Lista de obras - An Goris - Dominio Público Uruguay

A Dinucleotide Repeat Polymorphism Located in the IFN-α/β Gene Cluster at Chromosome 9p22 Is Not Associated with Multiple Sclerosis in Sardinia

article

A Taqman assay for high-throughput genotyping of the multiple sclerosis-associated HLA-DRB1*1501 allele

artículo científico publicado en 2008

A robust pipeline with high replication rate for detection of somatic variants in the adaptive immune system as a source of common genetic variation in autoimmune disease

scientific article published on 01 April 2019

A second major histocompatibility complex susceptibility locus for multiple sclerosis

artículo científico publicado en 2007

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.

artículo científico publicado en 2012

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

artículo científico publicado en 2016

Analysis of an IFN- gamma gene (IFNG) Polymorphism in Multiple Sclerosis in Europe: Effect of Population Structure on Association with Disease

article

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

artículo científico publicado en 2013

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study

artículo científico publicado en 2014

Apolipoprotein E genotype as a risk factor for susceptibility to and dementia in Parkinson's disease

artículo científico publicado en 2009

Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients

artículo científico publicado en 2013

Association of the human leucocyte antigen region with susceptibility to Parkinson's disease

artículo científico publicado en 2010

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

artículo científico publicado en 2007

Author Correction: The cellular composition of the human immune system is shaped by age and cohabitation

artículo científico publicado en 2020

Burden of risk variants correlates with phenotype of multiple sclerosis

artículo científico publicado en 2015

CD24 Ala/Val polymorphism and multiple sclerosis

artículo científico publicado en 2006

CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity

scientific article published on 08 February 2020

Chromosome 7q21–22 and multiple sclerosis: evidence for a genetic susceptibility effect in vicinity to the protachykinin-1 gene

article

Class II HLA interactions modulate genetic risk for multiple sclerosis

artículo científico publicado en 2015

Comment: the HLA region in multiple sclerosis.

artículo científico publicado en 2012

Cytokine gene polymorphisms in multifactorial diseases: gateways to novel targets for immunotherapy?

artículo científico publicado en 2003

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

artículo científico publicado en 2012

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation. ⬇️

artículo científico publicado en 2016

Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study

artículo científico publicado en 2013

Gelatinase B, PECAM-1 and MCP-3 gene polymorphisms in Belgian multiple sclerosis

article

Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators

article by Vasiliki Lagou et al published 16 October 2018 in Cell Reports

Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice

artículo científico publicado en 2016

Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation

artículo científico publicado en 2018

Genetic burden mirrors epidemiology of multiple sclerosis

artículo científico publicado en 2015

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

artículo científico publicado en 2017

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

artículo científico publicado en 2011

Genetic variants are major determinants of CSF antibody levels in multiple sclerosis

artículo científico publicado en 2015

Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis

artículo científico publicado en 2012

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

artículo científico publicado en 2016

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

artículo científico publicado en 2007

HERV-K113 Is Not Associated with Multiple Sclerosis in a Large Family-Based Study

scientific article published on 01 March 2008

HLA-DRB1 and multiple sclerosis in Malta

artículo científico publicado en 2007

HLA-E restricted CD8+ T cell subsets are phenotypically altered in multiple sclerosis patients.

artículo científico publicado en 2013

High-resolution analysis of IL-6 minisatellite polymorphism in Sardinian multiple sclerosis: effect on course and onset of disease

article

IFN-γ stimulates CpG-induced IL-10 production in B cells via p38 and JNK signalling pathways

scientific article published on 01 August 2018

IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosis

artículo científico publicado en 2005

Immunologic profiles of multiple sclerosis treatments reveal shared early B cell alterations

artículo científico publicado en 2016

Inflammatory Gene Expression Profile and Defective Interferon-γ and Granzyme K in Natural Killer Cells From Systemic Juvenile Idiopathic Arthritis Patients

artículo científico publicado en 2016

Interferon gamma gene in rheumatoid arthritis

artículo científico publicado en 2000

Interferon-? gene polymorphism-associated risk for multiple sclerosis in sardinia

article

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis

artículo científico publicado en 2007

Interleukin-12 p40 polymorphism and susceptibility to multiple sclerosis

scientific article published on 01 October 2002

Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson’s disease

article

KIR2DL4 (CD158d) polymorphisms and susceptibility to multiple sclerosis.

