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 101–200 of 879
- Impact of Advanced Paternal Age on Fertility and Risks of Genetic Disorders in OffspringAris Kaltsas, Efthalia Moustakli, Athanasios Zikopoulos, Ioannis A. Georgiou, Fotios Dimitriadis, Evangelos N. Symeonidis, Eleftheria Markou, Theologos M. Michaelidis, Dung Mai Ba Tien, Ioannis Giannakis et al. · 2023 · Genes
- The human clinical phenotypes of altered CHRNA7 copy numberMadelyn A. Gillentine, Christian Patrick Schaaf · 2015 · Biochemical Pharmacology
- De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophreniaGROUP Investigators, Rees, Elliott, Han, Jun, Morgan, Joanne, Carrera, Noa, Escott-Price, Valentina, Pocklington, Andrew J., Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E. et al. · 2020 · Nature Neuroscience
- Common alleles contribute to schizophrenia in CNV carriersTansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J et al. · 2016 · Molecular Psychiatry
- Integrated systems analysis reveals a molecular network underlying autism spectrum disordersLi, Jingjing, Shi, Minyi, Ma, Zhihai, Zhao, Shuchun, Euskirchen, Ghia, Ziskin, Jennifer, Urban, Alexander, Hallmayer, Joachim, Snyder, Michael · 2014 · Molecular Systems Biology
- Postsynaptic density proteins and their involvement in neurodevelopmental disordersKaizuka, Takeshi, Takumi, Toru · 2018 · The Journal of Biochemistry
- Transcriptome sequencing and genome-wide association analyses reveal lysosomal function and actin cytoskeleton remodeling in schizophrenia and bipolar disorderZhongming Zhao, Jia Xu, Jingchun Chen, S Kim, Mark Reimers, Silviu‐Alin Bacanu, H Yu, Chunyu Liu, Jingchun Sun, Quan Wang et al. · 2014 · Molecular Psychiatry
- High-resolution copy number variation analysis of schizophrenia in JapanItaru Kushima, Branko Aleksić, Masahiro Nakatochi, Teppei Shimamura, Tomoko Shiino, Akira Yoshimi, Hiroki Kimura, Yuto Takasaki, C Wang, J Xing et al. · 2016 · Molecular Psychiatry
- Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarraysGregory Costain, Anath Christopher Lionel, Daniele Merico, P. Forsythe, K. Russell, Chelsea Lowther, T. Yuen, Janice Husted, Dimitrios J. Stavropoulos, Marsha D. Speevak et al. · 2013 · Human Molecular Genetics
- Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston, Thomas Monfeuga, Donna M. McDonald‐McGinn, Raquel E. Gur, Bernice E. Morrow et al. · 2020 · Molecular Psychiatry
- Support for the N -Methyl-D-Aspartate Receptor Hypofunction Hypothesis of Schizophrenia From Exome Sequencing in Multiplex FamiliesAndrew E. Timms, Michael O. Dorschner, Jeremy Wechsler, Kyu Yeong Choi, Robert Kirkwood, Santhosh Girirajan, Carl A. Baker, Evan E. Eichler, Olena Korvatska, Katherine W. Roche et al. · 2013 · JAMA Psychiatry
- Caught in vicious circles: a perspective on dynamic feed-forward loops driving oxidative stress in schizophreniaMichel Cuénod, Pascal Steullet, Jan-Harry Cabungcal, Daniella Dwir, Inès Khadimallah, Paul Klauser, Philippe Conus, Kim Q. · 2021 · Molecular Psychiatry
- Treatment-resistant schizophrenia: current insights on the pharmacogenomics of antipsychoticsJohn Lally, Fiona Gaughran, Philip W. Timms, Sarah R Curran · 2016 · Pharmacogenomics and Personalized Medicine
- CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1Elliott Rees, James Walters, Kim Chambert, C O'Dushlaine, Jin Szatkiewicz, Alexander L. Richards, L. Georgieva, Gerwyn Mahoney‐Davies, Sophie E. Legge, Jennifer L. Moran et al. · 2013 · Human Molecular Genetics
- Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implicationsFátima Torres, Mafalda Barbosa, Patrı́cia Maciel · 2015 · Journal of Medical Genetics
- Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disordersJing Li, Wangshu Zhang, Hui Yang, Daniel P. Howrigan, Brent Wilkinson, Tade Souaiaia, Oleg Vadimovich Evgrafov, Giulio Genovese, Veronica A. Clementel, Jennifer C. Tudor et al. · 2017 · Nature Neuroscience
- Evolution of complexity in the zebrafish synapse proteomeÀlex Bayés, Mark O. Collins, Rita Reig‐Viader, Gemma Gou, David Goulding, Abril Izquierdo, Jyoti Sharma Choudhary, Richard David Emes, Seth G. N. Grant · 2017 · Nature Communications
- Tardive dyskinesia is caused by maladaptive synaptic plasticity: A hypothesisJames Teo, Mark John Edwards, Kailash P. Bhatia · 2012 · Movement Disorders
- Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number VariantsJoanna Martin, Miriam Cooper, Marian L. Hamshere, Andrew J. Pocklington, Stephen W. Scherer, Lindsey Kent, Michael Gill, Michael John Owen, Nigel M. Williams, Michael C. O’Donovan et al. · 2014 · Journal of the American Academy of Child & Adolescent Psychiatry
- Cognitive development prior to onset of psychosisJosephine Mollon, Abraham Reichenberg · 2017 · Psychological Medicine
- The proteome of schizophreniaJuliana Minardi Nascimento, Daniel Martins‐de‐Souza · 2015 · Schizophrenia
- The genetic variability and commonality of neurodevelopmental diseaseBradley P. Coe, Santhosh Girirajan, Evan E. Eichler · 2012 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
- Genetic Overlap Between Schizophrenia and Volumes of Hippocampus, Putamen, and Intracranial Volume Indicates Shared Molecular Genetic MechanismsOlav Bjerkehagen Smeland, Yunpeng Wang, Oleksandr Frei, Wen Li, Derrek P. Hibar, Barbara Franke, Francesco Bettella, Aree Witoelar, Srdjan Djurovic, Chi‐Hua Chen et al. · 2017 · Schizophrenia Bulletin
- Recent advances in quantitative neuroproteomicsGeorge E. Craft, Anshu Chen, Angus Clark Nairn · 2013 · Methods
- Spine pruning drives antipsychotic-sensitive locomotion via circuit control of striatal dopamineKim, Il Hwan, Rossi, Mark A, Aryal, Dipendra K, Racz, Bence, Kim, Namsoo, Uezu, Akiyoshi, Wang, Fan, Wetsel, William C, Weinberg, Richard J, Yin, Henry et al. · 2015 · Nature Neuroscience
- Developmental vulnerability of synapses and circuits associated with neuropsychiatric disordersPenzes, Peter, Buonanno, Andres, Passafaro, Maria, Sala, Carlo, Sweet, Robert A. · 2013 · Journal of Neurochemistry
- A brain atlas of synapse protein lifetime across the mouse lifespanBulovaite, Edita, Qiu, Zhen, Kratschke, Maximilian, Zgraj, Adrianna, Fricker, David G., Tuck, Eleanor J., Gokhale, Ragini, Koniaris, Babis, Jami, Shekib A., Merino-Serrais, Paula et al. · 2022 · Neuron
- Copy number variation and neuropsychiatric illnessElliott Rees, George Kirov · 2021 · Current Opinion in Genetics & Development
- Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous geneJess Nithianantharajah, Andrew G. McKechanie, Tiffany Stewart, Mandy Johnstone, Douglas Blackwood, David St Clair, Seth G. N. Grant, Timothy J. Bussey, Lisa M. Saksida · 2015 · Scientific Reports
- Glutamate in schizophrenia: Neurodevelopmental perspectives and drug developmentAlice Egerton, Anthony A. Grace, James M. Stone, Matthijs Geert Bossong, Michael S. Sand, Philip K. McGuire · 2020 · Schizophrenia Research
- Exome Sequencing of Familial Bipolar DisorderFernando S. Goes, Mehdi Pirooznia, Jennifer S. Parla, Melissa Kramer, Elena Ghiban, Senem Mavruk, Yun-Ching Chen, Eric T. Monson, Virginia L. Willour, Rachel Karchin et al. · 2016 · JAMA Psychiatry
- The genetics of neuropsychiatric disordersNicholas J. Bray, Michael C. O’Donovan · 2018 · Brain and Neuroscience Advances
- Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and SeizuresPetrovski, Slavé, Küry, Sébastien, Myers, Candace T., Anyane-Yeboa, Kwame, Cogné, Benjamin, Bialer, Martin, Xia, Fan, Hemati, Parisa, Riviello, James, Mehaffey, Michele et al. · 2016 · The American Journal of Human Genetics
- Defects in Bioenergetic Coupling in SchizophreniaCourtney R. Sullivan, Sinead Marie O'Donovan, Robert Erne McCullumsmith, Amy J. Ramsey · 2017 · Biological Psychiatry
- Exome sequence read depth methods for identifying copy number changesLatha Kadalayil, Sajjad Rafiq, Matthew J.J. Rose-Zerilli, Reuben J. Pengelly, Helen Parker, David Graham Oscier, Jonathan C. Strefford, William Tapper, J. Gibson, Sarah Ennis et al. · 2014 · Briefings in Bioinformatics
- Long-term potentiation modulates synaptic phosphorylation networks and reshapes the structure of the postsynaptic interactomeJing Li, Brent Wilkinson, Veronica A. Clementel, Junjie Hou, Thomas J. O’Dell, Marcelo P. Coba · 2016 · Science Signaling
- Implication of a Rare Deletion at Distal 16p11.2 in SchizophreniaSaurav Guha · 2013 · JAMA Psychiatry
- TNiK Is Required for Postsynaptic and Nuclear Signaling Pathways and Cognitive FunctionMarcelo P. Coba, Noboru H. Komiyama, Jess Nithianantharajah, Maksym V. Kopanitsa, Tim Indersmitten, Nathan Skene, Ellie J. Tuck, David G. Fricker, Kathryn A. Elsegood, Lianne E. Stanford et al. · 2012 · Journal of Neuroscience
- Identification and functional characterization of rare SHANK2 variants in schizophreniaSlavil Z. Peykov, Simone Berkel, Michael Schoen, K Weiss, Franziska Degenhardt, Jana Strohmaier, B Weiss, Christian Proepper, Gerhard M. Schratt, Markus Maria Nöthen et al. · 2015 · Molecular Psychiatry
- Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophreniaGregg W. Crabtree, Joseph A. Gogos · 2014 · Frontiers in Synaptic Neuroscience
- Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T. Nguyen, Julien Bryois, April Kim, Amanda L. Dobbyn, Laura M. Huckins, Ana B. Muñoz‐Manchado, Douglas M. Ruderfer, Giulio Genovese, Menachem Fromer, Xinyi Xu et al. · 2017 · Genome Medicine
- Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic ScalingMarco Benevento, Giovanni Iacono, Martijn M. Selten, Wei Ba, Astrid R. Oudakker, Monica Frega, Jason Keller, Roberta Mancini, Elly Lewerissa, Tjitske Kleefstra et al. · 2016 · Neuron
- Classics in Chemical Neuroscience: KetamineMarshall W. Tyler, Harmony B. Yourish, Dawn Flosnik Ionescu, Stephen J. Haggarty · 2017 · ACS Chemical Neuroscience
- A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental diseaseChee‐Seng Ku, Constantin Polychronakos, Eng‐King Tan, Nasheen Naidoo, Yudi Pawitan Y, Dimitrios H Roukos, Matthew E. Mort, D.N. Cooper · 2012 · Molecular Psychiatry
- Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) StudyTiffany A. Greenwood, Laura C. Lazzeroni, Adam X. Maihofer, Neal R. Swerdlow, Monica E. Calkins, Robert Freedman, Michael Foster Green, Gregory A. Light, Caroline M. Nievergelt, Keith H. Nuechterlein et al. · 2019 · JAMA Psychiatry
- Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion SyndromeAnne S. Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W.C. Chow, Thérèse van Amelsvoort, Donna M. McDonald‐McGinn, Raquel E. Gur, Ann Swillen, Marianne B. M. van den Bree et al. · 2017 · American Journal of Psychiatry
- Evidence of Mitochondrial Dysfunction within the Complex Genetic Etiology of SchizophreniaBrooke E. Hjelm, Brandi L. Rollins, Firoza Mamdani, Julie C. Lauterborn, George Kirov, GARY S. LYNCH, Christine M. Gall, Adolfo Sequeira, Marquis P. Vawter · 2015 · Complex Psychiatry
- What causes aberrant salience in schizophrenia? A role for impaired short-term habituation and the GRIA1 (GluA1) AMPA receptor subunitChris Barkus, David J. Sanderson, J. N. P. Rawlins, Mark E. Walton, Paul J. Harrison, David M. Bannerman · 2014 · Molecular Psychiatry
