De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia
Xu, Bin, Ionita-Laza, Iuliana, Roos, J Louw, Boone, Braden, Woodrick, Scarlet, Sun, Yan, Levy, Shawn, Gogos, Joseph A +1 more·2012·Nature Genetics
DOI 10.1038/ng.2446
Cited by (442)
Items 201–300 of 442
- Potentially repurposable drugs for schizophrenia identified from its interactomeKalyani Bindu Karunakaran, Srilakshmi Chaparala, Madhavi K. Ganapathiraju · 2019 · Scientific Reports
- Effects of Schizophrenia Risk Variation in the NRG1 Gene on NRG1-IV Splicing During Fetal and Early Postnatal Human Neocortical DevelopmentClare Paterson, Yanhong Wang, Joel E. Kleinman, Amanda J. Law · 2014 · American Journal of Psychiatry
- Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon Girard, Sylvia Dobrzeniecka, Amirthagowri Ambalavanan, Marie‐Odile Krebs, Ridha Joober, Julie Gauthier, Patrick A. Dion, Guy Armand Rouleau · 2013 · Behavioral and Brain Functions
- Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patientsMo Li, Lu Shen, Luan Chen, Cong Huai, Hailiang Huang, Xi Wu, Chao Yang, Jingsong Ma, Wei Zhou, Huihui Du et al. · 2020 · Translational Psychiatry
- Using human brain imaging studies as a guide toward animal models of schizophreniaScott S. Bolkan, Fernanda Carvalho Poyraz, Christoph Kellendonk · 2015 · Neuroscience
- Caveolin-1 regulation ofdisrupted-in-schizophrenia-1 as a potential therapeutic target for schizophreniaAdam Kassan, Junji Egawa, Zheng Zhang, Angels Almenar‐Queralt, Quynh My Nguyen, Yasaman Lajevardi, Kaitlyn Kim, Edmund Posadas, Dilip V. Jeste, David M. Roth et al. · 2016 · Journal of Neurophysiology
- Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa M. Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Deepro Banerjee, Laura Rohan, Emily Huber, Laïla El Khattabi, Paolo Prontera et al. · 2023 · The American Journal of Human Genetics
- Exome analysis of Smith–Magenis-like syndrome cohort identifies de novo likely pathogenic variantsNISC Comparative Sequencing Program, Seth Berger, Carla Ciccone, Karen Lyn Simon, May Christine V. Malicdan, Thierry Vilboux, Charles John Billington, Roxanne E. Fischer, Wendy J. Introne, Andrea Lynne Gropman et al. · 2017 · Human Genetics
- The Candidate Schizophrenia Risk Gene DGCR2 Regulates Early Steps of CorticogenesisAude Molinard‐Chenu, Alexandre G. Dayer · 2017 · Biological Psychiatry
- Exome Sequencing Identifies TENM4 as a Novel Candidate Gene for Schizophrenia in the SCZD2 Locus at 11q14-21Chao-Biao Xue, Zhou-Heng Xu, Jun Zhu, Yu Wu, Xi-Hang Zhuang, Qu-liang Chen, Cairu Wu, Hu Jintao, Hou-Shi Zhou, Wei-Hang Xie et al. · 2019 · Frontiers in Genetics
- Transcriptome Analysis of Post-Mortem Brain Tissue Reveals Up-Regulation of the Complement Cascade in a Subgroup of Schizophrenia PatientsEva Lindholm Carlström, Adnan Niazi, Mitra Etemadikhah, Jonatan Halvardson, Stefan Enroth, Craig A. Stockmeier, Grażyna Rajkowska, Bo Nilsson, Lars Feuk · 2021 · Genes
- Differentiation of human pluripotent stem cells into Medial Ganglionic Eminence vs. Caudal Ganglionic Eminence cellsSandra Ahn, Taegon Kim, Kwang‐Soo Kim, Sangmi Chung · 2015 · Methods
- Whole exome sequencing is necessary to clarify ID/DD cases with de novo copy number variants of uncertain significance: Two proof‐of‐concept examplesElisa Giorgio, Andrea Ciolfi, Elisa Biamino, Viviana Caputo, Eleonora Di Gregorio, Elga Fabia Belligni, Alessandro Calcia, Elena Gaidolfi, Alessandro Bruselles, Cecilia Mancini et al. · 2016 · American Journal of Medical Genetics Part A
- Genetics implicate common mechanisms in autism and schizophrenia: synaptic activity and immunityXiaoming Liu, Zhengwei Li, Conghai Fan, Dongli Zhang, Jiao Chen · 2017 · Journal of Medical Genetics
