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Times Cited: 158
Times Cited: 158
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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Genome-wide association study identifies 30 loci associated with bipolar disorder.
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A global reference for human genetic variation.
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
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Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
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Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia.
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Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
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Functional mapping and annotation of genetic associations with FUMA.
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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.
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Clinical use of current polygenic risk scores may exacerbate health disparities.
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Gene expression elucidates functional impact of polygenic risk for schizophrenia.
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An atlas of genetic correlations across human diseases and traits.
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15
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
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15
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
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14
Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
14
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Identification of common genetic risk variants for autism spectrum disorder.
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14
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
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Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
14
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
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13
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.
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Partitioning heritability by functional annotation using genome-wide association summary statistics.
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12
Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis.
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11
Schizophrenia risk from complex variation of complement component 4.
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Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders.
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10
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
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Genetic effects on gene expression across human tissues.
Alexis Battle, Christopher D Brown, Barbara E Engelhardt, Stephen B Montgomery. Nature 2017
Alexis Battle, Christopher D Brown, Barbara E Engelhardt, Stephen B Montgomery. Nature 2017
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10
Integrative analysis of 111 reference human epigenomes.
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Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register.
Rikke Hilker, Dorte Helenius, Birgitte Fagerlund, Axel Skytthe, Kaare Christensen, Thomas M Werge, Merete Nordentoft, Birte Glenthøj. Biol Psychiatry 2018
Rikke Hilker, Dorte Helenius, Birgitte Fagerlund, Axel Skytthe, Kaare Christensen, Thomas M Werge, Merete Nordentoft, Birte Glenthøj. Biol Psychiatry 2018
9
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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9
Multi-trait analysis of genome-wide association summary statistics using MTAG.
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9
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
Masashi Ikeda, Atsushi Takahashi, Yoichiro Kamatani, Yukihide Momozawa, Takeo Saito, Kenji Kondo, Ayu Shimasaki, Kohei Kawase, Takaya Sakusabe, Yoshimi Iwayama,[...]. Schizophr Bull 2019
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Second-generation PLINK: rising to the challenge of larger and richer datasets.
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Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
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De novo mutations in schizophrenia implicate synaptic networks.
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Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
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Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets.
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Genetic analyses of diverse populations improves discovery for complex traits.
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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
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9
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.