Michael J Gandal, Pan Zhang, Evi Hadjimichael, Rebecca L Walker, Chao Chen, Shuang Liu, Hyejung Won, Harm van Bakel, Merina Varghese, Yongjun Wang, Annie W Shieh, Jillian Haney, Sepideh Parhami, Judson Belmont, Minsoo Kim, Patricia Moran Losada, Zenab Khan, Justyna Mleczko, Yan Xia, Rujia Dai, Daifeng Wang, Yucheng T Yang, Min Xu, Kenneth Fish, Patrick R Hof, Jonathan Warrell, Dominic Fitzgerald, Kevin White, Andrew E Jaffe, Mette A Peters, Mark Gerstein, Chunyu Liu, Lilia M Iakoucheva, Dalila Pinto, Daniel H Geschwind. Science 2018
Times Cited: 311
Times Cited: 311
Times Cited
Times Co-cited
Similarity
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
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Gene expression elucidates functional impact of polygenic risk for schizophrenia.
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Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis.
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Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
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Comprehensive functional genomic resource and integrative model for the human brain.
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Schizophrenia risk from complex variation of complement component 4.
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Spatio-temporal transcriptome of the human brain.
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
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Integrative approaches for large-scale transcriptome-wide association studies.
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Genome-wide association study identifies 30 loci associated with bipolar disorder.
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Integrative functional genomic analysis of human brain development and neuropsychiatric risks.
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Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism.
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Genetic identification of brain cell types underlying schizophrenia.
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A global reference for human genetic variation.
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Genetic effects on gene expression across human tissues.
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Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
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Analysis of shared heritability in common disorders of the brain.
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Regional Heterogeneity in Gene Expression, Regulation, and Coherence in the Frontal Cortex and Hippocampus across Development and Schizophrenia.
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
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Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets.
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limma powers differential expression analyses for RNA-sequencing and microarray studies.
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Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.
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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
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Conserved cell types with divergent features in human versus mouse cortex.
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FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
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STAR: ultrafast universal RNA-seq aligner.
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Single-cell genomics identifies cell type-specific molecular changes in autism.
Dmitry Velmeshev, Lucas Schirmer, Diane Jung, Maximilian Haeussler, Yonatan Perez, Simone Mayer, Aparna Bhaduri, Nitasha Goyal, David H Rowitch, Arnold R Kriegstein. Science 2019
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Single-cell transcriptomic analysis of Alzheimer's disease.
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Comparative genetic architectures of schizophrenia in East Asian and European populations.
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De novo mutations in schizophrenia implicate synaptic networks.
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Post-mortem molecular profiling of three psychiatric disorders.
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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
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Massively parallel single-nucleus RNA-seq with DroNc-seq.
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A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.
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Functional mapping and annotation of genetic associations with FUMA.
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
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Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
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Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
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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.