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Dive into the research topics where Karen Woodward is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Studying Disease-Associated UBE3A Missense Variants Using Enhanced Sampling Molecular Simulations
Agostino, M., McKenzie, F., Buck, C., Woodward, K. J., Atkinson, V. J., Azmanov, D. N. & Heng, J.I.-T., 26 Jul 2022, In: ACS Omega. 7, 29, p. 25039-25045 7 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay
Singh, R., Cohen, A. S. A., Poulton, C., Hjortshøj, T. D., Akahira-Azuma, M., Mendiratta, G., Khan, W. A., Azmanov, D. N., Woodward, K. J., Kirchhoff, M., Shi, L., Edelmann, L., Baynam, G., Scott, S. A. & Jabs, E. W., Jun 2021, In: Cold Spring Harbor Molecular Case Studies. 7, 3, a005991.Research output: Contribution to journal › Article › peer-review
Open Access4 Link opens in a new tab Citations (Scopus) -
Further heterogeneity in Silver–Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement
Brereton, R. E., Nickerson, S. L., Woodward, K. J., Edwards, T., Sivamoorthy, S., Ramos Vasques Walters, F., Chabros, V., Marchin, V., Grumball, T., Kennedy, D., Uzaraga, J., Peverall, J., Arscott, G., Beilby, J., Choong, C. S., Townshend, S. & Azmanov, D. N., Oct 2021, In: American Journal of Medical Genetics Part A. 185, 10, p. 3136-3145 10 p.Research output: Contribution to journal › Article › peer-review
8 Link opens in a new tab Citations (Scopus) -
Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance
Woodward, K. J., Stampalia, J., Vanyai, H., Rijhumal, H., Potts, K., Taylor, F., Peverall, J., Grumball, T., Sivamoorthy, S., Alinejad-Rokny, H., Wray, J., Whitehouse, A., Nagarajan, L., Scurlock, J., Afchani, S., Edwards, M., Murch, A., Beilby, J., Baynam, G. & Kiraly-Borri, C. & 2 others, , Feb 2019, In: Molecular genetics & genomic medicine. 7, 2, 17 p., e00507.Research output: Contribution to journal › Article › peer-review
Open Access28 Link opens in a new tab Citations (Scopus) -
Author correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018)
Corbett, M. A., van Eyk, C. L., Webber, D. L., Bent, S. J., Newman, M., Harper, K., Berry, J. G., Azmanov, D. N., Woodward, K. J., Gardner, A. E., Slee, J., Perez-Jurado, L. A., MacLennan, A. H. & Gecz, J., 1 Dec 2019, In: npj Genomic Medicine. 4, 1, 1 p., 11.Research output: Contribution to journal › Letter › peer-review
Open Access2 Link opens in a new tab Citations (Web of Science)