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Using Machine Learning to Predict Noncoding Variant Associations with Sulcal Patterns in Congenital Heart Disease
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease
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From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline
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Association of genetic and sulcal traits with executive function in congenital heart disease
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Implication of LRRC4C and DPP6 in neurodevelopmental disorders
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Of mice and men: molecular genetics of congenital heart disease
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A convergent molecular network underlying autism and congenital heart disease
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Role of radial glial cells in cerebral cortex folding
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Hypoplastic Left Heart Syndrome Is Heritable
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An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest
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Quantitative comparison and analysis of sulcal patterns using sulcal graph matching: A twin study
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Spatial distribution and longitudinal development of deep cortical sulcal landmarks in infants
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The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors
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Neurodevelopmental outcome in children with congenital heart disease
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Regulation of cerebral cortex size and folding by expansion of basal progenitors
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Integrative analysis of 111 reference human epigenomes
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
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A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia
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The genetic architecture of structural left–right asymmetry of the human brain
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Establishment of H3K9-methylated heterochromatin and its functions in tissue differentiation and maintenance
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Genomic analyses implicate noncoding de novo variants in congenital heart disease
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Effective gene expression prediction from sequence by integrating long-range interactions
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PCDH7 interacts with GluN1 and regulates dendritic spine morphology and synaptic function
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Connectivity optimization and the positioning of cortical areas
inferredcites →https://doi.org/10.1073/pnas.1016071107openalex-extracted
Histone H3K27ac separates active from poised enhancers and predicts developmental state
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The protomap is propagated to cortical plate neurons through an Eomes -dependent intermediate map
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clusterProfiler: an R Package for Comparing Biological Themes Among Gene Clusters
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Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/cercor/bhaa328openalex-extracted
Intergenerational Transmission of Cortical Sulcal Patterns from Mothers to their Children
inferredcites →https://doi.org/10.1093/cercor/bhab114openalex-extracted
Abnormal Right-Hemispheric Sulcal Patterns Correlate with Executive Function in Adolescents with Tetralogy of Fallot
inferredcites →https://doi.org/10.1093/cercor/bhm225openalex-extracted
Cortical Folding Patterns and Predicting Cytoarchitecture
inferredcites →https://doi.org/10.1093/cercor/bhr126openalex-extracted
Emerging Cerebral Connectivity in the Human Fetal Brain: An MR Tractography Study
inferredcites →https://doi.org/10.1093/cercor/bhs292openalex-extracted
Quantification and Discrimination of Abnormal Sulcal Patterns in Polymicrogyria
inferredcites →https://doi.org/10.1093/cercor/bhu305openalex-extracted
Atypical Sulcal Pattern in Children with Developmental Dyslexia and At-Risk Kindergarteners
inferredcites →https://doi.org/10.1093/cercor/bhz101openalex-extracted
Abnormal Left-Hemispheric Sulcal Patterns Correlate with Neurodevelopmental Outcomes in Subjects with Single Ventricular Congenital Heart Disease
inferredcites →https://doi.org/10.1093/cvr/cvy061openalex-extracted
Slit–Robo signalling in heart development
inferredcites →https://doi.org/10.1097/mop.0000000000000530openalex-extracted
Genetic contribution to neurodevelopmental outcomes in congenital heart disease: are some patients predetermined to have developmental delay?
inferredcites →https://doi.org/10.1097/pcc.0000000000000800openalex-extracted
Neurodevelopmental Outcomes in Children With Congenital Heart Disease—What Can We Impact?
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-extracted
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
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inferredcites →https://doi.org/10.1126/science.abn6598openalex-extracted
Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images
inferredcites →https://doi.org/10.1136/jmedgenet-2017-104611openalex-extracted
Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects
inferredcites →https://doi.org/10.1161/circulationaha.109.857987openalex-extracted
Recurrence of Congenital Heart Defects in Families
inferredcites →https://doi.org/10.1161/circulationaha.109.865568openalex-extracted
Brain Volume and Metabolism in Fetuses With Congenital Heart Disease
inferredcites →https://doi.org/10.1186/1471-2105-9-559openalex-extracted
WGCNA: an R package for weighted correlation network analysis
inferredcites →https://doi.org/10.1212/wnl.0000000000001524openalex-extracted
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia
inferredcites →https://doi.org/10.1253/circj.cj-17-0250openalex-extracted
Familial Aggregation and Heritability of Congenital Heart Defects
inferredcites →https://doi.org/10.1371/journal.pcbi.1008050openalex-extracted
Cross-species regulatory sequence activity prediction
inferredcites →https://doi.org/10.1371/journal.pone.0030377openalex-extracted
Fast Computation and Applications of Genome Mappability
inferredcites →https://doi.org/10.1371/journal.pone.0123106openalex-extracted
Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in Neurodevelopment
inferredcites →https://doi.org/10.1371/journal.pone.0191319openalex-extracted
The Congenital Heart Disease Genetic Network Study: Cohort description
inferredcites →https://doi.org/10.1523/jneurosci.4682-09.2010openalex-extracted
A Surface-Based Analysis of Hemispheric Asymmetries and Folding of Cerebral Cortex in Term-Born Human Infants
inferredcites →https://doi.org/10.1542/peds.2016-4055openalex-extracted
Brain Injury and Neurodevelopmental Outcome in Congenital Heart Disease: A Systematic Review
inferredcites →https://doi.org/10.3389/fped.2023.1157630openalex-extracted
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system
inferredcites →https://doi.org/10.3390/cells9122711openalex-extracted
Right Place at the Right Time: How Changes in Protocadherins Affect Synaptic Connections Contributing to the Etiology of Neurodevelopmental Disorders
inferredcites →https://doi.org/10.3892/mmr.2021.12255openalex-extracted
H3K9me2 regulates early transcription factors to promote mesenchymal stem‑cell differentiation into cardiomyocytes
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Haplotype-based variant detection from short-read sequencing
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