Articles by Matti Pirinen | Synthical

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24

Refining fine-mapping: effect sizes and regional heritability

9 January 2025 by Christian Benner and others

Inherited infertility- mapping loci associated with impaired female reproduction

19 November 2024 by Santtu Ruotsalainen and others

Genetic and Genomic Medicine

Y chromosome sequencing data suggests dual paths of haplogroup N1a1 into Finland

28 October 2024 by A. Preussner and others

Lifestyle differences between co-twins are associated with decreased similarity in their internal and external exposome profiles

11 September 2024 by G. Drouard and others

Genome-wide association analysis of plasma lipidome identifies 495 genetic associations

31 October 2023 by L. Ottensmann and others

Genetic and Genomic Medicine

Estimating quantile treatment effect on the original scale of the outcome variable: a case study of common cold treatments

27 October 2023 by Harri Hemilä and Matti Pirinen

Leveraging global multi-ancestry meta-analysis in the study of Idiopathic Pulmonary Fibrosis genetics

12 October 2022 by J. Partanen and others

Genetic and Genomic Medicine

Lipidome- and genome-wide study to understand sex differences in circulatory lipids

4 October 2022 by Rana Tabassum and others

Genetic and Genomic Medicine

Genetic risk factors have a substantial impact on healthy life years

12 September 2022 by S. Jukarainen and others

Genetic and Genomic Medicine

Association of social isolation, loneliness, and genetic risk with incidence of dementia: UK Biobank cohort study

23 February 2022 by M. Elovainio and others at

University of Helsinki

Bayesian model comparison for rare variant association studies of multiple phenotypes

24 November 2021 by C. Deboever and others at

Stanford University

Polygenic risk, susceptibility genes, and breast cancer over the life course

14 December 2020 by N. Mars and others

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

28 November 2020 by Shahriar Hassan and others

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

16 November 2020 by Omer Weissbrod and others

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

27 October 2020 by S. Ruotsalainen and others

MetaPhat: Detecting and decomposing multivariate associations from univariate genome-wide association statistics

15 May 2020 by Jiadeng Lin and others

Geographic variation and bias in polygenic scores of complex diseases and traits in Finland

30 May 2019 by S. Kerminen and others

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

28 March 2019 by H. Trochet and others

Haplotype sharing provides insights into fine-scale population history and disease in Finland

25 April 2018 by A. Martin and others at

Massachusetts General Hospital

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

12 August 2017 by P. Ripatti and others

biMM: Efficient estimation of genetic variances andcovariances for cohorts with high-dimensional phenotype measurements

28 March 2017 by Matti Pirinen and others

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

1 February 2017 by Himanshu Chheda and others

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

19 February 2016 by Anna Cichońska and others

Multiple Output Regression with Latent Noise

3 February 2016 by Jussi Gillberg and others

Machine Learning

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

14 January 2016 by Christian Benner and others

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

27 March 2015 by Matti Pirinen and others

Bayesian Information Sharing Between Noise And Regression Models Improves Prediction of Weak Effects

16 October 2013 by Jussi Gillberg and others

Machine Learning

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

23 April 2013 by Matti Pirinen and others

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Genetics Genetic and Genomic Medicine Bioinformatics Machine Learning Applications Genomics Epidemiology Oncology