Lista de obras - Cordelia Langford - Dominio Público Uruguay

A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH.

artículo científico publicado en 2006

A cytogenetically characterized, genome-anchored 10-Mb BAC set and CGH array for the domestic dog.

artículo científico publicado en 2007

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

artículo científico publicado en 2013

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

artículo científico publicado en 2010

A novel CpG island set identifies tissue-specific methylation at developmental gene loci

artículo científico publicado en 2008

Accurate and reliable high-throughput detection of copy number variation in the human genome

artículo científico publicado en 2006

Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition

artículo científico publicado en 2009

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

artículo científico publicado en 2009

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

artículo científico publicado en 2013

Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays

artículo científico publicado en 2005

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

artículo científico publicado en 2012

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

artículo científico publicado en 2013

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

artículo científico publicado en 2010

Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution

artículo científico publicado en 2010

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

artículo científico publicado en 2011

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

artículo científico publicado en 2010

Distinct cytokine-driven responses of activated blood gammadelta T cells: insights into unconventional T cell pleiotropy

artículo científico publicado en 2007

Erratum: Corrigendum: The zebrafish reference genome sequence and its relationship to the human genome

scientific article published in Nature

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome

artículo científico publicado en 2005

Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype

artículo científico publicado en 2006

Gene expression profiling in polycythemia vera using cDNA microarray technology.

artículo científico publicado en 2003

Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology

article

Generation of a genomic tiling array of the human major histocompatibility complex (MHC) and its application for DNA methylation analysis

artículo científico publicado en 2008

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

artículo científico publicado en 2015

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

artículo científico publicado en 2011

Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles

artículo científico publicado en 2012

Genome-Wide Screening for Genetic Alterations in Esophageal Cancer by aCGH Identifies 11q13 Amplification Oncogenes Associated with Nodal Metastasis ⬇️

artículo científico publicado el 25 de junio de 2012

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

artículo científico publicado en 2013

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

artículo científico publicado en 2012

Genome-wide association study identifies five new breast cancer susceptibility loci

artículo científico publicado en 2010

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

artículo científico publicado en 2009

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic approaches uncover increasing complexities in the regulatory landscape at the human SCL (TAL1) locus

artículo científico publicado en 2010

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

artículo científico publicado en 2012

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.

artículo científico publicado en 2012

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

article

Improving the power to detect differentially expressed genes in comparative microarray experiments by including information from self-self hybridizations

artículo científico publicado en 2007

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

artículo científico publicado en 2011

Large-scale association analysis identifies new risk loci for coronary artery disease

artículo científico publicado en 2012

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Microarray-based cytogenetic profiling reveals recurrent and subtype-associated genomic copy number aberrations in feline sarcomas

artículo científico publicado en 2009

Neonates harbour highly active gammadelta T cells with selective impairments in preterm infants

artículo científico publicado en 2009

Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children

artículo científico publicado en 2016

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

artículo científico publicado en 2011

Selective nuclear export of specific classes of mRNA from mammalian nuclei is promoted by GANP.

artículo científico publicado en 2014

Spreading of mammalian DNA-damage response factors studied by ChIP-chip at damaged telomeres

artículo científico publicado en 2007

The DNA sequence of the human X chromosome

artículo científico publicado en 2005

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

artículo científico publicado en 2014

The zebrafish reference genome sequence and its relationship to the human genome

artículo científico publicado en 2013

Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function

artículo científico publicado en 2010

Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

artículo científico publicado en 2007

Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data

artículo científico publicado en 2003

Lista de obras de Cordelia Langford

A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH.

A cytogenetically characterized, genome-anchored 10-Mb BAC set and CGH array for the domestic dog.

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

A novel CpG island set identifies tissue-specific methylation at developmental gene loci

Accurate and reliable high-throughput detection of copy number variation in the human genome

Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

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

Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

Distinct cytokine-driven responses of activated blood gammadelta T cells: insights into unconventional T cell pleiotropy

Erratum: Corrigendum: The zebrafish reference genome sequence and its relationship to the human genome

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome

Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype

Gene expression profiling in polycythemia vera using cDNA microarray technology.

Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology

Generation of a genomic tiling array of the human major histocompatibility complex (MHC) and its application for DNA methylation analysis

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

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

Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles

Genome-Wide Screening for Genetic Alterations in Esophageal Cancer by aCGH Identifies 11q13 Amplification Oncogenes Associated with Nodal Metastasis ⬇️

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association study identifies five new breast cancer susceptibility loci

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genomic approaches uncover increasing complexities in the regulatory landscape at the human SCL (TAL1) locus

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

Improving the power to detect differentially expressed genes in comparative microarray experiments by including information from self-self hybridizations

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Large-scale association analysis identifies new risk loci for coronary artery disease

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Microarray-based cytogenetic profiling reveals recurrent and subtype-associated genomic copy number aberrations in feline sarcomas

Neonates harbour highly active gammadelta T cells with selective impairments in preterm infants

Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Selective nuclear export of specific classes of mRNA from mammalian nuclei is promoted by GANP.

Spreading of mammalian DNA-damage response factors studied by ChIP-chip at damaged telomeres

The DNA sequence of the human X chromosome

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

The zebrafish reference genome sequence and its relationship to the human genome

Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function

Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data