- Hidden Role of Gut Microbiome Dysbiosis in Schizophrenia: Antipsychotics or Psychobiotics as Therapeutics?Nayla Munawar, Khansa Ahsan, Khalid Muhammad, Aftab Ahmad, Munir Ahmad Anwar, Iltaf Shah, Ahlam Al Ameri, Fadwa Al Mughairbi · 2021 · International Journal of Molecular Sciences
- Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and IntelligenceEsperanza Fernández, Mark O. Collins, René Frank, Fei Zhu, Maksym V. Kopanitsa, Jess Nithianantharajah, Sarah A. Lemprière, David G. Fricker, Kathryn A. Elsegood, Catherine L. McLaughlin et al. · 2017 · Cell Reports
- Neurodevelopmental Disorders Associated with PSD-95 and Its Interaction PartnersAmanda M. Levy, Paulino Gómez‐Puertas, Zeynep Tümer · 2022 · International Journal of Molecular Sciences
- “Selfish Spermatogonial Selection”: A Novel Mechanism for the Association Between Advanced Paternal Age and Neurodevelopmental DisordersAnne Goriely, John Joseph McGrath, Christina M. Hultman, Andrew O.M. Wilkie, Dolores Malaspina · 2013 · American Journal of Psychiatry
- Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate GenesMichel Guipponi, Federico Andrea Santoni, Vincent Setola, Corinne Gehrig, Maud Rothärmel, Macarena Cuenca, Olivier Guillin, Dimitris G. Dikeos, Georgios Georgantopoulos, George N. Papadimitriou et al. · 2014 · PLoS ONE
- The Role of the Eukaryotic Translation Initiation Factor 4E (eIF4E) in Neuropsychiatric DisordersInês S. Amorim, Gilliard Lach, Christos G. Gkogkas · 2018 · Frontiers in Genetics
- Overexpression of LINE-1 Retrotransposons in Autism BrainSvitlana Shpyleva, Stepan Melnyk, Oleksandra Pavliv, Igor P. Pogribny, S. Jill James · 2017 · Molecular Neurobiology
- Zebrafish homologs of 16p11.2, a genomic region associated with brain disorders, are active during brain development, and include two deletion dosage sensor genesAlicia L. Blaker, Sunny Kumar Gupta, Jasmine M. McCammon, Gianluca De Rienzo, Hazel L. Sive · 2012 · Disease Models & Mechanisms
- Genetics of Eating DisordersCynthia Marie Bulik, Lauren E. Blake, Jehannine Austin · 2019 · Psychiatric Clinics of North America
- The interplay of dopamine metabolism abnormalities and mitochondrial defects in the pathogenesis of schizophreniaHaiyun Xu, Fan Yang · 2022 · Translational Psychiatry
- The genomics of schizophrenia: update and implicationsPaola Giusti‐Rodríguez, Patrick F. Sullivan · 2013 · Journal of Clinical Investigation
- Epigenetic Determinants of Healthy and Diseased Brain Aging and CognitionSchahram Akbarian, Michal Schnaider Beeri, Vahram H. Haroutunian · 2013 · JAMA Neurology
- Schizophrenia Genomics: Convergence on Synaptic Development, Adult Synaptic Plasticity, or Both?Jérémy Hall, Nicholas J. Bray · 2021 · Biological Psychiatry
- Specialized roles of neurofilament proteins in synapses: Relevance to neuropsychiatric disordersAidong Yuan, Ralph A. Nixon · 2016 · Brain Research Bulletin
- Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for NeurobiologySteven A. McCarroll, Steven E. Hyman · 2013 · Neuron
- Essential genetic findings in neurodevelopmental disordersAna R. Cardoso, Mónica Lopes‐Marques, Raquel Monteiro Silva, Catarina Serrano, António Amorim, Maria João Prata, Luı́sa Azevedo · 2019 · Human Genomics
- Scaffolding Proteins of the Post-synaptic Density Contribute to Synaptic Plasticity by Regulating Receptor Localization and Distribution: Relevance for Neuropsychiatric DiseasesFelice Iasevoli, Carmine Tomasetti, Andrea de Bartolomeis · 2012 · Neurochemical Research
- DNA methylation in schizophrenia: progress and challenges of epigenetic studiesMasaki Nishioka, Miki Bundo, Kiyoto Kasai, Kazuya Iwamoto · 2012 · Genome Medicine
