Kajiwara, Yuji
Icahn School of Medicine at Mount Sinai
7 papers on CoChatORCID 0000-0002-9307-8215
Most cited papers
- Verified
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
Bozdagi, O., Sakurai, T., Papapetrou, D., Wang, X., Dickstein, D. L., Takahashi, N., Kajiwara, Y., Yang, M., Katz, A. M., Scattoni, M. L., et al. (2010) · Molecular Autism
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 584
- Verified
Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer’s disease
Wang, M., Roussos, P., McKenzie, A., Zhou, X., Kajiwara, Y., Brennand, K. J., De Luca, G. C., Crary, J. F., Casaccia, P., Buxbaum, J. D., et al. (2016) · Genome Medicine
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 314
- Verified
Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators
Duffney, L. J., Zhong, P., Wei, J., Matas, E., Cheng, J., Qin, L., Ma, K., Dietz, D. M., Kajiwara, Y., Buxbaum, J. D., et al. (2015) · Cell Reports
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 281
- Verified
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder
Poultney, C. S., Goldberg, A. P., Drapeau, E., Kou, Y., Harony-Nicolas, H., Kajiwara, Y., De Rubeis, S., Durand, S., Stevens, C., Rehnström, K., et al. (2013) · The American Journal of Human Genetics
Genomic variations and chromosomal abnormalitiesGenomics and Rare Diseases
Cited by 169
- Verified
Canonical Inflammasomes Drive IFN-γ to Prime Caspase-11 in Defense against a Cytosol-Invasive Bacterium
Aachoui, Y., Kajiwara, Y., Leaf, I. A., Mao, D., Ting, J. P.-Y., Coers, J., Aderem, A., Buxbaum, J. D., & Miao, E. A. (2015) · Cell Host & Microbe
Inflammasome and immune disordersImmune Response and Inflammation
Cited by 125
- Verified
Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene
Buxbaum, J. D., Georgieva, L., Young, J. J., Plescia, C., Kajiwara, Y., Jiang, Y., Moskvina, V, Norton, N., Peirce, T., Williams, H., et al. (2008) · Molecular Psychiatry
Schizophrenia research and treatmentProtein Tyrosine Phosphatases
Cited by 86
- Verified
Characterization of SLITRK1 variation in obsessive-compulsive disorder
Ozomaro, U., Cai, G., Kajiwara, Y., Yoon, S., Makarov, V., Delorme, R., Betancur, C., Ruhrmann, S., Falkai, P., Grabe, H. J., et al. (2013) · PLoS ONE
Obsessive-Compulsive Spectrum DisordersGenetics and Neurodevelopmental Disorders
Cited by 52
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