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Woodward, Karen J.
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1

Clinical utility of prenatal SNP microarray by clinical ind..:

Tan, Brian ; Woodward, Karen ; Tracey Edwards, Sarah Nickerson...
Pathology.  56 (2024)  - p. S18 , 2024
Link: https://doi.org/10.1016/..
 
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2

Studying Disease-Associated UBE3A Missense Variants Using E..:

Agostino, Mark ; McKenzie, Fiona ; Buck, Chloe...
ACS Omega.  7 (2022)  29 - p. 25039-25045 , 2022
Link: https://doi.org/10.1021/..
 
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3

Further heterogeneity inSilver–Russellsyndrome:PLAG1deletio..:

Brereton, Rebecca E. ; Nickerson, Sarah L. ; Woodward, Karen J....
American Journal of Medical Genetics Part A.  185 (2021)  10 - p. 3136-3145 , 2021
Link: https://doi.org/10.1002/..
 
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4

Distinct patterns of complex rearrangements and a mutationa..:

Bahrambeigi, Vahid ; Song, Xiaofei ; Sperle, Karen...
Genome Medicine.  11 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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5

Author Correction: Pathogenic copy number variants that aff..:

Corbett, Mark A. ; van Eyk, Clare L. ; Webber, Dani L....
npj Genomic Medicine.  4 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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6

Atypical nested 22q11.2 duplications between LCR22B and LCR..:

Woodward, Karen J. ; Stampalia, Julie ; Vanyai, Hannah...
Molecular Genetics & Genomic Medicine.  7 (2019)  2 - p. , 2019
Link: https://doi.org/10.1002/..
 
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7

Pathogenic copy number variants that affect gene expression..:

Corbett, Mark A. ; van Eyk, Clare L. ; Webber, Dani L....
npj Genomic Medicine.  3 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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8

A review of structural brain abnormalities in Pallister‐Kil..:

Poulton, Cathryn ; Baynam, Gareth ; Yates, Clarissa...
Molecular Genetics & Genomic Medicine.  6 (2017)  1 - p. 92-98 , 2017
Link: https://doi.org/10.1002/..
 
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9

Reinforcing the association between distal 1q CNVs and stru..:

Hemming, Isabel A. ; Forrest, Alistair R. R. ; Shipman, Peter...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  171 (2016)  3 - p. 458-467 , 2016
Link: https://doi.org/10.1002/..
 
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10

The changing landscape of chromosome markers:

Azmanov, Dimitar N. ; Ngo, Con ; Sivamoorty, Soruba...
Pathology.  47 (2015)  - p. S27 , 2015
Link: https://doi.org/10.1097/..
 
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11

Mosaic Genome-Wide uniparental disomy (GW-UPD): Heterogenei..:

Azmanov, Dimitar ; Edwards, Caitlin ; Stampalia, Julie...
Pathology.  46 (2014)  - p. S91 , 2014
Link: https://doi.org/10.1097/..
 
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12

The molecular and cellular defects underlying Pelizaeus–Mer..:

Woodward, Karen J.
Expert Reviews in Molecular Medicine.  10 (2008)  - p. , 2008
Link: https://doi.org/10.1017/..
 
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13

Frameshift mutation in GJA12 leading to nystagmus, spastic ..:

Wolf, Nicole I. ; Cundall, Maria ; Rutland, Paul...
Neurogenetics.  8 (2006)  1 - p. 39-44 , 2006
Link: https://doi.org/10.1007/..
 
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14

DNA microarrays with stem–loop DNA probes: preparation and ..:

Broude, Natalia E. ; Woodward, Karen ; Cavallo, Robert..
Nucleic Acids Research.  29 (2001)  19 - p. e92-e92 , 2001
Link: https://doi.org/10.1093/..
 
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15

Multiplex allele-specific target amplification based on PCR..:

Broude, Natalia E. ; Zhang, Lingang ; Woodward, Karen..
Proceedings of the National Academy of Sciences.  98 (2001)  1 - p. 206-211 , 2001
Link: https://doi.org/10.1073/..
 
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