Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gillian P. Crockford"'
Autor:
D. Timothy Bishop, Radka Lohynska, Robert Huddart, Douglas F. Easton, Ludmila Liubchenko, Katherine L. Nathanson, Michael R. Stratton, Barbara L. Weber, Kelly-Anne Phillips, Parry Guilford, Michael Friedlander, Hans Stoll, Stéphane Richard, Catherine Bonaïti-Pellié, T. Oliver, Wilma Ormiston, Katherine M. Tucker, Mark H. Greene, Joan Kramer, David Forman, Elizabeth A. Rapley, Lawrence H. Einhorn, Gedske Daugaard, Axel Heidenreich, Sergei Tjulandin, Walter P. Weber, Michael A.S. Jewett, David W. Hogg, Sophie D. Fosså, Peter Albers, Rachel Linger, Lajos Géczi, Lola Johnson, Darshna Dudakia, Mary L. McMaster, Ketil Heimdal, István Bodrogi, Victoria K. Cortessis, Edith Olah, Peter A. Daly, Gillian P. Crockford, Agnès Chompret, Sarah Hockley
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2006, 15 (3), pp.443-51. ⟨10.1093/hmg/ddi459⟩
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15 (3), pp.443-51. ⟨10.1093/hmg/ddi459⟩
Human Molecular Genetics, 2006, 15 (3), pp.443-51. ⟨10.1093/hmg/ddi459⟩
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15 (3), pp.443-51. ⟨10.1093/hmg/ddi459⟩
A family history of disease is a strong risk factor for testicular germ cell tumour (TGCT). In order to identify the location of putative TGCT susceptibility gene(s) we conducted a linkage search in 237 pedigrees with two or more cases of TGCT. One h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1669ed70edbf7d179085b8ddd1c8754
http://doc.rero.ch/record/292102/files/ddi459.pdf
http://doc.rero.ch/record/292102/files/ddi459.pdf
Autor:
Michael R. Stratton, Elizabeth A. Rapley, Douglas F. Easton, D. Timothy Bishop, Gillian P. Crockford
Publikováno v:
APMIS. 111:128-135
Approximately 1700 men in the United Kingdom develop testicular germ cell tumours (TGCT) per year. Among the known risk factors a family history of disease remains one of the strongest (1, 2). Two-percent of TGCT cases report another affected family
Publikováno v:
Genetic Epidemiology. 17:S527-S532
We approached the simulation as though it were an international study with similar but not identical information being collected from different populations. In keeping with this we analyzed one replicate from each population. Initially we examined th
Autor:
Douglas F. Easton, Gillian P. Crockford, Michael R. Stratton, Elizabeth A. Rapley, Robert Huddart, J. G. Bodmer, Michael Leahy, Colin Cooper, Michael Friedlander, Paul Goss, Jenny Donald, D. Timothy Bishop, Ian Thomlinson, David Hogg, Sandeep Patel, R. Timothy D. Oliver, Sophie D. Fosså, Dawn Teare, Jonathon Moses, Fellicity Collins, Rita Barfoot, Susan Tonks, Rachael Hunter, Ketil Heimdal, Rifat Hamoudi, Hong Qi Peng, Katherine M. Tucker, Sandra Gill, Sheila Seal, Patrick J. Biggs, David Forman
Publikováno v:
APMIS. 106:64-72
Although the aetiology of testicular cancer is unknown, a clear familial component has been identified in a number of studies. In an effort to identify susceptibility genes for testicular cancer, the International Testis Cancer Linkage Consortium has
Autor:
David J. Vaughn, Parry Guilford, Michael Friedlander, Chu Chen, Wilma Ormiston, Sophie D. Fosså, Ludmila Liubchenko, Ketil Heimdal, Mark H. Greene, Robert Huddart, Stéphane Richard, Gedske Daugaard, Malcolm C. Pike, Elizabeth A. Rapley, David Forman, István Bodrogi, Rachel Hawes, Lawrence H. Einhorn, Axel Heidenreich, J. Wolter Oosterhuis, Barbara L. Weber, David W. Hogg, Ad J. M. Gillis, Peter A. Daly, Joan Kramer, Agnès Chompret, Leendert H. J. Looijenga, D. Timothy Oliver, Sergei Tjulandin, Katherine M. Tucker, D. Timothy Bishop, Richard Letrero, Matthew Rudd, Radka Lohynska, Douglas F. Easton, Michael R. Stratton, Kelly-Anne Phillips, Hans Stoll, Catherine Bonaïti-Pellié, Katherine L. Nathanson, Walter P. Weber, Michael A.S. Jewett, Lajos Géczi, Peter A. Kanetsky, Victoria K. Cortessis, Edith Olah, Gillian P. Crockford, Mary L. McMaster, Stephen M. Schwartz
