De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K +22 more·2012·Molecular Psychiatry
Cited by (879)
Items 201–300 of 879
- Genome-wide association studies in schizophrenia: Recent advances, challenges and future perspectiveCharlotte A. Dennison, Sophie E. Legge, Antonio F. Pardiñas, James Walters · 2019 · Schizophrenia Research
- A meta-analysis of gene expression quantitative trait loci in brainKim, Y, Xia, K, Tao, R, Giusti-Rodriguez, P, Vladimirov, V, van den Oord, E, Sullivan, P F · 2014 · Translational Psychiatry
- Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD PopulationNori Matsunami, Dexter Hadley, Charles H. Hensel, G. Bryce Christensen, Cecilia Kim, Edward C. Frackelton, Kelly Thomas, Renata Pellegrino da Silva, Jeff Stevens, Lisa Morrison Baird et al. · 2013 · PLoS ONE
- Copy Number Variable MicroRNAs in Schizophrenia and Their Neurodevelopmental Gene TargetsW. David Warnica, Daniele Merico, Gregory Costain, Simon E. Alfred, John Wei, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett · 2014 · Biological Psychiatry
- Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with SchizophreniaJennifer G. Mullé, Ann E. Pulver, John A. McGrath, Paula S Wolyniec, Anne Dodd, David J. Cutler, Jonathan L. Sebat, Dheeraj Malhotra, Gerald Nestadt, Donald F. Conrad et al. · 2013 · Biological Psychiatry
- Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular eraAnne S. Bassett, Gregory Costain · 2012 · The Application of Clinical Genetics
- Psychiatric gene discoveries shape evidence on ADHD’s biologyAnita Thapar, Joanna Martin, Eric O. Mick, Alejandro Arias Vásquez, K. Langley, Stephen W. Scherer, Russell James Schachar, Jennifer Crosbie, Nigel M. Williams, Barbara Franke et al. · 2015 · Molecular Psychiatry
- Cyfip1 Regulates Presynaptic Activity during DevelopmentHsiao, Kuangfu, Harony-Nicolas, Hala, Buxbaum, Joseph D., Bozdagi-Gunal, Ozlem, Benson, Deanna L. · 2016 · The Journal of Neuroscience
- Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genesTune H. Pers, Pascal N. Timshel, Stephan Ripke, Patrick F. Sullivan, Michael C. O’Donovan, Lude Franke, Joel N. Hirschhorn · 2016 · Human Molecular Genetics
- Genetics of schizophreniaElliott Rees, Michael C. O’Donovan, Michael John Owen · 2014 · Current Opinion in Behavioral Sciences
- Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on GeneticsIna Giegling, Ladislav Hosák, Rainald Mößner, Alessandro Serretti, Frank Bellivier, Stephan J. Claes, David Andrew Collier, Alejo Corrales, Lynn E. DeLisi, Carla Gallo et al. · 2017 · The World Journal of Biological Psychiatry
- Beyond antipsychotics: a twenty-first century update for preclinical development of schizophrenia therapeuticsDaisy L. Spark, Alex Fornito, Christopher J. Langmead, Gregory D. Stewart · 2022 · Translational Psychiatry
- Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in TaiwanShih‐Pin Chen, Jong‐Ling Fuh, Ming‐Yi Chung, Ying–Chao Lin, Yi‐Chu Liao, Yen-Feng Wang, Chia‐Lin Hsu, Ueng‐Cheng Yang, Ming‐Wei Lin, Jen-Jie Chiou et al. · 2017 · Cephalalgia
- Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum DisordersJingrui Xing, Hiroki Kimura, Chenyao Wang, Kanako Ishizuka, Itaru Kushima, Yuko Arioka, Akira Yoshimi, Yukako Nakamura, Tomoko Shiino, Tomoko Oya‐Ito et al. · 2016 · Scientific Reports
