Author details

Full Name

Tim Hubbard

Affiliation

ORCID

Career Start Year

1985

Papers

157

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37115922	The genomic landscape of familial glioma.	Sci Adv	2023
36420896	GENCODE: reference annotation for the human and mouse genomes in 2023.	Nucleic Acids Res	2023
34907575	Pharmacogenomic testing in paediatrics: Clinical implementation strategies.	Br J Clin Pharmacol	2022
33270111	GENCODE 2021.	Nucleic Acids Res	2021
32728065	Transcriptional activity and strain-specific history of mouse pseudogenes.	Nat Commun	2020
32854092	Mining Social Media Data to Study the Consequences of Dementia Diagnosis on Caregivers and Relatives.	Dement Geriatr Cogn Disord	2020
30357393	GENCODE reference annotation for the human and mouse genomes.	Nucleic Acids Res	2019
29691228	The 100â¿¿000 Genomes Project: bringing whole genome sequencing to the NHS.	BMJ	2018
30052801	Scientists on the Spot: Sequencing the human genome to influence patient healthcare.	Cardiovascular Research	2018
28207753	Analysis of diagnoses extracted from electronic health records in a large mental health case register.	PLoS One	2017
28507325	Corrigendum: Characterisation of mental health conditions in social media using Informed Deep Learning.	Sci Rep	2017
28365743	Automated PDF highlighting to support faster curation of literature for Parkinson's and Alzheimer's disease.	Database (Oxford)	2017
28327593	Characterisation of mental health conditions in social media using Informed Deep Learning.	Sci Rep	2017
28396521	Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.	Genome Res	2017
27821178	Erratum to: Making sense of big data in health research: towards an EU action plan.	Genome Med	2016
27338147	Making sense of big data in health research: Towards an EU action plan.	Genome Med	2016
26041702	Global implementation of genomic medicine: We are not alone.	Sci Transl Med	2015
26315906	An interactive genome browser of association results from the UK10K cohorts project.	Bioinformatics	2015
25164755	Comparative analysis of the transcriptome across distant species.	Nature	2014
25275169	Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease.	Proc Natl Acad Sci U S A	2014
24316576	Ensembl 2014.	Nucleic Acids Res	2014
24217909	Current status and new features of the Consensus Coding Sequence database.	Nucleic Acids Res	2014
24634402	Characterizing genetic variants for clinical action.	Am J Med Genet C Semin Med Genet	2014
24810143	A comparison of peak callers used for DNase-Seq data.	PLoS ONE	2014
24753594	Defining functional DNA elements in the human genome.	Proc Natl Acad Sci U S A	2014
25157146	Comparative analysis of pseudogenes across three phyla.	Proc Natl Acad Sci U S A	2014
23203987	Ensembl 2013.	Nucleic Acids Res	2013
24185837	Assessment of transcript reconstruction methods for RNA-seq.	Nat Methods	2013
24185836	Systematic evaluation of spliced alignment programs for RNA-seq data.	Nat Methods	2013
23922824	Chromatin accessibility data sets show bias due to sequence specificity of the DNase I enzyme.	PLoS ONE	2013
22238572	Evidence for transcript networks composed of chimeric RNAs in human cells.	PLoS One	2012
22955988	The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expression.	Genome Res	2012
22955987	GENCODE: the reference human genome annotation for The ENCODE Project.	Genome Res	2012
22955982	Combining RT-PCR-seq and RNA-seq to catalog all genic elements encoded in the human genome.	Genome Res	2012
22955620	Landscape of transcription in human cells.	Nature	2012
22951037	The GENCODE pseudogene resource.	Genome Biol	2012
22086963	Ensembl 2012.	Nucleic Acids Res	2012
21551269	The origins, evolution, and functional potential of alternative splicing in vertebrates.	Mol Biol Evol	2011
21045057	Ensembl 2011.	Nucleic Acids Res	2011
21252075	Dalliance: interactive genome viewing on the web.		2011
21460061	Shotgun proteomics aids discovery of novel protein-coding genes, alternative splicing, and "resurrected" pseudogenes in the mouse genome.	Genome Res	2011
21364695	The GENCODE exome: sequencing the complete human exome.	Eur J Hum Genet	2011
21955348	Developing and implementing an institute-wide data sharing policy.	Genome Med	2011
21750661	Modernizing reference genome assemblies.	PLoS Biol	2011
19906699	Ensembl's 10th year.	Nucleic Acids Res	2010
20923551	AnnoTrack--a tracking system for genome annotation.	BMC Genomics	2010
20106815	iMotifs: an integrated sequence motif visualization and analysis environment.		2010
20103622	Novel candidate cancer genes identified by a large-scale cross-species comparative oncogenomics approach.	Cancer Res	2010
19909804	Genome-wide end-sequenced BAC resources for the NOD/MrkTac() and NOD/ShiLtJ() mouse genomes.	Genomics	2010
20579334	Metamotifs--a generative model for building families of nucleotide position weight matrices.	BMC Bioinformatics	2010