- De novo CNVs in bipolar affective disorder and schizophreniaLyudmila Georgieva, Elliott Rees, Jennifer L. Moran, Kimberly D. Chambert, Vihra Krumova Milanova, Nick J. Craddock, Shaun Purcell, Pamela B. Sklar, Steven A. McCarroll, Peter Holmans et al. · 2014 · Human Molecular Genetics
- Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophreniaMatthew Halvorsen, Ruth Huh, Nikolay Oskolkov, Jia Wen, Sergiu Netotea, Paola Giusti‐Rodríguez, Robert Karlsson, Julien Bryois, Björn Nystedt, Adam Ameur et al. · 2020 · Nature Communications
- Proteomic analysis of postsynaptic proteins in regions of the human neocortexMarcia M. Roy, Oksana Sorokina, Nathan Skene, Clémence Simonnet, Francesca Mazzo, Ruud Zwart, Emanuele Sher, Colin Smith, J. Douglas Armstrong, Seth G. N. Grant · 2017 · Nature Neuroscience
- Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disordersAmit Lotan, Michaela Fencková, Janita Bralten, Aet O’Leary, Luanna Dixson, Robert W. Williams, Monique van der Voet · 2014 · Frontiers in Neuroscience
- Non-synaptic function of the autism spectrum disorder-associated gene SYNGAP1 in cortical neurogenesisMarcella Birtele, Ashley Del Dosso, Tiantian Xu, Tuan N. Nguyen, Brent Wilkinson, Negar Hosseini, Sarah C. Nguyen, Jean‐Paul Urenda, Gavin T. Knight, Camilo Rojas et al. · 2023 · Nature Neuroscience
- Epigenetic mechanisms in schizophreniaSchahram Akbarian · 2014 · Dialogues in Clinical Neuroscience
- Translating insights from neuropsychiatric genetics and genomics for precision psychiatryElliott Rees, Michael John Owen · 2020 · Genome Medicine
- Revitalizing Psychiatric TherapeuticsSteven E. Hyman · 2013 · Neuropsychopharmacology
- Schizophrenia genetics: emerging themes for a complex disorderDavid H. Kavanagh, Katherine E. Tansey, Michael C. O’Donovan, Michael John Owen · 2014 · Molecular Psychiatry
- A genetic model for neurodevelopmental diseaseBradley P. Coe, Santhosh Girirajan, Evan E. Eichler · 2012 · Current Opinion in Neurobiology
- Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autismIuliana Ionita‐Laza, Bin Xu, Vlad Makarov, Joseph D. Buxbaum, Johannes Lodewikus Roos, Joseph A. Gogos, Maria Karayiorgou · 2013 · Proceedings of the National Academy of Sciences
- Mechanisms Underlying the Comorbidity of Schizophrenia and Type 2 Diabetes MellitusYutaka Mizuki, Shinji Sakamoto, Yuko Okahisa, Yuji Yada, Nozomu Hashimoto, Manabu Takaki, Norihito Yamada · 2020 · The International Journal of Neuropsychopharmacology
- Clozapine’s multiple cellular mechanisms: What do we know after more than fifty years? A systematic review and critical assessment of translational mechanisms relevant for innovative strategies in treatment-resistant schizophreniaAndrea de Bartolomeis, Licia Vellucci, Annarita Barone, Mirko Manchia, Vincenzo De Luca, Felice Iasevoli, Christoph Ulrich Correll · 2022 · Pharmacology & Therapeutics
- Fifty Years of Research on Schizophrenia: The Ascendance of the Glutamatergic SynapseJoseph T. Coyle, W. Brad Ruzicka, Darrick T. Balu · 2020 · American Journal of Psychiatry
- Genetics of Bipolar DisorderFernando S. Goes · 2016 · Psychiatric Clinics of North America
- Recent Advances in the Genetics of SchizophreniaDimitrios Avramopoulos · 2018 · Complex Psychiatry
- Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteinsWilliam David Hill, Gail Davies, Louie N. van de Lagemaat, A Christoforou, Riccardo Emilio Marioni, Carla P. D. Fernandes, David C M Liewald, Mike D. R. Croning, Antony Payton, Leone C. A. Craig et al. · 2014 · Translational Psychiatry
- Recent Advances in the Genetics of Autism Spectrum DisorderSilvia De Rubeis, Joseph D. Buxbaum · 2015 · Current Neurology and Neuroscience Reports
