Lista de obras - Matti Pirinen - Dominio Público Uruguay

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

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

artículo científico publicado en 2020

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Assessing allele-specific expression across multiple tissues from RNA-seq read data

artículo científico publicado en 2015

Assessing association between protein truncating variants and quantitative traits

artículo científico publicado en 2013

Assessing multivariate gene-metabolome associations with rare variants using Bayesian reduced rank regression

artículo científico publicado en 2014

Bayesian meta-analysis across genome-wide association studies of diverse phenotypes

scientific article published on 28 March 2019

Bayesian refinement of association signals for 14 loci in 3 common diseases

artículo científico publicado en 2012

Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation

artículo científico publicado en 2014

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

Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland

artículo científico publicado en 2019

Coronary Artery Disease Risk and Lipidomic Profiles Are Similar in Hyperlipidemias With Family History and Population-Ascertained Hyperlipidemias

artículo científico publicado en 2019

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

correction of a scientific article; published on 30 May 2019

Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis

artículo científico publicado en 2016

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

Does evaluation of tumour budding in diagnostic biopsies have a clinical relevance? A systematic review

artículo científico publicado en 2019

Efficient computation with a linear mixed model on large-scale data sets with applications to genetic studies

article

Estimating genealogies from unlinked marker data: a Bayesian approach

artículo científico publicado en 2007

Estimating haplotype frequencies by combining data from large DNA pools with database information.

artículo científico publicado en 2011

Estimating population haplotype frequencies from pooled DNA samples using PHASE algorithm.

artículo científico publicado en 2008

Estimating population haplotype frequencies from pooled SNP data using incomplete database information

artículo científico publicado en 2009

Exome sequencing of Finnish isolates enhances rare-variant association power

scientific article published on 31 July 2019

FINEMAP: efficient variable selection using summary data from genome-wide association studies

artículo científico publicado en 2016

Finding consistent gene transmission patterns on large and complex pedigrees

artículo científico publicado en 2006

Fine-Scale Genetic Structure in Finland

artículo científico publicado en 2017

Functionally informed fine-mapping and polygenic localization of complex trait heritability

artículo científico publicado en 2020

Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population

artículo científico publicado en 2015

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

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 support for the causal role of insulin in coronary heart disease

artículo científico publicado en 2016

Genetic variation in is associated with bacteremia secondary to diverse pathogens in African children

article published in the Proceedings of the National Academy of Sciences of the United States of America

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

artículo científico publicado en 2013

Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent

artículo científico publicado en 2020

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

artículo científico publicado en 2012

Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.

artículo científico publicado en 2016

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland

artículo científico publicado en 2019

Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

scholarly article by Alicia R Martin et al published 3 May 2018 in American Journal of Human Genetics

Healthcare costs and outcomes in adult patients with juvenile idiopathic arthritis: a population-based study

scientific article published on 02 August 2018

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

artículo científico publicado en 2020

Human genetic and metabolite variation reveals that methylthioadenosine is a prognostic biomarker and an inflammatory regulator in sepsis

artículo científico publicado en 2017

Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome

artículo científico publicado en 2015

Imputation-based meta-analysis of severe malaria in three African populations

artículo científico publicado en 2013

Including known covariates can reduce power to detect genetic effects in case-control studies

artículo científico publicado en 2012

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

artículo científico publicado en 2018

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

preprint published 25 September 2016

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

Lipidome‐ and Genome‐Wide Study to Understand Sex Differences in Circulatory Lipids

artículo científico publicado en 2022

Patients with rheumatic diseases share similar patterns of healthcare resource utilization

scientific article published on 05 March 2019

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

artículo científico publicado en 2016

Prognostic value of blood and lymphatic vessel markers in tongue cancer: A systematic review

scientific article published on 30 September 2019

Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies

artículo científico publicado en 2017

Risk of nontyphoidal Salmonella bacteraemia in African children is modified by STAT4. ⬇️

