← back to search

Ian Dunham

European Bioinformatics Institute · GB
Area of research
Molecular Biology · Genetics
Research interest
Research interests include Genomics and Chromatin Dynamics, Genetic Associations and Epidemiology, Genomic variations and chromosomal abnormalities, and RNA and protein synthesis mechanisms.
h-index
77
citations
85,647
works
351
NIH funding
primary concept
Biology
email

Recent publications

CACHE (Critical Assessment of Computational Hit-finding Experiments): A public–private partnership benchmarking initiative to enable the development of computational methods for hit-finding
Nature Reviews Chemistry 2022cited by 99position: middledoi
Multi-ancestry Mendelian randomization of omics traits revealing drug targets of COVID-19 severity
EBioMedicine 2022cited by 30position: middledoi
Mapping the human genetic architecture of COVID-19
Nature 2021cited by 1,112position: middledoi
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
Nature Communications 2019cited by 40position: middledoi
The Human Cell Atlas
bioRxiv (Cold Spring Harbor Laboratory) 2017cited by 76position: middledoi
Author response: The Human Cell Atlas
2017cited by 13position: middledoi
The UK10K project identifies rare variants in health and disease
Nature 2015cited by 1,186position: middledoi
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Nature Communications 2015cited by 384position: middledoi
Whole-genome sequence-based analysis of thyroid function
Nature Communications 2015cited by 107position: middledoi
Defining functional DNA elements in the human genome
Proceedings of the National Academy of Sciences 2014cited by 747position: middledoi
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Nature Communications 2014cited by 74position: middledoi
Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease
Proceedings of the National Academy of Sciences 2014cited by 27position: middledoi
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Nature Genetics 2013cited by 415position: middledoi
Integrative annotation of chromatin elements from ENCODE data
Nucleic Acids Research 2012cited by 619position: middledoi
Large-Scale Identification of MicroRNA Targets in Murine Dgcr8-Deficient Embryonic Stem Cell Lines
PLoS ONE 2012cited by 8position: lastdoi

Grants

No grants ingested yet.

Frequent collaborators

George Davey Smith · Laboratoire d’immunologie intégrative du cancer1 papers (2022–2022)Ross C. Hardison · Pennsylvania State University1 papers (2012–2012)Cei Abreu‐Goodger · Centre for Immunity, Infection and Evolution1 papers (2012–2012)Huiling Zhao · University of Bristol1 papers (2022–2022)Pentao Liu · Jinan University1 papers (2012–2012) · 1 papers (2012–2012)Matthew P. Davis · European Bioinformatics Institute1 papers (2012–2012)Mohd Anisul Karim · Tabriz University of Medical Sciences1 papers (2022–2022)Belinda Giardine · Pennsylvania State University1 papers (2012–2012)Steven P. Wilder · Centre for Human Genetics1 papers (2012–2012) · 1 papers (2012–2012)Tom R. Gaunt · University Hospitals Bristol NHS Foundation Trust1 papers (2022–2022)Jeremy Schwartzentruber · Illumina (United States)1 papers (2022–2022)Felix Miller-Molloy · University of Bristol1 papers (2022–2022)Claudia Kutter · Science for Life Laboratory1 papers (2012–2012)Michael M. Hoffman · University Health Network1 papers (2012–2012)Nenad Bartoniček · Garvan Institute of Medical Research1 papers (2012–2012)Katherine Roberts · University of Bristol1 papers (2022–2022)Anton J. Enright · University of Cambridge1 papers (2012–2012)Stijn van Dongen · Wellcome Sanger Institute1 papers (2012–2012)