Tao Wang

Associate Professor

19942018
If you made any changes in Pure these will be visible here soon.

Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 6 Similar Profiles
Intellectual Disability Medicine & Life Sciences
Gyrate Atrophy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Retinal Degeneration Medicine & Life Sciences
Genes Medicine & Life Sciences
Ornithine-Oxo-Acid Transaminase Medicine & Life Sciences
AMPA Receptors Medicine & Life Sciences
Chromosome Banding Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1994 2018

FRMPD4 mutations cause X-linked intellectual disability and disrupt dendritic spine morphogenesis

Piard, J. , Hu, J. H. , Campeau, P. M. , Rzońca, S. , Esch, H. V. , Vincent, E. , Han, M. , Rossignol, E. , Castaneda, J. , Chelly, J. , Skinner, C. , Kalscheuer, V. M. , Wang, R. , Lemyre, E. , Kosińska, J. , Stawinski, P. , Bal, J. , Hoffman, D. A. , Schwartz, C. E. , Maldergem, L. V. & 2 others Wang, T. & Worley, P. F. Feb 15 2018 In : Human Molecular Genetics. 27, 4, p. 589-600 12 p., ddx426

Research output: Contribution to journalArticle

Dendritic Spines
Morphogenesis
Intellectual Disability
Frameshift Mutation
Mutation

GRASP1 Regulates Synaptic Plasticity and Learning through Endosomal Recycling of AMPA Receptors

Chiu, S. L., Diering, G. H., Ye, B., Takamiya, K., Chen, C. M., Jiang, Y., Niranjan, T., Schwartz, C. E., Wang, T. & Huganir, R. L. Mar 22 2017 In : Neuron. 93, 6, p. 1405-1419.e8

Research output: Contribution to journalArticle

Neuronal Plasticity
AMPA Receptors
Endosomes
Learning
Intellectual Disability

Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability

Vaidyanathan, K., Niranjan, T., Selvan, N., Teo, C. F., May, M., Patel, S., Weatherly, B., Skinner, C., Opitz, J., Carey, J., Viskochil, D., Gecz, J., Shaw, M., Peng, Y., Alexov, E., Wang, T., Schwartz, C. & Wells, L. May 26 2017 In : Journal of Biological Chemistry. 292, 21, p. 8948-8963 16 p.

Research output: Contribution to journalArticle

Acetylglucosamine
Missense Mutation
Intellectual Disability
Genes
Post Translational Protein Processing

Mice lacking GRIP1/2 show increased social interactions and enhanced phosphorylation at GluA2-S880

Han, M., Mejias, R., Chiu, S. L., Rose, R., Adamczyk, A., Huganir, R. & Wang, T. Mar 15 2017 In : Behavioural Brain Research. 321, p. 176-184 9 p.

Research output: Contribution to journalArticle

Interpersonal Relations
Knockout Mice
Autistic Disorder
Phosphorylation
Social Behavior

A distinct X-linked syndrome involving joint contractures, keloids, large optic cup-to-disc ratio, and renal stones results from a filamin A (FLNA) mutation

Lah, M., Niranjan, T., Srikanth, S., Holloway, L., Schwartz, C. E., Wang, T. & Weaver, D. D. Apr 1 2016 In : American Journal of Medical Genetics, Part A. 170, 4, p. 881-890 10 p.

Research output: Contribution to journalArticle

Filamins
Keloid
Contracture
Joints
Exome