List of works - M. Geoffrey Hayes

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

scientific article

Genome partitioning of genetic variation for complex traits using common SNPs

scientific article

Insulin gene mutations as a cause of permanent neonatal diabetes

scholarly article

Detectable clonal mosaicism from birth to old age and its relationship to cancer

scientific article

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

scientific article

Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study

scientific article published on 19 November 2011

Quality control procedures for genome-wide association studies

scientific article published in 2011

The genetic prehistory of the New World Arctic

scientific article

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

scientific article (publication date: May 2010)

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

scientific article

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

scientific article

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

scientific article published on 30 October 2011

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

scientific article published on March 2016

Worldwide allele frequencies of the human apolipoprotein E gene: climate, local adaptations, and evolutionary history

scientific article

Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies

scientific article published on 10 September 2007

Delayed paternal age of reproduction in humans is associated with longer telomeres across two generations of descendants

scientific article

eMERGEing progress in genomics-the first seven years

scientific article

Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from

scientific article

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

scientific article

Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas

scientific article

Comparative analysis of the human saliva microbiome from different climate zones: Alaska, Germany, and Africa

scientific article

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

scientific article published on 3 October 2014

Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort

scientific article

Practical challenges in integrating genomic data into the electronic health record

scientific article

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

scientific article

Genetics of chronic rhinosinusitis: state of the field and directions forward

scientific article published on April 2013

Genetic variation associated with circulating monocyte count in the eMERGE Network

scientific article published on 12 January 2013

Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci

scientific article published on 09 June 2006

Improving qPCR telomere length assays: Controlling for well position effects increases statistical power

scientific article

Ethnic variation in allele distribution of the androgen receptor (AR) (CAG)n repeat

scientific article published on 19 May 2011

Coordinated regulatory variation associated with gestational hyperglycaemia regulates expression of the novel hexokinase HKDC1

scientific article

Linkage of calpain 10 to type 2 diabetes: the biological rationale

scientific article

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

scientific article

Substantial variation in qPCR measured mean blood telomere lengths in young men from eleven European countries

scientific article published on 10 January 2011

Genetic variation in the HLA region is associated with susceptibility to herpes zoster

scientific article

Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans

scientific article published on 28 March 2013

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

scientific article published on 01 May 2019

The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study

scientific article published on 10 April 2013

Genetics of Gestational Diabetes Mellitus and Maternal Metabolism

scientific article

Constitutively decreased TGFBR1 allelic expression is a common finding in colorectal cancer and is associated with three TGFBR1 SNPs

scientific article

The short-chain fatty acid receptor, FFA2, contributes to gestational glucose homeostasis

scientific article published on 22 September 2015

The role of testosterone in coordinating male life history strategies: The moderating effects of the androgen receptor CAG repeat polymorphism

scientific article published on 26 October 2016

The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy

scientific article (publication date: 2012)

Testing the null hypothesis: comments on 'Culture-gene coevolution of individualism-collectivism and the serotonin transporter gene'.

scientific article

A candidate gene study reveals association between a variant of the Peroxisome Proliferator-Activated Receptor Gamma (PPAR-γ) gene and systemic sclerosis

scientific article published on 19 May 2015

A genomewide screen for chronic rhinosinusitis genes identifies a locus on chromosome 7q.

scientific article

Genome-wide study of resistant hypertension identified from electronic health records

scientific article

Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans

scientific article published on March 2017

Atopic Dermatitis Susceptibility Variants in Filaggrin Hitchhike Hornerin Selective Sweep.

scientific article published on 27 September 2016

Pathogenic Anti-Müllerian Hormone Variants in Polycystic Ovary Syndrome

scientific article published on 12 May 2017

List of works by M. Geoffrey Hayes

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

Genome partitioning of genetic variation for complex traits using common SNPs

Insulin gene mutations as a cause of permanent neonatal diabetes

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study

Quality control procedures for genome-wide association studies

The genetic prehistory of the New World Arctic

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

Worldwide allele frequencies of the human apolipoprotein E gene: climate, local adaptations, and evolutionary history

Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies

Delayed paternal age of reproduction in humans is associated with longer telomeres across two generations of descendants

eMERGEing progress in genomics-the first seven years

Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas

Comparative analysis of the human saliva microbiome from different climate zones: Alaska, Germany, and Africa

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

Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort

Practical challenges in integrating genomic data into the electronic health record

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Genetics of chronic rhinosinusitis: state of the field and directions forward

Genetic variation associated with circulating monocyte count in the eMERGE Network

Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci

Improving qPCR telomere length assays: Controlling for well position effects increases statistical power

Ethnic variation in allele distribution of the androgen receptor (AR) (CAG)n repeat

Coordinated regulatory variation associated with gestational hyperglycaemia regulates expression of the novel hexokinase HKDC1

Linkage of calpain 10 to type 2 diabetes: the biological rationale

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

Substantial variation in qPCR measured mean blood telomere lengths in young men from eleven European countries

Genetic variation in the HLA region is associated with susceptibility to herpes zoster

Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study

Genetics of Gestational Diabetes Mellitus and Maternal Metabolism

Constitutively decreased TGFBR1 allelic expression is a common finding in colorectal cancer and is associated with three TGFBR1 SNPs

The short-chain fatty acid receptor, FFA2, contributes to gestational glucose homeostasis

The role of testosterone in coordinating male life history strategies: The moderating effects of the androgen receptor CAG repeat polymorphism

The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy

Testing the null hypothesis: comments on 'Culture-gene coevolution of individualism-collectivism and the serotonin transporter gene'.

A candidate gene study reveals association between a variant of the Peroxisome Proliferator-Activated Receptor Gamma (PPAR-γ) gene and systemic sclerosis

A genomewide screen for chronic rhinosinusitis genes identifies a locus on chromosome 7q.

Genome-wide study of resistant hypertension identified from electronic health records

Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans

Atopic Dermatitis Susceptibility Variants in Filaggrin Hitchhike Hornerin Selective Sweep.

Pathogenic Anti-Müllerian Hormone Variants in Polycystic Ovary Syndrome