Rate My Professor Tim Morgan

Morgan has co-authored over 30 peer-reviewed publications in prestigious journals such as Brain, Nature Genetics, American Journal of Human Genetics, and European Journal of Human Genetics. Key contributions include 'A functional role for septin-2 in the maintenance of the axon initial segment and in human cognitive development' (Brain, 2025), 'The hinge-1 domain of Flna is not necessary for diverse physiological functions in mice' (European Journal of Clinical Investigation, 2024), 'Pathogenic FLNA variants affecting the hinge region of filamin A are associated with male survival' (American Journal of Medical Genetics Part A, 2024), 'FLNA-filaminopathy skeletal phenotypes are not due to an osteoblast autonomous loss-of-function' (Bone Reports, 2023), 'Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia' (European Journal of Human Genetics, 2022), 'Impaired retinoic acid receptor-γ signalling underlies a heritable form of urothelial carcinoma' (HGG Advances, 2026), 'Mutations in genes encoding the cadherin receptor-ligand pair CDH4 and CDH6 cause skeletal dysplasia' (Nature Genetics, 2013), 'Germline mutations in WTX cause a sclerosing skeletal dysplasia' (Nature Genetics, 2009), 'Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome' (American Journal of Human Genetics, 2015), 'Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype' (2017), and 'Exon skip-inducing variants in FLNA in an attenuated form of frontometaphyseal dysplasia' (2021). These works have significantly impacted the field by identifying disease-causing mutations and characterizing phenotypes in skeletal dysplasias, filaminopathies, and other developmental conditions.