Manju Kurian

41PUBLICATIONS
253CO-AUTHORS
NeurogeneticsCellular nervous systemNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (41)

|Apr 17, 2026
Longitudinal Phenotypic Trajectories in GNAO1-Related Disorders: Defining Disease Progression and Clinical Profiles.

|Feb 03, 2026
An in vivo and in vitro spatiotemporal profile of human midbrain development.

Dimitri Budinger, Pau Puigdevall, George T Hall

|Jan 19, 2026
International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.

Laia Nou-Fontanet, Claudia Ravelli, Lydie Burglen

|Dec 12, 2025
Atypical GNAO1 variants in severe childhood speech disorders: clinical, genetic, and molecular insights.

Yonika A Larasati, Moritz Thiel, Ainara Salazar-Villacorta

|Sep 13, 2025
Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study.

Adeline Ngoh, Maria Clark, Rebecca Greenaway

|May 14, 2025
Development and Preliminary Validation of a Parkinsonism-Dystonia Scale for Infants and Young Children.

Roser Pons, Toni S Pearson, Belen Perez-Dueñas

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Frequent Collaborators

9 joint publications

Robert V V Spaull

5 joint publications

Apostolos Papandreou

4 joint publications

Belén Pérez-Dueñas

4 joint publications

Victor S C Fung