Rinaldo Catta-Preta
Affiliations: | 2016-2020 | Center for Neuroscience | University of California, Davis, Davis, CA |
| 2020- | Genetics | Harvard Medical School |
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"Rinaldo Catta-Preta"Parents
Sign in to add mentor| Dennis A. Laskowski | research assistant | 1991-1994 | The Dow Chemical Company |
| Alexander Nord | grad student | 2016-2020 | UC Davis |
| Ayellet V. Falcovitz-Segre | post-doc | 2024- | Harvard Medical School - Massachusetts Eye and Ear (Cell Biology Tree) |
| Constance L. Cepko | post-doc | 2020-2024 | Harvard Medical School (Neurotree) |
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Publications
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| Catta-Preta R, Lindtner S, Ypsilanti A, et al. (2023) Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis. Biorxiv : the Preprint Server For Biology |
| Su-Feher L, Rubin AN, Silberberg SN, et al. (2022) Single cell enhancer activity distinguishes GABAergic and cholinergic lineages in embryonic mouse basal ganglia. Proceedings of the National Academy of Sciences of the United States of America. 119: e2108760119 |
| Ypsilanti AR, Pattabiraman K, Catta-Preta R, et al. (2021) Transcriptional network orchestrating regional patterning of cortical progenitors. Proceedings of the National Academy of Sciences of the United States of America. 118 |
| Catta-Preta R, Zdilar I, Jenner B, et al. (2021) Transcriptional Pathology Evolves over Time in Rat Hippocampus after Lateral Fluid Percussion Traumatic Brain Injury. Neurotrauma Reports. 2: 512-525 |
| Markenscoff-Papadimitriou E, Binyameen F, Whalen S, et al. (2021) Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes. Cell Reports. 37: 110089 |
| Haigh JL, Adhikari A, Copping NA, et al. (2021) Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice. Genome Medicine. 13: 69 |
| Lindtner S, Catta-Preta R, Tian H, et al. (2019) Genomic Resolution of DLX-Orchestrated Transcriptional Circuits Driving Development of Forebrain GABAergic Neurons. Cell Reports. 28: 2048-2063.e8 |
| Wade AA, Lim K, Catta-Preta R, et al. (2018) Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of Haploinsufficiency. Frontiers in Molecular Neuroscience. 11: 481 |
| Fazel Darbandi S, Robinson Schwartz SE, Qi Q, et al. (2018) Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity. Neuron |
| Gompers AL, Su-Feher L, Ellegood J, et al. (2017) Germline Chd8 haploinsufficiency alters brain development in mouse. Nature Neuroscience |