Year |
Citation |
Score |
2023 |
Catta-Preta R, Lindtner S, Ypsilanti A, Price J, Abnousi A, Su-Feher L, Wang Y, Juric I, Jones IR, Akiyama JA, Hu M, Shen Y, Visel A, Pennacchio LA, Dickel D, et al. Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis. Biorxiv : the Preprint Server For Biology. PMID 37425940 DOI: 10.1101/2023.06.28.546894 |
0.349 |
|
2022 |
Su-Feher L, Rubin AN, Silberberg SN, Catta-Preta R, Lim KJ, Ypsilanti AR, Zdilar I, McGinnis CS, McKinsey GL, Rubino TE, Hawrylycz MJ, Thompson C, Gartner ZJ, Puelles L, Zeng H, et al. 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. PMID 35377797 DOI: 10.1073/pnas.2108760119 |
0.366 |
|
2021 |
Ypsilanti AR, Pattabiraman K, Catta-Preta R, Golonzhka O, Lindtner S, Tang K, Jones IR, Abnousi A, Juric I, Hu M, Shen Y, Dickel DE, Visel A, Pennachio LA, Hawrylycz M, et al. Transcriptional network orchestrating regional patterning of cortical progenitors. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34921112 DOI: 10.1073/pnas.2024795118 |
0.407 |
|
2021 |
Catta-Preta R, Zdilar I, Jenner B, Doisy ET, Tercovich K, Nord AS, Gurkoff GG. Transcriptional Pathology Evolves over Time in Rat Hippocampus after Lateral Fluid Percussion Traumatic Brain Injury. Neurotrauma Reports. 2: 512-525. PMID 34909768 DOI: 10.1089/neur.2021.0021 |
0.41 |
|
2021 |
Markenscoff-Papadimitriou E, Binyameen F, Whalen S, Price J, Lim K, Ypsilanti AR, Catta-Preta R, Pai EL, Mu X, Xu D, Pollard KS, Nord AS, State MW, Rubenstein JL. Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes. Cell Reports. 37: 110089. PMID 34879283 DOI: 10.1016/j.celrep.2021.110089 |
0.61 |
|
2021 |
Haigh JL, Adhikari A, Copping NA, Stradleigh T, Wade AA, Catta-Preta R, Su-Feher L, Zdilar I, Morse S, Fenton TA, Nguyen A, Quintero D, Agezew S, Sramek M, Kreun EJ, et al. Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice. Genome Medicine. 13: 69. PMID 33910599 DOI: 10.1186/s13073-021-00884-0 |
0.51 |
|
2019 |
Lindtner S, Catta-Preta R, Tian H, Su-Feher L, Price JD, Dickel DE, Greiner V, Silberberg SN, McKinsey GL, McManus MT, Pennacchio LA, Visel A, Nord AS, Rubenstein JLR. Genomic Resolution of DLX-Orchestrated Transcriptional Circuits Driving Development of Forebrain GABAergic Neurons. Cell Reports. 28: 2048-2063.e8. PMID 31433982 DOI: 10.1016/J.Celrep.2019.07.022 |
0.614 |
|
2018 |
Wade AA, Lim K, Catta-Preta R, Nord AS. Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of Haploinsufficiency. Frontiers in Molecular Neuroscience. 11: 481. PMID 30692911 DOI: 10.3389/Fnmol.2018.00481 |
0.61 |
|
2018 |
Fazel Darbandi S, Robinson Schwartz SE, Qi Q, Catta-Preta R, Pai EL, Mandell JD, Everitt A, Rubin A, Krasnoff RA, Katzman S, Tastad D, Nord AS, Willsey AJ, Chen B, State MW, et al. Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity. Neuron. PMID 30318412 DOI: 10.1016/J.Neuron.2018.09.027 |
0.594 |
|
2017 |
Gompers AL, Su-Feher L, Ellegood J, Copping NA, Riyadh MA, Stradleigh TW, Pride MC, Schaffler MD, Wade AA, Catta-Preta R, Zdilar I, Louis S, Kaushik G, Mannion BJ, Plajzer-Frick I, et al. Germline Chd8 haploinsufficiency alters brain development in mouse. Nature Neuroscience. PMID 28671691 DOI: 10.1038/Nn.4592 |
0.568 |
|
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