Marisa S. Bartolomei
Affiliations: | Cell and Molecular Biology | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Molecular Biology, Genetics, Human DevelopmentGoogle:
"Marisa Bartolomei"Children
Sign in to add trainee| Ivona Percec | grad student | 2002 | Penn |
| Andrew Fedoriw | grad student | 2004 | Penn |
| Leisha Nolen | grad student | 2004 | Penn |
| Le-Ben Wan | grad student | 2008 | Penn |
| Jamie R. Weaver | grad student | 2012 | Penn |
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Publications
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| Caldwell BA, Bartolomei MS. (2022) DNA methylation reprogramming of genomic imprints in the mammalian germline: A TET-centric view. Andrology |
| Juan AM, Foong YH, Thorvaldsen JL, et al. (2022) Tissue-specific Grb10/Ddc insulator drives allelic architecture for cardiac development. Molecular Cell |
| Zhou W, Hinoue T, Barnes B, et al. (2022) DNA methylation dynamics and dysregulation delineated by high-throughput profiling in the mouse. Cell Genomics. 2 |
| Vrooman LA, Rhon-Calderon EA, Suri KV, et al. (2022) Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model. Frontiers in Cell and Developmental Biology. 10: 884088 |
| Robles-Matos N, Artis T, Simmons RA, et al. (2021) Environmental Exposure to Endocrine Disrupting Chemicals Influences Genomic Imprinting, Growth, and Metabolism. Genes. 12 |
| Bertozzi TM, Becker JL, Blake GET, et al. (2021) Variably methylated retrotransposons are refractory to a range of environmental perturbations. Nature Genetics |
| Freschi A, Del Prete R, Pignata L, et al. (2021) The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model. Human Molecular Genetics |
| Chang S, Hur SK, Naveh NSS, et al. (2020) Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome. Epigenetics |
| Bartolomei MS, Oakey RJ, Wutz A. (2020) Genomic imprinting: An epigenetic regulatory system. Plos Genetics. 16: e1008970 |
| Prasasya R, Grotheer KV, Siracusa LD, et al. (2020) Temple Syndrome and Kagami-Ogata Syndrome: Clinical Presentations, Genotypes, Models and Mechanisms. Human Molecular Genetics |