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References from Dosage-sensitive molecular mechanisms are associated with the tissue-specificity of traits and diseases. Local targets link to admitted publications; unresolved targets remain external evidence.
OMIM.org: leveraging knowledge across phenotype-gene relationships
10.1093/nar/gky1151 · 2019 · External reference
10.1093/nar/gky1120
10.1093/nar/gky1120 · External reference
10.1126/science.aaw3472
10.1126/science.aaw3472 · External reference
A large-scale analysis of tissue-specific pathology and gene expression of human disease genes and complexes
10.1073/pnas.0810772105 · 2008 · External reference
Comparative analysis of human tissue interactomes reveals factors leading to tissue-specific manifestation of hereditary diseases
10.1371/journal.pcbi.1003632 · 2014 · External reference
10.1038/ng.3259
10.1038/ng.3259 · External reference
10.1038/s41588-018-0154-4
10.1038/s41588-018-0154-4 · External reference
10.1038/s41576-019-0200-9
10.1038/s41576-019-0200-9 · External reference
10.1038/nature24277
10.1038/nature24277 · External reference
10.1126/science.1260419
10.1126/science.1260419 · External reference
10.1101/612143
10.1101/612143 · External reference
10.1002/jez.b.22555
10.1002/jez.b.22555 · External reference
Paralog dependency indirectly affects the robustness of human cells
10.15252/msb.20198871 · 2019 · External reference
10.1126/science.aac7041
10.1126/science.aac7041 · External reference
10.1371/journal.pgen.1008466
10.1371/journal.pgen.1008466 · External reference
A common framework for understanding the origin of genetic dominance and evolutionary fates of gene duplications
10.1016/j.tig.2004.05.001 · 2004 · External reference
Comments on “Human dominant disease genes are enriched in paralogs originating from whole genome duplication”
2014 · External reference
Human dominant disease genes are enriched in paralogs originating from whole genome duplication
10.1371/journal.pcbi.1003754 · 2014 · External reference
10.1073/pnas.0914697107
10.1073/pnas.0914697107 · External reference
10.1371/journal.pgen.1007327
10.1371/journal.pgen.1007327 · External reference
Unresolved reference
2010 · External reference
Human monogenic disease genes have frequently functionally redundant paralogs
2013 · External reference
10.1038/s41576-019-0127-1
10.1038/s41576-019-0127-1 · External reference
10.1038/nmeth.3799
10.1038/nmeth.3799 · External reference
A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia
10.1371/journal.pgen.1000642 · 2009 · External reference
10.1093/nar/gkn851
10.1093/nar/gkn851 · External reference
10.1038/nature09144
10.1038/nature09144 · External reference
Network analysis of pseudogene-gene relationships: from pseudogene evolution to their functional potentials
2018 · External reference
10.1126/science.aad8411
10.1126/science.aad8411 · External reference
10.1038/s41588-018-0081-4
10.1038/s41588-018-0081-4 · External reference
10.1056/nejmoa1702752
10.1056/nejmoa1702752 · External reference
10.1056/nejmoa1710504
10.1056/nejmoa1710504 · External reference
10.1158/1078-0432.ccr-16-1193
10.1158/1078-0432.ccr-16-1193 · External reference
Harnessing synthetic lethality to predict the response to cancer treatment
2018 · External reference
Fast and rigorous computation of gene and pathway scores from SNP-based summary statistics
10.1371/journal.pcbi.1004714 · 2016 · External reference
10.1093/nar/gky1079
10.1093/nar/gky1079 · External reference