- Genetic association of FMRP targets with psychiatric disordersNicholas E. Clifton, Elliott Rees, Peter Holmans, Antonio F. Pardiñas, Janet C Harwood, Arianna Di Florio, George Kirov, James Walters, Michael C. O’Donovan, Michael John Owen et al. · 2020 · Molecular Psychiatry
- A dual-activity topoisomerase complex regulates mRNA translation and turnoverShuaikun Su, Yutong Xue, Alexei A. Sharov, Yongqing Zhang, Seung Kyu Lee, Jennifer L. Martindale, Wen Li, Wai Lim Ku, Keji Zhao, Supriyo De et al. · 2022 · Nucleic Acids Research
- The Role of Metabotropic Glutamate Receptor Genes in SchizophreniaCarlo Maj, Alessandra Minelli, Edoardo Giacopuzzi, Emilio Sacchetti, Massimo Gennarelli · 2015 · Current Neuropharmacology
- Neurogenetic analysis of childhood disintegrative disorderAbha R. Gupta, Alexander Westphal, Daniel Y.‐J. Yang, Catherine A.W. Sullivan, Jeffrey A. Eilbott, Samir Zaidi, Avery C. Voos, Brent C. Vander Wyk, Pam Ventola, Zainulabedin Waqar et al. · 2017 · Molecular Autism
- Revisiting Schizophrenia from an Evolutionary Perspective: An Association Study of Recent Evolutionary Markers and SchizophreniaUpasana Bhattacharyya, Smita Neelkanth Deshpande, Triptish Bhatia A, Bittianda Kuttapa Thelma · 2020 · Schizophrenia Bulletin
- Conservation of the coding regions of the glycine N-acyltransferase gene further suggests that glycine conjugation is an essential detoxification pathwayRencia van der Sluis, Christoffel P. S. Badenhorst, Elardus Erasmus, Etresia van Dyk, Francois Hendrikus van der Westhuizen, Alberdina Aike van Dijk · 2015 · Gene
- Novel treatment strategies for schizophrenia from improved understanding of genetic riskBillah Morris, Judith A. Pratt · 2014 · Clinical Genetics
- An interaction network of mental disorder proteins in neural stem cellsMaaike J. Moen, Hieab H.H. Adams, Johannes H. Brandsma, Dick H. W. Dekkers, Umut Akinci, Sofia Karkampouna, Martí Quevedo, Christel E. M. Kockx, Zeliha Özgür, Wilfred F. J. van IJcken et al. · 2017 · Translational Psychiatry
- Modeling schizophrenia pathogenesis using patient-derived induced pluripotent stem cells (iPSCs)Haneul Noh, Zhicheng Shao, Joseph T. Coyle, Sangmi Chung · 2017 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Transcriptome analysis of fibroblasts from schizophrenia patients reveals differential expression of schizophrenia-related genesMitra Etemadikhah, Adnan Niazi, Lennart Wetterberg, Lars Feuk · 2020 · Scientific Reports
- System-based proteomic and metabonomic analysis of the Df(16)A+/− mouse identifies potential miR-185 targets and molecular pathway alterationsH Wesseling, Bin Xu, Elizabeth J. Want, Elaine C. Holmes, Paul C. Guest, Maria Karayiorgou, Joseph A. Gogos, Sabine Bahn · 2016 · Molecular Psychiatry
- Gene expression profiling of the dorsolateral and medial orbitofrontal cortex in schizophreniaMihovil Mladinov, Goran Sedmak, Heidi R. Fuller, Mirjana Babić Leko, Davor Mayer, Jason Kirincich, Andrija Štajduhar, Fran Borovečki, Patrick R. Hof, Goran Šimić · 2016 · Translational Neuroscience
- Identification of somatic mutations in monozygotic twins discordant for psychiatric disordersMasaki Nishioka, Miki Bundo, Junko Ueda, Akane Yoshikawa, Fumichika Nishimura, Tsukasa Sasaki, Chihiro Kakiuchi, Kiyoto Kasai, Tadafumi Kato, Kazuya Iwamoto · 2018 · Schizophrenia
- A Disc1 mutation differentially affects neurites and spines in hippocampal and cortical neuronsAude-Marie Lepagnol-Bestel, Mirna Kvajo, Maria Karayiorgou, Michel Simonneau, Joseph A. Gogos · 2013 · Molecular and Cellular Neuroscience
- Bioinformatics and genomic databasesJason Chen, Giovanni Coppola · 2018 · Handbook of clinical neurology
- Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophreniaJiewei Liu, Shiwu Li, Xiaoyan Li, Wenqiang Li, Yongfeng Yang, Suqin Guo, Luxian Lv, Xiao Xiao, Yong‐Gang Yao, Fanglin Guan et al. · 2021 · BMC Medicine
