Filtros de búsqueda

Lista de obras de

118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

artículo científico publicado en 2009

A Child's HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus

artículo científico publicado en 2016

A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis

artículo científico publicado en 2010

A case-control study of dietary salt intake in pediatric-onset multiple sclerosis

artículo científico publicado en 2016

A germ-line deletion of APOBEC3B does not contribute to subtype-specific childhood acute lymphoblastic leukemia etiology

artículo científico publicado en 2017

A high-density screen for linkage in multiple sclerosis

artículo científico publicado en 2005

A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis

artículo científico publicado en 2010

A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus

artículo científico publicado en 2019

A second major histocompatibility complex susceptibility locus for multiple sclerosis

artículo científico publicado en 2007

A second-generation genomic screen for multiple sclerosis

artículo científico publicado en 2004

A validation study for remote testing of cognitive function in multiple sclerosis

artículo científico publicado en 2020

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers

artículo científico publicado en 2006

Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry

scientific article published on 17 January 2019

Adverse socioeconomic position during the life course is associated with multiple sclerosis

artículo científico publicado en 2014

Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis

artículo científico publicado en 2006

Allergies and Childhood Acute Lymphoblastic Leukemia: A Case–Control Study and Meta-analysis

artículo científico publicado en 2018

Alloreactive fetal T cells promote uterine contractility in preterm labor via IFN-γ and TNF-α.

artículo científico publicado en 2018

An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings

artículo científico publicado en 2010

Analysis of IL4R haplotypes in predisposition to multiple sclerosis

artículo científico publicado en 2004

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

artículo científico publicado en 2013

Analysis of maternal-offspring HLA compatibility, parent-of-origin and non-inherited maternal effects for the classical HLA loci in type 1 diabetes

artículo científico publicado en 2009

Analysis of maternal-offspring HLA compatibility, parent-of-origin effects, and noninherited maternal antigen effects for HLA-DRB1 in systemic lupus erythematosus

artículo científico publicado en 2010

Annotation of functional variation within non-MHC MS susceptibility loci through bioinformatics analysis.

artículo científico publicado en 2014

Association between celiac disease and iron deficiency in Caucasians, but not non-Caucasians

artículo científico publicado en 2013

Association mapping of disease loci, by use of a pooled DNA genomic screen

artículo científico publicado en 1997

Association mapping with a pooled DNA genomic screen of the non-HLA genes in IDDM, RA and MS

article

Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children

artículo científico publicado en 2015

Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis

artículo científico publicado en 2002

Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15.

artículo científico publicado en 2005

Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations

artículo científico publicado en 2012

Author Correction: A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus

scientific article published on 27 February 2020

BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia

artículo científico publicado en 2018

Breastfeeding is associated with reduced risk of multiple sclerosis in males, predominantly among HLA-DRB1*15:01 carriers

artículo científico publicado en 2020

CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group

artículo científico publicado en 2000

CIITA is not associated with risk of developing rheumatoid arthritis ⬇️

artículo científico publicado el 20 de enero de 2011

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

artículo científico publicado en 2010

CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification

artículo científico publicado en 2009

Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility

artículo científico publicado en 2017

Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology

artículo científico publicado en 2019

Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients.

artículo científico publicado en 1997

Chromosome 7q21-22 and multiple sclerosis

artículo científico publicado en 2004

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

artículo científico publicado en 2006

Clustering of inflammatory bowel disease with immune mediated diseases among members of a northern california-managed care organization

artículo científico publicado en 2007

Comparison of DNA methylation measured by Illumina 450K and EPIC BeadChips in blood of newborns and 14-year-old children

artículo científico publicado en 2018

Comparison of statistical methods for estimating genetic admixture in a lung cancer study of African Americans and Latinos

artículo científico publicado en 2008

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

article

Considerations for normalization of DNA methylation data by Illumina 450K BeadChip assay in population studies.

artículo científico publicado en 2013

Contribution of dietary intake to relapse rate in early paediatric multiple sclerosis

artículo científico publicado en 2017

DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis

artículo científico publicado en 2016

Dietary salt intake and time to relapse in paediatric multiple sclerosis

artículo científico publicado en 2016

Differential methylation of interferon-related genes is associated with autoantibody production in systemic lupus erythematosus.

artículo científico publicado en 2014

Effects of PON polymorphisms and haplotypes on molecular phenotype in Mexican‐American mothers and children ⬇️

artículo científico publicado el 1 de marzo de 2011

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

article

Epigenetic Signatures of Salivary Gland Inflammation in Sjögren's Syndrome

artículo científico publicado en 2016

Epstein-Barr virus, cytomegalovirus, and multiple sclerosis susceptibility: A multiethnic study

artículo científico publicado en 2017

Evaluating the association of allergies with multiple sclerosis susceptibility risk and disease activity in a pediatric population

artículo científico publicado en 2017

Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Evidence for a complex interaction between HLA-DRB1 and environmental factors in MS

scientific article published on 01 January 2008

Evidence for the genetic role of human leukocyte antigens in low frequency DRB1*1501 multiple sclerosis patients in Israel

artículo científico publicado en 1999

Evolution of the CCR5 Delta32 mutation based on haplotype variation in Jewish and Northern European population samples

artículo científico publicado en 2001

Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44

scientific article published on 01 January 2006

Familial effects on the clinical course of multiple sclerosis

artículo científico publicado en 2007

Feasibility study for remote assessment of cognitive function in multiple sclerosis

artículo científico publicado en 2016

Fetal growth and body size genes and risk of childhood acute lymphoblastic leukemia

artículo científico publicado en 2012

Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects

artículo científico publicado en 2013

GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL.

artículo científico publicado en 2013

GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.

artículo científico publicado en 2018

Gene copy number regulates the production of the human chemokine CCL3-L1

artículo científico publicado en 2002

Genetic Analysis of Multiple Sclerosis in Europeans ⬇️

artículo científico publicado el 1 de octubre de 2003

Genetic aspects of multiple sclerosis

artículo científico publicado en 1999

Genetic basis for clinical expression in multiple sclerosis

artículo científico publicado en 2002

Genetic polymorphisms in adaptive immunity genes and childhood acute lymphoblastic leukemia

artículo científico publicado en 2010

Genetic predictors of relapse rate in pediatric MS.

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Genetic risk and longitudinal disease activity in systemic lupus erythematosus using targeted maximum likelihood estimation.

scientific article published on 28 July 2016

Genetic risk factors for pediatric-onset multiple sclerosis

artículo científico publicado en 2017

Genetic variability and linkage disequilibrium within the HLA-DP region: analysis of 15 different populations.

artículo científico publicado en 2001

Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics

artículo científico publicado en 2013

Genetic variants in the folate pathway and risk of childhood acute lymphoblastic leukemia

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis.

artículo científico publicado en 2017

Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes.

artículo científico publicado en 2010

Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus

artículo científico publicado en 2015

Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis

artículo científico publicado en 2015

Genome-wide association study identifies genetic loci associated with iron deficiency

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Genome-wide profiling identifies associations between lupus nephritis and differential methylation of genes regulating tissue hypoxia and type 1 interferon responses.

scientific article published on 07 December 2016

Genomewide association study of HLA alloimmunization in previously pregnant blood donors

artículo científico publicado en 2017

Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia

artículo científico publicado en 2014

Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs

scientific article published on 31 March 2020

HLA-DP genetic variation, proxies for early life immune modulation and childhood acute lymphoblastic leukemia risk

artículo científico publicado en 2012

HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course

artículo científico publicado en 2003

Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia

artículo científico publicado en 2011

Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome

scientific article published on 11 July 2019

Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis

artículo científico publicado en 2006

Heterogeneity in association of remote herpesvirus infections and pediatric MS

High consumption of coffee is associated with decreased multiple sclerosis risk; results from two independent studies

artículo científico publicado en 2016

High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions

artículo científico publicado en 2009

Human Epistatic Interaction Controls IL7R Splicing and Increases Multiple Sclerosis Risk.

artículo científico publicado en 2017

Hypomethylation of CYP2E1 and DUSP22 promoters associated with disease activity and erosive disease among rheumatoid arthritis patients

artículo científico publicado en 2017

Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twins.

artículo científico publicado en 2016

Immune mediated conditions in autism spectrum disorders

artículo científico publicado en 2015

Incorporating machine learning approaches to assess putative environmental risk factors for multiple sclerosis

artículo científico publicado en 2018

Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients

artículo científico publicado en 2018

Increased alloreactive and autoreactive antihuman leucocyte antigen antibodies associated with systemic lupus erythematosus and rheumatoid arthritis

scholarly article by Rachael P Jackman et al published 2018 in Lupus science & medicine

Increased risk of rheumatoid arthritis among mothers with children who carry DRB1 risk-associated alleles

artículo científico publicado en 2017

Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome

scientific article published on 01 October 2019

Interaction between adolescent obesity and HLA risk genes in the etiology of multiple sclerosis

artículo científico publicado en 2014

Interaction between passive smoking and two HLA genes with regard to multiple sclerosis risk

artículo científico publicado en 2014

Interactions between genetic, lifestyle and environmental risk factors for multiple sclerosis

artículo científico publicado en 2016

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

artículo científico publicado en 2007

Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex

artículo científico publicado en 2011

Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study

artículo científico publicado en 2003

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

artículo científico publicado en 2010

Linkage and association analysis of chromosome 19q13 in multiple sclerosis

artículo científico publicado en 2001

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

artículo científico publicado en 2004

Low frequency and rare coding variation contributes to multiple sclerosis risk

MHC associations with clinical and autoantibody manifestations in European SLE.

