De novo mutations in schizophrenia implicate synaptic networks
Fromer, Menachem, Pocklington, Andrew J., Kavanagh, David H., Williams, Hywel J., Dwyer, Sarah, Gormley, Padhraig, Georgieva, Lyudmila, Rees, Elliott, Palta, Priit, Ruderfer, Douglas M., Carrera, Noa, Humphreys, Isla, Johnson, Jessica S., Roussos, Panos, Barker, Douglas D., Banks, Eric, Milanova, Vihra, Grant, Seth G., Hannon, Eilis, Rose, Samuel A., Chambert, Kimberly, Mahajan, Milind, Scolnick, Edward M., Moran, Jennifer L., Kirov, George, Palotie, Aarno, McCarroll, Steven A., Holmans, Peter, Sklar, Pamela, Owen, Michael J., Purcell, Shaun M., O’Donovan, Michael C.·2014·Nature
Cited by (1,004)
Items 801–900 of 1,004
- Disrupted-in-Schizophrenia-1 (DISC1) protein disturbs neural function in multiple disease-risk pathwaysLisha Shao, Binyan Lu, Zhexing Wen, Shaolei Teng, Lingling Wang, Yi Chen Zhao, Liyuan Wang, Koko Ishizuka, Xiufeng Xu, Akira Sawa et al. · 2017 · Human Molecular Genetics
- Prevalence and Architecture of De Novo Mutations in Developmental DisordersDeciphering Developmental Disorders Study · 2017 · Obstetrical & Gynecological Survey
- Overexpression of the Type 1 Adenylyl Cyclase in the Forebrain Leads to Deficits of Behavioral InhibitionChen, Xuanmao, Cao, Hong, Saraf, Amit, Zweifel, Larry S., Storm, Daniel R. · 2015 · The Journal of Neuroscience
- Cognitive endophenotypes inform genome-wide expression profiling in schizophrenia.Amanda B. Zheutlin, Rachael Viehman, Rebecca G. Fortgang, Jacqueline Borg, Desmond Smith, Jaana Suvisaari, Sebastian Therman, Christina M. Hultman, Tyrone D. Cannon · 2015 · Neuropsychology
- Exome array analysis suggests an increased variant burden in families with schizophreniaNina S. McCarthy, Phillip E. Melton, Sarah V. Ward, Spencer M. Allan, Milan Dragović, Melanie L. Clark, Bharti Morar, Justin P. Rubio, John Blangero, Johanna Claire Badcock et al. · 2016 · Schizophrenia Research
- Emerging roles for long noncoding RNAs in learning, memory and associated disordersEddie Grinman, Isabel Espadas, Sathyanarayanan V. Puthanveettil · 2019 · Neurobiology of Learning and Memory
- Regulatory Variant rs2535629 in ITIH3 Intron Confers Schizophrenia Risk By Regulating CTCF Binding and SFMBT1 ExpressionYifan Li, Changguo Ma, Shiwu Li, Junyang Wang, Wenqiang Li, Yongfeng Yang, Xiaoyan Li, Jiewei Liu, Jinfeng Yang, Yixing Liu et al. · 2022 · Advanced Science
- The TALE never ends: A comprehensive overview of the role of PBX1, a TALE transcription factor, in human developmental defectsLaura Mary, Delphine Leclerc, David Gilot, Marc‐Antoine Belaud‐Rotureau, Sylvie Jaillard · 2022 · Human Mutation
- Dysfunction of cAMP–Protein Kinase A–Calcium Signaling Axis in Striatal Medium Spiny Neurons: A Role in Schizophrenia and Huntington’s Disease NeuropathologyMarija Fjodorova, Zoe Noakes, Daniel Cabezas de la Fuente, Adam C. Errington, Meng Li · 2022 · Biological Psychiatry Global Open Science
- Identification of activity-induced Egr3-dependent genes reveals genes associated with DNA damage response and schizophreniaKetan K. Marballi, Khaled Alganem, Samuel J. Brunwasser, Arhem Barkatullah, Kimberly T. Meyers, Janet M. Campbell, Annika B. Ozols, Robert Erne McCullumsmith, Amelia L. Gallitano · 2022 · Translational Psychiatry
- Molecular evidence for decreased synaptic efficacy in the postmortem olfactory bulb of individuals with schizophreniaChijioke N. Egbujo, Duncan Sinclair, Karin E. Borgmann‐Winter, Steven Edward Arnold, Bruce I. Turetsky, Chang-Gyu Hahn · 2015 · Schizophrenia Research
