Very small deletions within the NESP55 gene in pseudohypoparathyroidism type 1b

Por Rezwan, Faisal I, Poole, Rebecca L, Prescott, Trine, Walker, Joanna M, Karen Temple, I, Mackay, Deborah JG
Publicado no Eur J Hum Genet (2015)

An atypical case of hypomethylation at multiple imprinted loci

Por Baple, Emma L, Poole, Rebecca L, Mansour, Sahar, Willoughby, Catherine, Temple, I Karen, Docherty, Louise E, Taylor, Rohan, Mackay, Deborah J G
Publicado em 2011

Beckwith–Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1

Por Poole, Rebecca L, Leith, Donald J, Docherty, Louise E, Shmela, Mansur E, Gicquel, Christine, Splitt, Miranda, Temple, I Karen, Mackay, Deborah J G
Publicado em 2012

A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders

Por Rezwan, Faisal I, Docherty, Louise E, Poole, Rebecca L, Lockett, Gabrielle A, Arshad, S Hasan, Holloway, John W, Temple, I Karen, Mackay, Deborah JG
Publicado no Clin Epigenetics (2015)

Analysis of wheat SAGE tags reveals evidence for widespread antisense transcription

Por Poole, Rebecca L, Barker, Gary LA, Werner, Kay, Biggi, Gaia F, Coghill, Jane, Gibbings, J George, Berry, Simon, Dunwell, Jim M, Edwards, Keith J
Publicado em 2008

Transcriptome analysis of grain development in hexaploid wheat

Por Wan, Yongfang, Poole, Rebecca L, Huttly, Alison K, Toscano-Underwood, Claudia, Feeney, Kevin, Welham, Sue, Gooding, Mike J, Mills, Clare, Edwards, Keith J, Shewry, Peter R, Mitchell, Rowan AC
Publicado em 2008

Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

Por Docherty, Louise E, Rezwan, Faisal I, Poole, Rebecca L, Jagoe, Hannah, Lake, Hannah, Lockett, Gabrielle A, Arshad, Hasan, Wilson, David I, Holloway, John W, Temple, I Karen, Mackay, Deborah J G
Publicado em 2014

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci

Por Turner, Claire Louise Susan, Mackay, Deborah M, Callaway, Jonathan L A, Docherty, Louise E, Poole, Rebecca L, Bullman, Hilary, Lever, Margaret, Castle, Bruce M, Kivuva, Emma C, Turnpenny, Peter D, Mehta, Sarju G, Mansour, Sahar, Wakeling, Emma L, Mathew, Verghese, Madden, Jackie, Davies, Justin H, Temple, I Karen
Publicado em 2010

Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans

Por Docherty, Louise E., Rezwan, Faisal I., Poole, Rebecca L., Turner, Claire L. S., Kivuva, Emma, Maher, Eamonn R., Smithson, Sarah F., Hamilton-Shield, Julian P., Patalan, Michal, Gizewska, Maria, Peregud-Pogorzelski, Jaroslaw, Beygo, Jasmin, Buiting, Karin, Horsthemke, Bernhard, Soellner, Lukas, Begemann, Matthias, Eggermann, Thomas, Baple, Emma, Mansour, Sahar, Temple, I. Karen, Mackay, Deborah J. G.
Publicado no Nat Commun (2015)