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 KIAA0350 as a type 1 diabetes gene

artículo científico publicado en 2007

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

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

artículo científico publicado en 2008

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

artículo científico publicado en 2008

Association analysis of type 2 diabetes Loci in type 1 diabetes.

artículo científico publicado en 2008

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.

artículo científico publicado en 2009

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

artículo científico publicado en 2007

Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis

scientific article published on 01 July 2008

Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease

artículo científico publicado en 2007

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

artículo científico publicado en 2009

BMD-associated variation at the Osterix locus is correlated with childhood obesity in females

artículo científico publicado en 2011

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

artículo científico publicado en 2008

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

artículo científico publicado en 2009

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

scientific journal article

Common variants at five new loci associated with early-onset inflammatory bowel disease

artículo científico publicado en 2009

Common variants in HSPB7 and FRMD4B associated with advanced heart failure

artículo científico publicado en 2010

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

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

artículo científico publicado en 2010

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

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

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

artículo científico publicado en 2008

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

artículo científico publicado en 2011

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

artículo científico publicado en 2009

In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics Consortium.

artículo científico publicado en 2010

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

artículo científico publicado en 2010

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

artículo científico publicado en 2009

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

artículo científico publicado en 2008

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

artículo científico publicado en 2010

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 missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry.

artículo científico publicado en 2013

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

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 KIAA0350 as a type 1 diabetes gene

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

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

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

Association analysis of type 2 diabetes Loci in type 1 diabetes.

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis

Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease

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

BMD-associated variation at the Osterix locus is correlated with childhood obesity in females

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

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

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

Common variants at five new loci associated with early-onset inflammatory bowel disease

Common variants in HSPB7 and FRMD4B associated with advanced heart failure

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

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

Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

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

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.

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

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

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

In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics Consortium.

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

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

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

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

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

Strong synaptic transmission impact by copy number variations in schizophrenia

The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry.

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