- Autoantibodies to central nervous system neuronal surface antigens: psychiatric symptoms and psychopharmacological implicationsThomas Arthur Pollak, Katherine Beck, Sarosh R. Irani, Oliver David Howes, Anthony S. David, Philip K. McGuire · 2015 · Psychopharmacology
- DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to SullivanDavid John Porteous, Pippa A. Thomson, J. Kirsty Millar, Kathryn Louise Evans, William Hennah, Dinesh C. Soares, S McCarthy, William Richard McCombie, Steven J. Clapcote, Carsten Korth et al. · 2014 · Molecular Psychiatry
- Src kinase as a mediator of convergent molecular abnormalities leading to NMDAR hypoactivity in schizophreniaAnamika Banerjee, H-Y Wang, Karin E. Borgmann‐Winter, M L MacDonald, Hagop Kaprielian, Andres Stucky, Jessica Kvasic, Chijioke N. Egbujo, Rubik Ray, Konrad Talbot et al. · 2014 · Molecular Psychiatry
- Common developmental genome deprogramming in schizophrenia — Role of Integrative Nuclear FGFR1 Signaling (INFS)Sridhar Tatarao Narla, Y.W. Lee, Courtney A. Benson, Pinaki Sarder, Kristen Brennand, Ewa K. Stachowiak, Michal K. Stachowiak · 2017 · Schizophrenia Research
- Synapse diversity and synaptome architecture in human genetic disordersGrant, Seth G N · 2019 · Human Molecular Genetics
- Chronic LSD alters gene expression profiles in the mPFC relevant to schizophreniaMartin, David A., Marona-Lewicka, Danuta, Nichols, David E., Nichols, Charles D. · 2014 · Neuropharmacology
- Genetic analysis of schizophrenia and bipolar disorder reveals polygenicity but also suggests new directions for molecular interrogationBenjamin M. Neale, Pamela B. Sklar · 2014 · Current Opinion in Neurobiology
- Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic reviewJordi Soler, Lourdes Fañanás, Mara Parellada, Marie‐Odile Krebs, Guy Armand Rouleau, Mar Fatjó‐Vilas · 2018 · Journal of Psychiatry and Neuroscience
- Altered Glutamate Protein Co-Expression Network Topology Linked to Spine Loss in the Auditory Cortex of SchizophreniaMatthew L. MacDonald, Ying Ding, Jason T. Newman, Scott E. Hemby, Peter Penzes, David A. Lewis, Nathan A. Yates, Robert A. Sweet · 2014 · Biological Psychiatry
- Reversal of synaptic and behavioral deficits in a 16p11.2 duplication mouse model via restoration of the GABA synapse regulator Npas4Rein, Benjamin, Tan, Tao, Yang, Fengwei, Wang, Wei, Williams, Jamal, Zhang, Freddy, Mills, Alea, Yan, Zhen · 2021 · Molecular Psychiatry
- The relationship between synaptic density marker SV2A, glutamate and N-acetyl aspartate levels in healthy volunteers and schizophrenia: a multimodal PET and magnetic resonance spectroscopy brain imaging studyOnwordi, Ellis Chika, Whitehurst, Thomas, Mansur, Ayla, Statton, Ben, Berry, Alaine, Quinlan, Marina, O’Regan, Declan P., Rogdaki, Maria, Marques, Tiago Reis, Rabiner, Eugenii A. et al. · 2021 · Translational Psychiatry
- Roles for Arc in metabotropic glutamate receptor-dependent LTD and synapse elimination: Implications in health and diseaseJulia R. Wilkerson, Joseph P. Albanesi, Kimberly M. Huber · 2017 · Seminars in Cell and Developmental Biology
- An mGlu5-Positive Allosteric Modulator Rescues the Neuroplasticity Deficits in a Genetic Model of NMDA Receptor Hypofunction in SchizophreniaDarrick T. Balu, Yan Li, Shunsuke Takagi, Kendall Taylor Presti, Teniel S Ramikie, Jerri M. Rook, Carrie K. Jones, Craig W. Lindsley, Peter Jeffrey Conn, Vadim Y. Bolshakov et al. · 2016 · Neuropsychopharmacology
