| Enhanced prime editing systems by manipulating cellular determinants of editing outcomes PJ Chen, JA Hussmann, J Yan, F Knipping, P Ravisankar, PF Chen, ... Cell 184 (22), 5635-5652. e29, 2021 | 408 | 2021 |
| Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes SJ Chamberlain, PF Chen, KY Ng, F Bourgois-Rocha, F Lemtiri-Chlieh, ... Proceedings of the National Academy of Sciences 107 (41), 17668-17673, 2010 | 333 | 2010 |
| Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13. 1 ND Germain, PF Chen, AM Plocik, H Glatt-Deeley, J Brown, JJ Fink, ... Molecular autism 5 (1), 1-19, 2014 | 97 | 2014 |
| Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion K Martins-Taylor, JS Hsiao, PF Chen, H Glatt-Deeley, AJ De Smith, ... Human molecular genetics 23 (9), 2364-2373, 2014 | 73 | 2014 |
| Biallelic mutations in TSC2 lead to abnormalities associated with cortical tubers in human iPSC-derived neurons KD Winden, M Sundberg, C Yang, SMA Wafa, S Dwyer, PF Chen, ... Journal of Neuroscience 39 (47), 9294-9305, 2019 | 71 | 2019 |
| Balancing serendipity and reproducibility: Pluripotent stem cells as experimental systems for intellectual and developmental disorders NC Anderson, PF Chen, K Meganathan, WA Saber, AJ Petersen, ... Stem cell reports 16 (6), 1446-1457, 2021 | 25 | 2021 |
| RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing PF Chen, JS Hsiao, CL Sirois, SJ Chamberlain Scientific reports 6 (1), 1-13, 2016 | 20 | 2016 |
| A quantitative single-cell assay for retrograde membrane traffic enables rapid detection of defects in cellular organization P Luong, Q Li, PF Chen, PJ Wrighton, D Chang, S Dwyer, MT Bayer, ... Molecular biology of the cell 31 (7), 511-519, 2020 | 8 | 2020 |
| Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 Deficiency Disorder (CDD) PF Chen, T Chen, TE Forman, AC Swanson, B O'Kelly, SA Dwyer, ... Stem Cell Research 53, 102276, 2021 | 7 | 2021 |
| Colchicine-induced degeneration of the micronucleus during conjugation in Tetrahymena PF Chen, S Singhal, D Bushyhead, S Broder-Fingert, J Wolfe Biology open 3 (5), 353-361, 2014 | 5 | 2014 |
| Modeling genomic imprinting disorders using induced pluripotent stem cells SJ Chamberlain, ND Germain, PF Chen, JS Hsiao, H Glatt-Deeley Patient-Specific Induced Pluripotent Stem Cell Models, 45-64, 2014 | 4 | 2014 |
| Adaptor Protein Complex 4 Deficiency: A Paradigm of Complex Hereditary Spastic Paraplegia Associated With Defective Protein Trafficking (S19. 009) D Ebrahimi-Fakhari, R Behne, J Teinert, M Wimmer, A Diplock, ... Neurology 92 (15 Supplement), 2019 | | 2019 |
| Modeling Neurodevelopmental Disorders Involving Genomic Imprinting at Human Chromosome 15q11-q13 Using iPSC and CRISPR/Cas9 Technology PF Chen | | 2016 |
