Author: Matti Pirinen

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Preprints

Bayesian model comparison for rare variant association studies of multiple phenotypes

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  • Site-wide: 5,926
  • In genetics: 286
• Year to date:
  • Site-wide: 30,552
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  • Site-wide: 35,695

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

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  • Site-wide: 5,952
  • In genetics: 287
• Year to date:
  • Site-wide: 17,449
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  • Site-wide: None

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

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  • Site-wide: 7,127
  • In bioinformatics: 877
• Year to date:
  • Site-wide: 96,363
• Since beginning of last month:
  • Site-wide: 97,785

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

• Downloaded 1,576 times
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  • Site-wide: 10,011
  • In bioinformatics: 1,236
• Year to date:
  • Site-wide: 82,260
• Since beginning of last month:
  • Site-wide: 93,133

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

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  • Site-wide: 10,437
  • In genetics: 517
• Year to date:
  • Site-wide: 91,690
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  • Site-wide: 74,419

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 11,309
  • In genomics: 1,258
• Year to date:
  • Site-wide: 60,929
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  • Site-wide: 57,717

Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

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  • Site-wide: 11,497
  • In genomics: 1,279
• Year to date:
  • Site-wide: 36,902
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  • Site-wide: 25,139

Refining fine-mapping: effect sizes and regional heritability

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  • Site-wide: 11,695
  • In genetics: 584
• Year to date:
  • Site-wide: 34,340
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  • Site-wide: 37,137

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

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  • Site-wide: 14,085
  • In genetics: 719
• Year to date:
  • Site-wide: 91,593
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  • Site-wide: 74,944

Genetics of human plasma lipidome: Understanding lipid metabolism and its link to diseases beyond traditional lipids

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  • Site-wide: 16,000
  • In genetics: 810
• Year to date:
  • Site-wide: 58,021
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  • Site-wide: None

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

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  • Site-wide: 17,084
  • In genetics: 867
• Year to date:
  • Site-wide: 62,165
• Since beginning of last month:
  • Site-wide: 57,855

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

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  • Site-wide: 19,163
  • In genetics: 953
• Year to date:
  • Site-wide: 121,028
• Since beginning of last month:
  • Site-wide: None

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

• Downloaded 816 times
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  • Site-wide: 26,345
  • In oncology: 26
• Year to date:
  • Site-wide: 31,264
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  • Site-wide: 33,181

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

• Downloaded 666 times
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  • Site-wide: 34,832
  • In genetics: 1,702
• Year to date:
  • Site-wide: 94,165
• Since beginning of last month:
  • Site-wide: 102,954

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

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  • Site-wide: 37,911
  • In genetics: 1,847
• Year to date:
  • Site-wide: 14,132
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  • Site-wide: 8,648

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

• Downloaded 590 times
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  • Site-wide: 40,675
  • In bioinformatics: 4,430
• Year to date:
  • Site-wide: 95,165
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  • Site-wide: 61,209

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

• Downloaded 571 times
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  • Site-wide: 42,349
  • In genetics: 2,036
• Year to date:
  • Site-wide: 118,652
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  • Site-wide: None

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

• Downloaded 532 times
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  • Site-wide: 46,279
  • In genetics: 2,222
• Year to date:
  • Site-wide: 119,820
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  • Site-wide: None

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

• Downloaded 477 times
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  • Site-wide: 52,477
  • In genetics: 2,495
• Year to date:
  • Site-wide: 116,367
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  • Site-wide: 96,254

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

• Downloaded 450 times
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  • Site-wide: 55,988
  • In epidemiology: 2,396
• Year to date:
  • Site-wide: 24,726
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  • Site-wide: 18,755

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

• Downloaded 316 times
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  • Site-wide: 77,543
  • In genomics: 5,178
• Year to date:
  • Site-wide: 89,842
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  • Site-wide: 68,523

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

• Downloaded 291 times
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  • Site-wide: 82,384
  • In genomics: 5,359
• Year to date:
  • Site-wide: 70,456
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  • Site-wide: 79,379

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

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  • Site-wide: 90,994
  • In genetic and genomic medicine: 318
• Year to date:
  • Site-wide: 3,419
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  • Site-wide: 6,259

Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

• Downloaded 123 times
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  • Site-wide: 117,202
  • In genetic and genomic medicine: 523
• Year to date:
  • Site-wide: 59,332
• Since beginning of last month:
  • Site-wide: 69,571