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Publications by David E. Godler
Incomplete Silencing of Full Mutation Alleles in Males With Fragile X Syndrome Is Associated With Autistic Features
Molecular Autism
Psychiatry
Mental Health
Developmental Neuroscience
Developmental Biology
Molecular Biology
Exploring Autism Symptoms in an Australian Cohort of Patients With Prader-Willi and Angelman Syndromes
Journal of Neurodevelopmental Disorders
Pediatrics
Cognitive Neuroscience
Perinatology
Neurology
Forensic Medicine
Child Health
Pathology
Analysis of the Prader-Willi Syndrome Imprinting Center Using Droplet Digital PCR and Next-Generation Whole-Exome Sequencing
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Linking the FMR1 Alleles With Small CGG Expansions With Neurodevelopmental Disorders: Preliminary Data Suggest an Involvement of Epigenetic Mechanisms
American Journal of Medical Genetics, Part A
Genetics
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Molecular Control of Endothelial Cell Behaviour During Blood Vessel Morphogenesis
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Multidimensional Proteomics for Cell Biology
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DNA Methylation Pathways and Their Crosstalk With Histone Methylation
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Transcriptional Integration of Metabolism by the Nuclear Sterol-Activated Receptors LXR and FXR
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Tail-Anchored Membrane Protein Insertion Into the Endoplasmic Reticulum
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Dynamin, a Membrane-Remodelling GTPase
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Regulating the Regulator: Post-Translational Modification of RAS
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Trithorax Group Proteins: Switching Genes on and Keeping Them Active
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