- Unlocking the Treasure Trove: From Genes to Schizophrenia BiologyS. E. McCarthy, William Richard McCombie, Aiden Peter Corvin · 2014 · Schizophrenia Bulletin
- Rare UNC13B variations and risk of schizophrenia: Whole‐exome sequencing in a multiplex family and follow‐up resequencing and a case–control studyJun Egawa, Satoshi Hoya, Yuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, Masashi Ikeda, Emiko Inoue, Shujiro Okuda, Kenji Kondo, Takeo Saito et al. · 2016 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Protein Interaction Networks Link Schizophrenia Risk Loci to Synaptic FunctionEmanuel Schwarz, Rauf Izmailov, Píetro Lió, Andreas Meyer‐Lindenberg · 2016 · Schizophrenia Bulletin
- IQSEC2 and X-linked syndromal intellectual disabilityAaron F. Alexander‐Bloch, Christopher J. McDougle, Zhanna Ullman, David A. Sweetser · 2016 · Psychiatric Genetics
- Identification of a de novo DYNC1H1 mutation via WES according to published guidelinesDongxue Ding, Chen Zhao, Kai Li, Zhe Long, Wei Ye, Zhaoli Tang, Kun Xia, Rong Qiu, Beisha Tang, Hong Feng Jiang · 2016 · Scientific Reports
- Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophreniaGanna Leonenko, Alexander L. Richards, James Walters, Andrew J. Pocklington, Kimberly Chambert, Mariam M. AlEissa, Sally Isabel Sharp, Niamh Louise O’Brien, David Curtis, Nicholas James Bass et al. · 2017 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Assessment of somatic single-nucleotide variation in brain tissue of cases with schizophreniaJohn F. Fullard, Alexander W. Charney, Georgios Voloudakis, Andrew V. Uzilov, Vahram H. Haroutunian, Panos Roussos · 2019 · Translational Psychiatry
- A brief report: de novo copy number variants in children with attention deficit hyperactivity disorderJoanna Martin, Grace Hosking, Megan E. Wadon, Sharifah Shameem Agha, K. Langley, Elliott Rees, Michael John Owen, Michael C. O’Donovan, George Kirov, Anita Thapar · 2020 · Translational Psychiatry
- Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent PhenotypesAna Isabel Silva, Friederike Ehrhart, Magnus Orn Ulfarsson, Hreinn Stefánsson, Kāri Stefánsson, Lawrence S. Wilkinson, Jérémy Hall, David E.J. Linden · 2022 · Biological Psychiatry
- Quantitative electroencephalography parameters as neurophysiological biomarkers of schizophrenia-related deficits: A Phase II substudy of patients treated with iclepertin (BI 425809)Christian Schultheis, Holger Rosenbrock, Salome Rebecca Mack, Richard Vinisko, Niklas Schuelert, Andrea Plano, Sigurd D. Süßmuth · 2022 · Translational Psychiatry
- PSYCHIATRIC GENETICS AND THE FUTURE OF PERSONALIZED TREATMENTJordan W. Smoller · 2014 · Depression and Anxiety
- Cell migration in schizophrenia: Patient-derived cells do not regulate motility in response to extracellular matrixJing Yang Tee, Ratneswary Sutharsan, Yongjun Fan, Alan Mackay‐Sim · 2017 · Molecular and Cellular Neuroscience
- De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsySheng Luo, Wen‐Jun Zhang, Mi Jiang, Rong-Na Ren, Lei Liu, Yulan Li, Wenhui Liu, Pengyu Wang, Yujie Gu, Li‐Zhi Chen et al. · 2025 · Epilepsia
- mTADA is a framework for identifying risk genes from de novo mutations in multiple traitsTan-Hoang Nguyen, Amanda L. Dobbyn, Ruth C. Brown, Brien P. Riley, Joseph D. Buxbaum, Dalila Pinto, Shaun Purcell, Patrick F. Sullivan, Xin He, Eli A. Stahl · 2020 · Nature Communications
- Prioritizing the development of mouse models for childhood brain disordersKevin K. Ogden, Emin D. Ozkan, Gavin Rumbaugh · 2015 · Neuropharmacology
- Copy Number Variation in Syndromic Forms of Psychiatric Illness: The Emerging Value of Clinical Genetic Testing in PsychiatryChristian G. Bouwkamp, Anneke J.A. Kievit, Sander Markx, Joseph I. Friedman, Laura J. C. M. van Zutven, Rick van Minkelen, Terry Vrijenhoek, Bin Xu, Ineke M Sterrenburg-v.d.Nieuwegiessen, Joris A. Veltman et al. · 2017 · American Journal of Psychiatry
- Methods for the Analysis and Interpretation for Rare Variants Associated with Complex TraitsJ. Dylan Weissenkampen, Yu Jiang, Scott Eckert, Bibo Jiang, Bingshan Li, Dajiang J. Liu · 2019 · Current Protocols in Human Genetics
- Current challenges and possible future developments in personalized psychiatry with an emphasis on psychotic disordersАnastasia Levchenko, Timur Nurgaliev, Alexander A Kanapin, Anastasia A. Samsonova, Raul R. Gainetdinov · 2020 · Heliyon
- Association of SHANK Family with Neuropsychiatric Disorders: An Update on Genetic and Animal Model DiscoveriesLily Wan, Du Liu, Wenbiao Xiao, Boxin Zhang, Xiao‐Xin Yan, Zhaohui Luo, Bo Xiao · 2021 · Cellular and Molecular Neurobiology
- Co-barcoded sequence reads from long DNA fragments: a cost-effective solution for “perfect genome” sequencingBrock A. Peters, Jia Liu, Radoje Drmanac · 2015 · Frontiers in Genetics
- The Genetic Architecture of Neurodevelopmental DisordersKevin J. Mitchell · 2015 · Wiley eBooks
- Receptor Tyrosine Kinase MET Interactome and Neurodevelopmental Disorder Partners at the Developing SynapseZhihui Xie, Jing Li, Jonathan Scott Baker, Kathie L. Eagleson, Marcelo P. Coba, Pat R. Levitt · 2016 · Biological Psychiatry
- Distinct selective forces and Neanderthal introgression shaped genetic diversity at genes involved in neurodevelopmental disordersMozzi, Alessandra, Forni, Diego, Cagliani, Rachele, Pozzoli, Uberto, Clerici, Mario, Sironi, Manuela · 2017 · Scientific Reports
- Development of a highly automated and multiplexed targeted proteome pipeline and assay for 112 rat brain synaptic proteinsChristopher M. Colangelo, Gordana Ivosev, Lisa M. Chung, Thomas B. Abbott, Mark A. Shifman, Fumika Sakaue, David Cox, Robert R. Kitchen, Lyle Burton, Stephen A. Tate et al. · 2014 · PROTEOMICS
- Disturbed Prefrontal Cortex Activity in the Absence of Schizophrenia-Like Behavioral Dysfunction inArc/Arg3.1Deficient MiceXiaoyan Gao, Jasper Grendel, Mary Muhia, Sergio Castro‐Gomez, Ute Süsens, Dirk Isbrandt, Matthias Kneussel, Dietmar Kuhl, Ora Ohana · 2019 · Journal of Neuroscience
- miR-132 Regulates PTSD-like Behaviors in Rats Following Single-Prolonged Stress Through Fragile X-Related Protein 1Peng-Yin Nie, Li-Li Ji, Chang-Hai Fu, Junbo Peng, Zhenyu Wang, Lei Tong · 2020 · Cellular and Molecular Neurobiology
- Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S. Goes, Adam E. Locke, Duncan S. Palmer, Weiqing Wang, Sarah Cohen‐Woods, Giulio Genovese, Anne Jackson, J Chen, Mark N. Kvale et al. · 2021 · Molecular Psychiatry
- Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic TestingMerlin G. Butler, Daniel Moreno‐De‐Luca, Antonio Maria Persico · 2022 · Genes
- Genetic disorders of neurotransmitter release machineryBurak Uzay, Ege T. Kavalali · 2023 · Frontiers in Synaptic Neuroscience
- The pleiotropic spectrum of proximal 16p11.2 CNVsChiara Auwerx, Zoltán Kutalik, Alexandre Reymond · 2024 · The American Journal of Human Genetics