- Human post-mortem synapse proteome integrity screening for proteomic studies of postsynaptic complexesÀlex Bayés, Mark O. Collins, Clare M. Galtrey, Clémence Simonnet, Marcia M. Roy, Mike D. R. Croning, Gemma Gou, Louie N. van de Lagemaat, David Milward, Ian Roger Whittle et al. · 2014 · Molecular Brain
- Proteomic analysis of the postsynaptic density implicates synaptic function and energy pathways in bipolar disorderMelanie Föcking, Patrick Dicker, Lorna M. Lopez, Magdalena Hryniewiecka, Kieran J. Wynne, J A English, Gerard Cagney, David Cotter · 2016 · Translational Psychiatry
- Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplicationon behalf of the Simons VIP consortium, Green Snyder, LeeAnne, D’Angelo, Debra, Chen, Qixuan, Bernier, Raphael, Goin-Kochel, Robin P., Wallace, Arianne Stevens, Gerdts, Jennifer, Kanne, Stephen, Berry, Leandra et al. · 2016 · Journal of Autism and Developmental Disorders
- DLG4-related synaptopathy: a new rare brain disorderAgustí Rodríguez‐Palmero, Melissa M. Boerrigter, David Gómez‐Andrés, Kimberly A. Aldinger, Íñigo Marcos‐Alcalde, Bernt Popp, David B. Everman, Alysia Kern Lovgren, Stéphanie Arpin, Vahid Bahrambeigi et al. · 2021 · Genetics in Medicine
- Inhibition of 14-3-3 Proteins Leads to Schizophrenia-Related Behavioral Phenotypes and Synaptic Defects in MiceMolly M. Foote, Haifa Qiao, Kourtney C. Graham, Yuying Wu, Yi Zhou · 2015 · Biological Psychiatry
- The molecular pathology of schizophrenia: an overview of existing knowledge and new directions for future researchTakumi Nakamura, Atsushi Takata · 2023 · Molecular Psychiatry
- Genetics of psychiatric disorders in the GWAS era: an update on schizophreniaSibylle G. Schwab, Dieter B. Wildenauer · 2013 · European Archives of Psychiatry and Clinical Neuroscience
- Genetics of Schizophrenia: Ready to Translate?Claire Foley, Aiden Peter Corvin, Shigeki Nakagome · 2017 · Current Psychiatry Reports
- Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity PhenotypeMonica Frega, Martijn M. Selten, Britt Mossink, Jason M. Keller, Katrin Linda, Rebecca Moerschen, Jieqiong Qu, Pierre Koerner, Sophie Martina Johanna Jansen, Elske Bijvank et al. · 2020 · Cell Reports
- A genomic lifespan program that reorganises the young adult brain is targeted in schizophreniaNathan Skene, Marcia M. Roy, Seth G. N. Grant · 2017 · eLife
- Exome arrays capture polygenic rare variant contributions to schizophreniaRichards, A. L., Leonenko, G., Walters, J. T., Kavanagh, D. H., Rees, E. G., Evans, A., Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M. et al. · 2016 · Human Molecular Genetics
- Genetics of SchizophreniaEscudero, Irene, Johnstone, Mandy · 2014 · Current Psychiatry Reports
- Implications of Genetic Findings for Understanding SchizophreniaMichael John Owen · 2012 · Schizophrenia Bulletin
- Postsynaptic density levels of the NMDA receptor NR1 subunit and PSD-95 protein in prefrontal cortex from people with schizophreniaCatts, Vibeke Sørensen, Derminio, Dominique Suzanne, Hahn, Chang-Gyu, Weickert, Cynthia Shannon · 2015 · npj Schizophrenia
- De Novo Mutation in SchizophreniaElliott Rees, George Kirov, Michael C. O’Donovan, Michael John Owen · 2012 · Schizophrenia Bulletin
- NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis modelsMayanglambam Dhruba Singh, Matthew Jensen, Micaela C. Lasser, Emily Huber, Tanzeen Yusuff, Lucilla Pizzo, Brian Lifschutz, Inshya Desai, Alexis Kubina, Sneha Yennawar et al. · 2020 · PLoS Genetics
- Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registrythe Emory 3q29 Project, Rebecca M. Pollak, Melissa M. Murphy, Michael P. Epstein, Michael E. Zwick, Cheryl Klaiman, Celine A. Saulnier, Jennifer G. Mullé · 2019 · Molecular Autism
- What have we learned from the Psychiatric Genomics ConsortiumMichael C. O’Donovan · 2015 · World Psychiatry
- Dlgap1 knockout mice exhibit alterations of the postsynaptic density and selective reductions in sociabilityMarcelo P. Coba, Marcia J. Ramaker, Emily V. Ho, Summer L. Thompson, Noboru H. Komiyama, Seth G. N. Grant, James A. Knowles, Stephanie C. Dulawa · 2018 · Scientific Reports
- High-frequency neural oscillations and visual processing deficits in schizophreniaHeng‐Ru May Tan, Luiz Lana, Peter J. Uhlhaas · 2013 · Frontiers in Psychology
- The synapse in schizophreniaAndrew J. Pocklington, Michael C. O’Donovan, Michael John Owen · 2014 · European Journal of Neuroscience
- A Neurodevelopment Approach for a Transitional Model of Early Onset SchizophreniaDomenico De Berardis, Sergio De Filippis, Gabriele Masi, Stefano Vicari, Alessandro Zuddas · 2021 · Brain Sciences
- Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutationCarroll, Liam S., Woolf, Rebecca, Ibrahim, Yousef, Williams, Hywel J., Dwyer, Sarah, Walters, James, Kirov, George, O’Donovan, Michael C., Owen, Michael J. · 2016 · Psychiatric Genetics
- A Longitudinal Imaging Genetics Study of Neuroanatomical Asymmetry in Alzheimer’s DiseaseChristian Wachinger, Kwangsik T. Nho, Andrew J. Saykin, Martin Reuter, Anna Rieckmann · 2018 · Biological Psychiatry
- Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum DisorderItaru Kushima, Masahiro Nakatochi, Branko Aleksić, Takashi Okada, Hiroki Kimura, Hidekazu Kato, Mako Morikawa, Toshiya Inada, Kanako Ishizuka, Youta Torii et al. · 2022 · Biological Psychiatry
- Repint of “Reframing autism as a behavioral syndrome and not a specific mental disorder: Implications of genetic and phenotypic heterogeneity”Sylvie Tordjman, David Cohen, George M. Anderson, Michel Botbol, Roberto Canitano, Nathalie Coulon, Pierre L. Roubertoux · 2018 · Neuroscience & Biobehavioral Reviews
- Role of estrogen in sex differences in memory, emotion and neuropsychiatric disordersJaved Iqbal, Geng-Di Huang, Yan-Xue Xue, Mei Yang, Xiao-Jian Jia · 2024 · Molecular Biology Reports
- Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia RiskHuentelman, Matthew J., Muppana, Leela, Corneveaux, Jason J., Dinu, Valentin, Pruzin, Jeremy J., Reiman, Rebecca, Borish, Cassie N., De Both, Matt, Ahmed, Amber, Todorov, Alexandre et al. · 2015 · PLOS ONE
- Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?Claire Amiet, Isabelle Gourfinkel‐An, Claudine Laurent‐Levinson, Nicolas Bodeau, Bérengère Génin, Éric Leguern, Sylvie Tordjman, David Cohen · 2013 · Molecular Autism
- Identification and characterization of three inherited genomic copy number variations associated with familial schizophreniaHsiao-Mei Liao, Yu-Lin Chao, Ai-Ling Huang, Min-Chih Cheng, Yann-Jang Chen, Kuei-Fang Lee, Jye‐Siung Fang, Chih-Hao Hsu, Chia‐Hsiang Chen · 2012 · Schizophrenia Research
