ArticleNature genetics2015
The European Genome-phenome Archive of human data consented for biomedical research.
Abstract read
In one paragraph
Article in Nature genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 219 papers, 3 of them syntheses that pooled it.
0numbers the graph read from it
0cells of the map it votes in
219citing papers in PubMed, 3 pooled it
–field-weighted citation impact
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
219 citing papers in PubMed, 3 syntheses or guidelines pooled it.
- Loss of p53-DREAM-mediated repression of cell cycle genes as a driver of lymph node metastasis in head and neck cancer.Genome medicine · 2023Pooled it
- Teaching genomics to life science undergraduates using cloud computing platforms with open datasets.Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology · 2022Pooled it
- Flimma: a federated and privacy-aware tool for differential gene expression analysis.Genome biology · 2021Pooled it
- Alterations to the Bronchial Gene-Expression Effects of Tobacco Smoking in People Living With HIV.Journal of acquired immune deficiency syndromes (1999) · 2026Trial
- Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.Circulation. Genomic and precision medicine · 2021Trial
- Molecular profiling of longitudinally observed small colorectal polyps: A cohort study.EBioMedicine · 2019Trial
- Integration of Multiomics Datasets to Identify Allergy Biomarkers and Protective Signatures.Methods in molecular biology (Clifton, N.J.) · 2027Article
- Cancer genomic data systems in precision oncology: from integration to clinical implementation.EBioMedicine · 2026Review
- Ethical Governance of Open Data Across Biomedical Research, Healthcare, and Public Health: Privacy, Equity, Trust, and Controlled Access.Health care analysis : HCA : journal of health philosophy and policy · 2026Article
- AI and neuroimaging in autism spectrum disorder: advances in diagnosis, methodological challenges and future directions.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026Review
- DNAviWEB: sequencing-free clinical screening of liquid biopsies.Nucleic acids research · 2026Article
- Eras of bioinformatics technologies from command-line interfaces to artificial intelligence (AI) chatbots.Briefings in bioinformatics · 2026Review
- HUPA: A corpus of disordered and normophonic voices in Castilian Spanish.Data in brief · 2026Review
- AI and Big Data in Oncology: A Physician-Centered Perspective on Emerging Clinical and Research Applications.Cancer innovation · 2026Review
- Federated, governed, and interoperable? The emerging architecture of public human genomic data infrastructures: a European perspective.Frontiers in genetics · 2026Review
- A FAIR gold-standard benchmark for geographic entity recognition in cancer genomics literature for biomedical NLP.Bioinformatics advances · 2026Article
- The Impact of Variant Calling on Substitution Mutational Signature Inference.bioRxiv : the preprint server for biology · 2025Article
- Lessons learned: Recommendations for reproducible paleogenomic data analyses.American journal of human genetics · 2025Review
- Fusion transcripts landscape in hepatocellular carcinoma and potential impact on the expression of fusion partners.RNA biology · 2025Article
- The italian national genomic strategy: current status, challenges, and future perspectives in clinical practice and public health.Journal of community genetics · 2025Article
159 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
26 authors.
Ilkka LappalainenEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Jeff Almeida-KingEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Vasudev KumanduriEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Alexander SenfEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
John Dylan SpaldingEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Saif Ur-RehmanEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.ORCID 0000000276988671
Gary SaundersEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Jag KandasamyEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Mario CaccamoEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Rasko LeinonenEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Brendan VaughanEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Thomas LaurentEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Francis RowlandEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Pablo Marin-GarciaEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.ORCID 0000000339882365
Jonathan BarkerEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Petteri JokinenEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Angel Carreño TorresCentre for Genomic Regulation, Barcelona, Spain.
Jordi Rambla de ArgilaCentre for Genomic Regulation, Barcelona, Spain.
Oscar Martinez LlobetCentre for Genomic Regulation, Barcelona, Spain.
Ignacio MedinaEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Marc Sitges PuyCentre for Genomic Regulation, Barcelona, Spain.
Mario AlberichCentre for Genomic Regulation, Barcelona, Spain.
Sabela de la TorreCentre for Genomic Regulation, Barcelona, Spain.
Arcadi Navarro1] Centre for Genomic Regulation, Barcelona, Spain. [2] Institute of Evolutionary Biology, Universitat Pompeu Fabra-Consejo Superior de Investigaciones Científicas (CSIC), Barcelona, Spain. [3] Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.
Justin PaschallEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Paul FlicekEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Hinxton, UK.
Funding
Biotechnology and Biological Sciences Research Council BB/H008802/1Medical Research Council G0800681Wellcome TrustWellcome Trust WT 085475/C/08/Z
Abstract
PubMed holds no abstract for this paper.
Indexed as
Databases, GeneticAccess to InformationBiomedical ResearchEuropeGenome, HumanHumans
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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.