Tamara Beck

机构：Walter and Eliza Hall Institute of Medical Research · ORCID：0000-0002-1125-1871

发表论文 26 篇 · 总被引 809 次 · h-index 13

代表论文

• Using long-read sequencing to detect imprinted DNA methylation (2019 · Nucleic Acids Research · 被引 142)
• De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development (2017 · Nature Genetics · 被引 136)
• Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters (2018 · Nature Structural & Molecular Biology · 被引 109)
• Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects (2019 · Cell Reports · 被引 61)
• Unique properties of a subset of human pluripotent stem cells with high capacity for self-renewal (2020 · Nature Communications · 被引 49)
• A pooled shRNA screen for regulators of primary mammary stem and progenitor cells identifies roles for Asap1 and Prox1 (2015 · BMC Cancer · 被引 42)