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Publications by Astrid S. Plomp
Equivalent Missense Variant in the FOXP2 and FOXP1 Transcription Factors Causes Distinct Neurodevelopmental Disorders
Human Mutation
Genetics
Pathogenic Effect of a TGFBR1 Mutation in a Family With Loeys–Dietz Syndrome
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Related publications
The Distinct and Overlapping Phenotypic Spectra of FOXP1 and FOXP2 in Cognitive Disorders
Human Genetics
Genetics
The Arg1038Gly Missense Variant in the NF1 Gene Causes a Mild Phenotype Without Neurofibromas
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Overview of the Role of Environmental Factors in Neurodevelopmental Disorders
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy
American Journal of Human Genetics
Genetics
miR-191 Modulates B-Cell Development and Targets Transcription Factors E2A, Foxp1, and Egr1
European Journal of Immunology
Allergy
Immunology
Cardiofaciocutaneous Syndrome With Rare Structural Variant in DOCK8 Gene Associated With Neurodevelopmental Disorders
Clinical Case Reports
Medicine
Somatosensory Processing in Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
Pediatrics
Cognitive Neuroscience
Perinatology
Neurology
Forensic Medicine
Child Health
Pathology
Missense Variant in CCDC22 Causes X-Linked Recessive Intellectual Disability With Features of Ritscher-Schinzel/3c Syndrome
European Journal of Human Genetics
Genetics
Cross Talk: The Microbiota and Neurodevelopmental Disorders
Frontiers in Neuroscience
Neuroscience