- Embryonic and larval exposure to propylparaben induces developmental and long-term neurotoxicity in zebrafish modelCarmine Merola, Giulia Caioni, Cristiano Bertolucci, Tyrone Lucon‐Xiccato, Beste Başak Savaşçı, Sabrina Tait, Marialuisa Casella, Serena Camerini, Elisabetta Benedetti, Monia Perugini · 2023 · The Science of The Total Environment
- Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf MatingQing Jie, Denise Lu Shun Yan, Yuan Zhou, Qiong Liu, Weijing Wu, Zian Xiao, Yuyuan Liu, Jia Liu, Lilin Du, Dinghua Xie et al. · 2014 · PLoS ONE
- Genome-wide burden of deleterious coding variants increased in schizophreniaLoes M. Olde Loohuis, Jacob A. S. Vorstman, Anil P. S. Ori, Kim A. Staats, Tina Wang, Alexander L. Richards, Ganna Leonenko, James Walters, Joseph A. DeYoung, René S. Kahn et al. · 2015 · Nature Communications
- Estimating contribution of rare non‐coding variants to neuropsychiatric disordersAtsushi Takata · 2018 · Psychiatry and Clinical Neurosciences
- De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activityAkira Nishi, Shusuke Numata, Atsushi Tajima, Xiaolei Zhu, Koki Ito, Atsushi Saito, Yusuke Kato, Makoto Kinoshita, Shinji Shimodera, Shinji Ono et al. · 2017 · Scientific Reports
- Genome sequencing broadens the range of contributing variants with clinical implications in schizophreniaBahareh A. Mojarad, Yue Yin, Roozbeh Manshaei, Ian Backstrom, Gregory Costain, Tracy Heung, Daniele Merico, Christian R. Marshall, Anne S. Bassett, Ryan K. C. Yuen · 2021 · Translational Psychiatry
- iPhemap: an atlas of phenotype to genotype relationships of human iPSC models of neurological diseasesEthan W. Hollingsworth, Jacob Vaughn, Joshua C. Orack, Chelsea Skinner, Jamil Khouri, Sofia B. Lizarraga, Mark E. Hester, Fumihiro Watanabe, Kenneth S. Kosik, Jaime Imitola · 2017 · EMBO Molecular Medicine
- Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar DisorderCecilia Salvoro, Stefania Bortoluzzi, Alessandro Coppe, Giorgio Valle, Erika Feltrin, Maria Luisa Mostacciuolo, Giovanni Vazza · 2018 · Molecular Neurobiology
- The Effect of Paternal Age on Offspring Intelligence and Personality when Controlling for Parental Trait LevelsRuben C. Arslan, Lars Penke, Wendy Johnson, William G. Iacono, Matt K. McGue · 2014 · PLoS ONE
- A method to delineate de novo missense variants across pathways prioritizes genes linked to autismAmanda M. Koire, Christie Buchovecky, Panagiotis Katsonis, Young Won Kim, Stephen Joseph Wilson, Olivier Lichtarge · 2021 · Science Translational Medicine
- Unlocking the Treasure Trove: From Genes to Schizophrenia BiologyS. E. McCarthy, William Richard McCombie, Aiden Peter Corvin · 2014 · Schizophrenia Bulletin
- Targeted sequencing and integrative analysis of 3,195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genesTao Wang, Yi Zhang, Liqui Liu, Yan Wang, Huiqian Chen, Tianda Fan, Jinchen Li, Kun Xia, Zhong Sheng Sun · 2021 · Journal of genetics and genomics/Journal of Genetics and Genomics
- Tdrd3-null mice show post-transcriptional and behavioral impairments associated with neurogenesis and synaptic plasticityXingliang Zhu, Yuyoung Joo, Simone Bossi, Ross A. McDevitt, Ao‐Ji Xie, Yue Wang, Yutong Xue, Shuaikun Su, Seung Kyu Lee, Nirnath Sah et al. · 2023 · Progress in Neurobiology
- Mutation Burden of Rare Variants in Schizophrenia Candidate GenesSimon Girard, Patrick A. Dion, Cynthia V. Bourassa, Steve Geoffroy, Pamela Lachance‐Touchette, Amina Barhdadi, Mathieu Langlois, Ridha Joober, Marie‐Odile Krebs, Marie‐Pierre Dubé et al. · 2015 · PLoS ONE
