| Topoisomerases facilitate transcription of long genes linked to autism IF King, CN Yandava, AM Mabb, JS Hsiao, HS Huang, BL Pearson, ... Nature 501 (7465), 58-62, 2013 | 455 | 2013 |
| The murine polycomb group protein Eed is required for global histone H3 lysine-27 methylation ND Montgomery, D Yee, A Chen, S Kalantry, SJ Chamberlain, AP Otte, ... Current Biology 15 (10), 942-947, 2005 | 420 | 2005 |
| Polycomb repressive complex 2 is dispensable for maintenance of embryonic stem cell pluripotency SJ Chamberlain, D Yee, T Magnuson Stem cells 26 (6), 1496-1505, 2008 | 391 | 2008 |
| 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 | 331 | 2010 |
| The Prader–Willi Syndrome Imprinting Center Activates the Paternally Expressed Murine Ube3a Antisense Transcript but Represses Paternal Ube3a SJ Chamberlain, CI Brannan Genomics 73 (3), 316-322, 2001 | 242 | 2001 |
| Expression and imprinting of MAGEL2 suggest a role in Prader–Willi syndrome and the homologous murine imprinting phenotype S Lee, S Kozlov, L Hernandez, SJ Chamberlain, CI Brannan, CL Stewart, ... Human Molecular Genetics 9 (12), 1813-1819, 2000 | 178 | 2000 |
| Prader-Willi, Angelman, and 15q11-q13 duplication syndromes L Kalsner, SJ Chamberlain Pediatric Clinics 62 (3), 587-606, 2015 | 167 | 2015 |
| Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11–q13 SJ Chamberlain, M Lalande Neurobiology of disease 39 (1), 13-20, 2010 | 126 | 2010 |
| Angelman syndrome, a genomic imprinting disorder of the brain SJ Chamberlain, M Lalande Journal of Neuroscience 30 (30), 9958-9963, 2010 | 125 | 2010 |
| Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders JM LaSalle, LT Reiter, SJ Chamberlain Epigenomics 7 (7), 1213-1228, 2015 | 117 | 2015 |
| Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency T Wang, H Wu, Y Li, KE Szulwach, L Lin, X Li, IP Chen, IS Goldlust, ... Nature cell biology 15 (6), 700-711, 2013 | 107 | 2013 |
| Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells JJ Fink, TM Robinson, ND Germain, CL Sirois, KA Bolduc, AJ Ward, ... Nature Communications 8 (1), 15038, 2017 | 100 | 2017 |
| 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, 1-19, 2014 | 97 | 2014 |
| A mono‐allelic bivalent chromatin domain controls tissue‐specific imprinting at Grb10 LA Sanz, S Chamberlain, JC Sabourin, A Henckel, T Magnuson, ... The EMBO journal 27 (19), 2523-2532, 2008 | 91 | 2008 |
| Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus EY Smith, CR Futtner, SJ Chamberlain, KA Johnstone, JL Resnick PLoS genetics 7 (12), e1002422, 2011 | 87 | 2011 |
| Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders SJ Chamberlain, XJ Li, M Lalande Neurogenetics 9, 227-235, 2008 | 78 | 2008 |
| 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 |
| 15q duplication syndrome and related disorders BM Finucane, L Lusk, D Arkilo, S Chamberlain, O Devinsky, S Dindot, ... GeneReviews, 1993-2019, 2016 | 72 | 2016 |
| Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice SJ Chamberlain, KA Johnstone, AJ DuBose, TA Simon, MS Bartolomei, ... Human molecular genetics 13 (23), 2971-2977, 2004 | 64 | 2004 |
| Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs E Cruvinel, T Budinetz, N Germain, S Chamberlain, M Lalande, ... Human molecular genetics 23 (17), 4674-4685, 2014 | 61 | 2014 |
Marc LalandeProfessor of Genetics and Genome Sciences, University of ConnecticutVerified email at uchc.edu
