ArticleNucleic acids research2018
JASPAR 2018: update of the open-access database of transcription factor binding profiles and its web framework.
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Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 237 papers.
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237citing papers in PubMed
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Who cites it
237 citing papers in PubMed.
- GHT-SELEX demonstrates unexpectedly high intrinsic sequence specificity and complex DNA binding of many human transcription factors.Nature methods · 2026Article
- Genome-wide profiling of histone modifications and transcription factor binding at single-cell resolution by DeChIC-seq.Cell research · 2026Article
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- Distinct roles of Atf3, Zfp711 and Bcl6b in early embryonic hematopoietic and endothelial lineage specification.Development (Cambridge, England) · 2025Article
- Characterization of induced cohesin loop extrusion trajectories in living cells.Nature genetics · 2025Article
- Shedding Light on Patterns of Unconventional Expression of Opsin Genes in Hydra vulgaris.Integrative and comparative biology · 2025Article
- Ox-LDL induces a non-inflammatory response enriched for coronary artery disease risk in human endothelial cells.Scientific reports · 2025Article
- Characterizing DNA recognition preferences of transcription factors using global couplings and high-throughput sequencing.Nucleic acids research · 2025Article
- Screening of common genomic biomarkers to explore common drugs for the treatment of pancreatic and kidney cancers with type-2 diabetes through bioinformatics analysis.Scientific reports · 2025Article
- SP7 transcription factor ameliorates bone defect healing in low-density lipoprotein receptor-related protein 5 (LRP5)-dependent osteoporosis mice.Journal of Zhejiang University. Science. B · 2025Article
- Genomic clustering tendency of transcription factors reflects phase-separated transcriptional condensates at super-enhancers.Nucleic acids research · 2025Article
- N6-methyladenosine RNA modification regulates the transcription of SLC7A11 through KDM6B and GATA3 to modulate ferroptosis.Journal of biomedical science · 2025Article
- Systematic functional characterization of non-coding regulatory SNPs associated with central obesity.American journal of human genetics · 2025Article
- Article
- Chronologically inappropriate morphogenesis (Proceedings of the National Academy of Sciences of the United States of America · 2024Article
- Discovery of key molecular signatures for diagnosis and therapies of glioblastoma by combining supervised and unsupervised learning approaches.Scientific reports · 2024Article
- Integrative pan-cancer analysis reveals a common architecture of dysregulated transcriptional networks characterized by loss of enhancer methylation.PLoS computational biology · 2024Article
- MethylSeqLogo: DNA methylation smart sequence logos.BMC bioinformatics · 2024Article
- TWIST1+FAP+ fibroblasts in the pathogenesis of intestinal fibrosis in Crohn's disease.The Journal of clinical investigation · 2024Article
- Structure-based learning to predict and model protein-DNA interactions and transcription-factor co-operativity inNAR genomics and bioinformatics · 2024Article
177 more citing papers are in PubMed but not listed here.
Corrections and comments
- Erratum for
Authors and funding
19 authors.
Aziz KhanCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, 0318 Oslo, Norway.
Oriol FornesCentre for Molecular Medicine and Therapeutics, Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, 950 28th Ave W, Vancouver, BC V5Z 4H4, Canada.
Arnaud StiglianiUniversity of Grenoble Alpes, CNRS, CEA, INRA, BIG-LPCV, 38000 Grenoble, France.
Marius GheorgheCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, 0318 Oslo, Norway.
Jaime A Castro-MondragonCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, 0318 Oslo, Norway.
Robin van der LeeCentre for Molecular Medicine and Therapeutics, Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, 950 28th Ave W, Vancouver, BC V5Z 4H4, Canada.
Adrien BessyUniversity of Grenoble Alpes, CNRS, CEA, INRA, BIG-LPCV, 38000 Grenoble, France.
Jeanne ChènebyINSERM, UMR1090 TAGC, Marseille, F-13288, France.
Shubhada R KulkarniGhent University, Department of Plant Biotechnology and Bioinformatics, Technologiepark 927, 9052 Ghent, Belgium.
Ge TanInstitute of Clinical Sciences, Faculty of Medicine, Imperial College London, London W12 0NN, UK.
Damir BaranasicInstitute of Clinical Sciences, Faculty of Medicine, Imperial College London, London W12 0NN, UK.
David J ArenillasCentre for Molecular Medicine and Therapeutics, Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, 950 28th Ave W, Vancouver, BC V5Z 4H4, Canada.
Albin SandelinThe Bioinformatics Centre, Department of Biology and Biotech Research & Innovation Centre, University of Copenhagen, DK2200 Copenhagen N, Denmark.
Klaas VandepoeleGhent University, Department of Plant Biotechnology and Bioinformatics, Technologiepark 927, 9052 Ghent, Belgium.
Boris LenhardInstitute of Clinical Sciences, Faculty of Medicine, Imperial College London, London W12 0NN, UK.
Benoît BallesterINSERM, UMR1090 TAGC, Marseille, F-13288, France.
Wyeth W WassermanCentre for Molecular Medicine and Therapeutics, Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, 950 28th Ave W, Vancouver, BC V5Z 4H4, Canada.
François ParcyUniversity of Grenoble Alpes, CNRS, CEA, INRA, BIG-LPCV, 38000 Grenoble, France.
Anthony MathelierCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, 0318 Oslo, Norway.
Funding
Medical Research Council MC_UP_1102/1
Abstract
PubMed holds no abstract for this paper.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.