| Year |
Citation |
Score |
| 2022 |
Parnell E, Culotta L, Forrest MP, Jalloul HA, Eckman BL, Loizzo DD, Horan KKE, Dos Santos M, Piguel NH, Tai DJC, Zhang H, Gertler TS, Simkin D, Sanders AR, Talkowski ME, et al. Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived Neurons. Biological Psychiatry. PMID 36581494 DOI: 10.1016/j.biopsych.2022.11.005 |
0.642 |
|
| 2022 |
Parnell E, Voorn RA, Martin-de-Saavedra MD, Loizzo DD, Dos Santos M, Penzes P. A developmental delay linked missense mutation in Kalirin-7 disrupts protein function and neuronal morphology. Frontiers in Molecular Neuroscience. 15: 994513. PMID 36533124 DOI: 10.3389/fnmol.2022.994513 |
0.699 |
|
| 2021 |
Martín-de-Saavedra MD, Dos Santos M, Culotta L, Varea O, Spielman BP, Parnell E, Forrest MP, Gao R, Yoon S, McCoig E, Jalloul HA, Myczek K, Khalatyan N, Hall EA, Turk LS, et al. Shed CNTNAP2 ectodomain is detectable in CSF and regulates Ca homeostasis and network synchrony via PMCA2/ATP2B2. Neuron. PMID 34921780 DOI: 10.1016/j.neuron.2021.11.025 |
0.644 |
|
| 2020 |
Jolly LA, Parnell E, Gardner AE, Corbett MA, Pérez-Jurado LA, Shaw M, Lesca G, Keegan C, Schneider MC, Griffin E, Maier F, Kiss C, Guerin A, Crosby K, Rosenbaum K, et al. Missense variant contribution to USP9X-female syndrome. Npj Genomic Medicine. 5: 53. PMID 33298948 DOI: 10.1038/s41525-020-00162-9 |
0.535 |
|
| 2020 |
Parnell E, Shapiro LP, Voorn RA, Forrest MP, Jalloul HA, Loizzo DD, Penzes P. KALRN: A central regulator of synaptic function and synaptopathies. Gene. 145306. PMID 33189799 DOI: 10.1016/j.gene.2020.145306 |
0.732 |
|
| 2020 |
Yoon S, Parnell E, Penzes P. TGF-β-Induced Phosphorylation of Usp9X Stabilizes Ankyrin-G and Regulates Dendritic Spine Development and Maintenance. Cell Reports. 31: 107685. PMID 32460012 DOI: 10.1016/j.celrep.2020.107685 |
0.572 |
|
| 2019 |
Yoon S, Parnell E, Kasherman M, Forrest MP, Myczek K, Premarathne S, Sanchez Vega MC, Piper M, Burne THJ, Jolly LA, Wood SA, Penzes P. Usp9X Controls Ankyrin-Repeat Domain Protein Homeostasis during Dendritic Spine Development. Neuron. PMID 31813652 DOI: 10.1016/J.Neuron.2019.11.003 |
0.722 |
|
| 2019 |
Johnson BV, Kumar R, Oishi S, Alexander S, Kasherman M, Vega MS, Ivancevic A, Gardner A, Domingo D, Corbett M, Parnell E, Yoon S, Oh T, Lines M, Lefroy H, et al. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling. Biological Psychiatry. PMID 31443933 DOI: 10.1016/J.Biopsych.2019.05.028 |
0.573 |
|
| 2018 |
Forrest MP, Parnell E, Penzes P. Dendritic structural plasticity and neuropsychiatric disease. Nature Reviews. Neuroscience. 19: 215-234. PMID 29545546 DOI: 10.1038/Nrn.2018.16 |
0.732 |
|
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