Browsing by Author "Berry, Jesia G."

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  • Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy
    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, Luis Alberto; MacLennan, Alastair H.; Gecz, Jozef (Nature Research, 2018)
    Cerebral palsy (CP) is the most frequent movement disorder of childhood affecting 1 in 500 live births in developed countries. We previously identified likely pathogenic de novo or inherited single nucleotide variants (SNV) ...
  • Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing
    van Eyk, Clare L.; Webber, Dani L.; Minoche, André E.; Pérez Jurado, Luis Alberto; Corbett, Mark A.; Gardner, Alison E.; Berry, Jesia G.; Harper, Kelly; MacLennan, Alastair H.; Gecz, Jozef (Nature Research, 2021)
    Cerebral palsy (CP) is the most common cause of childhood physical disability, with incidence between 1/500 and 1/700 births in the developed world. Despite increasing evidence for a major contribution of genetics to CP ...

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