Sithara Ramdas

10PUBLICATIONS
45CO-AUTHORS
Gene and molecular therapyCancer diagnosisMedical infection agents (incl. prions)Neurology and neuromuscular diseasesMedical molecular engineering of nucleic acids and proteins
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Publications (10)

|Feb 04, 2026
Optimal strategies for treatment discontinuation in MOG antibody-associated disease.

Wei Z Yeh, Anna Francis, Sarah Cooper

|Feb 03, 2026
Congenital myasthenic syndrome: is it time for a name change to genetic myasthenic syndrome?

Sithara Ramdas, Yin Yao Dong, Pinki Munot

|Nov 18, 2025
Prevalence and Geographical Distribution of Patients With Congenital Myasthenic Syndromes in the United Kingdom.

Elena Rossini, Leighann Henehan, Yin Yao Dong

|Nov 03, 2025
Paramagnetic Rim Lesions in Pediatric Multiple Sclerosis and Their Association With Brain Tissue Atrophy.

Riccardo Nistri, Ermelinda De Meo, Nee Na Kim

|Dec 12, 2024
Quantitative Contribution of Clinical Attacks to Residual Disability in Patients With AQP4-Antibody Neuromyelitis Optica Spectrum Disorder.

Bo Chen, Anna Francis, Sarah A Cooper

|Nov 27, 2024
Assessing the Utility of ColabFold and AlphaMissense in Determining Missense Variant Pathogenicity for Congenital Myasthenic Syndromes.

Finlay Ryan-Phillips, Leighann Henehan, Sithara Ramdas

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Frequent Collaborators

4 joint publications

David Beeson

3 joint publications

Yael Hacohen

2 joint publications

Theodora Markati

2 joint publications

Gemma Fisher