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Karen Woodward

Dr

  • The University of Western Australia (M504), 35 Stirling Highway,

    6009 Perth

    Australia

  • 5 Citations
  • 1 h-Index
20182019
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Fingerprint 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.

Proteolipids Medicine & Life Sciences
Cerebral Palsy Medicine & Life Sciences
Gene Expression Medicine & Life Sciences
Exome Medicine & Life Sciences
Nucleotide Mapping Medicine & Life Sciences
Proteins Medicine & Life Sciences
Pelizaeus-Merzbacher Disease Medicine & Life Sciences
Nucleotides Medicine & Life Sciences

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Research Output 2018 2019

  • 5 Citations
  • 1 h-Index
  • 4 Article
  • 1 Letter
3 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 othersMcKenzie, F. & Heng, J. I. T., Feb 2019, In : Molecular genetics & genomic medicine. 7, 2, 17 p., 507.

Research output: Contribution to journalArticle

Open Access

Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants

Bahrambeigi, V., Song, X., Sperle, K., Beck, C. R., Hijazi, H., Grochowski, C. M., Gu, S., Seeman, P., Woodward, K. J., Carvalho, C. M. B., Hobson, G. M. & Lupski, J. R., 9 Dec 2019, In : Genome Medicine. 11, 1, 80.

Research output: Contribution to journalArticle

Open Access
Proteolipids
Nucleotide Mapping
Proteins
Pelizaeus-Merzbacher Disease
Human Genome

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., 31 May 2019, In : npj Genomic Medicine. 4, 1 p., 11.

Research output: Contribution to journalLetter

Open Access
1 Citation (Scopus)

A review of structural brain abnormalities in Pallister-Killian syndrome

Poulton, C., Baynam, G., Yates, C., Alinejad-Rokny, H., Williams, S., Wright, H., Woodward, K. J., Sivamoorthy, S., Peverall, J., Shipman, P., Ravine, D., Beilby, J. & Heng, J. I-T., Jan 2018, In : Molecular genetics & genomic medicine. 6, 1, p. 92-98 7 p.

Research output: Contribution to journalArticle

Open Access
1 Citation (Scopus)

Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy

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., Pérez-Jurado, L. A., MacLennan, A. H. & Gecz, J., 1 Dec 2018, In : npj Genomic Medicine. 3, 1, 33.

Research output: Contribution to journalArticle

Open Access
Cerebral Palsy
Gene Expression
Exome
Nucleotides
RNA Sequence Analysis