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A Haplotype-Based Analysis of the PTPN22 Locus in Type 1 Diabetes

article

A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes

artículo científico publicado en 2014

A high frequency of distinct ATM gene mutations in ataxia-telangiectasia

artículo científico publicado en 1996

A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples

artículo científico publicado en 2014

A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations

artículo científico publicado en 2014

Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk

artículo científico publicado en 2015

Cytomegalovirus infection enhances the immune response to influenza.

artículo científico publicado en 2015

Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians

artículo científico publicado en 2000

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

artículo científico publicado en 2011

Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis.

artículo científico publicado en 2013

Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.

artículo científico publicado en 2013

Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping

artículo científico publicado en 2015

ELMO1 signaling is a promoter of osteoclast function and bone loss

artículo científico publicado en 2021

Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes

artículo científico publicado en 2018

Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes

artículo científico publicado en 2021

Genetic Contribution to the Divergence in Type 1 Diabetes Risk Between Children From the General Population and Children From Affected Families

artículo científico publicado en 2019

Genome-wide association study of subclinical interstitial lung disease in MESA.

artículo científico publicado en 2017

Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32

artículo científico publicado en 2004

In situ 10-cell RNA sequencing in tissue and tumor biopsy samples

artículo científico publicado en 2019

Neuromedin B expression defines the mouse retrotrapezoid nucleus.

artículo científico publicado en 2017

Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes

artículo científico publicado en 2015

Plasma Soluble Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis

artículo científico publicado en 2017

Systems genetics in diversity outbred mice inform BMD GWAS and identify determinants of bone strength

artículo científico publicado en 2021

Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score

scientific article published on 18 January 2019

Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship.

artículo científico publicado en 2012

Lista de obras de

A Haplotype-Based Analysis of the PTPN22 Locus in Type 1 Diabetes

A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes

A high frequency of distinct ATM gene mutations in ataxia-telangiectasia

A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples

A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations

Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk

Cytomegalovirus infection enhances the immune response to influenza.

Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis.

Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.

Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping

ELMO1 signaling is a promoter of osteoclast function and bone loss

Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes

Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes

Genetic Contribution to the Divergence in Type 1 Diabetes Risk Between Children From the General Population and Children From Affected Families

Genome-wide association study of subclinical interstitial lung disease in MESA.

Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32

In situ 10-cell RNA sequencing in tissue and tumor biopsy samples

Neuromedin B expression defines the mouse retrotrapezoid nucleus.

Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes

Plasma Soluble Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis

Systems genetics in diversity outbred mice inform BMD GWAS and identify determinants of bone strength

Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score

Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship.