Lista de obras -

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

article

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

artículo científico publicado en 2009

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

scientific journal article

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

scientific journal article

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

artículo científico publicado en 2017

Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies

artículo científico publicado en 2015

Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy

artículo científico publicado en 2015

Copy number variations in alternative splicing gene networks impact lifespan

artículo científico publicado en 2013

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

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

artículo científico publicado en 2017

Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

artículo científico publicado en 2009

Examination of genetic variants influencing lipid traits in pediatric populations.

artículo científico publicado en 2012

Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

artículo científico publicado en 2009

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

artículo científico publicado en 2015

Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry

artículo científico publicado en 2009

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

artículo científico publicado en 2008

Strong synaptic transmission impact by copy number variations in schizophrenia

artículo científico publicado en 2010

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

artículo científico publicado en 2014

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

artículo científico publicado en 2016

Variants of DENND1B associated with asthma in children

artículo científico publicado en 2009

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

artículo científico publicado en 2013

Lista de obras de

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

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

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

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies

Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy

Copy number variations in alternative splicing gene networks impact lifespan

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

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

Examination of genetic variants influencing lipid traits in pediatric populations.

Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.

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

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry

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

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

Strong synaptic transmission impact by copy number variations in schizophrenia

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

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

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

Variants of DENND1B associated with asthma in children

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement