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

  • 1 Similar Profiles
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Proteins Medicine & Life Sciences
Gyrate Atrophy Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Retinal Degeneration Medicine & Life Sciences
Brain Medicine & Life Sciences

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

Research Output 1994 2017

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: Research - peer-reviewArticle

Neuronal Plasticity
AMPA Receptors
Learning
Endosomes
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: Research - peer-reviewArticle

Acetylglucosamine
Missense Mutation
Intellectual Disability
Genes
O-GlcNAc transferase

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: Research - peer-reviewArticle

Interpersonal Relations
Knockout Mice
Phosphorylation
Mouse Grip2 protein
Mouse Grip1 protein

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: Research - peer-reviewArticle

Filamins
Keloid
Contracture
Joints
Kidney

Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes

Niranjan, T. S., Skinner, C., May, M., Turner, T., Rose, R., Stevenson, R., Schwartz, C. E. & Wang, T. Feb 13 2015 In : PLoS One. 10, 2, e0116454

Research output: Research - peer-reviewArticle

Chromosomes, Human, X
Exome
Intellectual Disability
Genes
X chromosome