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Author Details

Tuuli Lappalainen
Columbia University
2006
82
41
Emma Lundberg (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36778406Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.bioRxiv2023
37601969Multiset correlation and factor analysis enables exploration of multi-omics data.Cell Genom2023
37995684Increasing diversity of functional genetics studies to advance biological discovery and human health.Am J Hum Genet2023
37905013Large-scale causal discovery using interventional data sheds light on the regulatory network architecture of blood traits.bioRxiv2023
37719147Identifying genetic regulatory variants that affect transcription factor activity.Cell Genom2023
37868038The functional impact of rare variation across the regulatory cascade.Cell Genom2023
37348055Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.Genetics2023
37216410Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.PLoS Genet2023
36778406Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.bioRxiv2023
37268414Pulmonary emphysema subtypes defined by unsupervised machine learning on CT scans.Thorax2023
37141313Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens.Science2023
36698131Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis.Respir Res2023
37425716Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects.bioRxiv2023
37719147Identifying genetic regulatory variants that affect transcription factor activity.Cell Genom2023
37905013Large-scale causal discovery using interventional data sheds light on the regulatory network architecture of blood traits.bioRxiv2023
37995684Increasing diversity of functional genetics studies to advance biological discovery and human health.Am J Hum Genet2023
37601969Multiset correlation and factor analysis enables exploration of multi-omics data.Cell Genom2023
37868038The functional impact of rare variation across the regulatory cascade.Cell Genom2023
37425716Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects.bioRxiv2023
37216410Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.PLoS Genet2023
37348055Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.Genetics2023
37141313Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens.Science2023
37268414Pulmonary emphysema subtypes defined by unsupervised machine learning on CT scans.Thorax2023
36698131Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis.Respir Res2023
35100260Transcription factor regulation of eQTL activity across individuals and tissues.PLoS Genet2022
35658476Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease.Circ Res2022
35385699Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.Am J Hum Genet2022
35483347Functional Characterization of Genetic Variant Effects on Expression.Annu Rev Biomed Data Sci2022
35922509Transcriptome variation in human tissues revealed by long-read sequencing.Nature2022
35100260Transcription factor regulation of eQTL activity across individuals and tissues.PLoS Genet2022
35658476Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease.Circ Res2022
35483347Functional Characterization of Genetic Variant Effects on Expression.Annu Rev Biomed Data Sci2022
35385699Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.Am J Hum Genet2022
35922509Transcriptome variation in human tissues revealed by long-read sequencing.Nature2022
33147445Identification of Required Host Factors for SARS-CoV-2 Infection in Human Cells.Cell2021
33499903Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.Genome Biol2021
33147445Identification of Required Host Factors for SARS-CoV-2 Infection in Human Cells.Cell2021
34554789From variant to function in human disease genetics.Science2021
34425859Integrative approach identifies SLC6A20 and CXCR6 as putative causal genes for the COVID-19 GWAS signal in the 3p21.31 locus.Genome Biol2021
34415308Epigenome-wide association study of mitochondrial genome copy number.Hum Mol Genet2021
33499903Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.Genome Biol2021
34554789From variant to function in human disease genetics.Science2021
34425859Integrative approach identifies SLC6A20 and CXCR6 as putative causal genes for the COVID-19 GWAS signal in the 3p21.31 locus.Genome Biol2021
34415308Epigenome-wide association study of mitochondrial genome copy number.Hum Mol Genet2021
32912286A polyclonal allelic expression assay for detecting regulatory effects of transcript variants.Genome Med2020
32913075Cell type-specific genetic regulation of gene expression across human tissues.Science2020
32913072The impact of sex on gene expression across human tissues.Science2020
32912332A vast resource of allelic expression data spanning human tissues.Genome Biol2020
32912333Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx.Genome Biol2020
32912286A polyclonal allelic expression assay for detecting regulatory effects of transcript variants.Genome Med2020
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Collaborators

Emmanouil T Dermitzakis
University of Geneva
Co-authored papers 24
Kristin G Ardlie
Co-authored papers 17
François Aguet
Co-authored papers 15
Silva Kasela
Co-authored papers 14
Stephen B Montgomery
Stanford University
Co-authored papers 14
Stephane E Castel
Co-authored papers 13
Pejman Mohammadi
Co-authored papers 11
Stephen S Rich
Co-authored papers 11
Daniel G MacArthur
Broad Institute of MIT and Harvard
Co-authored papers 9
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 8
Roderic Guig??
Barcelona Institute of Science and Technology
Co-authored papers 8
Russell P Tracy
Co-authored papers 8
Sarah Kim-Hellmuth
Co-authored papers 7
David Van Den Berg
Co-authored papers 7
Mark I McCarthy
Co-authored papers 7
Manuel A Rivas
Stanford University School of Medicine
Co-authored papers 7
Kent D Taylor
Co-authored papers 7
Peter Durda
Co-authored papers 6
Jerome I Rotter
Co-authored papers 6
Robert G Barr
Co-authored papers 6
Stylianos E Antonarakis
Co-authored papers 6
Juha Kere
Folkhalsan Research Center, University of Helsinki
Co-authored papers 6
Taru Tukiainen
Co-authored papers 5
Andrew A Brown
Co-authored papers 5
Michael Sammeth
Co-authored papers 5
Edwin K Silverman
Brigham and Women's Hospital
Co-authored papers 5
Pedro G Ferreira
Co-authored papers 5
W Craig Johnson
Co-authored papers 5
Stefan Schreiber
Co-authored papers 5
Ana Viñuela
Co-authored papers 4
Release 1.2