- No evidence for rare recessive and compound heterozygous disruptive variants in schizophreniaDouglas M. Ruderfer, Elaine T. Lim, Giulio Genovese, Jennifer L. Moran, Christina M. Hultman, Patrick F. Sullivan, Steven A. McCarroll, Peter Holmans, Pamela B. Sklar, Shaun Purcell · 2014 · European Journal of Human Genetics
- Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum DisordersKanako Ishizuka, Hiroki Kimura, Chenyao Wang, Jingrui Xing, Itaru Kushima, Yuko Arioka, Tomoko Oya‐Ito, Yota Uno, Takashi Okada, Daisuke Mori et al. · 2016 · PLoS ONE
- mirDNMR: a gene-centered database of backgroundde novomutation rates in humanYiyi Jiang, Zhongshan Li, Zhenwei Liu, Denghui Chen, Wanying Wu, Yaoqiang Du, Liying Ji, Zi‐Bing Jin, Wei Li, Jinyu Wu · 2016 · Nucleic Acids Research
- Translating advances in the molecular basis of schizophrenia into novel cognitive treatment strategiesColm M. P. O’Tuathaigh, Paula M. Moran, Xuechu Zhen, John L. Waddington · 2017 · British Journal of Pharmacology
- Inter-hemispherical asymmetry in default-mode functional connectivity and BAIAP2 gene are associated with anger expression in ADHD adultsRoland Hasler, Maria Giulia Preti, Djalel Eddine Meskaldji, Julien Prados, Wafae Adouan, Cristelle K. Rodriguez, S. Toma, N. Hiller, T. Ismaili, Jérémy Hofmeister et al. · 2017 · Psychiatry Research Neuroimaging
- Convergent roles of de novo mutations and common variants in schizophrenia in tissue-specific and spatiotemporal co-expression networkPeilin Jia, Xiangning Chen, Ayman H. Fanous, Zhongming Zhao · 2018 · Translational Psychiatry
- Are FXR Family Proteins Integrators of Dopamine Signaling and Glutamatergic Neurotransmission in Mental Illnesses?Jivan Khlghatyan, Jean‐Martin Beaulieu · 2018 · Frontiers in Synaptic Neuroscience
- The Arc gene: Retroviral heritage in cognitive functionsAlexander V. Kedrov, Mikhail O. Durymanov, K. V. Anokhin · 2019 · Neuroscience & Biobehavioral Reviews
- Convergence and Divergence in the Genetics of Psychiatric Disorders From Pathways to Developmental StagesShahar Shohat, Alana Amelan, Sagiv Shifman · 2020 · Biological Psychiatry
- The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorderDanyang Li, Nora Choque Olsson, Hong Jiao, Nina Norgren, Ulf Jonsson, Sven Bölte, Kristiina Tammimies · 2020 · npj Genomic Medicine
- Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disordersHalie J. May, Jaehoon Jeong, Anya Revah‐Politi, Julie S. Cohen, Anna Chassevent, Júlia Baptista, Evan H. Baugh, Louise Bier, Armand Bottani, Maria resa Te Carminho A. Rodrigues et al. · 2021 · Genetics in Medicine
- Brain-specific deletion of GIT1 impairs cognition and alters phosphorylation of synaptic protein networks implicated in schizophrenia susceptibilityDaniel M. Fass, Michael C. Lewis, Rushdy Ahmad, Matthew J. Szucs, Qiangge Zhang, Morgan Fleishman, Dongqing Wang, Myung Jong Kim, Jonathan D. Biag, Steven A. Carr et al. · 2022 · Molecular Psychiatry
- Advancing psychiatric genetics through dissecting heterogeneityKaren Hodgson, Peter McGuffin, Cathryn M. Lewis · 2017 · Human Molecular Genetics
- Synaptic proteomics as a means to identify the molecular basis of mental illness: Are we getting there?Rita Reig‐Viader, Carlos Balet Sindreu, Àlex Bayés · 2017 · Progress in Neuro-Psychopharmacology and Biological Psychiatry
- iMEGES: integrated mental-disorder GEnome score by deep neural network for prioritizing the susceptibility genes for mental disorders in personal genomesAtlas Khan, Qian Liu, Kai Wang · 2018 · BMC Bioinformatics
- Region-specific inhibition of 14-3-3 proteins induces psychomotor behaviors in miceKourtney Graham, Jiajing Zhang, Haifa Qiao, Yuying Wu, Yi Zhou · 2019 · Schizophrenia
- Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T Nguyen, Julien Bryois, April Kim, Amanda Dobbyn, Laura M Huckins, Ana B. Muñoz‐Manchado, Douglas M Ruderfer, Giulio Genovese, Menachem Fromer, Xinyi Xu et al. · 2017 · bioRxiv (Cold Spring Harbor Laboratory)
- Effects of chronic exposure to haloperidol, olanzapine or lithium on SV2A and NLGN synaptic puncta in the rat frontal cortexHalff, Els F., Cotel, Marie-Caroline, Natesan, Sridhar, McQuade, Richard, Ottley, Chris J., Srivastava, Deepak P., Howes, Oliver D., Vernon, Anthony C. · 2021 · Behavioural Brain Research
- Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibilitySuárez-Rama, José Javier, Arrojo, Manuel, Sobrino, Beatriz, Amigo, Jorge, Brenlla, Julio, Agra, Santiago, Paz, Eduardo, Brión, María, Carracedo, Ángel, Páramo, Mario et al. · 2015 · Journal of Psychiatric Research
- Disease severity across psychiatric disorders is linked to pro-inflammatory cytokinesPierre Solomon, Monika Budde, Mojtaba Oraki Kohshour, Kristina Adorjan, Maria Heilbronner, Alba Navarro‐Flores, Sergi Papiol, Daniela Reich‐Erkelenz, Eva Christina Schulte, Fanny Senner et al. · 2025 · Brain Behavior and Immunity
- Using model systems to understand errant plasticity mechanisms in psychiatric disordersBruno B. Averbeck, Matthew V. Chafee · 2016 · Nature Neuroscience
- Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencingYosuke Eriguchi, Hitoshi Kuwabara, Aya Inai, Yuki Kawakubo, Fumichika Nishimura, Chihiro Kakiuchi, Mamoru Tochigi, Jun Ohashi, Naoto Aoki, Kayoko Kato et al. · 2017 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- SAP97 regulates behavior and expression of schizophrenia risk enriched gene sets in mouse hippocampusPreetika Gupta, Ogul Ersin Uner, Soumyashant Nayak, Gregory R. Grant, Robert Gordon Kalb · 2018 · PLoS ONE
- Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disordersGregory Costain, Susan Walker, Bob Argiropoulos, Danielle A. Baribeau, Anne S. Bassett, Erik Boot, Koenraad Devriendt, Barbara Kellam, Christian R. Marshall, Aparna Prasad et al. · 2019 · Journal of Neurodevelopmental Disorders
- IRSp53 Deletion in Glutamatergic and GABAergic Neurons and in Male and Female Mice Leads to Distinct Electrophysiological and Behavioral PhenotypesYangsik Kim, Young Woo Noh, Kyungdeok Kim, Esther Yang, Hyun Kim, Eunjoon Kim · 2020 · Frontiers in Cellular Neuroscience
- Neuronal Differentiation of Induced Pluripotent Stem Cells from Schizophrenia Patients in Two-Dimensional and in Three-Dimensional Cultures Reveals Increased Expression of the Kv4.2 Subunit DPP6 That Contributes to Decreased Neuronal ActivityMaximilian Naujock, Anna Speidel, Sandra Elisabeth Fischer, Valeria Kizner, Cornelia Dorner‐Ciossek, Frank Gillardon · 2020 · Stem Cells and Development
- In vitro fluorescence assay to measure GDP/GTP exchange of guanine nucleotide exchange factors of Rho family GTPasesAlyssa M. Blaise, Ellen E Corcoran, Eve S. Wattenberg, Yan-Ling Zhang, Jeffrey R. Cottrell, Anthony J. Koleske · 2021 · Biology Methods and Protocols
- Etiology of Autism Spectrum Disorder: A Genomics PerspectiveJohn J. Connolly, Hakon H. Hakonarson · 2014 · Current Psychiatry Reports
- The impact of epigenomic next‐generation sequencing approaches on our understanding of neuropsychiatric disordersAnne‐Laure Schang, Délara Sabéran‐Djoneidi, Valérie Mezger · 2017 · Clinical Genetics
