Monogenic diabetes in New Zealand - An audit based revision of the monogenic diabetes genetic testing pathway in New Zealand

por Harrington, Francesca, Greenslade, Mark, Colclough, Kevin, Paul, Ryan, Jefferies, Craig, Murphy, Rinki
Publicado 2023

Current Challenges in Glioblastoma: Intratumour Heterogeneity, Residual Disease, and Models to Predict Disease Recurrence

por Ellis, Hayley P., Greenslade, Mark, Powell, Ben, Spiteri, Inmaculada, Sottoriva, Andrea, Kurian, Kathreena M.
Publicado 2015

BRAF Fusion Analysis in Pilocytic Astrocytomas: KIAA1549-BRAF 15-9 Fusions Are More Frequent in the Midline Than Within the Cerebellum

por Faulkner, Claire, Ellis, Hayley Patricia, Shaw, Abigail, Penman, Catherine, Palmer, Abigail, Wragg, Christopher, Greenslade, Mark, Haynes, Harry Russell, Williams, Hannah, Lowis, Stephen, White, Paul, Williams, Maggie, Capper, David, Kurian, Kathreena Mary
Publicado 2015

Genetic heterogeneity of motor neuropathies

por Bansagi, Boglarka, Griffin, Helen, Whittaker, Roger G., Antoniadi, Thalia, Evangelista, Teresinha, Miller, James, Greenslade, Mark, Forester, Natalie, Duff, Jennifer, Bradshaw, Anna, Kleinle, Stephanie, Boczonadi, Veronika, Steele, Hannah, Ramesh, Venkateswaran, Franko, Edit, Pyle, Angela, Lochmüller, Hanns, Chinnery, Patrick F., Horvath, Rita
Publicado 2017

PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features

por Low, Karen J, Ansari, Morad, Abou Jamra, Rami, Clarke, Angus, El Chehadeh, Salima, FitzPatrick, David R, Greenslade, Mark, Henderson, Alex, Hurst, Jane, Keller, Kory, Kuentz, Paul, Prescott, Trine, Roessler, Franziska, Selmer, Kaja K, Schneider, Michael C, Stewart, Fiona, Tatton-Brown, Katrina, Thevenon, Julien, Vigeland, Magnus D, Vogt, Julie, Willems, Marjolaine, Zonana, Jonathan, Study, D D D, Smithson, Sarah F
Publicado 2017