Aitana Alonso-Gonzalez, Manuel Calaza, Cristina Rodriguez-Fontenla, Angel Carracedo. Front Genet 2019
Times Cited: 11
Times Cited: 11
Times Cited
Times Co-cited
Similarity
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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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
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Functional mapping and annotation of genetic associations with FUMA.
Kyoko Watanabe, Erdogan Taskesen, Arjen van Bochoven, Danielle Posthuma. Nat Commun 2017
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
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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
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
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Pathway Network Analyses for Autism Reveal Multisystem Involvement, Major Overlaps with Other Diseases and Convergence upon MAPK and Calcium Signaling.
Ya Wen, Mohamad J Alshikho, Martha R Herbert. PLoS One 2016
Ya Wen, Mohamad J Alshikho, Martha R Herbert. PLoS One 2016
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Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014.
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Common genetic variants on 5p14.1 associate with autism spectrum disorders.
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Small-conductance Ca2+-activated K+ channel type 2 (SK2) modulates hippocampal learning, memory, and synaptic plasticity.
Rebecca S Hammond, Chris T Bond, Timothy Strassmaier, Thu Jennifer Ngo-Anh, John P Adelman, James Maylie, Robert W Stackman. J Neurosci 2006
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Activation mechanism of a human SK-calmodulin channel complex elucidated by cryo-EM structures.
Chia-Hsueh Lee, Roderick MacKinnon. Science 2018
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Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels.
Marek Szatanik, Nicolas Vibert, Isabelle Vassias, Jean-Louis Guénet, Daniel Eugène, Catherine de Waele, Jean Jaubert. Neurogenetics 2008
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Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome.
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KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia.
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Tremor dominant Kyoto (Trdk) rats carry a missense mutation in the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channel.
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The contribution of de novo coding mutations to autism spectrum disorder.
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The familial co-aggregation of ASD and ADHD: a register-based cohort study.
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
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Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
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Genetic contributions to autism spectrum disorder.
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Behçet disease-associated MHC class I residues implicate antigen binding and regulation of cell-mediated cytotoxicity.
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Detection of gene-environment interactions in the presence of linkage disequilibrium and noise by using genetic risk scores with internal weights from elastic net regression.
Anke Hüls, Katja Ickstadt, Tamara Schikowski, Ursula Krämer. BMC Genet 2017
Anke Hüls, Katja Ickstadt, Tamara Schikowski, Ursula Krämer. BMC Genet 2017
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Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray.
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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
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zCall: a rare variant caller for array-based genotyping: genetics and population analysis.
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Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index.
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Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.
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Accommodating linkage disequilibrium in genetic-association analyses via ridge regression.
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Performing different kinds of physical exercise differentially attenuates the genetic effects on obesity measures: Evidence from 18,424 Taiwan Biobank participants.
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Gene-environment interaction study for BMI reveals interactions between genetic factors and physical activity, alcohol consumption and socioeconomic status.
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Sex-specific autosomal genetic effects across 26 human complex traits.
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Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children.
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Genome-Wide Gene-Environment Interaction Analysis Using Set-Based Association Tests.
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Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases.
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Physical activity attenuates the body mass index-increasing influence of genetic variation in the FTO gene.
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Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration.
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Assessing the effect of interaction between an FTO variant (rs9939609) and physical activity on obesity in 15,925 Swedish and 2,511 Finnish adults.
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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.