Comparison of actionable events detected in cancer genomes by whole-genome sequencing, in silico whole-exome and mutation panels
Ramarao-Milne, P., Kondrashova, O., Patch, A.-M., Nones, K., Koufariotis, L.T., Newell, F., Addala, V., Lakis, V., Holmes, O., Leonard, C., Wood, S., Xu, Q., Mukhopadhyay, P., Naeini, M.M., Steinfort, D., Williamson, J.P., Bint, M., Pahoff, C., Nguyen, P.T., Twaddell, S., Arnold, D., Grainge, C., Basirzadeh, F., Fielding, D., Dalley, A.J., Chittoory, H., Simpson, P.T., Aoude, L.G., Bonazzi, V.F., Patel, K., Barbour, A.P., Fennell, D.A., Robinson, B.W., Creaney, J., Hollway, G., Pearson, J.V., Waddell, N.
Published in ESMO open (01.08.2022)
Published in ESMO open (01.08.2022)
Get full text
Journal Article
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2
Sutherland, G.R, Phillips, H.A, Mulley, J.C, Scheffer, I.E, Hollway, G.E, Berkovic, S.F
Published in Nature genetics (01.05.1995)
Published in Nature genetics (01.05.1995)
Get full text
Journal Article
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
MUENKE, M, GRIPP, K. W, LOSKEN, H. W, MULLIKEN, J. B, GUTTMACHER, A. E, WILROY, R. S, CLARKE, L. A, HOLLWAY, G, ADES, L. C, HAAN, E. A, MULLEY, J. C, COHEN, M. M, MCDONALD-MCGINN, D. M, BELLUS, G. A, FRANCOMANO, C. A, MOLONEY, D. M, WALL, S. A, WILKIE, A. O. M, ZACKAI, E. H, GAUDENZ, K, WHITAKER, L. A, BARTLETT, S. P, MARKOWITZ, R. I, ROBIN, N. H, NWOKORO, N, MULVIHILL, J. J
Published in American journal of human genetics (01.03.1997)
Get full text
Published in American journal of human genetics (01.03.1997)
Journal Article
Mutation detection in FGFR2 craniosynostosis syndromes
HOLLWAY, G. E, SUTHERS, G. K, HAAN, E. A, THOMPSON, E, DAVID, D. J, GECZ, J, MULLEY, J. C
Published in Human genetics (01.02.1997)
Published in Human genetics (01.02.1997)
Get full text
Journal Article
Deafness due to Pro250Arg mutation of FGFR3
Hollway, Georgina E, Suthers, Graeme K, Battese, Katie M, Turner, Anne M, David, David J, Mulley, John C
Published in The Lancet (British edition) (21.03.1998)
Published in The Lancet (British edition) (21.03.1998)
Get full text
Journal Article
Localization of craniosynostosis Adelaide type to 4p16
Hollway, G E, Phillips, H A, Adès, L C, Haan, E A, Mulley, J C
Published in Human molecular genetics (01.04.1995)
Published in Human molecular genetics (01.04.1995)
Get more information
Journal Article
Detection of actionable variants in various cancer types reveals value of whole-genome sequencing over in-silico whole-exome and hotspot panel sequencing
Ramarao-Milne, K.P., Patch, A-M, Nones, K., Koufariotis, R., Newell, F., Addala, V.R., Kondrashova, O., Mukhopadhyay, P., Kazakoff, S.H., Lakis, V., Holmes, O., Leonard, C., Wood, S., Xu, C., Pearson, J.V., Hollway, G., Waddell, N.
Published in Annals of oncology (01.11.2019)
Published in Annals of oncology (01.11.2019)
Get full text
Journal Article
115PDetection of actionable variants in various cancer types reveals value of whole-genome sequencing over in-silico whole-exome and hotspot panel sequencing
Ramarao-Milne, K P, Patch, A-M, Nones, K, Koufariotis, R, Newell, F, Addala, V R, Kondrashova, O, Mukhopadhyay, P, Kazakoff, S H, Lakis, V, Holmes, O, Leonard, C, Wood, S, Xu, C, Pearson, J V, Hollway, G, Waddell, N
Published in Annals of oncology (01.11.2019)
Published in Annals of oncology (01.11.2019)
Get full text
Journal Article
Choosing the rural route
Hollway, G., Klassen, R., Klassen, S., Newbery, S., Orrantia, E., Patel, R., Sylvester, M.
Published in Canadian Medical Association journal (CMAJ) (15.09.1997)
Get full text
Published in Canadian Medical Association journal (CMAJ) (15.09.1997)
Journal Article
Scube2 mediates Hedgehog signalling in the zebrafish embryo
Hollway, Georgina E., Maule, John, Gautier, Philippe, Evans, Timothy M., Keenan, David G., Lohs, Claudia, Fischer, Danielle, Wicking, Carol, Currie, Peter D.
Published in Developmental biology (01.06.2006)
Published in Developmental biology (01.06.2006)
Get full text
Journal Article
Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation
Kalscheuer, Vera M., Tao, Jiong, Donnelly, Andrew, Hollway, Georgina, Schwinger, Eberhard, Kübart, Sabine, Menzel, Corinna, Hoeltzenbein, Maria, Tommerup, Niels, Eyre, Helen, Harbord, Michael, Haan, Eric, Sutherland, Grant R., Ropers, Hans-Hilger, Gécz, Jozef
Published in American journal of human genetics (01.06.2003)
Published in American journal of human genetics (01.06.2003)
Get full text
Journal Article
Characterization of the Human Glutamate Receptor Subunit 3 Gene (GRIA3), a Candidate for Bipolar Disorder and Nonspecific X-Linked Mental Retardation
Gécz, Jozef, Barnett, Shaun, Liu, Jianjun, Hollway, Georgina, Donnelly, Andrew, Eyre, Helen, Eshkevari, Hadi S., Baltazar, Romulo, Grunn, Adina, Nagaraja, Ramaiah, Gilliam, Conrad, Peltonen, Leena, Sutherland, Grant R., Baron, Miron, Mulley, John C.
Published in Genomics (San Diego, Calif.) (15.12.1999)
Published in Genomics (San Diego, Calif.) (15.12.1999)
Get full text
Journal Article
Cadherin-Mediated Differential Cell Adhesion Controls Slow Muscle Cell Migration in the Developing Zebrafish Myotome
Cortés, Fernando, Daggett, David, Bryson-Richardson, Robert J., Neyt, Christine, Maule, John, Gautier, Phillipe, Hollway, Georgina E., Keenan, David, Currie, Peter D.
Published in Developmental cell (01.12.2003)
Published in Developmental cell (01.12.2003)
Get full text
Journal Article
Met and Hgf signaling controls hypaxial muscle and lateral line development in the zebrafish
Haines, Lynn, Neyt, Christine, Gautier, Philippe, Keenan, David G, Bryson-Richardson, Robert J, Hollway, Georgina E, Cole, Nicolas J, Currie, Peter D
Published in Development (Cambridge) (01.10.2004)
Published in Development (Cambridge) (01.10.2004)
Get full text
Journal Article
Deafness due to Pro250Arg mutation of FGFR3
Hollway, GE, Suthers, G K, Battese, K M, Turner, A M, David, D J, Mulley, J C
Published in The Lancet (North American edition) (21.03.1998)
Get full text
Published in The Lancet (North American edition) (21.03.1998)
Journal Article