Nana Matoba, Michael I Love, Jason L Stein. Hum Brain Mapp 2022
Times Cited: 9
Times Cited: 9
Times Cited
Times Co-cited
Similarity
The genetic architecture of the human cerebral cortex.
Katrina L Grasby, Neda Jahanshad, Jodie N Painter, Lucía Colodro-Conde, Janita Bralten, Derrek P Hibar, Penelope A Lind, Fabrizio Pizzagalli, Christopher R K Ching, Mary Agnes B McMahon,[...]. Science 2020
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Genome-wide association studies of brain imaging phenotypes in UK Biobank.
Lloyd T Elliott, Kevin Sharp, Fidel Alfaro-Almagro, Sinan Shi, Karla L Miller, Gwenaëlle Douaud, Jonathan Marchini, Stephen M Smith. Nature 2018
Lloyd T Elliott, Kevin Sharp, Fidel Alfaro-Almagro, Sinan Shi, Karla L Miller, Gwenaëlle Douaud, Jonathan Marchini, Stephen M Smith. Nature 2018
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
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Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
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The UK Biobank resource with deep phenotyping and genomic data.
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Clinical use of current polygenic risk scores may exacerbate health disparities.
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Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
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Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
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Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
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Functional mapping and annotation of genetic associations with FUMA.
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Kyoko Watanabe, Erdogan Taskesen, Arjen van Bochoven, Danielle Posthuma. Nat Commun 2017
33
Partitioning heritability by functional annotation using genome-wide association summary statistics.
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Hilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Farh,[...]. Nat Genet 2015
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MAGMA: generalized gene-set analysis of GWAS data.
Christiaan A de Leeuw, Joris M Mooij, Tom Heskes, Danielle Posthuma. PLoS Comput Biol 2015
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GCTA: a tool for genome-wide complex trait analysis.
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UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
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Image processing and Quality Control for the first 10,000 brain imaging datasets from UK Biobank.
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Fidel Alfaro-Almagro, Mark Jenkinson, Neal K Bangerter, Jesper L R Andersson, Ludovica Griffanti, Gwenaëlle Douaud, Stamatios N Sotiropoulos, Saad Jbabdi, Moises Hernandez-Fernandez, Emmanuel Vallee,[...]. Neuroimage 2018
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Richard Karlsson Linnér, Pietro Biroli, Edward Kong, S Fleur W Meddens, Robbee Wedow, Mark Alan Fontana, Maël Lebreton, Stephen P Tino, Abdel Abdellaoui, Anke R Hammerschlag,[...]. Nat Genet 2019
Richard Karlsson Linnér, Pietro Biroli, Edward Kong, S Fleur W Meddens, Robbee Wedow, Mark Alan Fontana, Maël Lebreton, Stephen P Tino, Abdel Abdellaoui, Anke R Hammerschlag,[...]. Nat Genet 2019
22
Genetic architecture of subcortical brain structures in 38,851 individuals.
Claudia L Satizabal, Hieab H H Adams, Derrek P Hibar, Charles C White, Maria J Knol, Jason L Stein, Markus Scholz, Muralidharan Sargurupremraj, Neda Jahanshad, Gennady V Roshchupkin,[...]. Nat Genet 2019
Claudia L Satizabal, Hieab H H Adams, Derrek P Hibar, Charles C White, Maria J Knol, Jason L Stein, Markus Scholz, Muralidharan Sargurupremraj, Neda Jahanshad, Gennady V Roshchupkin,[...]. Nat Genet 2019
22
Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model.
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Dominic Holland, Oleksandr Frei, Rahul Desikan, Chun-Chieh Fan, Alexey A Shadrin, Olav B Smeland, V S Sundar, Paul Thompson, Ole A Andreassen, Anders M Dale. PLoS Genet 2020
22
A global reference for human genetic variation.
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22
Integrating common and rare genetic variation in diverse human populations.
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22
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Mengzhen Liu, Yu Jiang, Robbee Wedow, Yue Li, David M Brazel, Fang Chen, Gargi Datta, Jose Davila-Velderrain, Daniel McGuire, Chao Tian,[...]. Nat Genet 2019
Mengzhen Liu, Yu Jiang, Robbee Wedow, Yue Li, David M Brazel, Fang Chen, Gargi Datta, Jose Davila-Velderrain, Daniel McGuire, Chao Tian,[...]. Nat Genet 2019
22
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
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22
Identification of common variants associated with human hippocampal and intracranial volumes.
