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Kathleen H. Wood

Observed names: Kathleen H Wood, Kathleen Wood
ORCID: 0000-0001-6566-4885
Observed ORCID: 0000-0001-6566-4885
OpenAlex ID: A5065166129
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
2023 · Mehul Sharma, Daniel Leung, et al. · The Journal of Experimental Medicine · 123
Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome
2017 · Brian S Johnson, Ying-Tao Zhao, et al. · Nature Medicine · 118
Emerging Molecular and Biological Functions of MBD2, a Reader of DNA Methylation
2016 · Kathleen H. Wood, Zhaolan Zhou · Frontiers in Genetics · 98
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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
2020 · Lisenka E.L.M. Vissers, Sreehari Kalvakuri, et al. · The American Journal of Human Genetics · 56
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Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema
2022 · Alicia B. Byrne, Pascal Brouillard, et al. · Science Translational Medicine · 40
Tagging Methyl-CpG-Binding Domain Proteins Reveals Different Spatiotemporal Expression and Supports Distinct Functions
2016 · Kathleen H Wood, Brian S Johnson, et al. · Epigenomics · 36
An Evi1-C/EBPβ Complex Controls Peroxisome Proliferator-Activated Receptor γ2 Gene Expression To Initiate White Fat Cell Differentiation
2012 · Jeff Ishibashi, Zeynep Firtina, et al. · Molecular and Cellular Biology · 23
A Novel Predicted Bromodomain-Related Protein Affects Coordination Between Meiosis and Spermiogenesis in Drosophila and Is Required for Male Meiotic Cytokinesis
2010 · Laura M. Bergner, F. Edward Hickman, et al. · DNA and Cell Biology · 10
Rapid targeted analysis of the genome: Rapid genomic sequencing in critically ill infants
2025 · K. Taylor Wild, Sara L. Reichert, et al. · Genetics in Medicine Open · 2
Loss-of-function variants in EPHX3 cause nonsyndromic epidermal differentiation disorders
2026 · Kunlun Lv, Karina M Forde, et al. · British Journal of Dermatology · 1
P532: Development, implementation, and preliminary results of rapid targeted genomic analysis in the newborn period
2024 · Emma Bedoukian, Sara Reichert, et al. · Genetics in Medicine Open · 1
218 Loss-of-function variants in EPHX3 cause nonsyndromic epidermal differentiation disorders
2026 · Kunlun Lv, Karina M. Forde, et al. · Journal of Investigative Dermatology
P164: Correlation of mitochondrial DNA content in muscle with genetic diagnosis*
2025 · Jiani Chen, Juliana Troiani, et al. · Genetics in Medicine Open
eP328: Establishing droplet digital PCR method for assessing mitochondrial DNA content in muscle
2022 · Ada Chan, Kathleen Wood, et al. · Genetics in Medicine
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eP313: Too few or too many? Variant reporting burden and diagnostic comparisons of an extensive gene panel with exome-sequencing in immunodeficiency
2022 · Erfan Aref-Eshghi, Kajia Cao, et al. · Genetics in Medicine
Insights into Mbd2 Function Revealed by a Novel Genetic Tagging Approach
2016 · Kathleen H. Wood · ScholarlyCommons (University of Pennsylvania)
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Works count: 17
Citation count: 508
H-index: 8
I10-index: 8
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