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Matti Pirinen

Showing results (1-10 of 129) with videos related to

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Bioinformatics (Oxford, England)|March 3, 2023
linemodels: clustering effects based on linear relationshipsMatti Pirinen
Bioinformatics (Oxford, England)|October 29, 2009
Estimating population haplotype frequencies from pooled SNP data using incomplete database informationMatti Pirinen
Bioinformatics (Oxford, England)|November 9, 2025
FINEMAP-miss: fine-mapping genome-wide association studies with missing genotype informationJoonas Kartau, Matti Pirinen
IEEE/ACM Transactions on Computational Biology and Bioinformatics|October 20, 2006
Finding consistent gene transmission patterns on large and complex pedigreesMatti Pirinen, Dario Gasbarra
Trials|November 25, 2025
Estimating quantile treatment effect on the original scale of the outcome variable: a case study of common cold treatmentsHarri Hemilä, Matti Pirinen
Plos Genetics|January 9, 2025
Refining fine-mapping: Effect sizes and regional heritabilityChristian Benner, Anubha Mahajan, Matti Pirinen
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variantsHeidi Hautakangas, , , et al.
Communications Biology|February 12, 2024
Disentangling the link between maternal influences on birth weight and disease risk in 36,211 genotyped mother-child pairsJaakko T Leinonen, , Matti Pirinen, et al.
Nature Genetics|July 24, 2012
Including known covariates can reduce power to detect genetic effects in case-control studiesMatti Pirinen, Peter Donnelly, Chris C A Spencer
Nucleic Acids Research|March 12, 2026
KANN: estimation of genetic ancestry profiles by nearest neighbor regressionJuha Riikonen, Sini Kerminen, Aki Havulinna, et al.
Pageof 13

Showing results (1-10 of 129) with videos related to

Sort By:
Pageof 13
Bioinformatics (Oxford, England)|March 3, 2023
linemodels: clustering effects based on linear relationshipsMatti Pirinen
Bioinformatics (Oxford, England)|October 29, 2009
Estimating population haplotype frequencies from pooled SNP data using incomplete database informationMatti Pirinen
Bioinformatics (Oxford, England)|November 9, 2025
FINEMAP-miss: fine-mapping genome-wide association studies with missing genotype informationJoonas Kartau, Matti Pirinen
IEEE/ACM Transactions on Computational Biology and Bioinformatics|October 20, 2006
Finding consistent gene transmission patterns on large and complex pedigreesMatti Pirinen, Dario Gasbarra
Trials|November 25, 2025
Estimating quantile treatment effect on the original scale of the outcome variable: a case study of common cold treatmentsHarri Hemilä, Matti Pirinen
Plos Genetics|January 9, 2025
Refining fine-mapping: Effect sizes and regional heritabilityChristian Benner, Anubha Mahajan, Matti Pirinen
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variantsHeidi Hautakangas, , , et al.
Communications Biology|February 12, 2024
Disentangling the link between maternal influences on birth weight and disease risk in 36,211 genotyped mother-child pairsJaakko T Leinonen, , Matti Pirinen, et al.
Nature Genetics|July 24, 2012
Including known covariates can reduce power to detect genetic effects in case-control studiesMatti Pirinen, Peter Donnelly, Chris C A Spencer
Nucleic Acids Research|March 12, 2026
KANN: estimation of genetic ancestry profiles by nearest neighbor regressionJuha Riikonen, Sini Kerminen, Aki Havulinna, et al.
Pageof 13