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Science, ISSN 0036-8075, 4/2008, Volume 320, Issue 5875, pp. 539 - 543
Schizophrenia is a devastating neurodevelopmental disorder whose genetic influences remain elusive. We hypothesize that individually rare structural variants... 
Autistic disorder | Genes | Genomics | DNA | Medical genetics | Schizophrenia | Amino acids | Reports | Genetic mutation | Chromosomes | Diseases | NEURONAL MIGRATION | NEUREGULIN | NMDA RECEPTOR | GLUTAMATE | NEUROTRANSMITTERS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | DIFFERENTIATION | CHILDHOOD-ONSET SCHIZOPHRENIA | EXPRESSION | COMMON DISEASE | Gene Duplication | Receptor, Epidermal Growth Factor - genetics | Oligonucleotide Array Sequence Analysis | Excitatory Amino Acid Transporter 1 - chemistry | Humans | Excitatory Amino Acid Transporter 1 - physiology | Molecular Sequence Data | Male | Neurons - cytology | Brain - growth & development | Excitatory Amino Acid Transporter 1 - genetics | Case-Control Studies | Brain - metabolism | Schizophrenia - genetics | Schizophrenia - physiopathology | Gene Deletion | Neurons - physiology | Adult | Female | Receptor, Epidermal Growth Factor - physiology | Child | Amino Acid Sequence | Brain - cytology | Genetic Predisposition to Disease | Signal Transduction | Receptor, Epidermal Growth Factor - chemistry | Adolescent | Age of Onset | Polymorphism, Single Nucleotide | Mutation | Genome, Human | Receptor, ErbB-4 | Chromosome replication | Gene mutations | Neurobiology | Physiological aspects | Influence | Genetic aspects | Chromosome deletion | Genetics | Psychiatry | Index Medicus
Journal Article
by Walsh, Tom and Gary, Sydney and Sutcliffe, James S and Addington, Anjene M and Chitkara, Nisha and Levy, Deborah L and Cichon, Sven and DeRosse, Pamela and Malhotra, Anil K and Leibenluft, Ellen and Dickel, Diane E and Lee, Yoon-ha and Zackai, Elaine H and Stroup, T Scott and McCarthy, Shane E and Crow, Timothy J and McMahon, Francis J and Lakshmi, B and Christian, Susan L and Malhotra, Dheeraj and McClellan, Jon and Goodell, Meredith and Spinner, Nancy B and Pearl, Justin and Wolff, Jessica and Bhandari, Abhishek and Iakoucheva, Lilia M and Deutsch, Curtis K and Pavon, Kevin and Nöthen, Markus M and Gallagher, Louise and Roccanova, Patricia and Lieberman, Jeffrey A and DeLisi, Lynn E and Puura, Kaija and Skuse, David and Rapoport, Judith and Willour, Virginia L and Kirov, George and Vacic, Vladimir and Makarov, Vladimir and Haldeman-Englert, Chad and Sullivan, Patrick F and Schulze, Thomas G and Craddock, Nick and Kendall, Jude and Perkins, Diana O and Kusenda, Mary and Lehtimäki, Terho and Kassem, Layla and Yoon, Seungtai and Krastoshevsky, Olga and Sebat, Jonathan and Owen, Michael J and Ganesh, Jaya and Gill, Michael and King, Mary-Claire and Steele, Jo and Krause, Verena and Susser, Ezra and Mendell, Nancy R and Leotta, Anthony and Shaikh, Tamim H and Kaplan, Paige and Potash, James B and Krantz, Ian D and Grozeva, Detelina and Lajonchere, Clara M and O'Donovan, Michael C and Kustanovich, Vlad and Rietschel, Marcella and Kumar, Ravinesh A and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium
Nature Genetics, ISSN 1061-4036, 11/2009, Volume 41, Issue 11, pp. 1223 - 1227
Journal Article
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