Evangeline Wassmer

Birmingham Children's Hospital — United Kingdom

Medicine · Health Sciences

62h-index14.0kcitations254works2.52yr avg
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Research Topics

Multiple Sclerosis Research Studies(69), Peripheral Neuropathies and Disorders(44), RNA regulation and disease(27), Systemic Lupus Erythematosus Research(21), Autoimmune Neurological Disorders and Treatments(21)

Publications237 total

A novel patient-Centered approach to clinical trial readiness in rare diseases: Application in Aicardi-Goutières Syndrome (AGS)
Molecular Genetics and Metabolism·2026Open Access
From Neonatal Encephalopathy to Adult Survival: Revisiting the Natural History of D‐Bifunctional Protein Deficiency in a Multicentre International Case Series
Journal of Inherited Metabolic Disease·2025
ATRX Deficiency Drives Aberrant Type I Interferon Signalling Through cGAS-Dependent Transcriptional Dysregulation
2025· 2 citedOpen Access
MRI cortical thickness in paediatric auto-immune encephalitis and acute disseminated encephalomyelitis
European Journal of Paediatric Neurology·2025Open Access
Paramagnetic Rim Lesions in Pediatric Multiple Sclerosis and Their Association With Brain Tissue Atrophy
Neurology Neuroimmunology & Neuroinflammation·2025Open Access
Observational evidence of the treatment efficacy of IVIG as maintenance therapy for pediatric MOGAD
European Journal of Paediatric Neurology·2025
Critical Functional Domains in Pediatric Onset TUBB4A-Related Leukodystrophy: A Clinical and Caregiver's Perspective
Pediatric Neurology·2025· 1 cited
Biallelic variants in the non-coding RNA gene <i>RNU4-2</i> cause a recessive neurodevelopmental syndrome with distinct white matter changes
2025· 3 citedOpen Access
Slowly Expanding Lesions in Pediatric-Onset Multiple Sclerosis
JAMA Neurology·2025· 1 citedOpen Access
Reduced brain volumes in children with radiologically isolated syndrome
Multiple Sclerosis Journal·2025
Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci
European Journal of Human Genetics·2025· 3 citedOpen Access
A first report of progressive multifocal leukoencephalopathy in childhood-onset NMOSD
Multiple Sclerosis Journal·2025· 1 citedOpen Access
Enabling new insights from old scans by repurposing clinical MRI archives for multiple sclerosis research
Nature Communications·2025· 10 citedOpen Access
Acute neurological deficit: is it demyelination? Review of demyelinating disorders of the central nervous system
Paediatrics and Child Health·2025
The natural history of variable subtypes in pediatric-onset TUBB4A-related leukodystrophy
Molecular Genetics and Metabolism·2025· 7 citedOpen Access
P334: Deep phenotyping of thirty-one cases of Aicardi-Goutières syndrome
Genetics in Medicine Open·2025Open Access
Interrogation of coded healthcare data to facilitate identification of patients with a rare neurotransmitter disorder; Aromatic L-Amino acid decarboxylase deficiency
Intelligence-Based Medicine·2025Open Access
Buccal midazolam vs rectal diazepam administered by parents for continuing and serial epileptic seizures: a randomised controlled trial of parental preferences
Exploration of neuroscience·2024Open Access
Pediatric MOG-Ab–Associated Encephalitis
Neurology Neuroimmunology & Neuroinflammation·2024· 13 citedOpen Access
Severe Pediatric Neurological Manifestations With SARS-CoV-2 or MIS-C Hospitalization and New Morbidity
Aston Publications Explorer (Aston University)·2024Open Access
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Frequent Co-authors

Ming Lim(22), Cheryl Hemingway(15), Yael Hacohen(12), Kumaran Deiva(10), Kevin Rostásy(8), Michael Absoud(8), Rinze F. Neuteboom(7), Marc Tardieu(6), Tanuja Chitnis(6), Angela Vincent(6), Brenda Banwell(5), Christian Lechner(5), Olga Ciccarelli(5), Banu Anlar(5), Patrick Waters(5), Paul Gissen(5), William Whitehouse(5), Lauren Krupp(4), Maria Pia Amato(4), Angelo Ghezzi(4)