| Year |
Citation |
Score |
| 2022 |
Babij R, Ferrer C, Donatelle A, Wacks S, Buch AM, Niemeyer JE, Ma H, Duan ZRS, Fetcho RN, Che A, Otsuka T, Schwartz TH, Huang BS, Liston C, De Marco García NV. Gabrb3 is required for the functional integration of pyramidal neuron subtypes in the somatosensory cortex. Neuron. PMID 36446382 DOI: 10.1016/j.neuron.2022.10.037 |
0.649 |
|
| 2021 |
Che A, De Marco García NV. An Calcium Imaging Approach for the Identification of Cell-Type Specific Patterns in the Developing Cortex. Frontiers in Neural Circuits. 15: 747724. PMID 34690708 DOI: 10.3389/fncir.2021.747724 |
0.81 |
|
| 2020 |
Inda MC, Joshi S, Wang T, Bolaender A, Gandu S, Koren Iii J, Che AY, Taldone T, Yan P, Sun W, Uddin M, Panchal P, Riolo M, Shah S, Barlas A, et al. The epichaperome is a mediator of toxic hippocampal stress and leads to protein connectivity-based dysfunction. Nature Communications. 11: 319. PMID 31949159 DOI: 10.1038/S41467-019-14082-5 |
0.737 |
|
| 2019 |
Duan ZRS, Che A, Chu P, Modol L, Bollmann Y, Babij R, Fetcho RN, Otsuka T, Fuccillo MV, Liston C, Pisapia DJ, Cossart R, De Marco García NV. GABAergic Restriction of Network Dynamics Regulates Interneuron Survival in the Developing Cortex. Neuron. PMID 31780329 DOI: 10.1016/J.Neuron.2019.10.008 |
0.743 |
|
| 2019 |
Modol L, Bollmann Y, Tressard T, Baude A, Che A, Duan ZRS, Babij R, De Marco García NV, Cossart R. Assemblies of Perisomatic GABAergic Neurons in the Developing Barrel Cortex. Neuron. PMID 31780328 DOI: 10.1016/j.neuron.2019.10.007 |
0.786 |
|
| 2018 |
Che A, Babij R, Iannone AF, Fetcho RN, Ferrer M, Liston C, Fishell G, De Marco García NV. Layer I Interneurons Sharpen Sensory Maps during Neonatal Development. Neuron. PMID 29937280 DOI: 10.1016/J.Neuron.2018.06.002 |
0.621 |
|
| 2017 |
Kabir ZD, Che A, Fischer DK, Rice RC, Rizzo BK, Byrne M, Glass MJ, De Marco Garcia NV, Rajadhyaksha AM. Rescue of impaired sociability and anxiety-like behavior in adult cacna1c-deficient mice by pharmacologically targeting eIF2α. Molecular Psychiatry. PMID 28584287 DOI: 10.1038/mp.2017.124 |
0.303 |
|
| 2015 |
Che A, Truong DT, Fitch RH, LoTurco JJ. Mutation of the Dyslexia-Associated Gene Dcdc2 Enhances Glutamatergic Synaptic Transmission Between Layer 4 Neurons in Mouse Neocortex. Cerebral Cortex (New York, N.Y. : 1991). PMID 26250775 DOI: 10.1093/cercor/bhv168 |
0.392 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2014 |
Che A, Girgenti MJ, Loturco J. The dyslexia-associated gene dcdc2 is required for spike-timing precision in mouse neocortex Biological Psychiatry. 76: 387-396. PMID 24094509 DOI: 10.1016/j.biopsych.2013.08.018 |
0.284 |
|
| 2015 |
Chen F, Rosiene J, Che A, Becker A, LoTurco J. Tracking and transforming neocortical progenitors by CRISPR/Cas9 gene targeting and PiggyBac transposase lineage labeling. Development (Cambridge, England). PMID 26400094 DOI: 10.1242/Dev.118836 |
0.217 |
|
| 2011 |
Gabel LA, Marin I, LoTurco JJ, Che A, Murphy C, Manglani M, Kass S. Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice. Genes, Brain, and Behavior. 10: 868-75. PMID 21883923 DOI: 10.1111/J.1601-183X.2011.00727.X |
0.213 |
|
| 2023 |
Ferrara NC, Che A, Briones B, Padilla-Coreano N, Lovett-Barron M, Opendak M. Neural Circuit Transitions Supporting Developmentally Specific Social Behavior. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 43: 7456-7462. PMID 37940586 DOI: 10.1523/JNEUROSCI.1377-23.2023 |
0.192 |
|
| 2014 |
Truong DT, Che A, Rendall AR, Szalkowski CE, LoTurco JJ, Galaburda AM, Holly Fitch R. Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability. Genes, Brain, and Behavior. 13: 802-11. PMID 25130614 DOI: 10.1111/Gbb.12170 |
0.137 |
|
| 2015 |
Schueler M, Braun DA, Chandrasekar G, Gee HY, Klasson TD, Halbritter J, Bieder A, Porath JD, Airik R, Zhou W, LoTurco JJ, Che A, Otto EA, Böckenhauer D, Sebire NJ, et al. DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling. American Journal of Human Genetics. 96: 81-92. PMID 25557784 DOI: 10.1016/J.Ajhg.2014.12.002 |
0.07 |
|
| Hide low-probability matches. |