Multiplex allele-specific target amplification based on PCR suppression

מאת Broude, Natalia E., Zhang, Lingang, Woodward, Karen, Englert, David, Cantor, Charles R.
יצא לאור 2001

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

מאת Broude, Natalia E., Woodward, Karen, Cavallo, Robert, Cantor, Charles R., Englert, David
יצא לאור 2001

Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human Genome

מאת Dhami, Pawandeep, Coffey, Alison J., Abbs, Stephen, Vermeesch, Joris R., Dumanski, Jan P., Woodward, Karen J., Andrews, Robert M., Langford, Cordelia, Vetrie, David
יצא לאור 2005

A review of structural brain abnormalities in Pallister‐Killian syndrome

מאת Poulton, Cathryn, Baynam, Gareth, Yates, Clarissa, Alinejad‐Rokny, Hamid, Williams, Simon, Wright, Helen, Woodward, Karen J., Sivamoorthy, Soruba, Peverall, Joanne, Shipman, Peter, Ravine, David, Beilby, John, Heng, Julian Ik‐Tsen
הוצא לאור ב Mol Genet Genomic Med (2017)

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

מאת Bahrambeigi, Vahid, Song, Xiaofei, Sperle, Karen, Beck, Christine R., Hijazi, Hadia, Grochowski, Christopher M., Gu, Shen, Seeman, Pavel, Woodward, Karen J., Carvalho, Claudia M. B., Hobson, Grace M., Lupski, James R.
הוצא לאור ב Genome Med (2019)

Additional Copies of the Proteolipid Protein Gene Causing Pelizaeus-Merzbacher Disease Arise by Separate Integration into the X Chromosome

מאת Hodes, M. E., Woodward, Karen, Spinner, Nancy B., Emanuel, Beverly S., Enrico-Simon, Agnes, Kamholz, John, Stambolian, Dwight, Zackai, Elaine H., Pratt, Victoria M., Thomas, I. T., Crandall, Kerry, Dlouhy, Stephen R., Malcolm, Sue
יצא לאור 2000

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

מאת Singh, Ram, Cohen, Ana S.A., Poulton, Cathryn, Hjortshøj, Tina Duelund, Akahira-Azuma, Moe, Mendiratta, Geetu, Khan, Wahab A., Azmanov, Dimitar N., Woodward, Karen J., Kirchhoff, Maria, Shi, Lisong, Edelmann, Lisa, Baynam, Gareth, Scott, Stuart A., Jabs, Ethylin Wang
הוצא לאור ב Cold Spring Harb Mol Case Stud (2021)

Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination

מאת Woodward, Karen J., Cundall, Maria, Sperle, Karen, Sistermans, Erik A., Ross, Mark, Howell, Gareth, Gribble, Susan M., Burford, Deborah C., Carter, Nigel P., Hobson, Donald L., Garbern, James Y., Kamholz, John, Heng, Henry, Hodes, M. E., Malcolm, Sue, Hobson, Grace M.
יצא לאור 2005

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

מאת Corbett, Mark A., van Eyk, Clare L., Webber, Dani L., Bent, Stephen J., Newman, Morgan, Harper, Kelly, Berry, Jesia G., Azmanov, Dimitar N., Woodward, Karen J., Gardner, Alison E., Slee, Jennie, Pérez-Jurado, Luís A., MacLennan, Alastair H., Gecz, Jozef
הוצא לאור ב NPJ Genom Med (2018)

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

מאת Corbett, Mark A., van Eyk, Clare L., Webber, Dani L., Bent, Stephen J., Newman, Morgan, Harper, Kelly, Berry, Jesia G., Azmanov, Dimitar N., Woodward, Karen J., Gardner, Alison E., Slee, Jennie, Pérez-Jurado, Luís A., MacLennan, Alastair H., Gecz, Jozef
הוצא לאור ב NPJ Genom Med (2019)

Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism

מאת Woods, Kathryn S., Cundall, Maria, Turton, James, Rizotti, Karine, Mehta, Ameeta, Palmer, Rodger, Wong, Jacqueline, Chong, W. K., Al-Zyoud, Mahmoud, El-Ali, Maryam, Otonkoski, Timo, Martinez-Barbera, Juan-Pedro, Thomas, Paul Q., Robinson, Iain C., Lovell-Badge, Robin, Woodward, Karen J., Dattani, Mehul T.
יצא לאור 2005

Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance

מאת Woodward, Karen J., Stampalia, Julie, Vanyai, Hannah, Rijhumal, Hashika, Potts, Kim, Taylor, Fiona, Peverall, Joanne, Grumball, Tanya, Sivamoorthy, Soruba, Alinejad‐Rokny, Hamid, Wray, John, Whitehouse, Andrew, Nagarajan, Lakshmi, Scurlock, Jacqueline, Afchani, Sabine, Edwards, Matthew, Murch, Ashleigh, Beilby, John, Baynam, Gareth, Kiraly‐Borri, Cathy, McKenzie, Fiona, Heng, Julian I. T.
הוצא לאור ב Mol Genet Genomic Med (2019)