Kathleen H. Wood

Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome

Brian S. Johnson, Ying-Tao Zhao, Maria Fasolino et al. · Nature Medicine · 2017 · 121 citations · Full text

Transcriptional Regulation, Functional Genomics, Developmental Biology +8

Human germline heterozygous gain-of-function <i>STAT6</i> variants cause severe allergic disease

Mehul Sharma, Daniel Leung, Mana Momenilandi et al. · The Journal of Experimental Medicine · 2023 · 99 citations · Full text

De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay

Lisenka E.L.M. Vissers, Sreehari Kalvakuri, Elke de Boer et al. · The American Journal of Human Genetics · 2020 · 47 citations · Full text

Developmental Biology, Cause Neurodevelopmental Delay, Genetic Disorder +9

Pathogenic variants in <i>MDFIC</i> cause recessive central conducting lymphatic anomaly with lymphedema

Alicia B. Byrne, Pascal Brouillard, Drew L. Sutton et al. · Science Translational Medicine · 2022 · 39 citations · Full text

Tagging Methyl-CpG-Binding Domain Proteins Reveals Different Spatiotemporal Expression and Supports Distinct Functions

Kathleen H. Wood, Brian S. Johnson, Sarah A. Welsh et al. · Epigenomics · 2016 · 31 citations · Full text