Lisa Cooper-Charles

New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies

R. Holt, P. Calvas, N. Chassaing, 2018, Human Genetics.

Evidence for 28 genetic disorders discovered by combining healthcare and research data

Patrick J. Short, M. Hurles, L. Vissers, 2020, Nature.

The contribution of X-linked coding variation to severe developmental disorders

M. Hurles, R. Sandford, D. Baralle, 2020, Nature Communications.

Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome

J. Morton, D. McMullan, C. Patel, 2011, European Journal of Human Genetics.

New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies

Luciana Rodrigues da Silva, R. Holt, P. Calvas, 2018, Human Genetics.

The deployment of adenovirus‐containing gene activated matrices onto severed axons after central nervous system injury leads to transgene expression in target neuronal cell bodies

O. Berlanga, M. Berry, A. Logan, 2009, The journal of gene medicine.

In vitro evaluation of a ‘stealth’ adenoviral vector for targeted gene delivery to adult mammalian neurones

Z. Ahmed, M. Berry, A. Logan, 2009, The journal of gene medicine.