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Bioinformatics (Oxford, England)|June 10, 2011
The variant call format and VCFtoolsPetr Danecek, Adam Auton, Goncalo Abecasis, et al.
European Journal of Ageing|November 28, 2024
Lifestyle factors and incident multimorbidity related to chronic disease: a population-based cohort studyYihui Du, Geertruida H de Bock, Judith M Vonk, et al.
Ebiomedicine|December 17, 2025
A genome- and phenome-wide association study of plasma procalcitonin concentrations in individuals of European ancestryWenbo Zhang, Peter J van der Most, Siqi Wang, et al.
Scientific Reports|March 20, 2021
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphomaHannah E Roberts, Maria Lopopolo, Alistair T Pagnamenta, et al.
Ebiomedicine|April 1, 2025
Genetic association studies in critically ill patients: a systematic reviewWenbo Zhang, Nam Nguyen-Hoang, Sean C S Rivrud, et al.
Genome Biology|March 24, 2012
The fine-scale architecture of structural variants in 17 mouse genomesBinnaz Yalcin, Kim Wong, Amarjit Bhomra, et al.
Plos Genetics|October 12, 2012
Cofilin-1: a modulator of anxiety in miceMartin Goodson, Marco B Rust, Walter Witke, et al.
Plos Genetics|March 14, 2012
The human pancreatic islet transcriptome: expression of candidate genes for type 1 diabetes and the impact of pro-inflammatory cytokinesDécio L Eizirik, Michael Sammeth, Thomas Bouckenooghe, et al.
BMJ Open|September 2, 2025
Propofol-based versus sevoflurane-based anaesthesia for deceased donor kidney transplantation: the VAPOR-2 study protocol for an international multicentre randomised controlled trialGerrie Joelle Julia Huisman, Stefan P Berger, Peter S Thyrrestrup, et al.
Plos Genetics|February 6, 2013
Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutationsKatherine R Bull, Andrew J Rimmer, Owen M Siggs, et al.
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