On the public citation graph

Implicating candidate genes at GWAS signals by leveraging topologically associating domains

https://doi.org/10.1101/087718
0 signed · 24 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1007/s00125-016-4077-2openalex-snapshot
The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5
inferredcites →https://doi.org/10.1016/j.cell.2014.11.021openalex-snapshot
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
inferredcites →https://doi.org/10.1016/j.cmet.2015.09.018openalex-snapshot
Making Biological Sense of GWAS Data: Lessons from the FTO Locus
inferredcites →https://doi.org/10.1016/s0140-6736(08)60599-1openalex-snapshot
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study
inferredcites →https://doi.org/10.1038/75556openalex-snapshot
Gene Ontology: tool for the unification of biology
inferredcites →https://doi.org/10.1038/nature11082openalex-snapshot
Topological domains in mammalian genomes identified by analysis of chromatin interactions
inferredcites →https://doi.org/10.1038/nature12124openalex-snapshot
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits
inferredcites →https://doi.org/10.1038/nature13415openalex-snapshot
Comparative analysis of metazoan chromatin organization
inferredcites →https://doi.org/10.1038/nbt.2422openalex-snapshot
Interpreting noncoding genetic variation in complex traits and human disease
inferredcites →https://doi.org/10.1038/ng.2249openalex-snapshot
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
inferredcites →https://doi.org/10.1038/ng.446openalex-snapshot
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
inferredcites →https://doi.org/10.1038/nm.3074openalex-snapshot
WNT signaling in bone homeostasis and disease: from human mutations to treatments
inferredcites →https://doi.org/10.1056/nejmoa1502214openalex-snapshot
FTO Obesity Variant Circuitry and Adipocyte Browning in Humans
inferredcites →https://doi.org/10.1093/bioinformatics/btl574openalex-snapshot
LdCompare: rapid computation of single- and multiple-markerr2 and genetic coverage
inferredcites →https://doi.org/10.1093/nar/gkt1229openalex-snapshot
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
inferredcites →https://doi.org/10.1093/nar/gkt439openalex-snapshot
WEB-based GEne SeT AnaLysis Toolkit (WebGestalt): update 2013
inferredcites →https://doi.org/10.1093/nar/gkw500openalex-snapshot
How far from the SNP may the causative genes be?
inferredcites →https://doi.org/10.1101/074450openalex-snapshot
Local genetic effects on gene expression across 44 human tissues
inferredcites →https://doi.org/10.1111/j.1749-6632.2011.06383.xopenalex-snapshot
Accurate evaluation and analysis of functional genomics data and methods
inferredcites →https://doi.org/10.1126/science.1181369openalex-snapshot
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
inferredcites →https://doi.org/10.1371/journal.pcbi.1002375openalex-snapshot
Ten Years of Pathway Analysis: Current Approaches and Outstanding Challenges
inferredcites →https://doi.org/10.1371/journal.pone.0062161openalex-snapshot
Assessing Methods for Assigning SNPs to Genes in Gene-Based Tests of Association Using Common Variants

What points at this work

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

inferred← backgroundhttps://doi.org/10.5281/zenodo.232520zenodo-depositor-declared
Data To Initialize A Tad_Pathways Analysis
inferred← citeshttps://doi.org/10.1186/s13040-019-0197-9openalex-snapshot
Innovative strategies for annotating the “relationSNP” between variants and molecular phenotypes
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.