On the public citation graph

Survey of the Heritability and Sparse Architecture of Gene Expression Traits Across Human Tissues

https://doi.org/10.1101/043653
0 signed · 55 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/gepi.21698openalex-snapshot
Performance and Robustness of Penalized and Unpenalized Methods for Genetic Prediction of Complex Human Disease
inferredcites →https://doi.org/10.1002/gepi.21808openalex-snapshot
Poly-Omic Prediction of Complex Traits: OmicKriging
inferredcites →https://doi.org/10.1016/j.ajhg.2010.11.011openalex-snapshot
GCTA: A Tool for Genome-wide Complex Trait Analysis
inferredcites →https://doi.org/10.1016/j.ajhg.2012.10.010openalex-snapshot
Improved Heritability Estimation from Genome-wide SNPs
inferredcites →https://doi.org/10.1016/j.ajhg.2013.03.022openalex-snapshot
Sherlock: Detecting Gene-Disease Associations by Matching Patterns of Expression QTL and GWAS
inferredcites →https://doi.org/10.1016/j.ajhg.2014.10.001openalex-snapshot
Cross-Tissue and Tissue-Specific eQTLs: Partitioning the Heritability of a Complex Trait
inferredcites →https://doi.org/10.1016/j.ajhg.2014.10.004openalex-snapshot
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
inferredcites →https://doi.org/10.1038/nature04244openalex-snapshot
Mapping determinants of human gene expression by regional and genome-wide association
inferredcites →https://doi.org/10.1038/nature08185openalex-snapshot
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
inferredcites →https://doi.org/10.1038/ng.2232openalex-snapshot
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
inferredcites →https://doi.org/10.1038/ng.2310openalex-snapshot
Genome-wide efficient mixed-model analysis for association studies
inferredcites →https://doi.org/10.1038/ng.2354openalex-snapshot
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
inferredcites →https://doi.org/10.1038/ng.2383openalex-snapshot
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng.2951openalex-snapshot
Heritability and genomics of gene expression in peripheral blood
inferredcites →https://doi.org/10.1038/ng.3220openalex-snapshot
Identification of common genetic variants controlling transcript isoform variation in human whole blood
inferredcites →https://doi.org/10.1038/ng.3367openalex-snapshot
A gene-based association method for mapping traits using reference transcriptome data
inferredcites →https://doi.org/10.1038/ng.3506openalex-snapshot
Integrative approaches for large-scale transcriptome-wide association studies
inferredcites →https://doi.org/10.1038/ng.3538openalex-snapshot
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets
inferredcites →https://doi.org/10.1038/ng2142openalex-snapshot
Population genomics of human gene expression
inferredcites →https://doi.org/10.1038/nmeth.1785openalex-snapshot
A linear complexity phasing method for thousands of genomes
inferredcites →https://doi.org/10.1038/nprot.2011.457openalex-snapshot
Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses
inferredcites →https://doi.org/10.1038/nrg2898openalex-snapshot
Predicting genetic predisposition in humans: the promise of whole-genome markers
inferredcites →https://doi.org/10.1038/nrg3891openalex-snapshot
The role of regulatory variation in complex traits and disease
inferredcites →https://doi.org/10.1080/00401706.1970.10488635openalex-snapshot
Ridge Regression: Applications to Nonorthogonal Problems
inferredcites →https://doi.org/10.1093/bioinformatics/bts163openalex-snapshot
Matrix eQTL: ultra fast eQTL analysis via large matrix operations
inferredcites →https://doi.org/10.1093/bioinformatics/btu704openalex-snapshot
minimac2: faster genotype imputation
inferredcites →https://doi.org/10.1093/nar/gng015openalex-snapshot
Summaries of Affymetrix GeneChip probe level data
inferredcites →https://doi.org/10.1101/035170openalex-snapshot
A reference panel of 64,976 haplotypes for genotype imputation
inferredcites →https://doi.org/10.1101/gr.115337.110openalex-snapshot
Genetic architecture of regulatory variation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1101/gr.135350.111openalex-snapshot