artículo científico publicado en 2018

The Contribution of GWAS Loci in Familial Dyslipidemias

artículo científico publicado en 2016

The Prognostic Value of Immune Checkpoints in Oral Squamous Cell Carcinoma

article

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

artículo científico publicado en 2014

The fine-scale genetic structure of the British population

artículo científico publicado en 2015

The impact of low-frequency and rare variants on lipid levels

artículo científico publicado en 2015

The landscape of genomic imprinting across diverse adult human tissues

artículo científico publicado en 2015

Transcriptome and genome sequencing uncovers functional variation in humans

artículo científico publicado en 2013

Tumour budding in oral squamous cell carcinoma: a meta-analysis.

artículo científico publicado en 2017

Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

artículo científico publicado en 2017

biMM: efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements

artículo científico publicado en 2017

metaCCA: summary statistics-based multivariate meta-analysis of genome-wide association studies using canonical correlation analysis

artículo científico publicado en 2016

Lista de obras de Matti Pirinen

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.

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

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

Assessing allele-specific expression across multiple tissues from RNA-seq read data

Assessing association between protein truncating variants and quantitative traits

Assessing multivariate gene-metabolome associations with rare variants using Bayesian reduced rank regression

Bayesian meta-analysis across genome-wide association studies of diverse phenotypes

Bayesian refinement of association signals for 14 loci in 3 common diseases

Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation

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

Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland

Coronary Artery Disease Risk and Lipidomic Profiles Are Similar in Hyperlipidemias With Family History and Population-Ascertained Hyperlipidemias

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis

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

Does evaluation of tumour budding in diagnostic biopsies have a clinical relevance? A systematic review

Efficient computation with a linear mixed model on large-scale data sets with applications to genetic studies

Estimating genealogies from unlinked marker data: a Bayesian approach

Estimating haplotype frequencies by combining data from large DNA pools with database information.

Estimating population haplotype frequencies from pooled DNA samples using PHASE algorithm.

Estimating population haplotype frequencies from pooled SNP data using incomplete database information

Exome sequencing of Finnish isolates enhances rare-variant association power

FINEMAP: efficient variable selection using summary data from genome-wide association studies

Finding consistent gene transmission patterns on large and complex pedigrees

Fine-Scale Genetic Structure in Finland

Functionally informed fine-mapping and polygenic localization of complex trait heritability

Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

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

Genetic support for the causal role of insulin in coronary heart disease

Genetic variation in is associated with bacteremia secondary to diverse pathogens in African children

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

Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent

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

Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland

Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

Healthcare costs and outcomes in adult patients with juvenile idiopathic arthritis: a population-based study

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

Human genetic and metabolite variation reveals that methylthioadenosine is a prognostic biomarker and an inflammatory regulator in sepsis

Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome

Imputation-based meta-analysis of severe malaria in three African populations

Including known covariates can reduce power to detect genetic effects in case-control studies

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

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

Lipidome‐ and Genome‐Wide Study to Understand Sex Differences in Circulatory Lipids

Patients with rheumatic diseases share similar patterns of healthcare resource utilization

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

Prognostic value of blood and lymphatic vessel markers in tongue cancer: A systematic review

Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies

Risk of nontyphoidal Salmonella bacteraemia in African children is modified by STAT4. ⬇️

The Contribution of GWAS Loci in Familial Dyslipidemias

The Prognostic Value of Immune Checkpoints in Oral Squamous Cell Carcinoma

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

The fine-scale genetic structure of the British population

The impact of low-frequency and rare variants on lipid levels

The landscape of genomic imprinting across diverse adult human tissues

Transcriptome and genome sequencing uncovers functional variation in humans

Tumour budding in oral squamous cell carcinoma: a meta-analysis.

Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

biMM: efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements

metaCCA: summary statistics-based multivariate meta-analysis of genome-wide association studies using canonical correlation analysis