artículo científico publicado en 2009

Lack of association between variants in theVKORC1gene and cerebrovascular or coronary heart disease

article

Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis

artículo científico publicado en 2010

Leveraging human genetics to inform intervention strategies for multiple sclerosis

artículo científico publicado en 2019

Linkage disequilibrium analysis of chromosome 12q14-15 in multiple sclerosis: delineation of a 118-kb interval around interferon-gamma (IFNG) that is involved in male versus female differential susceptibility.

artículo científico publicado en 2002

Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans

artículo científico publicado en 2006

LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients

scientific article published on 27 August 2018

Low frequency and rare coding variation contributes to multiple sclerosis risk

Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes

artículo científico publicado en 2019

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.

artículo científico publicado en 2014

Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells

artículo científico publicado en 2018

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

scientific article published on 27 March 2019

New candidate loci for multiple sclerosis susceptibility revealed by a whole genome association screen in a Belgian population

artículo científico publicado en 2003

No alterations in α-synuclein gene dosage observed in sporadic Parkinson's disease

article

No evidence for a role of rareCYP27B1functional variations in multiple sclerosis

artículo científico publicado en 2013

No evidence for association between an MAOA functional polymorphism and susceptibility to Parkinson's disease.

artículo científico publicado en 2009

No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis

scientific article published on 31 May 2006

No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

artículo científico publicado en 2006

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

artículo científico publicado en 2013

Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency

artículo científico publicado en 2013

Novel Olig 1-coding variants and susceptibility to multiple sclerosis

artículo científico publicado en 2006

Novel polymorphisms in the IL-10 related AK155 gene (chromosome 12q15)

artículo científico publicado en 2001

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis

artículo científico publicado en 2010

Polymorphisms in the interferon-gamma/interleukin-26 gene region contribute to sex bias in susceptibility to rheumatoid arthritis

artículo científico publicado en 2003

Polymorphisms in the interleukin-4 and IL-4 receptor genes and multiple sclerosis: a study in Spanish-Basque, Northern Irish and Belgian populations

article

Polymorphisms in the neuromyelitis optica auto-antigen AQP4 and susceptibility to multiple sclerosis

artículo científico publicado en 2007

Power estimation for non-standardized multisite studies

artículo científico publicado en 2016

Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort.

artículo científico publicado en 2006

Progress in multiple sclerosis genetics

artículo científico publicado en 2012

Rare MEFV variants are not associated with risk to develop multiple sclerosis and severity of disease

artículo científico publicado en 2013

Refining genetic associations in multiple sclerosis

artículo científico publicado en 2008

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

scientific article published on 18 March 2009

Replication of KIF21B as a susceptibility locus for multiple sclerosis

artículo científico publicado en 2010

Reply to Dr Pandey

artículo científico publicado en 2013

SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis

scientific article published on 27 October 2005

Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with Amyotrophic Lateral Sclerosis

artículo científico publicado en 2018

Smoking and multiple sclerosis risk: a Mendelian randomization study

artículo científico publicado en 2020

TDP-43 M311V mutation in familial amyotrophic lateral sclerosis.

artículo científico publicado en 2009

TNFRSF1A coding variants in multiple sclerosis

artículo científico publicado en 2011

Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's disease

artículo científico publicado en 2007

Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouse.

artículo científico publicado en 2010

The cellular composition of the human immune system is shaped by age and cohabitation.

artículo científico publicado en 2016

The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort

artículo científico

The immunogenetic architecture of autoimmune disease

artículo científico

The occurrence of mutations inFUSin a Belgian cohort of patients with familial ALS

article

The origins of diversity in human immunity

scientific article published on 01 March 2018

The role of the CD58 locus in multiple sclerosis

artículo científico publicado en 2009

The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases

article

Transcript-specific regulation in T-cells in multiple sclerosis susceptibility

artículo científico publicado en 2020

Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke

artículo científico publicado en 2009

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

artículo científico publicado en 2012

“Omics” and the immunopathogenesis of multiple sclerosis

artículo científico publicado en 2011

Lista de obras de An Goris

A Dinucleotide Repeat Polymorphism Located in the IFN-α/β Gene Cluster at Chromosome 9p22 Is Not Associated with Multiple Sclerosis in Sardinia