Publikováno v:
American journal of human genetics. 77(6)
Testicular germ cell tumor (TGCT) is the most common cancer in young men. Despite a considerable familial component to TGCT risk, no genetic change that confers increased risk has been substantiated to date. The human Y chromosome carries a number of
Autor:
Lawrence H. Einhorn, Axel Heidenreich, István Bodrogi, Sophie D. Fosså, Stéphane Richard, Ludmila Liubchenko, Leendert H. J. Looijenga, Mary L. McMaster, Sergei Tjulandin, Wilma Ormiston, D T Bishop, Robert Huddart, Peter A. Daly, David W. Hogg, Barbara L. Weber, Parry Guilford, Michael Friedlander, E. Olah, Gillian P. Crockford, M. G. Leahy, Mark H. Greene, L. Johnson, David Forman, William H. Warren, Gedske Daugaard, S. Hockley, E. A. Rapley, Kelly-Anne Phillips, Nina Aass, Ketil Heimdal, Katherine M. Tucker, Walter P. Weber, Radka Lohynska, Michael A.S. Jewett, Doug Easton, Michael R. Stratton, Hans Stoll, D. T. Oliver, Lajos Géczi
Publikováno v:
Scopus-Elsevier
British Jounal of Cancer, 90(12), 2397-2401. Nature Publishing Group
British Journal of Cancer, 90, 2397-2401. Nature Publishing Group
British Journal of Cancer
British Jounal of Cancer, 90(12), 2397-2401. Nature Publishing Group
British Journal of Cancer, 90, 2397-2401. Nature Publishing Group
British Journal of Cancer
Somatic mutations of KIT in familial testicular germ cell tumours Somatic mutations of the KIT gene have been reported in mast cell diseases and gastrointestinal stromal tumours. Recently, they have also been found in mediastinal and testicular germ
Publikováno v:
Germ Cell Tumours V ISBN: 9781447132837
Testicular Germ Cell Tumours (TGCT) affect 1 in 400 men in the UK. Two per cent of TGCT cases report another affected family member. The familial relative risk is estimated to be 8–10 fold for brothers of cases and 4–6 fold for fathers and sons.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::741dfda2b356f4e0dada27bbf394d794
https://doi.org/10.1007/978-1-4471-3281-3_1
https://doi.org/10.1007/978-1-4471-3281-3_1
Autor:
Paul E. Goss, S. Edwards, R. Timothy D. Oliver, Robert Huddart, Sophie D. Fosså, Peter A. Daly, Michael R. Stratton, Michael Friedlander, Julia G. Bodmer, Douglas F. Easton, Patrick J. Biggs, Sheila Seal, Michael Leahy, D. Timothy Bishop, Ketil Heimdal, Gillian P. Crockford, Wilma Ormiston, Rifat Hamoudi, David Hogg, Dawn Teare, Elizabeth A. Rapley, Axel Heidenreich, David Forman, Felicity Collins, Katherine L. Tucker, Colin Cooper, Jenny Donald, Rita Barfoot
Publikováno v:
ResearcherID
Testicular germ-cell tumours (TGCT) affect 1 in 500 men and are the most common cancer in males aged 15-40 in Western European populations. The incidence of TGCT has risen dramatically over the last century. Known risk factors for TGCT include a hist
Autor:
Valerie Newton, Alex F. Markham, K. A. Brown, Gillian P. Crockford, D. T. Bishop, Gareth Parry, G. Karbani, Robert F. Mueller, A. Noble, A. H. Janjua
Publikováno v:
Human molecular genetics. 5(1)
Autosomal recessive non-syndromal hearing impairment (NSRD) is genetically heterogeneous. Five loci have been identified to date which map to chromosomes 13 (DFNB1), 11 (DFNB2), 17 (DFNB3), 7 (DFNB4) and 14 (DFBN5). We report definite linkage of NSRD