Bernice Morrow
Affiliations: | Yeshiva University, New York, NY, United States |
Area:
Human Development, Genetics, Neuroscience BiologyGoogle:
"Bernice Morrow"Mean distance: 15266.6
Children
Sign in to add trainee| Elizabeth M. Spiteri | grad student | 2002 | Yeshiva University |
| Jelena S. Arnold | grad student | 2006 | Yeshiva University |
| Melanie Babcock | grad student | 2006 | Yeshiva University |
| Evan M. Braunstein | grad student | 2008 | Yeshiva University |
| Laina Freyer | grad student | 2011 | Yeshiva University |
| Dennis C. Monks | grad student | 2011 | Yeshiva University |
| Christopher De Bono | post-doc | (DevTree) |
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Publications
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| Shi L, Song H, Zhou B, et al. (2023) regulates early angiogenesis in mouse embryos by accelerating endothelial cell maturation. Biorxiv : the Preprint Server For Biology |
| Zhao Y, Wang Y, Shi L, et al. (2023) Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. Npj Genomic Medicine. 8: 17 |
| Campbell IM, Crowley TB, Jobaliya C, et al. (2022) Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Clinical Genetics |
| Nomaru H, Liu Y, De Bono C, et al. (2021) Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm. Nature Communications. 12: 6645 |
| Oluwafemi OO, Musfee FI, Mitchell LE, et al. (2021) Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Genes. 12 |
| Pastor S, Tran O, Jin A, et al. (2020) Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR). Scientific Reports. 10: 12235 |
| Vervoort L, Demaerel W, Rengifo LY, et al. (2019) Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. Human Molecular Genetics. 28: 3724-3733 |
| Zhao Y, Diacou A, Johnston HR, et al. (2019) Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American Journal of Human Genetics |
| Demaerel W, Mostovoy Y, Yilmaz F, et al. (2019) The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29: 1389-1401 |
| Hasten E, Morrow BE. (2019) Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome. Plos Genetics. 15: e1008301 |