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Evidence of Syntaxin 1A Involvement in Migraine Susceptibility
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journal
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April 2010 |
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The human protein atlas: A spatial map of the human proteome: The Human Protein Atlas
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journal
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October 2017 |
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STarMir Tools for Prediction of microRNA Binding Sites
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book
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January 2016 |
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Rare variant association testing in the non-coding genome
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journal
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June 2020 |
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Familial analysis reveals rare risk variants for migraine in regulatory regions
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journal
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February 2020 |
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The SNAP25 Gene Is Linked to Working Memory Capacity and Maturation of the Posterior Cingulate Cortex During Childhood
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journal
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December 2010 |
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The Genetics of Transcription Factor DNA Binding Variation
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journal
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July 2016 |
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Where Are the Disease-Associated eQTLs?
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journal
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February 2021 |
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ChIP-seq accurately predicts tissue-specific activity of enhancers
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journal
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February 2009 |
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Integrative analysis of 111 reference human epigenomes
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February 2015 |
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The NIH Roadmap Epigenomics Mapping Consortium
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October 2010 |
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The Genotype-Tissue Expression (GTEx) project
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May 2013 |
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A general framework for estimating the relative pathogenicity of human genetic variants
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February 2014 |
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Meta-analysis of the heritability of human traits based on fifty years of twin studies
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journal
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May 2015 |
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Enhancer–promoter interactions are encoded by complex genomic signatures on looping chromatin
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journal
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April 2016 |
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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journal
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June 2016 |
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Functional annotation of noncoding sequence variants
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journal
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February 2014 |
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Expanded encyclopaedias of DNA elements in the human and mouse genomes
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journal
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July 2020 |
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CScape: a tool for predicting oncogenic single-point mutations in the cancer genome
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September 2017 |
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Association between SNAP-25 gene polymorphisms and cognition in autism: functional consequences and potential therapeutic strategies
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journal
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January 2015 |
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Prevalence and Burden of Migraine in the United States: Data From the American Migraine Study II
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July 2001 |
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MicroRNAs activate gene transcription epigenetically as an enhancer trigger
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journal
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May 2017 |
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Regulatory variants: from detection to predicting impact
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journal
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June 2018 |
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PROMO: detection of known transcription regulatory elements using species-tailored searches
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February 2002 |
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Predicting regulatory variants with composite statistic
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June 2016 |
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Non-coding genetic variants in human disease: Figure 1.
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July 2015 |
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SNPnexus: a web server for functional annotation of human genome sequence variation (2020 update)
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June 2020 |
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Ensembl 2022
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November 2021 |
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DIANA-miTED: a microRNA tissue expression database
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September 2021 |
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RNAhybrid: microRNA target prediction easy, fast and flexible
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July 2006 |
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MEME SUITE: tools for motif discovery and searching
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May 2009 |
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miRBase: integrating microRNA annotation and deep-sequencing data
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October 2010 |
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HOCOMOCO: towards a complete collection of transcription factor binding models for human and mouse via large-scale ChIP-Seq analysis
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journal
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November 2017 |
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IW-Scoring: an Integrative Weighted Scoring framework for annotating and prioritizing genetic variations in the noncoding genome
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journal
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January 2018 |
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Update of the FANTOM web resource: expansion to provide additional transcriptome atlases
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November 2018 |
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miRDB: an online database for prediction of functional microRNA targets
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August 2019 |
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Annotation of functional variation in personal genomes using RegulomeDB
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September 2012 |
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Going Deep into Synaptic Vesicle Machinery Genes and Migraine Susceptibility – A Case‐Control Association Study
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journal
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September 2020 |
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Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohorts
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journal
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April 2008 |
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Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
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journal
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September 2012 |
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The GTEx Consortium atlas of genetic regulatory effects across human tissues
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journal
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September 2020 |
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Family studies to find rare high risk variants in migraine
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March 2017 |
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Advances in genetics of migraine
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journal
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June 2019 |
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Enhancer RNAs: transcriptional regulators and workmates of NamiRNAs in myogenesis
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journal
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February 2021 |
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CTCF-mediated chromatin loops enclose inducible gene regulatory domains
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journal
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March 2016 |
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Functional relevance for central cornea thickness-associated genetic variants by using integrative analyses
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journal
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August 2018 |
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Gateways to the FANTOM5 promoter level mammalian expression atlas
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January 2015 |
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The Ensembl Variant Effect Predictor
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June 2016 |
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Prediction of functional microRNA targets by integrative modeling of microRNA binding and target expression data
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January 2019 |
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Editing GWAS: experimental approaches to dissect and exploit disease-associated genetic variation
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journal
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March 2021 |
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Recommendations for clinical interpretation of variants found in non-coding regions of the genome
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July 2022 |
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Migraine prevalence, disease burden, and the need for preventive therapy
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January 2007 |
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DNA Variation in the SNAP25 Gene Confers Risk to ADHD and Is Associated with Reduced Expression in Prefrontal Cortex
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journal
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April 2013 |
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Interaction between γ-Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility
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September 2013 |
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Genetic and Environmental Influences on Migraine: A Twin Study Across Six Countries
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journal
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October 2003 |
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Exploring the Hereditary Nature of Migraine
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April 2021 |
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Common features of microRNA target prediction tools
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January 2014 |
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Tools for Sequence-Based miRNA Target Prediction: What to Choose?
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December 2016 |
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miRNA Targets: From Prediction Tools to Experimental Validation
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journal
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December 2020 |