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Publications by Alica M. Goldman
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
American Journal of Human Genetics
Genetics
Channelopathy as a SUDEP Biomarker in Dravet Syndrome Patient-Derived Cardiac Myocytes
Stem Cell Reports
Biochemistry
Genetics
Developmental Biology
Cell Biology
Sudden Unexpected Death in Epilepsy Genetics: Molecular Diagnostics and Prevention
Epilepsia
Neurology
Brainstem Network Disruption: A Pathway to Sudden Unexplained Death in Epilepsy?
Human Brain Mapping
Nuclear Medicine
Radiology
Ultrasound Technology
Anatomy
Radiological
Neurology
Imaging
Mechanisms of Sudden Unexplained Death in Epilepsy
Current Opinion in Neurology
Neurology
De Novo Missense Variant in the GTPase Effector Domain (GED) of DNM1L Leads to Static Encephalopathy and Seizures
Cold Spring Harbor molecular case studies
Biochemistry
Molecular Medicine
Genetics
