about
Swedish population substructure revealed by genome-wide single nucleotide polymorphism dataTandem RNA chimeras contribute to transcriptome diversity in human population and are associated with intronic genetic variantsPopulation substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPsIntegrative annotation of variants from 1092 humans: application to cancer genomicsInsights into hominid evolution from the gorilla genome sequenceGenome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern EuropeRegional differences among the Finns: a Y-chromosomal perspectiveMigration waves to the Baltic Sea regionPopulation structure in contemporary Sweden--a Y-chromosomal and mitochondrial DNA analysisAssociating cellular epigenetic models with human phenotypesIdentification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data.Assessing allele-specific expression across multiple tissues from RNA-seq read dataGenetic interactions affecting human gene expression identified by variance association mapping.Distinct variants at LIN28B influence growth in height from birth to adulthood.Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcriptionRare and common regulatory variation in population-scale sequenced human genomesDistribution and medical impact of loss-of-function variants in the Finnish founder population.Transcriptome sequencing from diverse human populations reveals differentiated regulatory architectureGenomic landscape of positive natural selection in Northern European populations.Transcriptome and genome sequencing uncovers functional variation in humansAllelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies.Human genomics. The human transcriptome across tissues and individuals.Gene age predicts the strength of purifying selection acting on gene expression variation in humansJanus--a comprehensive tool investigating the two faces of transcription.Epistatic selection between coding and regulatory variation in human evolution and disease.Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicingTools and best practices for data processing in allelic expression analysis.The landscape of genomic imprinting across diverse adult human tissuesHuman genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeFunctional genomics bridges the gap between quantitative genetics and molecular biology.Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins.Sex-biased genetic effects on gene regulation in humans.Passive and active DNA methylation and the interplay with genetic variation in gene regulationHigh risk population isolate reveals low frequency variants predisposing to intracranial aneurysms.Evolutionary history of regulatory variation in human populations.Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.Concerted Genetic Function in Blood Traits.Voices of biotech.MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets.From trainee to tenure-track: ten tips.
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
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հետազոտող
@hy
name
Tuuli Lappalainen
@ast
Tuuli Lappalainen
@en
Tuuli Lappalainen
@es
Tuuli Lappalainen
@fr
Tuuli Lappalainen
@nl
Tuuli Lappalainen
@sl
type
label
Tuuli Lappalainen
@ast
Tuuli Lappalainen
@en
Tuuli Lappalainen
@es
Tuuli Lappalainen
@fr
Tuuli Lappalainen
@nl
Tuuli Lappalainen
@sl
prefLabel
Tuuli Lappalainen
@ast
Tuuli Lappalainen
@en
Tuuli Lappalainen
@es
Tuuli Lappalainen
@fr
Tuuli Lappalainen
@nl
Tuuli Lappalainen
@sl
P106
P21
P31
P496
0000-0002-7746-8109
P569
2000-01-01T00:00:00Z