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Genetic analysis of de novo variants reveals sex differences in complex and isolated congenital diaphragmatic hernia and indicates MYRF as a candidate gene
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471142905.hg0725s87openalex-snapshot
Interpreting de novo Variation in Human Disease Using denovolyzeR
inferredcites →https://doi.org/10.1002/ajmg.a.30778openalex-snapshot
Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia
inferredcites →https://doi.org/10.1002/ajmg.a.32896openalex-snapshot
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia
inferredcites →https://doi.org/10.1002/ajmg.c.30126openalex-snapshot
Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH
inferredcites →https://doi.org/10.1002/ajmg.c.30128openalex-snapshot
Development of the diaphragm and genetic mouse models of diaphragmatic defects
inferredcites →https://doi.org/10.1002/bdr2.1015openalex-snapshot
Survival Disparities Associated with Congenital Diaphragmatic Hernia
inferredcites →https://doi.org/10.1007/s00439-017-1774-yopenalex-snapshot
Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia
inferredcites →https://doi.org/10.1016/j.jpedsurg.2005.03.025openalex-snapshot
Cardiac anomalies in patients with congenital diaphragmatic hernia and their prognosis: a report from the Congenital Diaphragmatic Hernia Study Group
inferredcites →https://doi.org/10.1016/j.jpedsurg.2010.03.011openalex-snapshot
Neurodevelopmental outcome of infants with congenital diaphragmatic hernia prospectively enrolled in an interdisciplinary follow-up program
inferredcites →https://doi.org/10.1016/j.jpedsurg.2014.11.002openalex-snapshot
Improved mortality rate for congenital diaphragmatic hernia in the modern era of management: 15year experience in a single institution
inferredcites →https://doi.org/10.1016/j.jpedsurg.2015.02.025openalex-snapshot
The association between congenital diaphragmatic hernia and undescended testes
inferredcites →https://doi.org/10.1016/j.ydbio.2006.09.050openalex-snapshot
Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects
inferredcites →https://doi.org/10.1038/nature09298openalex-snapshot
Integrating common and rare genetic variation in diverse human populations
inferredcites →https://doi.org/10.1038/nature12141openalex-snapshot
De novo mutations in histone-modifying genes in congenital heart disease
inferredcites →https://doi.org/10.1038/nature13908openalex-snapshot
The contribution of de novo coding mutations to autism spectrum disorder
inferredcites →https://doi.org/10.1038/nature19057openalex-snapshot
Analysis of protein-coding genetic variation in 60,706 humans
inferredcites →https://doi.org/10.1038/ng.2892openalex-snapshot
A general framework for estimating the relative pathogenicity of human genetic variants
inferredcites →https://doi.org/10.1038/ng.3050openalex-snapshot
A framework for the interpretation of de novo mutation in human disease
inferredcites →https://doi.org/10.1038/ng.3250openalex-snapshot
Muscle connective tissue controls development of the diaphragm and is a source of congenital diaphragmatic hernias
inferredcites →https://doi.org/10.1038/ng.3970openalex-snapshot
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
inferredcites →https://doi.org/10.1038/ng1847openalex-snapshot
Principal components analysis corrects for stratification in genome-wide association studies
inferredcites →https://doi.org/10.1038/nn.4351openalex-snapshot
Rapid production of new oligodendrocytes is required in the earliest stages of motor-skill learning
inferredcites →https://doi.org/10.1053/j.sempedsurg.2007.01.004openalex-snapshot
Diaphragm development and congenital diaphragmatic hernia
inferredcites →https://doi.org/10.1053/jpsu.2000.8725openalex-snapshot
Congenital diaphragmatic hernia: A meta-analysis of mortality factors
inferredcites →https://doi.org/10.1073/pnas.0507832102openalex-snapshot
Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia
inferredcites →https://doi.org/10.1073/pnas.1121621109openalex-snapshot
Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes
inferredcites →https://doi.org/10.1073/pnas.1211070110openalex-snapshot
Examining and interpreting the female protective effect against autistic behavior
inferredcites →https://doi.org/10.1086/429842openalex-snapshot
Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization
inferredcites →https://doi.org/10.1086/497082openalex-snapshot
Narrowing the Candidate Region for Congenital Diaphragmatic Hernia in Chromosome 15q26: Contradictory Results
inferredcites →https://doi.org/10.1086/519795openalex-snapshot
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/hmg/ddv196openalex-snapshot
Increased burden ofde novopredicted deleterious variants in complex congenital diaphragmatic hernia
inferredcites →https://doi.org/10.1093/nar/gkq603openalex-snapshot
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
inferredcites →https://doi.org/10.1093/nar/gkx080openalex-snapshot
Homo-trimerization is essential for the transcription factor function of Myrf for oligodendrocyte differentiation
inferredcites →https://doi.org/10.1101/gr.078212.108openalex-snapshot
Mapping short DNA sequencing reads and calling variants using mapping quality scores
inferredcites →https://doi.org/10.1101/gr.080531.108openalex-snapshot
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes
inferredcites →https://doi.org/10.1126/science.1254960openalex-snapshot
Motor skill learning requires active central myelination
inferredcites →https://doi.org/10.1126/science.aac9396openalex-snapshot
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
inferredcites →https://doi.org/10.1136/jmedgenet-2012-101135openalex-snapshot
De novo copy number variants are associated with congenital diaphragmatic hernia
inferredcites →https://doi.org/10.1152/ajplung.00027.2008openalex-snapshot
Gene expression in the developing diaphragm: significance for congenital diaphragmatic hernia
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/10.1186/s40748-017-0045-1openalex-snapshot
Congenital Diaphragmatic hernia – a review
inferredcites →https://doi.org/10.1371/journal.pbio.1001624openalex-snapshot
A Bacteriophage Tailspike Domain Promotes Self-Cleavage of a Human Membrane-Bound Transcription Factor, the Myelin Regulatory Factor MYRF
inferredcites →https://doi.org/10.1371/journal.pbio.1001625openalex-snapshot
MYRF Is a Membrane-Associated Transcription Factor That Autoproteolytically Cleaves to Directly Activate Myelin Genes
inferredcites →https://doi.org/10.1371/journal.pgen.0010010openalex-snapshot
Fog2 Is Required for Normal Diaphragm and Lung Development in Mice and Humans
inferredcites →https://doi.org/10.1371/journal.pgen.0010058openalex-snapshot
Canine Genomics and Genetics: Running with the Pack
inferredcites →https://doi.org/10.1371/journal.pgen.1003907openalex-snapshot
The Transcription Factors Sox10 and Myrf Define an Essential Regulatory Network Module in Differentiating Oligodendrocytes
inferredcites →https://doi.org/10.1542/peds.2016-3659openalex-snapshot
Congenital Diaphragmatic Hernia and Growth to 12 Years
inferredcites →https://doi.org/10.7554/elife.16009openalex-snapshot
Conditional deletion of WT1 in the septum transversum mesenchyme causes congenital diaphragmatic hernia in mice
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1038/s41598-018-31477-4openalex-snapshot
Elucidating the transactivation domain of the pleiotropic transcription factor Myrf
inferred← citeshttps://doi.org/10.1136/archdischild-2017-313933openalex-snapshot
Early population-based outcomes of infants born with congenital diaphragmatic hernia
inferred← citeshttps://doi.org/10.1161/jaha.119.012941openalex-snapshot
Spatiotemporal Gene Coexpression and Regulation in Mouse Cardiomyocytes of Early Cardiac Morphogenesis
inferred← citeshttps://doi.org/10.1167/iovs.18-26275openalex-snapshot
Detection of Clinically Relevant Genetic Variants in Chinese Patients With Nanophthalmos by Trio-Based Whole-Genome Sequencing Study
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