Lista de obras -

Active immunisation targeting nerve growth factor attenuates chronic pain behaviour in murine osteoarthritis.

artículo científico publicado en 2019

Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci

artículo científico publicado en 2016

Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations

artículo científico publicado en 2015

Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank

artículo científico publicado en 2017

Bayesian meta-analysis across genome-wide association studies of diverse phenotypes

scientific article published on 28 March 2019

Class II HLA interactions modulate genetic risk for multiple sclerosis

artículo científico publicado en 2015

Comparison of LABORAS with static incapacitance testing for assessing spontaneous pain behaviour in surgically-induced murine osteoarthritis

artículo científico publicado en 2020

Constructing custom-made radiotranscriptomic signatures of vascular inflammation from routine CT angiograms: a prospective outcomes validation study in COVID-19

artículo científico publicado en 2022

Correction: Imputation-Based Meta-Analysis of Severe Malaria in Three African Populations.

artículo científico publicado en 2013

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

correction of a scientific article; published on 30 May 2019

Defective tumor necrosis factor release from Crohn's disease macrophages in response to Toll-like receptor activation: relationship to phenotype and genome-wide association susceptibility loci

artículo científico publicado en 2012

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis

artículo científico publicado en 2012

Dispatches from the functional phase of genome biology

artículo científico publicado en 2012

Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.

artículo científico publicado en 2017

Fine-mapping inflammatory bowel disease loci to single-variant resolution

artículo científico publicado en 2017

GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome

publication published on 08 December 2021

Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families

artículo científico publicado en 2016

Genetic risk prediction in complex disease

artículo científico publicado en 2011

Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.

artículo científico publicado en 2017

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

article

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.

artículo científico publicado en 2017

Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

artículo científico publicado en 2016

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

artículo científico publicado en 2010

Genomic profiling of T cell activation reveals dependency of memory T cells on CD28 costimulation

Genomic profiling of T-cell activation suggests increased sensitivity of memory T cells to CD28 costimulation

artículo científico publicado en 2020

Graphical Model Selection for Gaussian Conditional Random Fields in the Presence of Latent Variables

scientific article published on 11 July 2018

High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis

artículo científico publicado en 2015

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

artículo científico publicado en 2012

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

artículo científico publicado en 2011

Imputation-based meta-analysis of severe malaria in three African populations

artículo científico publicado en 2013

Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study

artículo científico publicado en 2015

Innate immune activity conditions the effect of regulatory variants upon monocyte gene expression

artículo científico publicado en 2014

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

artículo científico publicado en 2018

Microindel detection in short-read sequence data

artículo científico publicado en 2010

Misuse of hierarchical linear models overstates the significance of a reported association between OXTR and prosociality

artículo científico publicado en 2012

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

artículo científico publicado en 2013

Next-generation sequencing and the era of personal Y genomes.

artículo científico publicado en 2010

Resolving TYK2 locus genotype-to-phenotype differences in autoimmunity

artículo científico publicado en 2016

Reverse engineering a gene network using an asynchronous parallel evolution strategy

artículo científico publicado en 2010

Trinculo: Bayesian and frequentist multinomial logistic regression for genome-wide association studies of multi-category phenotypes

artículo científico publicado en 2016

Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments

artículo científico publicado en 2013

Lista de obras de

Active immunisation targeting nerve growth factor attenuates chronic pain behaviour in murine osteoarthritis.

Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci

Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations

Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank

Bayesian meta-analysis across genome-wide association studies of diverse phenotypes

Class II HLA interactions modulate genetic risk for multiple sclerosis

Comparison of LABORAS with static incapacitance testing for assessing spontaneous pain behaviour in surgically-induced murine osteoarthritis

Constructing custom-made radiotranscriptomic signatures of vascular inflammation from routine CT angiograms: a prospective outcomes validation study in COVID-19

Correction: Imputation-Based Meta-Analysis of Severe Malaria in Three African Populations.

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Defective tumor necrosis factor release from Crohn's disease macrophages in response to Toll-like receptor activation: relationship to phenotype and genome-wide association susceptibility loci

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis

Dispatches from the functional phase of genome biology

Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.

Fine-mapping inflammatory bowel disease loci to single-variant resolution

GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome

Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families

Genetic risk prediction in complex disease

Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.

Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Genomic profiling of T cell activation reveals dependency of memory T cells on CD28 costimulation

Genomic profiling of T-cell activation suggests increased sensitivity of memory T cells to CD28 costimulation

Graphical Model Selection for Gaussian Conditional Random Fields in the Presence of Latent Variables

High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

Imputation-based meta-analysis of severe malaria in three African populations

Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study

Innate immune activity conditions the effect of regulatory variants upon monocyte gene expression

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Microindel detection in short-read sequence data

Misuse of hierarchical linear models overstates the significance of a reported association between OXTR and prosociality

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

Next-generation sequencing and the era of personal Y genomes.

Resolving TYK2 locus genotype-to-phenotype differences in autoimmunity

Reverse engineering a gene network using an asynchronous parallel evolution strategy

Trinculo: Bayesian and frequentist multinomial logistic regression for genome-wide association studies of multi-category phenotypes

Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments