Catalina Sakai, Sundas Ijaz, Ellen J Hoffman. Front Mol Neurosci 2018
Times Cited: 36
Times Cited: 36
Times Cited
Times Co-cited
Similarity
The zebrafish reference genome sequence and its relationship to the human genome.
Kerstin Howe, Matthew D Clark, Carlos F Torroja, James Torrance, Camille Berthelot, Matthieu Muffato, John E Collins, Sean Humphray, Karen McLaren, Lucy Matthews,[...]. Nature 2013
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Whole-brain activity mapping onto a zebrafish brain atlas.
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Zebrafish models of autism spectrum disorder.
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Zebrafish as an emerging model for studying complex brain disorders.
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CRISPR/Cas9-induced shank3b mutant zebrafish display autism-like behaviors.
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Stages of embryonic development of the zebrafish.
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Pentylenetetrazole induced changes in zebrafish behavior, neural activity and c-fos expression.
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Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2.
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Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment.
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Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.
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Development of social behavior in young zebrafish.
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Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish.
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Disruptive CHD8 mutations define a subtype of autism early in development.
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Guidelines for morpholino use in zebrafish.
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Towards a comprehensive catalog of zebrafish behavior 1.0 and beyond.
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Efficient genome editing in zebrafish using a CRISPR-Cas system.
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Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system.
Li-En Jao, Susan R Wente, Wenbiao Chen. Proc Natl Acad Sci U S A 2013
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Large-Scale Phenotype-Based Antiepileptic Drug Screening in a Zebrafish Model of Dravet Syndrome
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Mecp2 regulates tnfa during zebrafish embryonic development and acute inflammation.
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Whole-brain functional imaging at cellular resolution using light-sheet microscopy.
Misha B Ahrens, Michael B Orger, Drew N Robson, Jennifer M Li, Philipp J Keller. Nat Methods 2013
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Animal models in epilepsy research: legacies and new directions.
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The Utility of Zebrafish as a Model for Screening Developmental Neurotoxicity.
Marta d'Amora, Silvia Giordani. Front Neurosci 2018
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Zebrafish knockout of Down syndrome gene, DYRK1A, shows social impairments relevant to autism.
Oc-Hee Kim, Hyun-Ju Cho, Enna Han, Ted Inpyo Hong, Krishan Ariyasiri, Jung-Hwa Choi, Kyu-Seok Hwang, Yun-Mi Jeong, Se-Yeol Yang, Kweon Yu,[...]. Mol Autism 2017
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Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish.
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Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency.
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Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions.
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Live imaging of neuronal degradation by microglia reveals a role for v0-ATPase a1 in phagosomal fusion in vivo.
Francesca Peri, Christiane Nüsslein-Volhard. Cell 2008
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De novo mutations in epileptic encephalopathies.
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Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism.
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Acute inflammation initiates the regenerative response in the adult zebrafish brain.
Nikos Kyritsis, Caghan Kizil, Sara Zocher, Volker Kroehne, Jan Kaslin, Dorian Freudenreich, Anne Iltzsche, Michael Brand. Science 2012
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The dorsal pallium in zebrafish, Danio rerio (Cyprinidae, Teleostei).
Thomas Mueller, Zhiqiang Dong, Michael A Berberoglu, Su Guo. Brain Res 2011
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Potential of zebrafish as a model for exploring the role of the amygdala in emotional memory and motivational behavior.
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Impaired constitutive and regenerative neurogenesis in adult hyperglycemic zebrafish.
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The developing utility of zebrafish models of neurological and neuropsychiatric disorders: A critical review.
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Zebrafish Behavior: Opportunities and Challenges.
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Transgenic tools to characterize neuronal properties of discrete populations of zebrafish neurons.
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CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
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De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.
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Developmental and behavioral alterations in zebrafish embryonically exposed to valproic acid (VPA): An aquatic model for autism.
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Judith S Eisen, James C Smith. Development 2008
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Embryonic exposure to valproic acid affects the histaminergic system and the social behaviour of adult zebrafish (Danio rerio).
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Function and regulation of AUTS2, a gene implicated in autism and human evolution.
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Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling.
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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
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A phylotypic stage in vertebrate brain development: GABA cell patterns in zebrafish compared with mouse.
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KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
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8
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.