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Author/Creator Barry, Brenda

1. Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant. Issue 4 (13th July 2019)

Authors:
Thomas, Mervyn G; Maconachie, Gail D E; Constantinescu, Cris S; Chan, Wai-Man; Barry, Brenda; Hisaund, Michael; Sheth, Viral; Kuht, Helen J; Dineen, Rob A; Harieaswar, Sreemathi; Engle, Elizabeth C; Gottlob, Irene
Journal:
British journal of ophthalmology
Issue:
Volume 104:Issue 4(2020)
Page Start:
547
Record Type:
Journal Article
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2. G‐protein coupled receptor 56 promotes myoblast fusion through serum response factor‐ and nuclear factor of activated T‐cell‐mediated signalling but is not essential for muscle development in vivo. (8th October 2013)

Authors:
Wu, Melissa P.; Doyle, Jamie R.; Barry, Brenda; Beauvais, Ariane; Rozkalne, Anete; Piao, Xianhua; Lawlor, Michael W.; Kopin, Alan S.; Walsh, Christopher A.; Gussoni, Emanuela
Journal:
FEBS journal
Issue:
Volume 280:Number 23(2013)
Page Start:
6097
Record Type:
Journal Article
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4. MAGEL2‐related disorders: A study and case series. Issue 6 (22nd August 2019)

Authors:
Patak, Jameson; Gilfert, James; Byler, Melissa; Neerukonda, Vamsee; Thiffault, Isabelle; Cross, Laura; Amudhavalli, Shivarajan; Pacio‐Miguez, Marta; Palomares‐Bralo, Maria; Garcia‐Minaur, Sixto; Santos‐Simarro, Fernando; Powis, Zoe; Alcaraz, Wendy; Tang, Sha; Jurgens, Julie; Barry, Brenda; Englan...
Journal:
Clinical genetics
Issue:
Volume 96:Issue 6(2019)
Page Start:
493
Record Type:
Journal Article
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6. SLC25A22 is a novel gene for migrating partial seizures in infancy. Issue 6 (17th October 2013)

Authors:
Poduri, Annapurna; Heinzen, Erin L.; Chitsazzadeh, Vida; Lasorsa, Francesco Massimo; Elhosary, P. Christina; LaCoursiere, Christopher M.; Martin, Emilie; Yuskaitis, Christopher J.; Hill, Robert Sean; Atabay, Kutay Deniz; Barry, Brenda; Partlow, Jennifer N.; Bashiri, Fahad A.; Zeidan, Radwan M.; E...
Journal:
Annals of neurology
Issue:
Volume 74:Issue 6(2013:Dec.)
Page Start:
873
Record Type:
Journal Article
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