Maria Karayiorgou, M.D.

Center for Human Genetics Columbia University, New York, NY 
"Maria Karayiorgou"
Mean distance: 15.89 (cluster 6)
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Diamantopoulou A, Sun Z, Mukai J, et al. (2017) Loss-of-function mutation in Mirta22/Emc10 rescues specific schizophrenia-related phenotypes in a mouse model of the 22q11.2 deletion. Proceedings of the National Academy of Sciences of the United States of America
Qi Y, Zhang XJ, Renier N, et al. (2017) Combined small-molecule inhibition accelerates the derivation of functional cortical neurons from human pluripotent stem cells. Nature Biotechnology
Wesseling H, Xu B, Want EJ, et al. (2016) System-based proteomic and metabonomic analysis of the Df(16)A(+/-) mouse identifies potential miR-185 targets and molecular pathway alterations. Molecular Psychiatry
Takata A, Ionita-Laza I, Gogos JA, et al. (2016) De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia. Neuron. 89: 940-7
Barr I, Weitz SH, Atkin T, et al. (2015) Cobalt(III) Protoporphyrin Activates the DGCR8 Protein and Can Compensate microRNA Processing Deficiency. Chemistry & Biology. 22: 793-802
Levy RJ, Kvajo M, Li Y, et al. (2015) Deletion of Rapgef6, a candidate schizophrenia susceptibility gene, disrupts amygdala function in mice. Translational Psychiatry. 5: e577
Mukai J, Tamura M, Fénelon K, et al. (2015) Molecular substrates of altered axonal growth and brain connectivity in a mouse model of schizophrenia. Neuron. 86: 680-95
Hsu PK, Xu B, Mukai J, et al. (2015) The BDNF Val66Met variant affects gene expression through miR-146b. Neurobiology of Disease. 77: 228-37
Malherbe PJ, Roos JL, Ehlers R, et al. (2015) Phenotypic features of patients with schizophrenia carrying de novo gene mutations: a pilot study. Psychiatry Research. 225: 108-14
Karayannis T, Au E, Patel JC, et al. (2014) Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission. Nature. 511: 236-40
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