- Antibodies to the N-Methyl-D-Aspartate Receptor and Other Synaptic Proteins in PsychosisJulia Deakin, Belinda Lennox, Michael S. Zandi · 2013 · Biological Psychiatry
- The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variantsBryan J. Mowry, Jacob Gratten · 2012 · Molecular Psychiatry
- Animal models of gene–environment interaction in schizophrenia: A dimensional perspectiveYavuz Ayhan, Ross McFarland, Mikhail V. Pletnikov · 2015 · Progress in Neurobiology
- Recurrent deletions of ULK4 in schizophrenia: a novel gene crucial for neuritogenesis and neuronal motilityBing Lang, Jin Pu, Irene Hunter, Min Liu, Cristina Martín‐Granados, Thomas James Reilly, Guodong Gao, Zhenlong Guan, Weidong Li, Yongyong Shi et al. · 2013 · Journal of Cell Science
- Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hubBlizinsky, Katherine D., Diaz-Castro, Blanca, Forrest, Marc P., Schürmann, Britta, Bach, Anthony P., Martin-de-Saavedra, Maria Dolores, Wang, Lei, Csernansky, John G., Duan, Jubao, Penzes, Peter · 2016 · Proceedings of the National Academy of Sciences
- Amelioration of autism-like social deficits by targeting histone methyltransferases EHMT1/2 in Shank3-deficient miceWang, Zi-Jun, Zhong, Ping, Ma, Kaijie, Seo, Ji-Seon, Yang, Fengwei, Hu, Zihua, Zhang, Freddy, Lin, Lin, Wang, Jie, Liu, Tao et al. · 2020 · Molecular Psychiatry
- Magnetic resonance spectroscopy and tissue protein concentrations together suggest lower glutamate signaling in dentate gyrus in schizophreniaAna D. Stan, Subroto Ghose, C Zhao, Keith Hulsey, Perry Mihalakos, Masaya Yanagi, Sidney Morris, John J. Bartko, Changho Choi, Carol A. Tamminga · 2014 · Molecular Psychiatry
- A Simple Cell-Based Assay Reveals That Diverse Neuropsychiatric Risk Genes Converge on Primary CiliaAaron Marley, Mark von Zastrow · 2012 · PLoS ONE
- Evidence for the role of EP HX2 gene variants in anorexia nervosaAshley A. Scott‐Van Zeeland, Cinnamon S. Bloss, Ryan Tewhey, Vikas Bansal, Ali Torkamani, Ondrej Libiger, Vikas Duvvuri, Nathan E. Wineinger, L Galvez, Burcu F. Darst et al. · 2013 · Molecular Psychiatry
- Intellectual disability and major psychiatric disorders: A continuum of neurodevelopmental causalityMichael John Owen · 2012 · The British Journal of Psychiatry
- Proteomics of the Synapse – A Quantitative Approach to Neuronal PlasticityDaniela C. Dieterich, Michael R. Kreutz · 2015 · Molecular & Cellular Proteomics
- Diagnostic and therapeutic potential of microRNAs in neuropsychiatric disorders: Past, present, and futureBegüm Alural, Şermin Genç, Stephen J. Haggarty · 2016 · Progress in Neuro-Psychopharmacology and Biological Psychiatry
- Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndromeMonique C.M. Balemans, Nael Nadif Kasri, Maksim V. Kopanitsa, Nurudeen O. Afinowi, G.J.A. Ramakers, Theo A. Peters, Andy J. Beynon, Sanne Marlijn Janssen, Rik C.J. van Summeren, Jorine M. Eeftens et al. · 2012 · Human Molecular Genetics
- Modulating Neuroinflammation to Treat Neuropsychiatric DisordersFranziska Radtke, Gareth Chapman, Jérémy Hall, Yasir Ahmed Syed · 2017 · BioMed Research International
- A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophreniaLynsey S. Hall, Christopher William Medway, Oliver Pain, Antonio F. Pardiñas, Elliott Rees, Valentina Escott‐Price, Andrew J. Pocklington, Nicholas J. Bray, Peter Holmans, James Walters et al. · 2019 · Human Molecular Genetics
- Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family StudyTiffany A. Greenwood, Laura C. Lazzeroni, Monica E. Calkins, Robert Freedman, Michael Foster Green, Raquel E. Gur, Ruben C. Gur, Gregory A. Light, Keith H. Nuechterlein, Ann Olincy M. D et al. · 2015 · Schizophrenia Research