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Publications by Fadi F. Hamdan
De Novo Mutations in FOXP1 in Cases With Intellectual Disability, Autism, and Language Impairment
American Journal of Human Genetics
Genetics
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons
American Journal of Human Genetics
Genetics
De Novo Mutations in the Gene Encoding the Synaptic Scaffolding proteinSHANK3in Patients Ascertained for Schizophrenia
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Re-Annotation of 191 Developmental and Epileptic Encephalopathy-Associated Genes Unmasks De Novo Variants in SCN1A
npj Genomic Medicine
Genetics
Molecular Biology
Conformational Changes That Occur During M3Muscarinic Acetylcholine Receptor Activation Probed by the Use of Anin SituDisulfide Cross-Linking Strategy
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
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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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Regulating the Regulator: Post-Translational Modification of RAS
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