GENCODE: The reference human genome annotation for The ENCODE Project
inferredcites →https://doi.org/10.1101/gr.155192.113openalex-snapshot
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals
inferredcites →https://doi.org/10.1109/sc.companion.2012.127openalex-snapshot
The Design of a Community Science Cloud: The Open Science Data Cloud Perspective
inferredcites →https://doi.org/10.1111/j.1467-9868.2005.00503.xopenalex-snapshot
Regularization and Variable Selection Via the Elastic Net
inferredcites →https://doi.org/10.1111/j.2517-6161.1996.tb02080.xopenalex-snapshot
Regression Shrinkage and Selection Via the Lasso
inferredcites →https://doi.org/10.1126/science.1262110openalex-snapshot
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
inferredcites →https://doi.org/10.1136/amiajnl-2013-002155openalex-snapshot
Bionimbus: a cloud for managing, analyzing and sharing large genomics datasets
inferredcites →https://doi.org/10.1186/s13742-015-0047-8openalex-snapshot
Second-generation PLINK: rising to the challenge of larger and richer datasets
inferredcites →https://doi.org/10.1371/journal.pgen.0030161openalex-snapshot
Capturing Heterogeneity in Gene Expression Studies by Surrogate Variable Analysis
inferredcites →https://doi.org/10.1371/journal.pgen.1000888openalex-snapshot
Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS
inferredcites →https://doi.org/10.1371/journal.pgen.1000895openalex-snapshot
Candidate Causal Regulatory Effects by Integration of Expression QTLs with Complex Trait Genetic Associations
inferredcites →https://doi.org/10.1371/journal.pgen.1002078openalex-snapshot
Identification, Replication, and Functional Fine-Mapping of Expression Quantitative Trait Loci in Primary Human Liver Tissue
inferredcites →https://doi.org/10.1371/journal.pgen.1003264openalex-snapshot
Polygenic Modeling with Bayesian Sparse Linear Mixed Models
inferredcites →https://doi.org/10.1371/journal.pgen.1003396openalex-snapshot
Robust Prediction of Expression Differences among Human Individuals Using Only Genotype Information
inferredcites →https://doi.org/10.1371/journal.pgen.1003486openalex-snapshot
A Statistical Framework for Joint eQTL Analysis in Multiple Tissues
inferredcites →https://doi.org/10.1371/journal.pgen.1003649openalex-snapshot
Integrative Modeling of eQTLs and Cis-Regulatory Elements Suggests Mechanisms Underlying Cell Type Specificity of eQTLs
inferredcites →https://doi.org/10.1371/journal.pgen.1003864openalex-snapshot
Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture
inferredcites →https://doi.org/10.1371/journal.pgen.1004322openalex-snapshot
Genetic Dissection of the Drosophila melanogaster Female Head Transcriptome Reveals Widespread Allelic Heterogeneity
inferredcites →https://doi.org/10.1371/journal.pgen.1004383openalex-snapshot
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
inferredcites →https://doi.org/10.1371/journal.pgen.1004818openalex-snapshot
Mediation Analysis Demonstrates That Trans-eQTLs Are Often Explained by Cis-Mediation: A Genome-Wide Analysis among 1,800 South Asians
inferredcites →https://doi.org/10.18637/jss.v033.i01openalex-snapshot
Regularization Paths for Generalized Linear Models via Coordinate Descent
inferredcites →https://doi.org/10.18637/jss.v039.i05openalex-snapshot
Regularization Paths for Cox's Proportional Hazards Model via Coordinate Descent

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1038/s41588-017-0004-9openalex-snapshot
Annotation-free quantification of RNA splicing using LeafCutter
inferred← citeshttps://doi.org/10.1101/2022.03.25.22272928openalex-snapshot
A comparison of the genes and genesets identified by EWAS and GWAS of fourteen complex traits
inferred← citeshttps://doi.org/10.1101/2022.10.21.22281371openalex-snapshot
Allele frequency differences of causal variants have a major impact on low cross-ancestry portability of PRS
inferred← citeshttps://doi.org/10.3390/ijms21218150openalex-snapshot
Genotype-Based Gene Expression in Colon Tissue—Prediction Accuracy and Relationship with the Prognosis of Colorectal Cancer Patients
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.