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Blended Learning Model Incorporating Online Learning for a Competency-Focused, Work-Based Learning (WBL) Programme -- Allied Healthcare Case-Study

Higher education, skills and work-based learning, 2022-07, Vol.12 (4), p.791

2022

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A Protein Domain and Family Based Approach to Rare Variant Association Analysis

PloS one, 2016-04, Vol.11 (4), p.e0153803-e0153803

2016

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Rab25 and CLIC3 Collaborate to Promote Integrin Recycling from Late Endosomes/Lysosomes and Drive Cancer Progression

Developmental cell, 2012-01, Vol.22 (1), p.131-145

2012

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Mining the human phenome using allelic scores that index biological intermediates

PLoS genetics, 2013-10, Vol.9 (10), p.e1003919-e1003919

2013

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Nature genetics, 2019-01, Vol.51 (1), p.63-75

2019

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WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

PLoS genetics, 2012-07, Vol.8 (7), p.e1002745-e1002745

2012

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Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

Nature genetics, 2016-11, Vol.48 (11), p.1303-1312

2016

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A genome-wide association meta-analysis identifies new childhood obesity loci

Nature genetics, 2012-05, Vol.44 (5), p.526-531

2012

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Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

Nature genetics, 2012-02, Vol.44 (2), p.187-192

2012

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Estimating telomere length from whole genome sequence data

Nucleic acids research, 2014-05, Vol.42 (9), p.e75

2014

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An interactive genome browser of association results from the UK10K cohorts project

Bioinformatics (Oxford, England), 2015-12, Vol.31 (24), p.4029-4031

2015

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Managing clinically significant findings in research: the UK10K example

European journal of human genetics : EJHG, 2014-01, Vol.22 (9), p.1100-1104

2014

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Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour

Nature human behaviour, 2021-12, Vol.5 (12), p.1717

2021

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Whole-genome sequence-based analysis of thyroid function

Nature communications, 2015-03, Vol.6 (1), p.5681-5681, Article 5681

2015

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A novel common variant in DCST2 is associated with length in early life and height in adulthood

Human molecular genetics, 2015-02, Vol.24 (4), p.1155-1168

2015

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Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

Scientific reports, 2017-11, Vol.7 (1), p.15351-15, Article 15351

2017

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Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

Diabetologia, 2023-07, Vol.66 (7), p.1260-1272

2023

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Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

Nature genetics, 2018-12, Vol.50 (12), p.1752-1752

2018

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The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects

European journal of epidemiology, 2019, Vol.34 (3), p.279-300

2019

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Managing clinically significant findings in research: the UK10K example

European journal of human genetics : EJHG, 2014-09, Vol.22 (9), p.1100-1104

2014

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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

Nature communications, 2014-09, Vol.5 (1), p.4871-4871, Article 4871

2014

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The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects

Molecular psychiatry, 2015-06, Vol.20 (6), p.735-743

2015

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Chlamydia trachomatis in the Age of the Genome: Application of Molecular Genotyping to Improve Our Understanding of the Immunopathogenesis of Chlamydia Genital Tract Disease

Sexually transmitted diseases, 2011-06, Vol.38 (6), p.495-498

2011

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Blended Learning Model Incorporating Online Learning for a Competency-Focused, Work-Based Learning (WBL) Programme -- Allied Healthcare Case-Study

A Protein Domain and Family Based Approach to Rare Variant Association Analysis

Rab25 and CLIC3 Collaborate to Promote Integrin Recycling from Late Endosomes/Lysosomes and Drive Cancer Progression

Mining the human phenome using allelic scores that index biological intermediates

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Identification of unique neoantigen qualities in long-term survivors of pancreatic cancer

WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

A genome-wide association meta-analysis identifies new childhood obesity loci

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

Estimating telomere length from whole genome sequence data

An interactive genome browser of association results from the UK10K cohorts project

Managing clinically significant findings in research: the UK10K example

Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour

Whole-genome sequence-based analysis of thyroid function

A novel common variant in DCST2 is associated with length in early life and height in adulthood

Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects

Managing clinically significant findings in research: the UK10K example

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects

Chlamydia trachomatis in the Age of the Genome: Application of Molecular Genotyping to Improve Our Understanding of the Immunopathogenesis of Chlamydia Genital Tract Disease

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