Lista de obras -

A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis

artículo científico publicado en 2011

A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome

artículo científico publicado en 2015

A second major histocompatibility complex susceptibility locus for multiple sclerosis

artículo científico publicado en 2007

A specific amino acid motif of mediates risk and interacts with smoking history in Parkinson's disease

scientific article published on 25 March 2019

A splice acceptor variant in HLA-DRA affects the conformation and cellular localization of the class II DR alpha-chain

artículo científico publicado en 2020

Abrogation of T cell quiescence characterizes patients at high risk for multiple sclerosis after the initial neurological event

artículo científico publicado en 2008

Aggregation of multiple sclerosis genetic risk variants in multiple and single case families

artículo científico publicado en 2011

An ImmunoChip study of multiple sclerosis risk in African Americans

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Association Between Serum Neurofilament Light Chain Levels and Long-term Disease Course Among Patients With Multiple Sclerosis Followed up for 12 Years

artículo científico publicado en 2019

Association of HLA Genetic Risk Burden With Disease Phenotypes in Multiple Sclerosis

artículo científico publicado en 2016

Ataxin-1 regulates B cell function and the severity of autoimmune experimental encephalomyelitis

scientific article published on 02 September 2020

Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls

artículo científico publicado en 2013

CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis

artículo científico publicado en 2010

Cell type-specific transcriptomics identifies neddylation as a novel therapeutic target in multiple sclerosis

artículo científico publicado en 2020

Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: a descriptive study.

artículo científico publicado en 2006

Complex gene–gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes

article

Copy number variation in African Americans

artículo científico publicado en 2009

Copy number variation in pediatric multiple sclerosis

artículo científico

Correction: Synergy or Independence? Deciphering the Interaction of HLA Class I and NK Cell KIR Alleles in Early HIV-1 Disease Progression.

artículo científico publicado en 2007

Deconstruction of HLA-DRB104:01:01 and HLA-DRB115:01:01 class II haplotypes using next-generation sequencing in European-Americans with multiple sclerosis

artículo científico publicado en 2018

Evaluating the genomic and sequence integrity of human ES cell lines; comparison to normal genomes

artículo científico publicado en 2011

Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS.

artículo científico publicado en 2017

Genetic risk factors for pediatric-onset multiple sclerosis

artículo científico publicado en 2017

Genetic risk variants in African Americans with multiple sclerosis

artículo científico publicado en 2013

Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis

artículo científico publicado en 2008

Genetic variation in the odorant receptors family 13 and the mhc loci influence mate selection in a multiple sclerosis dataset

artículo científico publicado en 2010

Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis

artículo científico publicado en 2018

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

artículo científico publicado en 2010

Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis

scientific journal article

Genome-wide network analysis reveals the global properties of IFN-beta immediate transcriptional effects in humans

artículo científico

Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis.

artículo científico publicado en 2008

Genotype-Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1HMR spectroscopy and MRI measures

artículo científico publicado en 2008

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

artículo científico publicado en 2007

Killer Cell Immunoglobulin-like Receptor Variants Are Associated with Protection from Symptoms Associated with More Severe Course in Parkinson Disease

artículo científico publicado en 2020

Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis

artículo científico publicado en 2004

Long-term evolution of multiple sclerosis disability in the treatment era.

artículo científico publicado en 2016

Low frequency and rare coding variation contributes to multiple sclerosis risk

MIF and D-DT are potential disease severity modifiers in male MS subjects

artículo científico publicado en 2017

Mitochondrial DNA sequence variation in multiple sclerosis.

artículo científico publicado en 2015

Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans

artículo científico publicado en 2006

Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies

artículo científico publicado en 2016

Multiple sclerosis susceptibility alleles in African Americans.

artículo científico publicado en 2009

Next-generation sequencing reveals new information about HLA allele and haplotype diversity in a large European American population

scientific article published on 22 July 2019

No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis

artículo científico publicado en 2013

Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis

artículo científico publicado en 2013

Opposite roles of NMDA receptors in relapsing and primary progressive multiple sclerosis

artículo científico publicado en 2013

Osteopontin polymorphisms and disease course in multiple sclerosis

artículo científico publicado en 2003

PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients

artículo científico publicado en 2001

Pharmacogenomic analysis of interferon receptor polymorphisms in multiple sclerosis.

