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Times Cited: 511
Times Cited: 511
Times Cited
Times Co-cited
Similarity
De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
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A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
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Analysis of copy number variations at 15 schizophrenia-associated loci.
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Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
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Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia.
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Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
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Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
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Gene expression elucidates functional impact of polygenic risk for schizophrenia.
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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
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Analysis of protein-coding genetic variation in 60,706 humans.
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Synaptic, transcriptional and chromatin genes disrupted in autism.
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Schizophrenia risk from complex variation of complement component 4.
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FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
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De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.
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Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies.
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CNVs: harbingers of a rare variant revolution in psychiatric genetics.
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Copy number variation in schizophrenia in Sweden.
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The penetrance of copy number variations for schizophrenia and developmental delay.
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Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways.
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Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
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Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
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Common alleles contribute to schizophrenia in CNV carriers.
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Microduplications of 16p11.2 are associated with schizophrenia.
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Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity.
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Large recurrent microdeletions associated with schizophrenia.
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De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
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Common variants conferring risk of schizophrenia.
Hreinn Stefansson, Roel A Ophoff, Stacy Steinberg, Ole A Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli P H Pietiläinen, Ole Mors, Preben B Mortensen,[...]. Nature 2009
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Finding the missing heritability of complex diseases.
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Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.
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Genetic identification of brain cell types underlying schizophrenia.
Nathan G Skene, Julien Bryois, Trygve E Bakken, Gerome Breen, James J Crowley, Héléna A Gaspar, Paola Giusti-Rodriguez, Rebecca D Hodge, Jeremy A Miller, Ana B Muñoz-Manchado,[...]. Nat Genet 2018
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
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Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
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High frequencies of de novo CNVs in bipolar disorder and schizophrenia.
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Microdeletions of 3q29 confer high risk for schizophrenia.
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Increased exonic de novo mutation rate in individuals with schizophrenia.
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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Alexander Gusev, Nicholas Mancuso, Hyejung Won, Maria Kousi, Hilary K Finucane, Yakir Reshef, Lingyun Song, Alexias Safi, Steven McCarroll, Benjamin M Neale,[...]. Nat Genet 2018
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A framework for the interpretation of de novo mutation in human disease.
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Characterization of the proteome, diseases and evolution of the human postsynaptic density.
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7
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.