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22
Common genetic variants influence human subcortical brain structures.
Derrek P Hibar, Jason L Stein, Miguel E Renteria, Alejandro Arias-Vasquez, Sylvane Desrivières, Neda Jahanshad, Roberto Toro, Katharina Wittfeld, Lucija Abramovic, Micael Andersson,[...]. Nature 2015
Derrek P Hibar, Jason L Stein, Miguel E Renteria, Alejandro Arias-Vasquez, Sylvane Desrivières, Neda Jahanshad, Roberto Toro, Katharina Wittfeld, Lucija Abramovic, Micael Andersson,[...]. Nature 2015
22
Mapping causal pathways from genetics to neuropsychiatric disorders using genome-wide imaging genetics: Current status and future directions.
Brandon D Le, Jason L Stein. Psychiatry Clin Neurosci 2019
Brandon D Le, Jason L Stein. Psychiatry Clin Neurosci 2019
22
Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits.
Yan Zhang, Guanghao Qi, Ju-Hyun Park, Nilanjan Chatterjee. Nat Genet 2018
Yan Zhang, Guanghao Qi, Ju-Hyun Park, Nilanjan Chatterjee. Nat Genet 2018
22
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
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
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
22
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
Bjarni J Vilhjálmsson, Jian Yang, Hilary K Finucane, Alexander Gusev, Sara Lindström, Stephan Ripke, Giulio Genovese, Po-Ru Loh, Gaurav Bhatia, Ron Do,[...]. Am J Hum Genet 2015
Bjarni J Vilhjálmsson, Jian Yang, Hilary K Finucane, Alexander Gusev, Sara Lindström, Stephan Ripke, Giulio Genovese, Po-Ru Loh, Gaurav Bhatia, Ron Do,[...]. Am J Hum Genet 2015
22
The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.
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Annalisa Buniello, Jacqueline A L MacArthur, Maria Cerezo, Laura W Harris, James Hayhurst, Cinzia Malangone, Aoife McMahon, Joannella Morales, Edward Mountjoy, Elliot Sollis,[...]. Nucleic Acids Res 2019
22
An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank.
Stephen M Smith, Gwenaëlle Douaud, Winfield Chen, Taylor Hanayik, Fidel Alfaro-Almagro, Kevin Sharp, Lloyd T Elliott. Nat Neurosci 2021
Stephen M Smith, Gwenaëlle Douaud, Winfield Chen, Taylor Hanayik, Fidel Alfaro-Almagro, Kevin Sharp, Lloyd T Elliott. Nat Neurosci 2021
22
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.
Edith Hofer, Gennady V Roshchupkin, Hieab H H Adams, Maria J Knol, Honghuang Lin, Shuo Li, Habil Zare, Shahzad Ahmad, Nicola J Armstrong, Claudia L Satizabal,[...]. Nat Commun 2020
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22
Comprehensive functional genomic resource and integrative model for the human brain.
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Daifeng Wang, Shuang Liu, Jonathan Warrell, Hyejung Won, Xu Shi, Fabio C P Navarro, Declan Clarke, Mengting Gu, Prashant Emani, Yucheng T Yang,[...]. Science 2018
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CHIMGEN: a Chinese imaging genetics cohort to enhance cross-ethnic and cross-geographic brain research.
Qiang Xu, Lining Guo, Jingliang Cheng, Meiyun Wang, Zuojun Geng, Wenzhen Zhu, Bing Zhang, Weihua Liao, Shijun Qiu, Hui Zhang,[...]. Mol Psychiatry 2020
Qiang Xu, Lining Guo, Jingliang Cheng, Meiyun Wang, Zuojun Geng, Wenzhen Zhu, Bing Zhang, Weihua Liao, Shijun Qiu, Hui Zhang,[...]. Mol Psychiatry 2020
25
Integrative analysis of 111 reference human epigenomes.
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Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits.
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A resource-efficient tool for mixed model association analysis of large-scale data.
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Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
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Quantifying the Polygenic Architecture of the Human Cerebral Cortex: Extensive Genetic Overlap between Cortical Thickness and Surface Area.
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Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
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11
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.
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Biobanks and electronic medical records: enabling cost-effective research.
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Genetic Markers of ADHD-Related Variations in Intracranial Volume.
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11
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.