- AMPA receptors control fear extinction through an Arc-dependent mechanismSimon Trent, Philip Barnes, Jérémy Hall, Kerrie L. Thomas · 2017 · Learning & Memory
- Family-based genome-wide association study of autism spectrum disorder in middle eastern familiesAl-Sarraj, Yasser, Al-Dous, Eman, Taha, Rowaida Z., Ahram, Dina, Alshaban, Fouad, Tolfat, Mohammed, El-Shanti, Hatem, Albagha, Omar M.E. · 2021 · Genes
- Regional Specificity of Cortical Layer 3 Dendritic Spine Deficits in SchizophreniaKenneth N. Fish, Robert A. Sweet, Matthew L. MacDonald, David A. Lewis · 2025 · JAMA Psychiatry
- Dopamine is Required for Activity-Dependent Amplification ofArcmRNA in Developing Postnatal Frontal CortexYizhou Ye, Surjeet S. Mastwal, Vania Y. Cao, Ming Ren, Qing Liu, Wenyu Zhang, ABDEL G. ELKAHLOUN, Kuan Hong Wang · 2016 · Cerebral Cortex
- The diverse pleiotropic effects of spliceosomal protein PUF60 : A case series of Verheij syndromeAndrew Paul Fennell, Anne Baxter, Samuel Frank Berkovic, Carolyn Ellaway, Caitlin Forwood, Michael S. Hildebrand, Smitha Kumble, Colina McKeown, David R. Mowat, Gemma Poke et al. · 2022 · American Journal of Medical Genetics Part A
- Suppressed prefrontal neuronal firing variability and impaired social representation in IRSp53-mutant miceWoohyun Kim, Jae Jin Shin, Yu Jin Jeong, Kyungdeok Kim, Jung Won Bae, Young Woo Noh, Seungjoon Lee, Woochul Choi, Se‐Bum Paik, Min Whan Jung et al. · 2022 · eLife
- Dysregulated nitric oxide signaling as a candidate mechanism of fragile X syndrome and other neuropsychiatric disordersSteven M. Colvin, Kenneth Y. Kwan · 2014 · Frontiers in Genetics
- Translating Genetic Risk Loci Into Molecular Risk Mechanisms for SchizophreniaNicholas J. Bray, Matthew Hill · 2015 · Schizophrenia Bulletin
- Expression Analyses of POGZ, A Responsible Gene for Neurodevelopmental Disorders, during Mouse Brain DevelopmentKyoko Ibaraki, Nanako Hamada, Ikuko Iwamoto, Hidenori Ito, Noriko Kawamura, Rika Morishita, Hidenori Tabata, Koh‐ichi Nagata · 2019 · Developmental Neuroscience
- A functional missense variant in ITIH3 affects protein expression and neurodevelopment and confers schizophrenia risk in the Han Chinese populationKaiqin Li, Yifan Li, Junyang Wang, Yongxia Huo, Di Huang, Shiwu Li, Jiewei Liu, Xiaoyan Li, Rong Liu, Xiaogang Chen et al. · 2020 · Journal of genetics and genomics/Journal of Genetics and Genomics
- De Novo Gene Variants and Familial Bipolar DisorderClaudio Toma A, Alex D. Shaw, Bronwyn J. Overs, Philip Bowden Mitchell, Peter R. Schofield, Antony A. Cooper, Janice M. Fullerton · 2020 · JAMA Network Open
- Extracellular vesicles in patients in the acute phase of psychosis and after clinical improvement: an explorative studyMette Elise Tunset, Hanne Haslene‐Hox, Tim Van Den Bossche, Arne Einar Vaaler, Einar Sulheim, Daniel Kondziella · 2020 · PeerJ
- ASH1L mutation caused seizures and intellectual disability in twin sistersHailing Liu, De-Tian Liu, Song Lan, Yanlian Yang, Jingjing Huang, Jinbo Huang, Ling Fang · 2021 · Journal of Clinical Neuroscience
- The U-shaped relationship between parental age and the risk of bipolar disorder in the offspring: A systematic review and meta-analysisGiovanna Fico, Vincenzo Oliva, Michele De Prisco, Anna Giménez‐Palomo, María Sagué‐Vilavella, Susana Gomes‐da‐Costa, Marina Garriga, Eva Solé, Marc Valentí, Giuseppe Fanelli et al. · 2022 · European Neuropsychopharmacology
- de novo variant calling identifies cancer mutation signatures in the 1000 Genomes ProjectJeffrey K. Ng, Pankaj Vats, Elyn Fritz‐Waters, Stephanie Sarkar, Eleanor I. Sams, Evin M. Padhi, Zachary L. Payne, Shawn Leonard, Marc A. West, Chandler Prince et al. · 2022 · Human Mutation
