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Publications

Effects of epigenetic pathway inhibitors on corticotroph tumour AtT20 cells

Lines KE. et al, (2020), Endocrine-Related Cancer, 27, 163 - 174

Sequencing of human genomes with nanopore technology

Bowden R. et al, (2019), Nature Communications, 10

A practical solution for preserving single cells for RNA sequencing

Attar M. et al, (2018), Scientific Reports, 8

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Flannick J. et al, (2018), Scientific Data, 5

Single cell RNA-seq reveals profound transcriptional similarity between Barrett’s oesophagus and oesophageal submucosal glands

Owen RP. et al, (2018), Nature Communications, 9

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

Schwerd T. et al, (2018), Mucosal Immunology, 11, 562 - 574

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Flannick J. et al, (2017), Scientific Data, 4

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

Manning A. et al, (2017), Diabetes, 66, 2019 - 2032

Comprehensive comparison of Pacific Biosciences and Oxford Nanopore Technologies and their applications to transcriptome analysis

Weirather JL. et al, (2017), F1000Research, 6, 100 - 100

Epigenetic pathway inhibitors represent potential drugs for treating pancreatic and bronchial neuroendocrine tumors

Lines KE. et al, (2017), Oncogenesis, 6, e332 - e332

Correction: Corrigendum: Rapid antibiotic-resistance predictions from genome sequence data for Staphylococcus aureus and Mycobacterium tuberculosis

Bradley P. et al, (2016), Nature Communications, 7

The genetic architecture of type 2 diabetes

Fuchsberger C. et al, (2016), Nature, 536, 41 - 47

Rapid antibiotic-resistance predictions from genome sequence data for Staphylococcus aureus and Mycobacterium tuberculosis

Bradley P. et al, (2015), Nature Communications, 6

MinION Analysis and Reference Consortium: Phase 1 data release and analysis

Ip CLC. et al, (2015), F1000Research, 4, 1075 - 1075

ve-SEQ: Robust, unbiased enrichment for streamlined detection and whole-genome sequencing of HCV and other highly diverse pathogens

Bonsall D. et al, (2015), F1000Research, 4, 1062 - 1062

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Taylor JC. et al, (2015), Nature Genetics, 47, 717 - 726

High-throughput DNA Sequencing Identifies Novel CtIP (RBBP8) Variants in Muscle-invasive Bladder Cancer Patients

Jevons SJ. et al, (2015), Bladder Cancer, 1, 31 - 44

Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus

Mahajan A. et al, (2015), PLOS Genetics, 11, e1004876 - e1004876

Erythrocytosis associated with a novel missense mutation in the BPGM gene

Petousi N. et al, (2014), Haematologica, 99, e201 - e204

Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden

Cazier J-B. et al, (2014), Nature Communications, 5

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