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1. The flowers of William Morris
by Baker, Derek W
1996, ISBN 9781899531035, 88
Morris, William, 1834-1896 | Textile fabrics | Decoration and ornament | Designers | Plant forms | History | Flowers in art
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2. Full Text Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment
by Whitton, Laura and Apostolova, Galina and Rieder, Dietmar and Dechant, Georg and Rea, Stephen and Donohoe, Gary and Morris, Derek W
PLoS Genetics, ISSN 1553-7390, 07/2018, Volume 14, Issue 7, pp. e1007515 - e1007515
SATB2 is associated with schizophrenia and is an important transcription factor regulating neocortical organization and circuitry. Rare mutations in SATB2... 
INDIVIDUALS | METAANALYSIS | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | PROJECTION NEURON IDENTITY | RISK | TRANSCRIPTION FACTOR SATB2 | SPECIFICATION | ASSOCIATION | EXPRESSION | CELL | Corpus Callosum - metabolism | Synaptic Transmission - genetics | Humans | Cognition | Neurodevelopmental Disorders - genetics | Schizophrenia - pathology | Academic Success | Schizophrenia - genetics | Gene Expression Regulation, Developmental | Female | Axon Guidance - genetics | Genomics - methods | Hippocampus - growth & development | Disease Models, Animal | Genetic Predisposition to Disease | Datasets as Topic | Matrix Attachment Region Binding Proteins - metabolism | Transcription Factors - genetics | Neurodevelopmental Disorders - pathology | Transcription Factors - metabolism | Hippocampus - metabolism | Animals | Matrix Attachment Region Binding Proteins - genetics | Corpus Callosum - growth & development | Mice | Mutation | Academic achievement | Educational aspects | Schizophrenia | Genetic aspects | Binding proteins | Genetic regulation | Neurogenesis | Health aspects | Neurosciences | Animal models | Mental disorders | Intellectual disabilities | Memory | Genomics | Genes | Cardiovascular disease | Biochemistry | Genomes | Neurodevelopmental disorders | Proteins | Developmental stages | Synaptic transmission | Genetics | Discipline | Cognitive therapy | Medical imaging | Neurons | Cortex | Ribonucleic acid--RNA | Corpus callosum | Educational attainment | Meta-analysis | Autism | Cognition & reasoning | Axon guidance | Binding sites | Index Medicus | RNA | Ribonucleic acid
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3. Full Text Genes encoding SATB2-interacting proteins in adult cerebral cortex contribute to human cognitive ability
by Cera, Isabella and Whitton, Laura and Whitton, Laura and Donohoe, Gary and Donohoe, Gary and Morris, Derek W and Morris, Derek W and Dechant, Georg and Apostolova, Galina and Apostolova, Galina
PLoS Genetics, ISSN 1553-7390, 02/2019, Volume 15, Issue 2, pp. e1007890 - e1007890
During CNS development, the nuclear protein SATB2 is expressed in superficial cortical layers and determines projection neuron identity. In the adult CNS,... 
ORGANIZATION | CLEFT-PALATE | METAANALYSIS | INTERACTS | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | PROJECTION NEURON IDENTITY | RISK | TRANSCRIPTION FACTOR SATB2 | EXPRESSION | GENOME-WIDE ASSOCIATION | Cerebral cortex | Demographic aspects | Analysis | Influence | Cognition | Genetic aspects | DNA binding proteins | Neonates | Chromatin | Neurosciences | Mental disorders | Laboratories | Funding | Genomics | Cognitive ability | Schizophrenia | Cardiovascular disease | Ontogeny | Biochemistry | Genomes | Kinases | Proteins | Publishing | Plasticity (cortical) | Genetics | Long term memory | Bioinformatics | Discipline | Supervision | Cognitive therapy | Medical imaging | Cortex | Gene expression | Gene silencing | Plasticity (synaptic) | Cognition & reasoning | Pyramidal cells | Index Medicus
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4. Full Text Pulmonary Radiofrequency Ablation - An International Study Survey
by KARIN STEINKE and PATRICK E. SEWELL and DAMIEN DUPUY and RICCARDO LENCIONI and THOMAS HELMBERGER and STEPHEN T. KEE and AUGUSTINUS L. JACOB and DEREK W. GLENN and JULIE KING and DAVID L. MORRIS
Anticancer Research, ISSN 0250-7005, 01/2004, Volume 24, Issue 1, pp. 339 - 343
Background: The lung is the most common site for primary cancer worldwide as well as being a common site of metastases for various malignancies. Percutaneous... 