A Taqman assay for high-throughput genotyping of the multiple sclerosis-associated HLA-DRB1*1501 allele

A robust pipeline with high replication rate for detection of somatic variants in the adaptive immune system as a source of common genetic variation in autoimmune disease

A second major histocompatibility complex susceptibility locus for multiple sclerosis

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

Analysis of an IFN- gamma gene (IFNG) Polymorphism in Multiple Sclerosis in Europe: Effect of Population Structure on Association with Disease

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study

Apolipoprotein E genotype as a risk factor for susceptibility to and dementia in Parkinson's disease

Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients

Association of the human leucocyte antigen region with susceptibility to Parkinson's disease

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Author Correction: The cellular composition of the human immune system is shaped by age and cohabitation

Burden of risk variants correlates with phenotype of multiple sclerosis

CD24 Ala/Val polymorphism and multiple sclerosis

CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity

Chromosome 7q21–22 and multiple sclerosis: evidence for a genetic susceptibility effect in vicinity to the protachykinin-1 gene

Class II HLA interactions modulate genetic risk for multiple sclerosis

Comment: the HLA region in multiple sclerosis.

Cytokine gene polymorphisms in multifactorial diseases: gateways to novel targets for immunotherapy?

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation. ⬇️

Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study

Gelatinase B, PECAM-1 and MCP-3 gene polymorphisms in Belgian multiple sclerosis

Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators

Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice

Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation

Genetic burden mirrors epidemiology of multiple sclerosis

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

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

Genetic variants are major determinants of CSF antibody levels in multiple sclerosis

Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

HERV-K113 Is Not Associated with Multiple Sclerosis in a Large Family-Based Study

HLA-DRB1 and multiple sclerosis in Malta

HLA-E restricted CD8+ T cell subsets are phenotypically altered in multiple sclerosis patients.

High-resolution analysis of IL-6 minisatellite polymorphism in Sardinian multiple sclerosis: effect on course and onset of disease

IFN-γ stimulates CpG-induced IL-10 production in B cells via p38 and JNK signalling pathways

IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosis

Immunologic profiles of multiple sclerosis treatments reveal shared early B cell alterations

Inflammatory Gene Expression Profile and Defective Interferon-γ and Granzyme K in Natural Killer Cells From Systemic Juvenile Idiopathic Arthritis Patients

Interferon gamma gene in rheumatoid arthritis

Interferon-? gene polymorphism-associated risk for multiple sclerosis in sardinia

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis

Interleukin-12 p40 polymorphism and susceptibility to multiple sclerosis

Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson’s disease

KIR2DL4 (CD158d) polymorphisms and susceptibility to multiple sclerosis.

Lack of association between variants in theVKORC1gene and cerebrovascular or coronary heart disease

Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis

Leveraging human genetics to inform intervention strategies for multiple sclerosis

Linkage disequilibrium analysis of chromosome 12q14-15 in multiple sclerosis: delineation of a 118-kb interval around interferon-gamma (IFNG) that is involved in male versus female differential susceptibility.

Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans

LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients

Low frequency and rare coding variation contributes to multiple sclerosis risk

Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.

Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

New candidate loci for multiple sclerosis susceptibility revealed by a whole genome association screen in a Belgian population

No alterations in α-synuclein gene dosage observed in sporadic Parkinson's disease

No evidence for a role of rareCYP27B1functional variations in multiple sclerosis

No evidence for association between an MAOA functional polymorphism and susceptibility to Parkinson's disease.

No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis

No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency

Novel Olig 1-coding variants and susceptibility to multiple sclerosis

Novel polymorphisms in the IL-10 related AK155 gene (chromosome 12q15)

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis

Polymorphisms in the interferon-gamma/interleukin-26 gene region contribute to sex bias in susceptibility to rheumatoid arthritis

Polymorphisms in the interleukin-4 and IL-4 receptor genes and multiple sclerosis: a study in Spanish-Basque, Northern Irish and Belgian populations

Polymorphisms in the neuromyelitis optica auto-antigen AQP4 and susceptibility to multiple sclerosis

Power estimation for non-standardized multisite studies

Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort.

Progress in multiple sclerosis genetics

Rare MEFV variants are not associated with risk to develop multiple sclerosis and severity of disease

Refining genetic associations in multiple sclerosis