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

  • 13 Similar Profiles
Neurogenesis Medicine & Life Sciences
Epilepsy Medicine & Life Sciences
Seizures Medicine & Life Sciences
Dentate Gyrus Medicine & Life Sciences
Lateral Ventricles Medicine & Life Sciences
Neurons Medicine & Life Sciences
Temporal Lobe Epilepsy Medicine & Life Sciences
Brain Medicine & Life Sciences

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Grants 2000 2021

Research Output 1994 2018

1 Citations

Critical roles of αII spectrin in brain development and epileptic encephalopathy

Wang, Y., Ji, T., Nelson, A. D., Glanowska, K., Murphy, G. G., Jenkins, P. M. & Parent, J. M. Feb 1 2018 In : Journal of Clinical Investigation. 128, 2, p. 760-773 14 p.

Research output: Contribution to journalArticle

Brain Diseases

Fibroblast growth factor 2 regulates activity and gene expression of human post-mitotic excitatory neurons

Gupta, S., M-Redmond, T., Meng, F., Tidball, A., Akil, H., Watson, S., Parent, J. M. & Uhler, M. May 1 2018 In : Journal of Neurochemistry. 145, 3, p. 188-203 16 p.

Research output: Contribution to journalArticle

Fibroblast Growth Factor 2
Gene expression
Gene Expression
Major Depressive Disorder

PlexinA2 Forward Signaling through Rap1 GTPases Regulates Dentate Gyrus Development and Schizophrenia-like Behaviors

Zhao, X. F., Kohen, R., Parent, R., Duan, Y., Fisher, G. L., Korn, M. J., Ji, L., Wan, G., Jin, J., Püschel, A. W., Dolan, D. F., Parent, J. M., Corfas, G., Murphy, G. G. & Giger, R. J. Jan 1 2018 In : Cell Reports. 22, 2, p. 456-470 15 p.

Research output: Contribution to journalArticle

GTPase-Activating Proteins
GTP Phosphohydrolases
Dentate Gyrus
Sensory Gating
2 Citations

Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data

Epi4K Consortium, Epilepsy Phenome Genome Project & EuroEPINOMICS-RES Consortium Jun 1 2017 In : European Journal of Human Genetics. 25, 7, p. 894-899 6 p.

Research output: Contribution to journalArticle

Brain Diseases
Infantile Spasms
Recessive Genes
Ion Channels

Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013))

Appenzeller, S. , Balling, R. , Barisic, N. , Baulac, S. , Caglayan, H. , Craiu, D. , De Jonghe, P. , Depienne, C. , Dimova, P. , Djémié, T. , Gormley, P. , Guerrini, R. , Helbig, I. , Hjalgrim, H. , Hoffman-Zacharska, D. , Jähn, J. , Klein, K. M. , Koeleman, B. , Komarek, V. , Krause, R. & 30 others Kuhlenbäumer, G., Leguern, E., Lehesjoki, A. E., Lemke, J. R., Lerche, H., Linnankivi, T., Marini, C., May, P., Møller, R. S., Muhle, H., Pal, D., Palotie, A., Pendziwiat, M., Robbiano, A., Roelens, F., Rosenow, F., Selmer, K., Serratosa, J. M., Sisodiya, S., Stephani, U., Sterbova, K., Striano, P., Suls, A., Talvik, T., von Spiczak, S., Weber, Y., Weckhuysen, S., Zara, F., Abou-Khalil, B. & Alldredge, B. K. Jan 5 2017 In : American journal of human genetics. 100, 1, 1 p.

Research output: Contribution to journalComment/debate

Medical Genetics
Brain Diseases
Synaptic Transmission