Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

Association of circulating neuregulin 4 with metabolic syndrome in obese adults: a cross-sectional study

(2016) Chengfu Cai et al.   BMC Medicine

The Geisinger MyCode community health initiative: an electronic health record–linked biobank for precision medicine research

(2016) David J. Carey et al.   GENETICS IN MEDICINE

Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151)

(2016) G Davies et al.   MOLECULAR PSYCHIATRY

A reference panel of 64,976 haplotypes for genotype imputation

(2016)   NATURE GENETICS

Prokineticin receptor-1 signaling promotes Epicardial to Mesenchymal Transition during heart development

(2016) Himanshu Arora et al.   Scientific Reports

Recent genomic heritage in Scotland

(2015) Carmen Amador et al.   BMC GENOMICS

Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant atCCND2Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion

(2015) Hanieh Yaghootkar et al.   DIABETES

Directional dominance on stature and cognition in diverse human populations

(2015) Peter K. Joshi et al.   NATURE

A global reference for human genetic variation

(2015) Richard A. Gibbs et al.   NATURE

The UK10K project identifies rare variants in health and disease

(2015)   NATURE

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

(2015) María Soler Artigas et al.   Nature Communications

Comparison of Heritability of Cystatin C- and Creatinine-Based Estimates of Kidney Function and Their Relation to Heritability of Cardiovascular Disease

(2015) J. Arpegard et al.   Journal of the American Heart Association

A GWAS Study on Liver Function Test Using eMERGE Network Participants

(2015) Bahram Namjou et al.   PLoS One

Efficient haplotype matching and storage using the positional Burrows-Wheeler transform (PBWT)

(2014) R. Durbin   BIOINFORMATICS

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

(2014) Valgerdur Steinthorsdottir et al.   NATURE GENETICS

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

(2014) Dan E Arking et al.   NATURE GENETICS

A Review of the Role of Electronic Health Record in Genomic Research

(2014) Parasuram Krishnamoorthy et al.   Journal of Cardiovascular Translational Research

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

(2014) Nicholas J. Timpson et al.   Nature Communications

Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study

(2013) Shona M Kerr et al.   BMC Medical Genetics

RegScan: a GWAS tool for quick estimation of allele effects on continuous traits and their combinations

(2013) T. Haller et al.   BRIEFINGS IN BIOINFORMATICS

Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders

(2013) Marcel den Hoed et al.   NATURE GENETICS

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

(2013) Danielle Welter et al.   NUCLEIC ACIDS RESEARCH

Prokineticin Receptor‐1 Is a New Regulator of Endothelial Insulin Uptake and Capillary Formation to Control Insulin Sensitivity and Cardiovascular and Kidney Functions

(2013) Mojdeh Dormishian et al.   Journal of the American Heart Association

Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness

(2012) Blair H Smith et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

(2012) Anna Köttgen et al.   NATURE GENETICS

Rapid variance components–based method for whole-genome association analysis

(2012) Gulnara R Svishcheva et al.   NATURE GENETICS

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

(2012) Robert A Scott et al.   NATURE GENETICS

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

(2012) Alisa K Manning et al.   NATURE GENETICS

Improved whole-chromosome phasing for disease and population genetic studies

(2012) Olivier Delaneau et al.   NATURE METHODS

Age-Dependent Association of the Polymorphisms in the Mitochondria-Shaping Gene, OPA1, With Blood Pressure and Hypertension in Korean Population

(2011) Hyun-Seok Jin et al.   AMERICAN JOURNAL OF HYPERTENSION

Genetic Inactivation of Prokineticin Receptor-1 Leads to Heart and Kidney Disorders

(2011) Mounia Boulberdaa et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

A linear complexity phasing method for thousands of genomes

(2011) Olivier Delaneau et al.   NATURE METHODS

A Novel Glycerophosphodiester Phosphodiesterase, GDE5, Controls Skeletal Muscle Development via a Non-enzymatic Mechanism

(2010) Yuri Okazaki et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Near-infrared (NIR) dye-labeled RNAs identify binding of ZBP1 to the noncoding Y3-RNA

(2010) M. Kohn et al.   RNA

Divergent roles of prokineticin receptors in the endothelial cells: angiogenesis and fenestration

(2009) Célia Guilini et al.   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

Genetic variations in ATP2B1, CSK, ARSG and CSMD1 loci are related to blood pressure and/or hypertension in two Korean cohorts

(2009) K-W Hong et al.   JOURNAL OF HUMAN HYPERTENSION

Junctin and the histidine-rich Ca2+binding protein: potential roles in heart failure and arrhythmogenesis

(2009) Tracy J. Pritchard et al.   JOURNAL OF PHYSIOLOGY-LONDON

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

(2008) Veronique Vitart et al.   NATURE GENETICS