List of works - Colin Palmer

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

scientific article

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

scientific article (publication date: November 2010)

Genetic studies of body mass index yield new insights for obesity biology

scientific article

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

scientific article

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

scientific article

Discovery and refinement of loci associated with lipid levels

scientific article

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

scientific article

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

scientific article

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scientific article

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

scientific article

Defining the role of common variation in the genomic and biological architecture of adult human height

scientific article

Replicating genotype-phenotype associations

scientific article (publication date: 7 June 2007)

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

scientific article published in October 2013

Large-scale association analysis identifies new risk loci for coronary artery disease

scientific article published on 02 December 2012

Common variants near MC4R are associated with fat mass, weight and risk of obesity

scientific article

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

scientific article

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

scientific article

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

scientific article

Observation of a new boson at a mass of 125 GeV with the CMS experiment at the LHC

scientific article

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

article

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

scientific article

Variants in MTNR1B influence fasting glucose levels

scientific article

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

scientific article

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

scientific journal article

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

scientific journal article

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

scientific article published on 18 June 2014

The genetic architecture of type 2 diabetes

scientific article (publication date: 11 July 2016)

Common variants associated with plasma triglycerides and risk for coronary artery disease

scientific article

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

scientific article published in June 2009

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

article

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

scientific article

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

scientific article

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

scientific article published on 5 October 2012

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

scientific article

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

scientific article

Common variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMI

scientific article

Rare and low-frequency coding variants alter human adult height

scientific article (publication date: February 2017)

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

scientific article published on 2 March 2016

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy.

scientific article

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

scientific article published on 12 September 2016

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

scientific article published on 08 October 2018

Inactivating mutations in NPC1L1 and protection from coronary heart disease

scientific article

Variation in TCF7L2 influences therapeutic response to sulfonylureas: a GoDARTs study

scientific article published on 22 May 2007

Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood

article

Genome-wide association and functional follow-up reveals new loci for kidney function

scientific article

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

scientific article

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

scientific article

Mouse p53 inhibits SV40 origin-dependent DNA replication

scientific article published in October 1987

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study

scientific article

List of works by Colin Palmer

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Genetic studies of body mass index yield new insights for obesity biology

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Discovery and refinement of loci associated with lipid levels

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

Defining the role of common variation in the genomic and biological architecture of adult human height

Replicating genotype-phenotype associations

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Large-scale association analysis identifies new risk loci for coronary artery disease

Common variants near MC4R are associated with fat mass, weight and risk of obesity

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

Observation of a new boson at a mass of 125 GeV with the CMS experiment at the LHC

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

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

Variants in MTNR1B influence fasting glucose levels

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

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

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

The genetic architecture of type 2 diabetes

Common variants associated with plasma triglycerides and risk for coronary artery disease

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

Common variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMI

Rare and low-frequency coding variants alter human adult height

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy.

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Inactivating mutations in NPC1L1 and protection from coronary heart disease

Variation in TCF7L2 influences therapeutic response to sulfonylureas: a GoDARTs study

Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood

Genome-wide association and functional follow-up reveals new loci for kidney function

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

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

Mouse p53 inhibits SV40 origin-dependent DNA replication

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study