Tuuli Lappalainen
Science · 2012–2021
A researcher in the Science corpus: 15 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Whom Tuuli Lappalainen trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Tuuli Lappalainen overall
Papers from Tuuli Lappalainen's perspective
Ordered by how strongly the researchers Tuuli Lappalainen trusts endorse each paper. Same corpus, a different order for every researcher.
- The Human Gene Mutation Database: 2008 update
- Exome sequencing as a tool for Mendelian disease gene discovery
- Mapping copy number variation by population scale genome sequencing (Nature)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (Nature Genetics)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- An integrated map of genetic variation from 1,092 human genomes
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
- Next-generation genotype imputation service and methods (Nature Genetics)
- Transcriptome genetics using second generation sequencing in a Caucasian population (Nature)
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
Their papers
- Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
- The Genotype-Tissue Expression (GTEx) project (2013) — 8,629 citations
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- Tools and best practices for data processing in allelic expression analysis (2015) — 359 citations
- Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
- The human transcriptome across tissues and individuals (2015) — 1,238 citations
- The GTEx Consortium atlas of genetic regulatory effects across human tissues (2019) — 4,770 citations
- Widespread dose-dependent effects of RNA expression and splicing on complex diseases and traits (2019) — 116 citations
- Landscape of X chromosome inactivation across human tissues (2016) — 943 citations
- Insights into hominid evolution from the gorilla genome sequence (2012) — 719 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Genome-wide association studies (2021) — 1,011 citations
- The impact of sex on gene expression across human tissues (2020) — 618 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations