List of works - Struan F.A. Grant

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

scientific article

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

scientific article (publication date: March 2006)

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

scientific article

Common genetic variants on 5p14.1 associate with autism spectrum disorders

scientific article

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

scientific article

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

scientific article

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

scientific article published on 10 July 2009

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

scientific article

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

article

Copy number variation at 1q21.1 associated with neuroblastoma

scientific article

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

scientific article

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

scientific journal article

Variants of DENND1B associated with asthma in children

scientific article

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

scientific article

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

scientific article

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

scientific article

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

scientific article

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

scientific article

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

scientific article

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

scientific article

A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci

scientific journal article

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

scientific article

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

scientific article

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

scientific article published on 2 December 2012

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

scientific article

From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.

scientific article

Relation of alleles of the collagen type Ialpha1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women

scientific article published on 01 April 1998

Genome-wide associations for birth weight and correlations with adult disease

scientific article

Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.

scientific article

Strong synaptic transmission impact by copy number variations in schizophrenia

scientific article

The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI

scientific article

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

scientific article published on 24 November 2015

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

scientific article

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

scientific article

A genome-wide association study on obesity and obesity-related traits

scientific article published on 28 April 2011

Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes

scientific article

A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study

scientific article

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

scientific article

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.

scientific article

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

scientific article

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 22 December 2017

Genome-wide association of body fat distribution in African ancestry populations suggests new loci

scientific article

Common variants at 12q15 and 12q24 are associated with infant head circumference

scientific article published on 15 April 2012

Directional dominance on stature and cognition in diverse human populations

scientific article published in July 2015

The genetics of human obesity

article

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

scientific article

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

scientific article

Role of BMI‐Associated Loci Identified in GWAS Meta‐Analyses in the Context of Common Childhood Obesity in European Americans

scientific article published on July 21, 2011

The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the β-Cell–Centric Classification Schema

scientific article published on February 1, 2016

List of works by Struan F.A. Grant

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

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Common genetic variants on 5p14.1 associate with autism spectrum disorders

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

Copy number variation at 1q21.1 associated with neuroblastoma

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

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

Variants of DENND1B associated with asthma in children

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.

Relation of alleles of the collagen type Ialpha1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women

Genome-wide associations for birth weight and correlations with adult disease

Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.

Strong synaptic transmission impact by copy number variations in schizophrenia

The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

A genome-wide association study on obesity and obesity-related traits

Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes

A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Genome-wide association of body fat distribution in African ancestry populations suggests new loci

Common variants at 12q15 and 12q24 are associated with infant head circumference

Directional dominance on stature and cognition in diverse human populations

The genetics of human obesity

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

Role of BMI‐Associated Loci Identified in GWAS Meta‐Analyses in the Context of Common Childhood Obesity in European Americans

The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the β-Cell–Centric Classification Schema