- Transcriptional targets of the schizophrenia risk gene MIR137A L Collins, Y Kim, Rachael J. Bloom, Samir N. P. Kelada, Praveen Sethupathy, Patrick F. Sullivan · 2014 · Translational Psychiatry
- Prefrontal Cortical Dysfunction After Overexpression of Histone Deacetylase 1Mira Jakovcevski, Rahul A. Bharadwaj, Juerg Straubhaar, Guangping Gao, David P. Gavin, Igor Jakovčevski, Amanda Mitchell, Schahram Akbarian · 2013 · Biological Psychiatry
- Magnetoencephalography as a Tool in Psychiatric Research: Current Status and PerspectivePeter J. Uhlhaas, Peter Francis Liddle, David E.J. Linden, Anna Christina Nobre, Krish D. Singh, Joachim Groß · 2017 · Biological Psychiatry Cognitive Neuroscience and Neuroimaging
- Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studiesXue Xiao, Hong Chang, Ming Li · 2017 · Molecular Psychiatry
- Integrated Post-GWAS Analysis Sheds New Light on the Disease Mechanisms of SchizophreniaJhih-Rong Lin, Ying Cai, Quanwei Zhang, Wen Zhang, Rubén Nogales‐Cadenas, Zhengdong D. Zhang · 2016 · Genetics
- Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selectionA. Pardiñas, P. Holmans, A. Pocklington et al. · 2016 · bioRxiv
- Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion SyndromeDaniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Matthew J. Gazzellone, Nancy J. Butcher, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Eva W.C. Chow et al. · 2015 · G3 Genes Genomes Genetics
- Functional analysis of schizophrenia genes using GeneAnalytics program and integrated databasesTharani Sundararajan, Ann M. Manzardo, Merlin G. Butler · 2017 · Gene
- Astrocytes as master modulators of neural networks: Synaptic functions and disease‐associated dysfunction of astrocytesJeffrey A. Stogsdill, Corey C. Harwell, Steven A. Goldman · 2023 · Annals of the New York Academy of Sciences
- MAGI1 Copy Number Variation in Bipolar Affective Disorder and SchizophreniaRobert Karlsson, Lisette Graae, Magnus Lekman, Dai Wang, Reyna Favis, Tomas Axelsson, Dagmar Galter, Andrea Carmine Belin, Silvia Paddock · 2012 · Biological Psychiatry
- Cognitive impairment in psychiatric diseases: Biomarkers of diagnosis, treatment, and preventionYafen Wang, Weicheng Meng, Zhixin Liu, Qunxing An, Xingbin Hu · 2022 · Frontiers in Cellular Neuroscience
- Blocking NMDAR Disrupts Spike Timing and Decouples Monkey Prefrontal Circuits: Implications for Activity-Dependent Disconnection in SchizophreniaZick, Jennifer L., Blackman, Rachael K., Crowe, David A., Amirikian, Bagrat, DeNicola, Adele L., Netoff, Theoden I., Chafee, Matthew V. · 2018 · Neuron
- Inverse synaptic tagging: An inactive synapse-specific mechanism to capture activity-induced Arc/arg3.1 and to locally regulate spatial distribution of synaptic weightsHiroyuki Okuno, Keiichiro Minatohara, Haruhiko Bito · 2017 · Seminars in Cell and Developmental Biology
- MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion SyndromeDaniele Merico, Gregory Costain, Nancy J. Butcher, W. David Warnica, Lucas Ogura, Simon E. Alfred, Linda M. Brzustowicz, Anne S. Bassett · 2014 · Frontiers in Neurology
- An opposing function of paralogs in balancing developmental synapse maturationPlinio D. Favaro, Xiaojie Huang, Leon Hosang, Sophia Katharina Stodieck, Lei Cui, Yu-zhang Liu, Karl-Alexander Engelhardt, Frank Schmitz, Yan Dong, Siegrid Löwel et al. · 2018 · PLoS Biology
- Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia PathogenesisElliott Rees, Noa Carrera, Joanne Morgan, Kirsty Hambridge, Valentina Escott‐Price, Andrew J. Pocklington, Alexander L. Richards, Antonio F. Pardiñas, Colm McDonald, Gary J Donohoe et al. · 2018 · Biological Psychiatry
- High Content Image Analysis Identifies Novel Regulators of Synaptogenesis in a High-Throughput RNAi Screen of Primary NeuronsThomas J.F. Nieland, David J. Logan, Jessica L. Saulnier, Daniel Lam, Caroline A. Johnson, David E. Root, Anne Elizabeth Carpenter, Bernardo Luis Sabatini · 2014 · PLoS ONE
- History of the Concept of Disconnectivity in SchizophreniaJoseph T. Coyle, Darrick T. Balu, Matthew D. Puhl, Glenn T. Konopaske · 2016 · Harvard Review of Psychiatry
- Somatic mutations in the human brain: implications for psychiatric researchMasaki Nishioka, Miki Bundo, Kazuya Iwamoto, Tadafumi Kato · 2018 · Molecular Psychiatry
- Novel Complex Interactions between Mitochondrial and Nuclear DNA in Schizophrenia and Bipolar DisorderAnton Schulmann, Euijung Ryu, Vanessa Faria Gonçalves, Brandi L. Rollins, Michael Christiansen, Mark A. Frye, Joanna M. Biernacka, Marquis P. Vawter · 2019 · Complex Psychiatry
- Prefrontal Cortex-Mediated Impairments in a Genetic Model of NMDA Receptor Hypofunction Are Reversed by the Novel M1PAM VU6004256Michael D. Grannan, Catharine A. Mielnik, Sean P. Moran, Robert W. Gould, Jacob Ball, Zhuoyan Lu, Michael Bubser, Amy J. Ramsey, Masahito Abe, Hyekyung P. Cho et al. · 2016 · ACS Chemical Neuroscience
- Systems Biology, Bioinformatics, and Biomarkers in NeuropsychiatryAli Mostafa Alawieh, Fadi A. Zaraket, Jian‐Liang Li, Stefania Mondello, Amaly Nokkari, Mahdi Razafsha, Bilal H. Fadlallah, Rose‐Mary Boustany, Firas H. Kobeissy · 2012 · Frontiers in Neuroscience
- A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesityElisa Biamino, Eleonora Di Gregorio, Elga Fabia Belligni, Roberto Keller, Evelise Riberi, Marina Gandione, Alessandro Calcia, Cecilia Mancini, Elisa Giorgio, Simona Cavalieri et al. · 2015 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Mitochondrial Complex I Deficiency in Schizophrenia and Bipolar Disorder and Medication InfluenceBrandi L. Rollins, Ling Morgan, Brooke E. Hjelm, Adolfo Sequeira, Alan F. Schatzberg, Jack D. Barchas, Francis S. Lee, Rick M. Myers, Stanley J. Watson, Huda Akil et al. · 2017 · Complex Psychiatry
- Molecular Risk Factors for SchizophreniaShira Modai, Noam Shomron · 2016 · Trends in Molecular Medicine
- The molecular evolution of the vertebrate behavioural repertoireSeth G. N. Grant · 2015 · Philosophical Transactions of the Royal Society B Biological Sciences
- Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophreniaAndrés Ingason, Ina Giegling, Annette M. Hartmann, Just Genius, Bettina Konte, M. Friedl, Stephan Ripke, Patrick F. Sullivan, David St Clair, David Andrew Collier et al. · 2015 · Translational Psychiatry
- Specific Roles of NMDA Receptor Subunits in Mental DisordersHideko Yamamoto, Yoko Hagino, Shinya Kasai, Kazutaka Ikeda · 2015 · Current Molecular Medicine
