Lista de obras - Jeanne C Latourelle - Dominio Público Uruguay

A comparison of visual and quantitative methods to identify interstitial lung abnormalities

artículo científico publicado en 2015

Absence of previously reported variants in theSCNA (G88C and G209A),NR4A2 (T291D and T245G) and theDJ-1 (T497C) genes in familial Parkinson's disease from theGenePD study

article

Assessment of cortical and striatal involvement in 523 Huntington disease brains

artículo científico publicado en 2012

Association Between Interstitial Lung Abnormalities and All-Cause Mortality

artículo científico publicado en 2016

BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study

article

Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset

artículo científico publicado en 2013

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

artículo científico publicado en 2012

Copy number variation in familial Parkinson disease

artículo científico publicado en 2011

Correction: RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression

artículo científico publicado en 2016

Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study

artículo científico publicado en 2011

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study

artículo científico publicado en 2016

Development and Progression of Interstitial Lung Abnormalities in the Framingham Heart Study.

artículo científico publicado en 2016

Dynamic equilibration of airway smooth muscle contraction during physiological loading

scientific article published on 01 February 2002

Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).

artículo científico publicado en 2009

Estrogen-related and other disease diagnoses preceding Parkinson's disease

artículo científico publicado en 2010

Evaluation of Parkinson disease risk variants as expression-QTLs

artículo científico publicado en 2012

Exact morphometric modeling of rat lungs for predicting mechanical impedance.

artículo científico publicado en 2001

Galectin-3 Is Associated with Restrictive Lung Disease and Interstitial Lung Abnormalities

artículo científico publicado en 2016

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

artículo científico publicado en 2012

Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

artículo científico publicado en 2017

Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction

artículo científico publicado en 2012

Genomewide association study for onset age in Parkinson disease

artículo científico publicado en 2009

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

artículo científico publicado en 2008

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

artículo científico publicado en 2011

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

artículo científico publicado en 2008

Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: The GenePD Study

article

Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study

artículo científico publicado en 2008

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study

artículo científico publicado en 2006

Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease

artículo científico publicado en 2016

Large Meta-Analysis in the CHARGE Consortium Provides Evidence For an Association of Serum Vitamin D With Pulmonary Function

Large-scale identification of clinical and genetic predictors of motor progression in patients with newly diagnosed Parkinson's disease: a longitudinal cohort study and validation.

artículo científico publicado en 2017

MUC5B promoter polymorphism and interstitial lung abnormalities

artículo científico publicado en 2013

Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function

artículo científico publicado en 2018

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

artículo científico publicado en 2012

Meta-analysis of exome array data identifies six novel genetic loci for lung function

scientific article published on 12 January 2018

Meta-analysis of exome array data identifies six novel genetic loci for lung function

MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study

artículo científico publicado en 2017

MicroRNAs located in the Hox gene clusters are implicated in huntington's disease pathogenesis.

artículo científico publicado en 2014

Multiethnic Meta-analysis Identifies New Loci for Pulmonary Function

Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

scientific article published in Nature Communications

Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study

artículo científico publicado en 2009

Network-guided sparse regression modeling for detection of gene-by-gene interactions

scientific article published on 18 April 2013

Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.

artículo científico publicado en 2016

Paraseptal emphysema: Prevalence and distribution on CT and association with interstitial lung abnormalities

artículo científico publicado en 2015

Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression

artículo científico publicado en 2016

Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study

artículo científico publicado en 2008

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

artículo científico publicado en 2012

Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain

artículo científico publicado en 2012

RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression

artículo científico publicado en 2015

Replication of association between ELAVL4 and Parkinson disease: the GenePD study

artículo científico publicado en 2008

Risk of Parkinson's disease after tamoxifen treatment

artículo científico publicado en 2010

Sepiapterin reductase expression is increased in Parkinson's disease brain tissue

artículo científico publicado en 2007

Study of plasma-derived miRNAs mimic differences in Huntington's disease brain

artículo científico publicado en 2015

The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane

artículo científico publicado en 2016

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study

artículo científico publicado en 2008

miR-10b-5p expression in Huntington's disease brain relates to age of onset and the extent of striatal involvement

artículo científico publicado en 2015

miR-149 and miR-29c as candidates for bipolar disorder biomarkers.

artículo científico publicado en 2017

microRNA Profiles in Parkinson's Disease Prefrontal Cortex

artículo científico publicado en 2016

Lista de obras de Jeanne C Latourelle

A comparison of visual and quantitative methods to identify interstitial lung abnormalities

Absence of previously reported variants in theSCNA (G88C and G209A),NR4A2 (T291D and T245G) and theDJ-1 (T497C) genes in familial Parkinson's disease from theGenePD study

Assessment of cortical and striatal involvement in 523 Huntington disease brains

Association Between Interstitial Lung Abnormalities and All-Cause Mortality

BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study

Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

Copy number variation in familial Parkinson disease

Correction: RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression

Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study

Development and Progression of Interstitial Lung Abnormalities in the Framingham Heart Study.

Dynamic equilibration of airway smooth muscle contraction during physiological loading

Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).

Estrogen-related and other disease diagnoses preceding Parkinson's disease

Evaluation of Parkinson disease risk variants as expression-QTLs

Exact morphometric modeling of rat lungs for predicting mechanical impedance.

Galectin-3 Is Associated with Restrictive Lung Disease and Interstitial Lung Abnormalities

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction

Genomewide association study for onset age in Parkinson disease

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: The GenePD Study

Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study

Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease

Large Meta-Analysis in the CHARGE Consortium Provides Evidence For an Association of Serum Vitamin D With Pulmonary Function

Large-scale identification of clinical and genetic predictors of motor progression in patients with newly diagnosed Parkinson's disease: a longitudinal cohort study and validation.

MUC5B promoter polymorphism and interstitial lung abnormalities

Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

Meta-analysis of exome array data identifies six novel genetic loci for lung function

Meta-analysis of exome array data identifies six novel genetic loci for lung function

MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study

MicroRNAs located in the Hox gene clusters are implicated in huntington's disease pathogenesis.

Multiethnic Meta-analysis Identifies New Loci for Pulmonary Function

Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study

Network-guided sparse regression modeling for detection of gene-by-gene interactions

Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.

Paraseptal emphysema: Prevalence and distribution on CT and association with interstitial lung abnormalities

Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression

Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain

RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression

Replication of association between ELAVL4 and Parkinson disease: the GenePD study

Risk of Parkinson's disease after tamoxifen treatment

Sepiapterin reductase expression is increased in Parkinson's disease brain tissue

Study of plasma-derived miRNAs mimic differences in Huntington's disease brain

The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study

miR-10b-5p expression in Huntington's disease brain relates to age of onset and the extent of striatal involvement

miR-149 and miR-29c as candidates for bipolar disorder biomarkers.

microRNA Profiles in Parkinson's Disease Prefrontal Cortex