Radiofrequency ablation | Tumor | Complications | Lung | Minimally invasive | lung | complications | ONCOLOGY | RESECTION | tumor | METASTASES | minimally invasive | radiofrequency ablation | Catheter Ablation - methods | Catheter Ablation - utilization | Lung Neoplasms - surgery | Catheter Ablation - adverse effects | Humans | Health Care Surveys | Index Medicus
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5. 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 | Index Medicus | Clinical Medicine | Psykiatri | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Psychiatry
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6. 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 | Index Medicus | Life Sciences | Biochemistry, Molecular Biology
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7. Full Text Identification of common variants associated with human hippocampal and intracranial volumes
by Stein, J.L and Medland, S.E and Arias Vasquez, A and Hibar, D.P and Senstad, R.E and Winkler, A.M and Toro, R and Appel, K and Bartecek, R and Bergmann, O and Bernard, M and Brown, A.A and Cannon, D.M and Chakravarty, M.M and Christoforou, A and Domin, M and Grimm, O and Hollinshead, M and Holmes, A.J and Homuth, G and Hottenga, J.J and Langan, C and Lopez, L.M and Hansell, N.K and Hwang, K.S and Kim, S and Laje, G and Lee, P.H and Liu, X and Loth, E and Lourdusamy, A and Mattingsdal, M and Mohnke, S and Maniega, S.M and Nho, K and Nugent, A.C and O'Brien, C and Papmeyer, M and Putz, B and Ramasamy, A and Rasmussen, J and Rijpkema, M.J.P and Risacher, S.L and Roddey, J.C and Rose, E.J and Ryten, M and Shen, L and Sprooten, E and Strengman, E and Teumer, A and Trabzuni, D and Turner, J and Eijk, K. van and Erp, T.G. van and Tol, M.J. van and Wittfeld, K and Wolf, C. de and Woudstra, S and Aleman, A and Alhusaini, S and Almasy, L and Binder, E.B and Brohawn, D.G and Cantor, R.M and Carless, M.A and Corvin, A and Czisch, M and Curran, J.E and Davies, G and Almeida, M.A. de and Delanty, N and Depondt, C and Duggirala, R and Dyer, T.D and Erk, S and Fagerness, J and Fox, P.T and Freimer, N.B and Gill, M and Goring, H.H and Hagler, D.J and Hoehn, D and Holsboer, F and Hoogman, M and Hosten, N and Jahanshad, N and Johnson, M.P and Kasperaviciute, D and Kent Jr., J.W and Kochunov, P and Lancaster, J.L and Lawrie, S.M and Liewald, D.C and Mandl, R.C.W and Matarin, M and Mattheisen, M and Meisenzahl, E and Melle, I and Moses, E.K and Muhleisen, T.W and ... and Cohorts Heart Aging Res Genomic Ep and EPIGEN Consortium and ADNI and Saguenay Youth Study Grp SYS and IMAGEN Consortium and Enhancing Neuro Imaging Genetics M and Alzheimer's Disease Neuroimaging Initiative and Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium and Saguenay Youth Study Group and Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium and the Alzheimer's Disease Neuroimaging Initiative (ADNI) and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and Saguenay Youth Study Group (SYS) and for the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium
Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 5, pp. 552 - 561
Identifying genetic variants influencing human brain structures may reveal new biological mechanisms underlying cognition and neuropsychiatric illness. The... 
AUTOMATED SEGMENTATION | HUMAN HEIGHT | FUNCTIONAL IMPLICATIONS | TEMPORAL-LOBE EPILEPSY | UNIFIED APPROACH | GENOTYPE IMPUTATION | ALZHEIMERS-DISEASE | GENETICS & HEREDITY | BRAIN VOLUME | NA+/H+ EXCHANGER | GENOME-WIDE ASSOCIATION | Neuroimaging | Genome-Wide Association Study | Meta-Analysis as Topic | Brain - physiopathology | Humans | Polymorphism, Single Nucleotide - genetics | Genetic Loci | Genetic Markers | Chromosomes, Human, Pair 12 - genetics | Hippocampus - physiopathology | Head | Genetic aspects | Hippocampus (Brain) | Genetic variation | Identification and classification | Body size | Studies | Haplotypes | Neurology | Brain | Genealogy | Statistical analysis | Quality control | Genetics | Genomes | Meta-analysis | Index Medicus | Life Sciences | Neurons and Cognition
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