- No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association datasetElizabeth A. Heron, Paul Cormican, Gary J Donohoe, F. Anthony O’Neill, Kenneth S. Kendler, Brien P. Riley, Michael Gill, Aiden Peter Corvin, Derek W. Morris · 2014 · Schizophrenia Research
- 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
- Nipped‐A regulates the Drosophila circadian clock via histone deubiquitinationBei Bu, Lixia Chen, Liubin Zheng, Weiwei He, Luoying Zhang · 2019 · The EMBO Journal
- Roles of Topoisomerases in Heterochromatin, Aging, and DiseasesSeung Kyu Lee, Weidong Wang · 2019 · Genes
- Role of carotenoids and retinoids during heart developmentIoan Ovidiu Sîrbu, Aimée Rodica Chiş, Alexander R. Moise · 2020 · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
- Deletion of Rapgef6, a candidate schizophrenia susceptibility gene, disrupts amygdala function in miceRebecca J. Levy, Mirna Kvajo, Yan Li, Evgeny Tsvetkov, Weifan Dong, Yoko Yoshikawa, Tohru Kataoka, Vadim Y. Bolshakov, Maria Karayiorgou, Joseph A. Gogos · 2015 · Translational Psychiatry
- Patterns of Variation Influencing Antipsychotic Treatment Outcomes in South African First-Episode Schizophrenia PatientsBritt I. Drögemöller, Dana J.H. Niehaus, Bonginkosi Chiliza, Lize van der Merwe, Laila Asmal, Anil K. Malhotra, Galen E.B. Wright, Robin Alexander Emsley, Louise Warnich · 2014 · Pharmacogenomics
- A literature search tool for intelligent extraction of disease-associated genesJae-Yoon Jung, Todd F. DeLuca, Tristan H. Nelson, Dennis Paul Wall · 2013 · Journal of the American Medical Informatics Association
- Molecular hypotheses to explain the shared pathways and underlying pathobiological causes in catatonia and in catatonic presentations in neuropsychiatric disordersE.M. Peter-Ross⁎ · 2018 · Medical Hypotheses
- Ethical issues in the use of genetic testing of patients with schizophrenia and their familiesLynn E. DeLisi · 2014 · Current Opinion in Psychiatry
- Advancing paternal age at birth is associated with poorer social functioning earlier and later in life of schizophrenia patients in a founder populationRudolf Liebenberg, Brigitte van Heerden, René Ehlers, Anna M.E. Du Plessis, Johannes Lodewikus Roos · 2016 · Psychiatry Research
- Resequencing and association analysis of MIR137 with schizophrenia in a J apanese populationJun Egawa, Ayako Nunokawa, Masako Shibuya, Yuichiro Watanabe, Naoshi Kaneko, Hirofumi Igeta, Toshiyuki Someya · 2013 · Psychiatry and Clinical Neurosciences
- 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
- Phenotypic features of patients with schizophrenia carrying de novo gene mutations: A pilot studyP.J. Malherbe, Johannes Lodewikus Roos, René Ehlers, Maria Karayiorgou, Johannes Lodewikus Roos · 2014 · Psychiatry Research
- Behavior genetics: Past, present, futureSara R. Jaffee, Thomas S. Price, Teresa M. Reyes · 2013 · Development and Psychopathology
- 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
- Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-functionNicholas E. Clifton, Matthew L. Bosworth, Niels Haan, Elliott Rees, Peter Holmans, Lawrence S. Wilkinson, Anthony R Isles, Mark O. Collins, Jérémy Hall · 2022 · Human Molecular Genetics
- Array-CGH in children with mild intellectual disability: a population-based studyCharles Coutton, Klaus D. Dieterich, Véronique Satre, Gaëlle Vieville, Florence Amblard, Marie David, Christine Cans, Pierre‐Simon Jouk, Françoise Devillard · 2014 · European Journal of Pediatrics
- Co-activator candidate interactions for orphan nuclear receptor NR2E1Ximena Corso‐Díaz, Charles N. de Leeuw, Vivian Alonso, Diana Melchers, Bibiana K. Y. Wong, René Houtman, Elizabeth M. Simpson · 2016 · BMC Genomics
- The abiding relevance of mouse models of rare mutations to psychiatric neuroscience and therapeuticsJoseph A. Gogos, Gregg W. Crabtree, Anastasia Diamantopoulou · 2019 · Schizophrenia Research
