Cox, Timothy C.

MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: Implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders

Short, K. M., Hopwood, B., Yi, Z., & Cox, T. C. (2002) · BMC Cell Biology

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 137

A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development

Ashe, A., Morgan, D. K., Whitelaw, N. C., Bruxner, T. J., Vickaryous, N. K., Cox, L. L., Butterfield, N. C., Wicking, C., Blewitt, M. E., Wilkins, S. J., et al. (2008) · Genome Biology

Epigenetics and DNA MethylationGenomics and Chromatin Dynamics

Cited by 117

Triplication of the interferon receptor locus contributes to hallmarks of Down syndrome in a mouse model

Waugh, K. A., Minter, R., Baxter, J., Chi, C., Galbraith, M. D., Tuttle, K. D., Eduthan, N. P., Kinning, K. T., Andrysik, Z., Araya, P., et al. (2023) · Nature Genetics

Down syndrome and intellectual disability researchinterferon and immune responses

Cited by 117

Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis

Nandadasa, S., Kraft, C. M., Wang, L. W., O’Donnell, A., Patel, R., Gee, H. Y., Grobe, K., Cox, T. C., Hildebrandt, F., & Apte, S. S. (2019) · Nature Communications

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 76

Transcriptional Regulation of the Human Erythroid 5-Aminolevulinate Synthase Gene

Surinya, K. H., Cox, T. C., & May, B. K. (1997) · Journal of Biological Chemistry

Hemoglobinopathies and Related DisordersGenomics and Chromatin Dynamics

Cited by 74

Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment

Shaffer, J. R., Li, J., Lee, M. K., Roosenboom, J., Orlova, E., Adhikari, K., Gallo, C., Poletti, G., Schuler-Faccini, L., Bortolini, M.-C., et al. (2017) · The American Journal of Human Genetics

Genetic Associations and EpidemiologyDermatoglyphics and Human Traits

Cited by 47

Somatic FGFR and TWIST Mutations are not a Common Cause of Isolated Nonsyndromic Single Suture Craniosynostosis

Anderson, P. J., Cox, T. C., Roscioli, T., Elakis, G., Smithers, L., David, D. J., & Powell, B. (2007) · Journal of Craniofacial Surgery

Craniofacial Disorders and Treatmentsdental development and anomalies

Cited by 23