Lista de obras - Céline Bellenguez - Dominio Público Uruguay

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

artículo científico publicado en 2016

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

artículo científico publicado en 2017

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 multiple splitting approach to linkage analysis in large pedigrees identifies a linkage to asthma on chromosome 12.

artículo científico publicado en 2009

A novel Alzheimer disease locus located near the gene encoding tau protein.

artículo científico publicado en 2015

A robust clustering algorithm for identifying problematic samples in genome-wide association studies

artículo científico publicado en 2011

ABCA7 rare variants and Alzheimer disease risk

artículo científico publicado en 2016

Accuracy of heritability estimations in presence of hidden population stratification.

artículo científico publicado en 2016

Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype

scientific article published on 10 June 2019

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

artículo científico publicado en 2013

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Common genetic determinants of intraocular pressure and primary open-angle glaucoma

artículo científico publicado en 2012

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

artículo científico publicado en 2012

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

artículo científico publicado en 2021

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

artículo científico publicado en 2013

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

artículo científico publicado en 2010

Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

artículo científico publicado en 2017

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

artículo científico publicado en 2019

Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443].

artículo científico publicado en 2015

Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease

artículo científico publicado en 2016

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

artículo científico publicado en 2014

Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology.

artículo científico publicado en 2016

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

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

artículo científico publicado en 2011

Genetic variants modulating CRIPTO serum levels identified by genome-wide association study in Cilento isolates

artículo científico publicado en 2015

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Genome-wide association interaction analysis for Alzheimer's disease

artículo científico publicado en 2014

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

artículo científico publicado en 2018

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

artículo científico publicado en 2012

Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways

artículo científico publicado en 2020

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

artículo científico publicado en 2009

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Identification and Replication of a Novel Obesity Locus on Chromosome 1q24 in Isolated Populations of Cilento

article by Marina Ciullo et al published 27 December 2007 in Diabetes

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

artículo científico publicado en 2013

Linkage analysis with dense SNP maps in isolated populations

artículo científico publicado en 2009

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

artículo científico publicado en 2013

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

artículo científico publicado en 2016

Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Missense variant in TREML2 protects against Alzheimer's disease

scientific article published on 21 December 2013

New insights into the genetic etiology of Alzheimer's disease and related dementias

artículo científico publicado en 2022

New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate

artículo científico publicado en 2006

PLD3 and sporadic Alzheimer's disease risk.

artículo científico publicado en 2015

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

artículo científico publicado en 2016

SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease.

artículo científico publicado en 2015

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

artículo científico publicado en 2014

Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies

artículo científico publicado en 2016

Strategies for phasing and imputation in a population isolate.

artículo científico publicado en 2018

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

artículo científico publicado en 2014

The role of ATM in response to metformin treatment and activation of AMPK.

artículo científico publicado en 2012

Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease

artículo científico publicado en 2019

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

article

Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy

article

Lista de obras de Céline Bellenguez

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

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 multiple splitting approach to linkage analysis in large pedigrees identifies a linkage to asthma on chromosome 12.

A novel Alzheimer disease locus located near the gene encoding tau protein.

A robust clustering algorithm for identifying problematic samples in genome-wide association studies

ABCA7 rare variants and Alzheimer disease risk

Accuracy of heritability estimations in presence of hidden population stratification.

Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype

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

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Common genetic determinants of intraocular pressure and primary open-angle glaucoma

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

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

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

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443].

Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology.

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

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

Genetic variants modulating CRIPTO serum levels identified by genome-wide association study in Cilento isolates

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

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

Genome-wide association interaction analysis for Alzheimer's disease

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

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

Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways

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

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Identification and Replication of a Novel Obesity Locus on Chromosome 1q24 in Isolated Populations of Cilento

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

Linkage analysis with dense SNP maps in isolated populations

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Missense variant in TREML2 protects against Alzheimer's disease

New insights into the genetic etiology of Alzheimer's disease and related dementias

New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate

PLD3 and sporadic Alzheimer's disease risk.

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

SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease.

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies

Strategies for phasing and imputation in a population isolate.

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

The role of ATM in response to metformin treatment and activation of AMPK.

Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy