S and Arias-Vasquez, A and Seshai, S and Desrivieres, S and Beecham, A.H and Jahanshad, N and Wittfeld, K and Lee, S.J. van der and Abramovic, L and Alhusaini, S and Amin, N and Andersson, M and Arfanakis, K and Aribisala, B.S and Armstrong, N.J and Athanasiu, L and Axelsson, T and Beiser, A and Bernard, M and Bis, J.C and Blanken, L.M and Blanton, S.H and Bohlken, M.M and Boks, M.P and Bralten, J and Brickman, A.M and Carmichael, O and Chakravarty, M.M and Chauhan, G and Chen, Q and Ching, C.R and Cuellar-Partida, G and Braber, A.D and Doan, N.T and Ehrlich, S and Filippi, I and Ge, T and Giddaluru, S and Goldman, A.L and Gottesman, R.F and Greven, C.U and Grimm, O and Griswold, M.E and Guadalupe, T.M and Hass, J and Haukvik, U.K and Hilal, S and Hofer, E and Hoehn, D and Holmes, A.J and Hoogman, M and Janowitz, D and Jia, T and Kasperaviciute, D and Kim, S and Klein, M and Kraemer, B and Lee, P.H and Liao, J and Liewald, D.C and Lopez, L.M and Luciano, M and Macare, C and Marquand, A and Matarin, M and Mather, K.A and Mattheisen, M and Mazoyer, B and McKay, D.R and McWhirter, R and Milaneschi, Y and Mirza-Schreiber, N and Muetzel, R.L and Maniega, S.M and Nho, K and Nugent, A.C and Loohuis, L.M and Oosterlaan, J and Papmeyer, M and Pappa, I and Pirpamer, L and Pudas, S and Putz, B and Rajan, K.B and Ramasamy, A and Richards, J.S and Risacher, S.L and Roiz-Santianez, R and Rommelse, N and Rose, E.J and Royle, N.A and Rundek, T and Samann, P.G and Satizabal, C.L and ... and EPIGEN and SYS and Alzheimer's Dis Neuroimaging Initi and IMAGEN and Mind Research Network, Albuquerque, NM (United States) and Medicinska fakulteten and Institutionen för integrativ medicinsk biologi (IMB) and Umeå centrum för funktionell hjärnavbildning (UFBI) and Umeå universitet
Nature Neuroscience, ISSN 1097-6256, 2016, Volume 19, Issue 12, pp. 1569 - 1582
Intracranial volume reflects the maximally attained brain size during development, and remains stable with loss of tissue in late life. It is highly heritable,... 
CONSORTIUM | COMMON VARIANTS | IGF-I | METAANALYSIS | ALZHEIMERS-DISEASE | 17Q21.31 MICRODELETION | BRAIN SIZE | HEIGHT | NEUROSCIENCES | HEAD CIRCUMFERENCE | PARKINSONS-DISEASE | Genetic Predisposition to Disease | Humans | Genetic Loci - genetics | European Continental Ancestry Group | Brain - growth & development | Parkinson Disease - genetics | Phosphatidylinositol 3-Kinases - genetics | Phenotype | Oncogene Protein v-akt - genetics | Brain - pathology | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Genome-Wide Association Study - methods | Research | Genetic variation | Genomics | Analysis | Neurophysiology | Neuroscience | Cognitive science | Neurosciences & Neurology | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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5. Full Text Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
by Maier, Wolfgang and Maier, Robert and Moser, Gerhard and Chen, Guo-Bo and Ripke, Stephan and Absher, Devin and Agartz, Ingrid and Akil, Huda and Amin, Farooq and Andreassen, Ole A and Anjorin, Adebayo and Anney, Richard and Arking, Dan E and Asherson, Philip and Azevedo, Maria H and Backlund, Lena and Badner, Judith A and Bailey, Anthony J and Banaschewski, Tobias and Barchas, Jack D and Barnes, Michael R and Barrett, Thomas B and Bass, Nicholas and Battaglia, Agatino and Bauer, Michael and Bayés, Mònica and Bellivier, Frank and Bergen, Sarah E and Berrettini, Wade and Betancur, Catalina and Bettecken, Thomas and Biederman, Joseph and Binder, Elisabeth B and Black, Donald W and Blackwood, Douglas H.R and Bloss, Cinnamon S and Boehnke, Michael and Boomsma, Dorret I and Breen, Gerome and Breuer, René and Bruggeman, Richard and Buccola, Nancy G and Buitelaar, Jan K and Bunney, William E and Buxbaum, Joseph D and Byerley, William F and Caesar, Sian and Cahn, Wiepke and Cantor, Rita M and Casas, Miguel and Chakravarti, Aravinda and Chambert, Kimberly and Choudhury, Khalid and Cichon, Sven and Cloninger, C. Robert and Collier, David A and Cook, Edwin H and Coon, Hilary and Cormand, Bru and Cormican, Paul and Corvin, Aiden and Coryell, William and Coryell, William H and Craddock, Nicholas and Craig, David W and Craig, Ian W and Crosbie, Jennifer and Cuccaro, Michael L and Curtis, David and Czamara, Darina and Daly, Mark J and Datta, Susmita and Dawson, Geraldine and Day, Richard and De Geus, Eco J and Degenhardt, Franziska and Devlin, Bernie and Djurovic, Srdjan and Donohoe, Gary J and Doyle, Alysa E and Duan, Jubao and Dudbridge, Frank and Duketis, Eftichia and Ebstein, Richard P and Edenberg, Howard J and Elia, Josephine and Ennis, Sean and Etain, Bruno and Fanous, Ayman and Faraone, Stephen V and Farmer, Anne E and Ferrier, I. Nicol and Flickinger, Matthew and Fombonne, Eric and Foroud, Tatiana and Frank, Josef and Franke, Barbara and Fraser, Christine and Freedman, Robert and Freimer, Nelson B and ... and Psychiat Genomics Consortium and Cross-Disorder Working Group of the Psychiatric Genomics Consortium and Institute of Neuroscience and Physiology and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institutionen för neurovetenskap och fysiologi
The American Journal of Human Genetics, ISSN 0002-9297, 02/2015, Volume 96, Issue 2, pp. 283 - 294
Genetic risk prediction has several potential applications in medical research and clinical practice and could be used, for example, to stratify a... 
POPULATION | DISEASES | GENETIC RISK | GENETICS & HEREDITY | LOCI | ALGORITHMS | TRAIT | SELECTION | GENOME-WIDE ASSOCIATION | Mental Disorders - genetics | Multifactorial Inheritance - genetics | Multivariate Analysis | Risk Assessment - methods | Genetics, Medical - methods | Schizophrenia - genetics | Depressive Disorder, Major - genetics | Humans | Polymorphism, Single Nucleotide - genetics | Linear Models | Bipolar Disorder - genetics | Genetic Testing - methods | Schizophrenia | Bipolar disorder | Risk factors | Major depressive disorder | Life Sciences | Neurons and Cognition | Report | INFORMATION | Genetics & Heredity | Klinisk medicin | IDENTIFICATION | RESTRICTED MAXIMUM-LIKELIHOOD | Clinical Medicine | MODELS | AVERAGE | TRAITS
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6. 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 de Haan, Lieuwe 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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