Lista de obras -

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

artículo científico publicado en 2007

A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changes

artículo científico publicado en 2010

Analysis of neuropeptide S receptor gene (NPSR1) polymorphism in rheumatoid arthritis

artículo científico publicado en 2010

Assessment of the neuropeptide S system in anxiety disorders

artículo científico publicado en 2010

Association of TNFSF15 polymorphism with irritable bowel syndrome

artículo científico publicado en 2011

Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families

article

Characterization of a common susceptibility locus for asthma-related traits

artículo científico publicado en 2004

Evidence for genetic association and interaction between the TYK2 and IRF5 genes in systemic lupus erythematosus

artículo científico publicado en 2009

Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts

artículo científico publicado en 2014

Expression analysis of the NLRP gene family suggests a role in human preimplantation development

artículo científico publicado en 2008

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene

artículo científico publicado en 2004

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

artículo científico publicado en 2009

Gene mapping with pooled samples on three genotyping platforms

artículo científico publicado en 2005

Genetic Susceptibility to Inflammation is Associated With Colonic Transit and Other Intermediate Phenotypes in Irritable Bowel Syndrome

artículo científico publicado en 2011

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

artículo científico publicado en 2013

Germline genetic contributions to risk for esophageal adenocarcinoma, Barrett's esophagus, and gastroesophageal reflux

artículo científico publicado en 2013

Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes

artículo científico publicado en 2005

Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE)

artículo científico publicado en 2009

In Vivo Differentiated Human Embryonic Stem Cells Can Acquire Chromosomal Aberrations More Frequently Than In Vitro During the Same Period

article

Interactions between glutathione S-transferase P1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease

artículo científico publicado en 2008

Large-Scale Zygosity Testing Using Single Nucleotide Polymorphisms

article by Ulf Hannelius et al published August 2007 in Twin Research and Human Genetics

Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1).

artículo científico publicado en 2011

Neuropeptide S receptor induces neuropeptide expression and associates with intermediate phenotypes of functional gastrointestinal disorders

artículo científico publicado en 2009

Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease

artículo científico publicado en 2007

No association between the eczema genes COL29A1 and IL31 and inflammatory bowel disease

artículo científico publicado en 2009

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease

artículo científico publicado en 2009

Perturbations of heart development and function in cardiomyocytes from human embryonic stem cells with trisomy 21.

artículo científico publicado en 2015

Potential role for the common cystic fibrosis ΔF508 mutation in Crohnʼs disease

artículo científico publicado en 2007

Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population

artículo científico

SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.

artículo científico publicado en 2011

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

artículo científico publicado en 2005

The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language

artículo científico publicado en 2012

The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus

artículo científico publicado en 2007

Transcriptome profiling of human pre-implantation development

artículo científico publicado en 2009

Variation in STAT4 is associated with systemic lupus erythematosus in a Finnish family cohort

artículo científico publicado en 2009

Lista de obras de

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changes

Analysis of neuropeptide S receptor gene (NPSR1) polymorphism in rheumatoid arthritis

Assessment of the neuropeptide S system in anxiety disorders

Association of TNFSF15 polymorphism with irritable bowel syndrome

Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families

Characterization of a common susceptibility locus for asthma-related traits

Evidence for genetic association and interaction between the TYK2 and IRF5 genes in systemic lupus erythematosus

Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts

Expression analysis of the NLRP gene family suggests a role in human preimplantation development

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

Gene mapping with pooled samples on three genotyping platforms

Genetic Susceptibility to Inflammation is Associated With Colonic Transit and Other Intermediate Phenotypes in Irritable Bowel Syndrome

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

Germline genetic contributions to risk for esophageal adenocarcinoma, Barrett's esophagus, and gastroesophageal reflux

Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes

Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE)

In Vivo Differentiated Human Embryonic Stem Cells Can Acquire Chromosomal Aberrations More Frequently Than In Vitro During the Same Period

Interactions between glutathione S-transferase P1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease

Large-Scale Zygosity Testing Using Single Nucleotide Polymorphisms

Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1).

Neuropeptide S receptor induces neuropeptide expression and associates with intermediate phenotypes of functional gastrointestinal disorders

Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease

No association between the eczema genes COL29A1 and IL31 and inflammatory bowel disease

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease

Perturbations of heart development and function in cardiomyocytes from human embryonic stem cells with trisomy 21.

Potential role for the common cystic fibrosis ΔF508 mutation in Crohnʼs disease

Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population

SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language

The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus

Transcriptome profiling of human pre-implantation development

Variation in STAT4 is associated with systemic lupus erythematosus in a Finnish family cohort