Alfred L George

50PUBLICATIONS
236CO-AUTHORS
NeurogeneticsAutonomic nervous systemNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Characterisation of biological macromolecules
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Publications (50)

|Oct 27, 2026
KCNH1 variants associated with neurodevelopmental disorders exhibit prominent gain of function.

|Oct 25, 2026
ATP1A3 dysfunction alters excitability and developmental trajectory of human neurons in alternating hemiplegia of childhood.

|Oct 24, 2026
Elevated neuronal excitability and seizure susceptibility in a mouse model of SCN2A -related developmental and epileptic encephalopathy.

|Jul 21, 2026
Classification models for KCNQ1 variants distinguish functional and trafficking effects to enhance pathogenicity interpretation.

|Jun 23, 2026
Protein-enhanced small molecule disruptors of ordered membrane domains.

|Jun 04, 2026
Excitatory Dysfunction and Phenotypic Rescue in a Human Neuronal Model of SCN2A-Related Disorders.

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Frequent Collaborators

13 joint publications

Carlos G Vanoye

8 joint publications

Charles R Sanders

6 joint publications

Christopher H Thompson

4 joint publications

Jens Meiler