Abstract
Yangyang Yuan, Liubin Zhang, Qihan Long
Abstract
Authors
Institutions
Provenance
crossref
Confidence 100%
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Confidence 99%
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A global genetic interaction network maps a wiring diagram of cellular function
10.1126/science.aaf1420 · 2016
10.1093/nar/gkx557
10.1093/nar/gkx557
10.1016/b978-1-4160-3080-5.50009-2
10.1016/b978-1-4160-3080-5.50009-2
Polygenic inheritance and micro/minisatellites
10.1038/sj.mp.4000289 · 1998
Systematic analysis of complex genetic interactions
10.1126/science.aao1729 · 2018
Monogenic traits are not simple lessons from phenylketonuria
10.1016/s0168-9525(99)01761-8 · 1999
10.1111/cge.13150
10.1111/cge.13150
Monogenic disorders: an overview
10.21474/ijar01/3294 · 2017
Unresolved referenced work
Kept as external metadata until matched
10.1038/nrg910
10.1038/nrg910
Common variant burden contributes to the familial aggregation of migraine in 1,589 families
pubmed
Confidence 98%
europepmc
Confidence 96%
openalex
Confidence 95%
unpaywall
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
10.1016/j.neuron.2018.08.029 · 2018
Machine learning for detecting gene-gene interactions: a review
10.2165/00822942-200605020-00002 · 2006
10.1016/j.yexcr.2014.11.006
10.1016/j.yexcr.2014.11.006
MYBPH acts as modifier of cardiac hypertrophy in hypertrophic cardiomyopathy (HCM) patients
10.1007/s00439-016-1649-7 · 2016
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis
10.1038/ncomms9382 · 2015
10.1126/science.1155085
10.1126/science.1155085
10.1093/nar/gkv1068
10.1093/nar/gkv1068
10.1073/pnas.1815601116
10.1073/pnas.1815601116
10.1016/j.ajhg.2021.08.010
10.1016/j.ajhg.2021.08.010
10.1136/jmedgenet-2013-101713
10.1136/jmedgenet-2013-101713
10.1073/pnas.0406614101
10.1073/pnas.0406614101
Genenames.org: the HGNC and VGNC resources in 2021
10.1093/nar/gkaa980 · 2021
10.1371/journal.pgen.1003709
10.1371/journal.pgen.1003709
10.1002/humu.21517
10.1002/humu.21517
10.1093/nar/gkw971
10.1093/nar/gkw971
10.1073/pnas.1518646112
10.1073/pnas.1518646112
10.1126/science.1215040
10.1126/science.1215040
10.1371/journal.pgen.1003484
10.1371/journal.pgen.1003484
10.1186/s13059-015-0772-4
10.1186/s13059-015-0772-4
Interpretation of genomic variants using a unified biological network approach
10.1371/journal.pcbi.1002886 · 2013
10.1038/75556
10.1038/75556
10.1093/bioinformatics/btq064
10.1093/bioinformatics/btq064
Identifying disease genes using machine learning and gene functional similarities, assessed through Gene Ontology
10.1371/journal.pone.0208626 · 2018
10.1093/nar/gkq537
10.1093/nar/gkq537
10.1093/nar/gkn698
10.1093/nar/gkn698
10.1371/journal.pgen.1001154
10.1371/journal.pgen.1001154
10.1186/1471-2164-15-256
10.1186/1471-2164-15-256
10.1038/nature19057
10.1038/nature19057
10.1093/bioinformatics/btv602
10.1093/bioinformatics/btv602
10.1093/nar/gky1079
10.1093/nar/gky1079
10.1038/nrg2085
10.1038/nrg2085 · doi-reference
10.1146/annurev-genom-082509-141730
10.1146/annurev-genom-082509-141730 · doi-reference
10.1146/annurev.genet.39.073003.114751
10.1146/annurev.genet.39.073003.114751 · doi-reference
10.1016/j.neuron.2014.11.027
10.1016/j.neuron.2014.11.027 · doi-reference
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles
10.7554/elife.20125 · doi-reference
Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes
10.1038/s10038-018-0436-9 · doi-reference
Beware of risk for increased false positive rates in genome-wide association studies for phenotypic variability
10.3389/fgene.2013.00093 · doi-reference
10.1038/nature08185
10.1038/nature08185 · doi-reference
The Undiagnosed Diseases Network of the National Institutes of Health: A National Extension
10.1001/jama.2015.12249 · doi-reference
10.1038/ng.2892
10.1038/ng.2892 · doi-reference
Machine learning and integrative analysis of biomedical big data
10.3390/genes10020087 · doi-reference
DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants
10.1093/nar/gkw943 · doi-reference
Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders
10.1111/epi.14074 · doi-reference
10.1111/epi.12089
10.1111/epi.12089 · doi-reference
10.1016/j.artmed.2019.06.006
10.1016/j.artmed.2019.06.006 · doi-reference
10.1172/jci60981
10.1172/jci60981 · doi-reference
10.1111/j.2517-6161.1995.tb02031.x
10.1111/j.2517-6161.1995.tb02031.x · doi-reference
Statistics notes – The odds ratio
10.1136/bmj.320.7247.1468 · doi-reference
10.1007/978-0-387-98141-3
10.1007/978-0-387-98141-3 · doi-reference
10.1038/s42256-019-0138-9
10.1038/s42256-019-0138-9 · doi-reference
10.1056/nejmoa1516767
10.1056/nejmoa1516767 · doi-reference
10.1093/nar/gkr1257
10.1093/nar/gkr1257 · doi-reference
A map of human genome variation from population-scale sequencing
10.1038/nature09534 · doi-reference
10.1038/ejhg.2013.209
10.1038/ejhg.2013.209 · doi-reference
UniProt: a worldwide hub of protein knowledge
10.1093/nar/gky1049 · doi-reference
UniProt: the universal protein knowledgebase
10.1093/nar/gkw1099 · doi-reference
10.1093/bioinformatics/btu684
10.1093/bioinformatics/btu684 · doi-reference
COXPRESdb v7: a gene coexpression database for 11 animal species supported by 23 coexpression platforms for technical evaluation and evolutionary inference
10.1093/nar/gky1155 · doi-reference
10.1002/pmic.201400441
10.1002/pmic.201400441 · doi-reference
10.1089/bio.2015.29031.hmm
10.1089/bio.2015.29031.hmm · doi-reference
The Pfam protein families database in 2019
10.1093/nar/gky995 · doi-reference
10.1093/nar/gky1100
10.1093/nar/gky1100 · doi-reference
The Reactome pathway knowledgebase
10.1093/nar/gkt1102 · doi-reference
STRING: known and predicted protein-protein associations, integrated and transferred across organisms
10.1093/nar/gki005 · doi-reference
10.1093/nar/gky1131
10.1093/nar/gky1131 · doi-reference