- Human Genetics and Clinical Aspects of Neurodevelopmental DisordersGholson J. Lyon, Jason O'Rawe · 2015 · Wiley eBooks
- Schizophrenia at a Genetics Crossroads: Where to Now?Aiden Peter Corvin · 2013 · Schizophrenia Bulletin
- Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort AnalysisJibin John, Aditya Kumar Sharma, Prachi Kukshal, Triptish Bhatia A, Vishwajit Laxmikant Nimgaonkar, Smita Neelkanth Deshpande, Bittianda Kuttapa Thelma · 2017 · Schizophrenia Bulletin
- Novel brain expressed RNA identified at the MIR137 schizophrenia-associated locusOlympia Gianfrancesco, Alix Warburton, David Andrew Collier, Vivien J. Bubb, John Peter Quinn · 2016 · Schizophrenia Research
- Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elementsG. Piluso, P. Monteleone, S. Galderisi, Teresa Giugliano, A. Bertolino, P. Rocca, A. Rossi, A. Mucci, E. Aguglia, I. Andriola et al. · 2019 · World Journal of Biological Psychiatry
- 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
- 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
- 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
- Novel rare variants in F-box protein 45 (FBXO45) in schizophreniaChenyao Wang, Takayoshi Koide, Hiroki Kimura, Shohko Kunimoto, Akira Yoshimi, Yukako Nakamura, Itaru Kushima, Masahiro Banno, Naoko Kawano, Yuto Takasaki et al. · 2014 · Schizophrenia Research
- Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspectiveJia Nee Foo, Jianjun Liu, Eng‐King Tan · 2013 · Human Genetics
- Phelan‐McDermid syndrome data network: Integrating patient reported outcomes with clinical notes and curated genetic reportsCartik R. Kothari, Maxime Wack, Claire Hassen‐Khodja, Sean Finan, Guergana Savova, Megan O'Boyle, Geraldine Bliss, Andria Cornell, Elizabeth J. Horn, Rebecca Davis et al. · 2017 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Whole-Genome Sequencing in PharmacogeneticsThomas Jacob Urban · 2013 · Pharmacogenomics
- cnvCapSeq: detecting copy number variation in long-range targeted resequencing dataEvangelos Bellos, Vikrant Kumar, Clarabelle Bitong Lin, Jordi Maggi, Zai Yang Phua, Ching‐Yu Cheng, Chui Ming Gemmy Cheung, Martin Lloyd Hibberd, Tien Yin Wong, Lachlan Coin et al. · 2014 · Nucleic Acids Research
- Impact of schizophrenia GWAS loci converge onto distinct pathways in cortical interneurons vs glutamatergic neurons during developmentDongxin Liu, Amy L. Zinski, Akanksha Mishra, Haneul Noh, Gun-Hoo Park, Yiren Qin, Oshoname Olorife, James M. Park, Chiderah P. Abani, Joy S. Park et al. · 2022 · Molecular Psychiatry
- De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case reportChrystal F. Mavros, Catherine A. Brownstein, Roshni Thyagrajan, Casie A. Genetti, Sahil K. Tembulkar, Kelsey M. Graber, Quinn Murphy, Kristin Cabral, Grace E. VanNoy, Matthew Neil Bainbridge et al. · 2018 · BMC Medical Genetics
- Two Genetic Mechanisms in Two Siblings with Intellectual Disability, Autism Spectrum Disorder, and PsychosisYu‐Shu Huang, Ting-Hsuan Fang, Belle Kung, Chia‐Hsiang Chen · 2022 · Journal of Personalized Medicine
- Microendophenotypes of Psychiatric Disorders: Phenotypes of Psychiatric Disorders at the Level of Molecular Dynamics, Synapses, Neurons, and Neural CircuitsSatoshi Kida, Tadafumi Kato · 2015 · Current Molecular Medicine
- Introduction to Epigenetics in PsychiatryRichard S. Lee, Dimitrios Avramopoulos · 2014 · Elsevier eBooks
- Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based studyJibin John, Prachi Kukshal, Aditya Kumar Sharma, Triptish Bhatia A, Vishwajit Laxmikant Nimgaonkar, S.N. Deshpande, Bittianda Kuttapa Thelma · 2018 · Schizophrenia Research
- Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 GenesJosep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Víctor J. Asensio, Bernat Ortega-Vila, Diego M. Marzese, Carme Vidal, Carmen Santos et al. · 2021 · Frontiers in Genetics
- Dysmaturational Longitudinal Epigenetic Aging During Transition to PsychosisAnton Iftimovici, Oussama Kébir, Chuan Jiao, Qin He, Marie‐Odile Krebs, Boris Chaumette · 2022 · Schizophrenia Bulletin Open
- Fitness Consequences of Advanced Ancestral Age over Three Generations in HumansAdam D. Hayward, Virpi Lummaa, Georgii A. Bazykin · 2015 · PLoS ONE
- The importance of de novo mutations for pediatric neurological disease—It is not all in utero or birth traumaRobert P. Erickson · 2016 · Mutation Research/Reviews in Mutation Research
- Derivation, Expansion, Cryopreservation and Characterization of Brain Microvascular Endothelial Cells from Human Induced Pluripotent Stem CellsSovannarath Pong, Paulo L. Lizano, Rakesh Karmacharya · 2020 · Journal of Visualized Experiments
- Overlapping Etiology of Neurodevelopmental DisordersEric Kelleher, Aiden Peter Corvin · 2015 · Wiley eBooks
- Paternal-age-related de novo mutations and risk for five disordersJacob L. Taylor, Jean-Christophe Debost, Sarah U. Morton, Emilie M. Wigdor, Henrike Heyne, Dennis Lal, Daniel P. Howrigan, Alex Bloemendal, Janne Tidselbak Larsen, Jack A. Kosmicki et al. · 2017 · bioRxiv (Cold Spring Harbor Laboratory)
- Impairment of translation in neurons as a putative causative factor for autismEugenia Poliakov, Eugene V. Koonin, Igor B. Rogozin · 2014 · Biology Direct
- Van laboratoriumbank tot siekbed: Genetiese bevindings in skisofrenieJohannes Lodewikus Roos · 2017 · Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie
- Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari CohortAfif Ben‐Mahmoud, Vijay R. Gupta, Alice K. Abdel Aleem, Ian Richard Thompson, Abdi Aden, Hamdi Mbarek, Chadi Saad, Mohamed Tolefat, Fouad A. W. Alshaban, Lawrence Walter Stanton et al. · 2024 · International Journal of Molecular Sciences
- Filamin A interacting protein plays a role in proper positioning of callosal projection neurons in the cortexHideshi Yagi, Yuichiro Oka, Munekazu Komada, Min-Jue Xie, Koichi Noguchi, Makoto Sato · 2015 · Neuroscience Letters
- Topoisomerase IIIβ Deficiency Induces Neuro-Behavioral Changes and Brain Connectivity Alterations in MiceFaiz Ur Rahman, You-Rim Kim, Eun-Kyeung Kim, Hae-rim Kim, Sang-Mi Cho, Chin-Soo Lee, Su Jin Kim, Kimi Araki, Ken‐ichi Yamamura, Mi-Ni Lee et al. · 2021 · International Journal of Molecular Sciences
- Genes positively regulated by Mef2c in cortical neurons are enriched for common genetic variation associated with IQ and educational attainmentLaura Fahey, Deema Ali, Gary J Donohoe, Pilib Ó Broin, Derek W. Morris · 2023 · Human Molecular Genetics
- SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new casesMark Ainsley Colijn, Prescilla B. Carrion, Guillaume Poirier‐Morency, Sanja Rogić, Ivan J. Torres, Mahesh Menon, Michelle Lisonek, Courtney B. Cook, Ashley DeGraaf, Subramanya Ponnachana Thammaiah et al. · 2023 · Progress in Neuro-Psychopharmacology and Biological Psychiatry
- GWAS, Cytomegalovirus Infection, and SchizophreniaJakob Grove, Anders Dupont Børglum, Brad D. Pearce · 2014 · Current Behavioral Neuroscience Reports
- Association of oligodendrocytes differentiation regulator geneDUSP15with autismYe Tian, Lifang Wang, Meixiang Jia, Tianlan Lu, Yanyan Ruan, Zhiliu Wu, Linyan Wang, Jing Liu, Dai Zhang · 2016 · The World Journal of Biological Psychiatry
- Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese populationYuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, Masashi Ikeda, Akitoyo Hishimoto, Kenji Kondo, Jun Egawa, Naoshi Kaneko, Tatsuyuki Muratake, Takeo Saito et al. · 2015 · Psychiatry Research