Zobrazeno 1 - 10
of 206
pro vyhledávání: '"Hodgson, Shirley V"'
Autor:
Frayling, Ian M., Beck, Nicholas E., Ilyas, Mohammad, Dove-Edwin, Isis, Goodman, Peter, Pack, Kevin, Bell, Jennifer A., Williams, Christopher B., Hodgson, Shirley V., Talbot, Ian C., Bodmer, Walter F.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1998 Sep 01. 95(18), 10722-10727.
Externí odkaz:
https://www.jstor.org/stable/45958
Akademický článek
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Autor:
Burn, John, Gerdes, Anne-Marie, Macrae, Finlay, Mecklin, Jukka-Pekka, Moeslein, Gabriela, Olschwang, Sylviane, Eccles, Diane, Evans, D Gareth, Maher, Eamonn R, Bertario, Lucio, Bisgaard, Marie-Luise, Dunlop, Malcolm G, Ho, Judy WC, Hodgson, Shirley V, Lindblom, Annika, Lubinski, Jan, Morrison, Patrick J, Murday, Victoria, Ramesar, Raj, Side, Lucy, Scott, Rodney J, Thomas, Huw JW, Vasen, Hans F, Barker, Gail, Crawford, Gillian, Elliott, Faye, Movahedi, Mohammad, Pylvanainen, Kirsi, Wijnen, Juul T, Fodde, Riccardo, Lynch, Henry T, Mathers, John C, Bishop, D Timothy
Publikováno v:
In The Lancet 2011 378(9809):2081-2087
Autor:
Hodgson, Shirley V.
Publikováno v:
In Clinical Molecular Medicine 2020:423-436
Autor:
Hodgson, Shirley V, Popat, Sanjay
Publikováno v:
In Clinical Medicine May 2003 3(3):260-264
Autor:
Andrews, Katrina A, Ascher, David B, Pires, Douglas Eduardo Valente, Barnes, Daniel R, Vialard, Lindsey, Casey, Ruth T, Bradshaw, Nicola, Adlard, Julian, Aylwin, Simon, Brennan, Paul, Brewer, Carole, Cole, Trevor, Cook, Jackie A, Davidson, Rosemarie, Donaldson, Alan, Fryer, Alan, Greenhalgh, Lynn, Hodgson, Shirley V, Irving, Richard, Lalloo, Fiona, McConachie, Michelle, McConnell, Vivienne PM, Morrison, Patrick J, Murday, Victoria, Park, Soo-Mi, Simpson, Helen L, Snape, Katie, Stewart, Susan, Tomkins, Susan E, Wallis, Yvonne, Izatt, Louise, Goudie, David, Lindsay, Robert S, Perry, Colin G, Woodward, Emma R, Antoniou, Antonis C, Maher, Eamonn R
Publikováno v:
JOURNAL OF MEDICAL GENETICS
Background: Germline pathogenic variants in SDHB/\ud SDHC/SDHD are the most frequent causes of inherited\ud phaeochromocytomas/paragangliomas. Insufficient\ud information regarding penetrance and phenotypic\ud variability hinders optimum management o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de75177a06328da680648a7dfef5ac27
https://eprints.gla.ac.uk/157129/1/157129.pdf
https://eprints.gla.ac.uk/157129/1/157129.pdf
Publikováno v:
BMC Cancer, Vol 8, Iss 1, p 257 (2008)
Abstract Background Fanconi anemia (FA) is an autosomal recessive DNA repair disorder with affected individuals having a high risk of developing acute myeloid leukaemia and certain solid tumours. Thirteen complementation groups have been identified a
Externí odkaz:
https://doaj.org/article/c6788c3c918a404a8309ccced35df95c
Autor:
Scott, Rodney J., Froggatt, Nicola J., Trembath, Richard C., Gareth Evans, Hodgson, Shirley V., Maher, Eamonn R.
Publikováno v:
University of Manchester-PURE
Desmoid tumours are generally very rare but occur about 100 times more frequently in the colorectal cancer predisposition syndrome familial adenomatous polyposis (MIM 175100), being represented in about 10% of patients. In addition to desmoid disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c6d8909304407bbb056341768e6c9bb8
http://doc.rero.ch/record/299015/files/5-12-1921.pdf
http://doc.rero.ch/record/299015/files/5-12-1921.pdf
Autor:
Painter, Jodie N, O'Mara, Tracy A, Marquart, Louise, Webb, Penelope M, Attia, John, Medland, Sarah E, Cheng, Timothy, Dennis, Joe, Holliday, Elizabeth G, McEvoy, Mark, Scott, Rodney J, Ahmed, Shahana, Healey, Catherine S, Shah, Mitul, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley V, Beckmann, Matthias W, Ekici, Arif B, Fasching, Peter A, Hein, Alexander, Rübner, Matthias, Czene, Kamila, Darabi, Hatef, Hall, Per, Li, Jingmei, Dörk, Thilo, Dürst, Matthias, Hillemanns, Peter, Runnebaum, Ingo B, Amant, Frederic, Annibali, Daniela, Depreeuw, Jeroen, Lambrechts, Diether, Neven, Patrick, Cunningham, Julie M, Dowdy, Sean C, Goode, Ellen L, Fridley, Brooke L, Winham, Stacey J, Njølstad, Tormund S, Salvesen, Helga B, Trovik, Jone, Werner, Henrica MJ, Ashton, Katie A, Otton, Geoffrey, Proietto, Anthony, Mints, Miriam, Tham, Emma, Bolla, Manjeet K, Michailidou, Kyriaki, Wang, Qin, Tyrer, Jonathan P, Hopper, John L, Peto, Julian, Swerdlow, Anthony J, Burwinkel, Barbara, Brenner, Hermann, Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Chang-Claude, Jenny, Couch, Fergus J, Giles, Graham G, Kristensen, Vessela N, Cox, Angela, Pharoah, Paul DP, Tomlinson, Ian, Dunning, Alison M, Easton, Douglas F, Thompson, Deborah J, Spurdle, Amanda B, AOCS Group, for RENDOCAS, National Study of Endometrial Cancer Genetics Group (NSECG), Australian National Endometrial Cancer Study Group (ANECS)
BACKGROUND: The strongest known risk factor for endometrial cancer is obesity. To determine whether SNPs associated with increased body mass index (BMI) or waist-hip ratio (WHR) are associated with endometrial cancer risk, independent of measured BMI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a2bcc5f54d715225ff97c9b16329754e
https://openaccess.sgul.ac.uk/id/eprint/113823/1/Painter_et_al-2016-Cancer_Epidemiology_Biomarkers_and_Prevention-AM.pdf
https://openaccess.sgul.ac.uk/id/eprint/113823/1/Painter_et_al-2016-Cancer_Epidemiology_Biomarkers_and_Prevention-AM.pdf