- Functional analysis of rare variants found in schizophrenia implicates a critical role for GIT1–PAK3 signaling in neuroplasticityM. J. Kim, Jonathan D. Biag, Daniel M. Fass, M C Lewis, Qiangge Zhang, Morgan Fleishman, Shanti Pal Gangwar, Mischa Machius, Menachem Fromer, Shaun Purcell et al. · 2016 · Molecular Psychiatry
- 22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basisSquarcione, Chiaras, Torti, Maria Chiara, Di Fabio, Fabio, Biondi, Massimo · 2013 · Neuropsychiatric Disease and Treatment
- Effects of common GRM5 genetic variants on cognition, hippocampal volume and mGluR5 protein levels in schizophreniaNatalie Matosin, Kelly Anne Newell, Yann Quidé, Jessica Lee Andrews, Nina Teroganova, Melissa J. Green, Francesca Fernandez · 2017 · Brain Imaging and Behavior
- Electrophysiological Endophenotypes for SchizophreniaEmily M. Owens, Peter Bachman, David C. Glahn, Carrie E. Bearden · 2016 · Harvard Review of Psychiatry
- Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptionsEduardo A. Maury, Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris, Prashanth Rajarajan, Erin K. Flaherty, Schahram Akbarian, Andrew J. Chess et al. · 2023 · Cell Genomics
- Temporal dynamics of miRNAs in human DLPFC and its association with miRNA dysregulation in schizophreniaZhonghua Hu, Shouguo Gao, Daniel M. Lindberg, Debabrata Panja, Yoshi Wakabayashi, Keshen Li, Joel E. Kleinman, Jun Zhu, Zheng Li · 2019 · Translational Psychiatry
- Molecular mechanisms of schizophrenia: Insights from human geneticsZohreh Farsi, Morgan Sheng · 2023 · Current Opinion in Neurobiology
- Assessment of copy number variations in the brain genome of schizophrenia patientsMiwako Sakai, Yuichiro Watanabe, Toshiyuki Someya, Kazuaki Araki, Masako Shibuya, Kazuhiro Niizato, Kenichi Oshima, Yasuto Kunii, Hirooki Yabe, Junya Matsumoto et al. · 2015 · Molecular Cytogenetics
- Neurodevelopmental synaptopathies: Insights from behaviour in rodent models of synapse gene mutationsJiaqi Keith Luo, Rebecca H C Norris, Sarah L. Gordon, Jess Nithianantharajah · 2017 · Progress in Neuro-Psychopharmacology and Biological Psychiatry
- Hippocampal Regulation of Postsynaptic Density Homer1 by Associative LearningNicholas E. Clifton, Darren Cameron, Simon Trent, Lucy Sykes, Kerrie L. Thomas, Jérémy Hall · 2017 · Neural Plasticity
- Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophreniaJinsong Tang, Yu Fan, Hong Li, Qun Xiang, Dengfeng Zhang, Zongchang Li, Ying He, Yanhui Liao, Ya Wang, Fan He et al. · 2017 · Journal of genetics and genomics/Journal of Genetics and Genomics
- Directly and Indirectly Targeting the Glycine Modulatory Site to Modulate NMDA Receptor Function to Address Unmet Medical Needs of Patients With SchizophreniaJu-Chun Pei, Da-Zhong Luo, Shiang-Shin Gau, Chia‐Yuan Chang, Wen‐Sung Lai · 2021 · Frontiers in Psychiatry
- Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disordersTimothy P. Rutkowski, Jason P. Schroeder, Georgette M. Gafford, Stephen T. Warren, David Weinshenker, Tamara Caspary, Jennifer G. Mullé · 2016 · Journal of Neuroscience Research
- Schizophrenia: A critical view on genetic effectsRoar Fosse, Jay Joseph, Mike Jones · 2015 · Psychosis
- Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in SchizophreniaCaitlin Rippey, Tom Walsh, Süleyman Gülsüner, Matt Brodsky, Alex S. Nord, Molly J. Gasperini, Sarah B. Pierce, Cailyn H. Spurrell, Bradley P. Coe, Niklas Krumm et al. · 2013 · The American Journal of Human Genetics