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Publications by Ulrike B. S. Hedrich
KCNC1 ‐related Disorders: New De Novo Variants Expand the Phenotypic Spectrum
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
Differential Activation of Projection Neurons by Two Sensory Pathways Contributes to Motor Pattern Selection
Journal of Neurophysiology
Neuroscience
Physiology
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Novel Variants and Phenotypes Widen the Phenotypic Spectrum of GABRG2-related Disorders
Seizure : the journal of the British Epilepsy Association
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Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay
American Journal of Human Genetics
Genetics
De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders
American Journal of Human Genetics
Genetics
Phenotypic Spectrum of the Tubulin-Related Disorders and Functional Implications of Disease-Causing Mutations
Current Opinion in Genetics and Development
Genetics
Developmental Biology
Expanding the Phenotypic Spectrum ofECEL1-related Congenital Contracture Syndromes
Clinical Genetics
Genetics
Causative and Common PHOX2B Variants Define a Broad Phenotypic Spectrum
Clinical Genetics
Genetics
Spectrum of Gluten-Related Disorders: Consensus on New Nomenclature and Classification
BMC Medicine
Medicine
Update on the Phenotypic Spectrum of Lesch-Nyhan Disease and Its Attenuated Variants
Current Rheumatology Reports
Rheumatology
De Novo Variants in Congenital Diaphragmatic Hernia Identify MYRF as a New Syndrome and Reveal Genetic Overlaps With Other Developmental Disorders
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior