Lista de obras - Stephen J. Newhouse - Dominio Público Uruguay

A Pathway Based Classification Method for Analyzing Gene Expression for Alzheimer's Disease Diagnosis

artículo científico publicado en 2015

A genome-wide association study for extremely high intelligence.

artículo científico publicado en 2017

Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease

artículo científico publicado en 2014

Alzheimer's disease biomarker discovery using SOMAscan multiplexed protein technology

artículo científico publicado en 2014

An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis

artículo científico publicado en 2016

An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.

artículo científico publicado en 2011

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

artículo científico publicado en 2018

Assessment of ZnT3 and PSD95 protein levels in Lewy body dementias and Alzheimer's disease: association with cognitive impairment.

artículo científico publicado en 2014

Blood pressure loci identified with a gene-centric array

artículo científico publicado en 2011

Calibrating longitudinal cognition in Alzheimer's disease across diverse test batteries and datasets

artículo científico publicado en 2014

Candidate blood proteome markers of Alzheimer's disease onset and progression: a systematic review and replication study

artículo científico

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

artículo científico publicado en 2010

Circulating Proteomic Signatures of Chronological Age.

artículo científico publicado en 2014

Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

artículo científico publicado en 2011

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

artículo científico publicado en 2009

Differential gene expression analysis in blood of first episode psychosis patients

artículo científico publicado en 2019

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: Meta-analysis of data from genome-wide association studies

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip

artículo científico publicado en 2009

Genes and hypertension

artículo científico publicado en 2003

Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study

artículo científico publicado en 2017

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a Mendelian randomization analysis

artículo científico publicado en 2014

Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study

artículo científico publicado en 2017

Genome-Wide Association of Heroin Dependence in Han Chinese

artículo científico publicado en 2016

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

artículo científico publicado en 2008

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 scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

artículo científico publicado en 2009

Immune signatures and disorder-specific patterns in a cross-disorder gene expression analysis

artículo científico publicado en 2016

Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study

article

Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension

artículo científico publicado en 2006

Linking Genetics of Brain Changes to Alzheimer's Disease: Sparse Whole Genome Association Scan of Regional MRI Volumes in the ADNI and AddNeuroMed Cohorts

artículo científico publicado en 2015

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

Mitochondrial dysfunction and immune activation are detectable in early Alzheimer's disease blood

artículo científico publicado en 2012

Multi-polygenic score approach to trait prediction ⬇️

artículo científico publicado en 2017

No Evidence to Suggest that the Use of Acetylcholinesterase Inhibitors Confounds the Results of Two Blood-Based Biomarker Studies in Alzheimer's Disease

artículo científico publicado en 2015

No differences in hippocampal volume between carriers and non-carriers of the ApoE ε4 and ε2 alleles in young healthy adolescents

artículo científico publicado en 2014

Pharmacogenetics of antidepressant response: A polygenic approach

artículo científico publicado en 2017

Pharmacogenetics of pemetrexed combination therapy in lung cancer: pathway analysis reveals novel toxicity associations

artículo científico publicado en 2014

Plasma based markers of [11C] PiB-PET brain amyloid burden

artículo científico publicado en 2012

Polygenic risk score analyses of symptoms and treatment response in an antipsychotic-naive first episode of psychosis cohort

scientific article published on 31 August 2018

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion

artículo científico publicado en 2009

Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray

artículo científico publicado en 2015

SLC2A9 is a high-capacity urate transporter in humans

artículo científico publicado en 2008

Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients

artículo científico publicado en 2012

Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array

artículo científico publicado en 2009

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

artículo científico publicado en 2012

Trajectories of dementia-related cognitive decline in a large mental health records derived patient cohort

artículo científico publicado en 2017

Lista de obras de Stephen J. Newhouse

A Pathway Based Classification Method for Analyzing Gene Expression for Alzheimer's Disease Diagnosis

A genome-wide association study for extremely high intelligence.

Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease

Alzheimer's disease biomarker discovery using SOMAscan multiplexed protein technology

An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis

An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

Assessment of ZnT3 and PSD95 protein levels in Lewy body dementias and Alzheimer's disease: association with cognitive impairment.

Blood pressure loci identified with a gene-centric array

Calibrating longitudinal cognition in Alzheimer's disease across diverse test batteries and datasets

Candidate blood proteome markers of Alzheimer's disease onset and progression: a systematic review and replication study

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

Circulating Proteomic Signatures of Chronological Age.

Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

Differential gene expression analysis in blood of first episode psychosis patients

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: Meta-analysis of data from genome-wide association studies

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip

Genes and hypertension

Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a Mendelian randomization analysis

Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study

Genome-Wide Association of Heroin Dependence in Han Chinese

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

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

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

Immune signatures and disorder-specific patterns in a cross-disorder gene expression analysis

Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study

Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension

Linking Genetics of Brain Changes to Alzheimer's Disease: Sparse Whole Genome Association Scan of Regional MRI Volumes in the ADNI and AddNeuroMed Cohorts

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Mitochondrial dysfunction and immune activation are detectable in early Alzheimer's disease blood

Multi-polygenic score approach to trait prediction ⬇️

No Evidence to Suggest that the Use of Acetylcholinesterase Inhibitors Confounds the Results of Two Blood-Based Biomarker Studies in Alzheimer's Disease

No differences in hippocampal volume between carriers and non-carriers of the ApoE ε4 and ε2 alleles in young healthy adolescents

Pharmacogenetics of antidepressant response: A polygenic approach

Pharmacogenetics of pemetrexed combination therapy in lung cancer: pathway analysis reveals novel toxicity associations

Plasma based markers of [11C] PiB-PET brain amyloid burden

Polygenic risk score analyses of symptoms and treatment response in an antipsychotic-naive first episode of psychosis cohort

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion

Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray

SLC2A9 is a high-capacity urate transporter in humans

Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients

Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

Trajectories of dementia-related cognitive decline in a large mental health records derived patient cohort