artículo científico publicado en 2014

MS Sunshine Study: Sun Exposure But Not Vitamin D Is Associated with Multiple Sclerosis Risk in Blacks and Hispanics.

artículo científico publicado en 2018

Male microchimerism in peripheral blood leukocytes from women with multiple sclerosis

artículo científico publicado en 2011

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans

artículo científico publicado en 2003

Matching on Race and Ethnicity in Case-Control Studies as a Means of Control for Population Stratification

artículo científico publicado en 2011

Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium

artículo científico publicado en 2017

Men transmit MS more often to their children vs women: the Carter effect

artículo científico publicado en 2006

Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk

artículo científico publicado en 2016

Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers

artículo científico publicado en 2019

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

artículo científico publicado en 2006

Multiple sclerosis genetics: leaving no stone unturned

artículo científico publicado en 2005

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

artículo científico publicado en 2016

Multiple sclerosis: genomic rewards

artículo científico publicado en 2001

Multiple susceptibility loci for multiple sclerosis

scientific article published on 01 September 2002

No differential gene expression for CD4+ T cells of MS patients and healthy controls

scientific article published on 01 April 2019

Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype

artículo científico publicado en 2013

OR.102. The CD58 Pathway is Implicated in MS Susceptibility

Obesity and Multiple Sclerosis Susceptibility: A Review

artículo científico publicado en 2016

Obesity during childhood and adolescence increases susceptibility to multiple sclerosis after accounting for established genetic and environmental risk factors

artículo científico publicado en 2014

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

Pathway Analysis of Genome-wide Association Study in Childhood Leukemia among Hispanics.

artículo científico publicado en 2016

Pharmacogenomic analysis of interferon receptor polymorphisms in multiple sclerosis.

artículo científico publicado en 2003

Pregnancy does not modify the risk of MS in genetically susceptible women

artículo científico publicado en 2020

Prenatal phthalate exposure and altered patterns of DNA methylation in cord blood.

artículo científico publicado en 2017

Remote assessment of verbal memory in MS patients using the California Verbal Learning Test

artículo científico publicado en 2017

Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes

scientific article published on 09 October 2016

Risk alleles for multiple sclerosis identified by a genomewide study

artículo científico publicado en 2007

SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children

artículo científico publicado en 2013

Seafood, fatty acid biosynthesis genes, and multiple sclerosis susceptibility

artículo científico publicado en 2019

Searching for additional disease loci in a genomic region

artículo científico publicado en 2008

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

artículo científico publicado en 2001

Seroprevalence of aquaporin-4-IgG in a northern California population representative cohort of multiple sclerosis

artículo científico publicado en 2014

Several household chemical exposures are associated with pediatric-onset multiple sclerosis

Sex differences in DNA methylation assessed by 450 K BeadChip in newborns

artículo científico publicado en 2015

Smoking and risk of multiple sclerosis: evidence of modification by NAT1 variants.

artículo científico publicado en 2014

Socioeconomic Status and Lung Cancer: Unraveling the Contribution of Genetic Admixture ⬇️

artículo científico publicado el 15 de agosto de 2013

Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis

artículo científico publicado en 2010

The Association of Refractive Error with Glaucoma in a Multiethnic Population

artículo científico publicado en 2015

The HLA locus and multiple sclerosis in Sicily.

artículo científico publicado en 2005

The HLA locus and multiple sclerosis in Spain. Role in disease susceptibility, clinical course and response to interferon-β

article

The MHC2TA -168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients and 9270 controls reveals no evidence for association

artículo científico publicado en 2007

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 interaction between smoking and HLA genes in multiple sclerosis: replication and refinement

artículo científico publicado en 2017

The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults

artículo científico publicado en 2017

The price of whole-genome sequencing may be decreasing, but who will be sequenced?

artículo científico publicado en 2017

The role of the CD58 locus in multiple sclerosis

artículo científico publicado en 2009

The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus.

artículo científico publicado en 2011

To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes

scholarly article by Amelia D Wallace et al published 2018 in Frontiers in Genetics

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

artículo científico publicado en 2008

Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans

artículo científico publicado en 2012

Variation in xenobiotic transport and metabolism genes, household chemical exposures, and risk of childhood acute lymphoblastic leukemia

artículo científico publicado en 2012

Variation within DNA repair pathway genes and risk of multiple sclerosis

artículo científico publicado en 2010

Vitamin D genes influence MS relapses in children

scientific article published on 13 May 2019

Vitamin D-Binding Protein Polymorphisms, 25-Hydroxyvitamin D, Sunshine and Multiple Sclerosis

artículo científico publicado en 2018

miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS

scientific article published on 15 May 2019

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda