Annie Godwin

Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome

Matthew O. Parker, D. Baralle, S. Ellard, 2022, American journal of human genetics.

Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders

J. Hehir-Kwa, B. D. de Vries, D. Baralle, 2020, American journal of human genetics.

Anaplastic lymphoma kinase (alk), a neuroblastoma associated gene, is expressed in neural crest domains during embryonic development of Xenopus.

W. Barrell, Karen J. Liu, M. Guille, 2021, Gene expression patterns : GEP.

Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

D. Baralle, S. Ellard, K. Stals, 2021, Genome medicine.

A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency

A. Pshezhetsky, E. Henckaerts, M. Agbandje-McKenna, 2018, Brain : a journal of neurology.

Monoallelic de novo variants in DDX17 cause a novel neurodevelopmental disorder

D. Koboldt, P. Sulem, A. O’Donnell-Luria, 2023, medRxiv.

Modelling human genetic disorders in Xenopus tropicalis

E. Seaby, H. Willsey, Annie Godwin, 2024, Disease models & mechanisms.