Tamara Beck
Walter and Eliza Hall Institute of Medical Research(AU)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Epigenetics and DNA Methylation, Prenatal Screening and Diagnostics, Genomics and Chromatin Dynamics, CRISPR and Genetic Engineering
Most-Cited Works
- → Using long-read sequencing to detect imprinted DNA methylation(2019)134 cited
- → De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development(2017)132 cited
- → Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters(2018)107 cited
- → EGF-mediated induction of Mcl-1 at the switch to lactation is essential for alveolar cell survival(2015)78 cited
- → Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects(2019)60 cited
- → Unique properties of a subset of human pluripotent stem cells with high capacity for self-renewal(2020)47 cited
- → A pooled shRNA screen for regulators of primary mammary stem and progenitor cells identifies roles for Asap1 and Prox1(2015)41 cited
- → Smchd1 is a maternal effect gene required for genomic imprinting(2020)37 cited
- → Integration of microRNA signatures of distinct mammary epithelial cell types with their gene expression and epigenetic portraits(2015)37 cited
- → BAF complex-mediated chromatin relaxation is required for establishment of X chromosome inactivation(2022)20 cited