Matti Pirinen
Genetics · 2010–2022
A researcher in the Science corpus: 15 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 199 citations into it; #5,638 of 6,854 by trust here, #663 by citations
Whom Matti Pirinen trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Matthew Stephens (in Genetics)
Who trusts Matti Pirinen
- Chris Wallace (in Genetics)
Papers from Matti Pirinen's perspective
Ordered by how strongly the researchers Matti Pirinen trusts endorse each paper. Same corpus, a different order for every researcher.
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- GCTA: a tool for genome-wide complex trait analysis. (American Journal of Human Genetics)
- Genome-partitioning of genetic variation for complex traits using common SNPs (Nature Genetics)
- Partitioning heritability by functional annotation using genome-wide association summary statistics (Nature Genetics)
- Bayesian variable selection regression for genome-wide association studies and other large-scale problems
- Genetic effects on gene expression across human tissues
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)
Their papers
- Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (2015) — 774 citations
- Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA (2016) — 691 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
- Functionally-informed fine-mapping and polygenic localization of complex trait heritability (2019) — 341 citations
- Multiple Sclerosis Genomic Map implicates peripheral immune cells & microglia in susceptibility (2019) — 1,186 citations
- Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
- Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland (2018) — 6 citations
- Geographic variation and bias in polygenic scores of complex diseases and traits in Finland (2018) — 32 citations
- Traumatic brain injury: integrated approaches to improve prevention, clinical care, and research (2017) — 2,023 citations
- Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity (2012) — 721 citations
- Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) — 508 citations
- Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility (2011) — 898 citations
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) — 2,780 citations
- A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 (2010) — 1,032 citations