artículo científico publicado en 2003

Prognostic biomarkers of IFNb therapy in multiple sclerosis patients

artículo científico publicado en 2014

Quantitative longitudinal analysis of T cell receptor repertoire expression in HIV-infected patients on antiretroviral and interleukin-2 therapy

artículo científico publicado en 2007

Refining the association of MHC with multiple sclerosis in African Americans

artículo científico publicado en 2010

SNP imputation bias reduces effect size determination

artículo científico publicado en 2015

SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients

artículo científico publicado en 2011

Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility

artículo científico publicado en 2001

Sex-specific Tau methylation patterns and synaptic transcriptional alterations are associated with neural vulnerability during chronic neuroinflammation

scientific article published on 19 April 2019

Synergy or independence? Deciphering the interaction of HLA Class I and NK cell KIR alleles in early HIV-1 disease progression

artículo científico publicado en 2007

Telomere Length Is Associated with Disability Progression in Multiple Sclerosis

scientific article published on 02 October 2019

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

scholarly article published 13 July 2017

The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis

artículo científico publicado en 2005

The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis

scientific article published on 08 October 2007

The killer immunoglobulin-like receptor KIR3DL1 in combination with HLA-Bw4 is protective against multiple sclerosis in African Americans

artículo científico publicado en 2016

Transcription-based prediction of response to IFNbeta using supervised computational methods

artículo científico publicado en 2005

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis

artículo científico publicado en 2008

miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS

scientific article published on 15 May 2019

Lista de obras de

A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis

A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome

A second major histocompatibility complex susceptibility locus for multiple sclerosis

A specific amino acid motif of mediates risk and interacts with smoking history in Parkinson's disease

A splice acceptor variant in HLA-DRA affects the conformation and cellular localization of the class II DR alpha-chain

Abrogation of T cell quiescence characterizes patients at high risk for multiple sclerosis after the initial neurological event

Aggregation of multiple sclerosis genetic risk variants in multiple and single case families

An ImmunoChip study of multiple sclerosis risk in African Americans

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

Association Between Serum Neurofilament Light Chain Levels and Long-term Disease Course Among Patients With Multiple Sclerosis Followed up for 12 Years

Association of HLA Genetic Risk Burden With Disease Phenotypes in Multiple Sclerosis

Ataxin-1 regulates B cell function and the severity of autoimmune experimental encephalomyelitis

Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls

CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis

Cell type-specific transcriptomics identifies neddylation as a novel therapeutic target in multiple sclerosis

Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: a descriptive study.

Complex gene–gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes

Copy number variation in African Americans

Copy number variation in pediatric multiple sclerosis

Correction: Synergy or Independence? Deciphering the Interaction of HLA Class I and NK Cell KIR Alleles in Early HIV-1 Disease Progression.

Deconstruction of HLA-DRB1*04:01:01 and HLA-DRB1*15:01:01 class II haplotypes using next-generation sequencing in European-Americans with multiple sclerosis

Evaluating the genomic and sequence integrity of human ES cell lines; comparison to normal genomes

Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS.

Genetic risk factors for pediatric-onset multiple sclerosis

Genetic risk variants in African Americans with multiple sclerosis

Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis

Genetic variation in the odorant receptors family 13 and the mhc loci influence mate selection in a multiple sclerosis dataset

Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis

Genome-wide network analysis reveals the global properties of IFN-beta immediate transcriptional effects in humans

Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis.

Genotype-Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1HMR spectroscopy and MRI measures

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

Killer Cell Immunoglobulin-like Receptor Variants Are Associated with Protection from Symptoms Associated with More Severe Course in Parkinson Disease

Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis

Long-term evolution of multiple sclerosis disability in the treatment era.

Low frequency and rare coding variation contributes to multiple sclerosis risk

MIF and D-DT are potential disease severity modifiers in male MS subjects

Mitochondrial DNA sequence variation in multiple sclerosis.

Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans

Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies

Multiple sclerosis susceptibility alleles in African Americans.

Next-generation sequencing reveals new information about HLA allele and haplotype diversity in a large European American population

No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis

Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis

Opposite roles of NMDA receptors in relapsing and primary progressive multiple sclerosis

Osteopontin polymorphisms and disease course in multiple sclerosis

PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients

Pharmacogenomic analysis of interferon receptor polymorphisms in multiple sclerosis.

Prognostic biomarkers of IFNb therapy in multiple sclerosis patients

Quantitative longitudinal analysis of T cell receptor repertoire expression in HIV-infected patients on antiretroviral and interleukin-2 therapy

Refining the association of MHC with multiple sclerosis in African Americans

SNP imputation bias reduces effect size determination

SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients

Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility

Sex-specific Tau methylation patterns and synaptic transcriptional alterations are associated with neural vulnerability during chronic neuroinflammation

Synergy or independence? Deciphering the interaction of HLA Class I and NK cell KIR alleles in early HIV-1 disease progression

Telomere Length Is Associated with Disability Progression in Multiple Sclerosis

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis

The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis

The killer immunoglobulin-like receptor KIR3DL1 in combination with HLA-Bw4 is protective against multiple sclerosis in African Americans

Transcription-based prediction of response to IFNbeta using supervised computational methods

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis

miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS

Deconstruction of HLA-DRB104:01:01 and HLA-DRB115:01:01 class II haplotypes using next-generation sequencing in European-Americans with multiple sclerosis