Tamara Beck

De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

Christopher T. Gordon, Shifeng Xue, Gökhan Yigit et al. · Nature Genetics · 2017 · 131 citations · Full text

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +5

Using long-read sequencing to detect imprinted DNA methylation

Scott Gigante, Quentin Gouil, Alexis Lucattini et al. · Nucleic Acids Research · 2019 · 127 citations · Full text

Epigenetic Change, Genetics, Dna Methylation +22

Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters

Natasha Jansz, Andrew Keniry, Marie Trussart et al. · Nature Structural & Molecular Biology · 2018 · 104 citations

Chromatin, Transcriptional Regulation, Genome Instability +15

EGF-mediated induction of Mcl-1 at the switch to lactation is essential for alveolar cell survival

Nai Yang Fu, Anne C. Rios, Bhupinder Pal et al. · Nature Cell Biology · 2015 · 77 citations

Developmental Biology, Cell Signaling, Egf-mediated Induction +9

Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects

Alex R. D. Delbridge, Andrew J. Kueh, Francine Ke et al. · Cell Reports · 2019 · 60 citations · Full text