- Whole-exome sequencing identifies a novel heterozygous missense variant of the EN2 gene in two unrelated patients with autism spectrum disorderAreerat Hnoonual, Thanya Sripo, Pornprot Limprasert · 2016 · Psychiatric Genetics
- A CRISPR view of gene regulationBudhaditya Banerjee, Richard I. Sherwood · 2017 · Current Opinion in Systems Biology
- Presynaptic disorders: a clinical and pathophysiological approach focused on the synaptic vesicleElisenda Cortès‐Saladelafont, Noa Lipstein, Àngels García‐Cazorla · 2018 · Journal of Inherited Metabolic Disease
- Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approachElena Michaelovsky, Miri Carmel, Amos Frisch, Mali Salmon‐Divon, Metsada Pasmanik, Abraham Weizman, Doron Gothelf · 2019 · Translational Psychiatry
- De novo deleterious variants that may alter the dopaminergic reward pathway are associated with anorexia nervosaThierry Bienvenu, Nicolas Lebrun, Julia Clarke, Philibert Duriez, Philip A. P. M. Gorwood, Nicolás Ramoz · 2019 · Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity
- Unraveling the Neurobiology of Sleep and Sleep Disorders Using DrosophilaLeela J. Chakravarti, Emilia H. Moscato, Matthew S. Kayser · 2016 · Current topics in developmental biology/Current Topics in Developmental Biology
- Genetic Feedback Regulation of Frontal Cortical Neuronal Ensembles Through Activity-Dependent Arc Expression and Dopaminergic InputSurjeet S. Mastwal, Vania Y. Cao, Kuan Hong Wang · 2016 · Frontiers in Neural Circuits
- Aberrant hippocampal transmission and behavior in mice with a stargazin mutation linked to intellectual disabilityGladys L. Caldeira, Ângela S. Inácio, Nuno Beltrão, Carlos A.V. Barreto, Marina Manuela Ventura Rodrigues, Tiago Rondão, Rosangela B. Macedo, Raquel P. Gouveia, Mohamed Edfawy, Joana Ribeiro Guedes et al. · 2022 · Molecular Psychiatry
- Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorderMasaki Nishioka, Jun Takayama, Naomi Sakai, An‐a Kazuno, Mizuho Ishiwata, Junko Ueda, Takashi Hayama, Kumiko Fujii, Toshiyuki Someya, Shinichi Kuriyama et al. · 2023 · Molecular Psychiatry
- FlyNet: a versatile network prioritization server for theDrosophilacommunityJunha Shin, Sunmo Yang, Eiru Kim, Chan Yeong Kim, Hongseok Shim, Ara Cho, Hyojin Kim, Sohyun Hwang, Jung Eun Shim, Insuk Lee · 2015 · Nucleic Acids Research
- Synaptic activity: An emerging player in schizophreniaAnindita Sarkar, Maria Carolina Marchetto, Fred H. Gage · 2015 · Brain Research
- Advances in the genetics of schizophrenia: toward a network and pathway view for drug discoveryDavid Andrew Collier, Brian J. Eastwood, Karim Malki, Younes Mokrab · 2016 · Annals of the New York Academy of Sciences
- Enrichment of rare genetic variants in astrocyte gene enriched co-expression modules altered in postmortem brain samples of schizophreniaJavier González‐Peñas, Javier Costas, María José Ginzo Villamayor, Bin Xu · 2018 · Neurobiology of Disease
- Novel Compound Heterozygous DST Variants Causing Hereditary Sensory and Autonomic Neuropathies VI in Twins of a Chinese FamilyJie‐Yuan Jin, Panfeng Wu, Jiqiang He, Liang‐Liang Fan, Zhuang‐Zhuang Yuan, Xiao-Yang Pang, Juyu Tang, Liyang Zhang · 2020 · Frontiers in Genetics
- Investigation of Schizophrenia with Human Induced Pluripotent Stem CellsSamuel K. Powell, Callan P. O’Shea, Sara Rose Shannon, Schahram Akbarian, Kristen Brennand · 2020 · Advances in neurobiology