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 Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.

artículo científico publicado en 2017

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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

artículo científico publicado en 2014

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

artículo científico publicado en 2008

A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity

scientific article published on 01 October 2019

A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius.

artículo científico publicado en 2015

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

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

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 12q15 and 12q24 are associated with infant head circumference

artículo científico publicado en 2012

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

artículo científico publicado en 2009

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

artículo científico publicado en 2009

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

artículo científico publicado en 2010

Copy number variation at 1q21.1 associated with neuroblastoma

artículo científico publicado en 2009

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

artículo científico publicado en 2017

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

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

scholarly article published in Nature 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

First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes

artículo científico publicado en 2018

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

artículo científico publicado en 2008

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

artículo científico publicado en 2009

GATA factors promote ER integrity and β-cell survival and contribute to type 1 diabetes risk.

artículo científico publicado en 2013

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

artículo científico publicado en 2019

Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC

scientific article published on 16 December 2019

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2009

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Genome-wide associations for birth weight and correlations with adult 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

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

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

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

artículo científico publicado en 2019

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

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

artículo científico publicado en 2012

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

artículo científico publicado en 2020

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

artículo científico publicado en 2008

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

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

artículo científico publicado en 2018

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

artículo científico publicado en 2019

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

scientific article published on 14 January 2020

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

The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

artículo científico publicado en 2019

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 Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.

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

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

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

A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity

A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius.

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

Associations of autozygosity with a broad range of human phenotypes

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 12q15 and 12q24 are associated with infant head circumference

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

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

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

Copy number variation at 1q21.1 associated with neuroblastoma

Directional dominance on stature and cognition in diverse human populations

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

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

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

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.

First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes

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

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

GATA factors promote ER integrity and β-cell survival and contribute to type 1 diabetes risk.

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC

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

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

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

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

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

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

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.

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

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

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

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

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

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

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

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

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

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

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

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

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

The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis

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

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

Variants of DENND1B associated with asthma in children