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Items Authored or Edited by Sushila Rigas

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Group by: Published Date | Item Type | Authors/Editors/Creators | No Grouping
Jump to: 2019 | 2018 | 2017 | 2016 | 2014 | 2012 | 2011 | 2010 | 2009 | 2008 | 2007 | 2006 | 2005 | 2004 | 2001
Number of items: 22.

2019

Silvestri, Roberto; Pucci, Perla; Venalainen, Erik; Matheou, Chrysanthi; Mather, Rebecca; Chandler, Stephen; Aceto, Romina; Rigas, Sushila; Wang, Yuzhuo; Rietdorf, Katja; Bootman, Martin and Crea, Francesco (2019). T-type calcium channels drive the proliferation of androgen-receptor negative prostate cancer cells. The Prostate (Early Access). restricted access item, not available for direct download

2018

Chandler, Stephen; Crea, Francesco; Hirst, Mark; Cox, Angela and Rigas, Sushila (2018). Identification of candidate genes that may function in ER- breast cancer. In: BACR Conference: Response and Resistance in Cancer Therapy, 10-12 Sep 2018, University of Kent, Canterbury.

2017

Paolicchi, Elisa; Fornaro, Lorenzo; Landi, Stefano; Rigas, Sushilaben and Crea, Francesco (2017). EZH2 Single Nucleotide Variants (SNVs): Diagnostic and Prognostic Role in 10 Solid Tumor Types. Epigenomes, 1(3), article no. 18. file

Chandler, Stephen; Crea, Francesco; Hirst, Mark; Cox, Angela and Rigas, Sushilaben (2017). Identification of putative functional genes in breast and other cancers with potentially shared aetiology. In: The Human Genome in Healthcare, 23-24 Nov 2017, The Royal Society, London, UK.

Pucci, Perla; Venalainen, Erik; Mather, Rebecca; Xue, Hui; Rigas, Sushila; Romero, Ignacio A; Wang, Yuzho and Crea, Francesco (2017). Identification of a long non-coding RNA that mediates response to therapy in castration-resistant prostate cancer. In: 3rd International Cancer Symposium, 25-27 Sep 2017, Lyon, France.

2016

Camp, Nicola J.; Lin, Wei-Yu; Bigelow, Alex; Burghel, George J.; Mosbruger, Timothy L.; Parry, Marina A.; Waller, Rosalie G.; Rigas, Sushilaben H.; Tai, Pei-Yi; Berrett, Kristofer; Rajamanickam, Venkatesh; Cosby, Rachel; Brock, Ian W.; Jones, Brandt; Connley, Dan; Sargent, Robert; Wang, Guoying; Factor, Rachel E.; Bernard, Philip S.; Cannon-Albright, Lisa; Knight, Stacey; Abo, Ryan; Werner, Theresa L.; Reed, Malcolm W. R.; Gertz, Jason and Cox, Angela (2016). Discordant Haplotype Sequencing Identifies Functional Variants at the 2q33 Breast Cancer Risk Locus. Cancer Research, 76(7) pp. 1916–1925. file

2014

Camp, Nicola J.; Lin, Wei-Yu; Bigelow, Alex; Parry, Marina A.; Mosbruger, Tim; Burghel, George; Rajamanickam, Venkatesh; Rigas, Sushilaben H.; Cosby, Rachel; Connley, Dan; Wang, Guoying; George, Tresa; Waller, Rosalie; Cannon-Albright, Lisa A.; Jones, Brandt; Sargent, Rob; Reed, Malcolm W. R. and Cox, Angela (2014). Targeted DNA and RNA sequencing identifies breast cancer risk variants associated with differential expression of CASP8 and CFLAR/CASP10. Cancer Research, 74(19 (Supp)), article no. 3267.

2012

Camp, Nicola J.; Parry, Marina; Knight, Stacey; Abo, Ryan; Elliott, Graeme; Rigas, Sushilaben H.; Balasubramanian, Sabapathy P.; Reed, Malcolm W. R.; McBurney, Helen; Latif, Ayse; Newman, William G.; Cannon-Albright, Lisa A.; Evans, D. Gareth and Cox, Angela (2012). Fine-Mapping CASP8 Risk Variants in Breast Cancer. Cancer Epidemiology, Biomarkers & Prevention, 21(1) pp. 176–181.

2011

Rigas, S.; Elliot, G.; Brock, I.; Parry, M.; Abo, R.; Knight, S.; Burghel, G.; Lin, W. Y.; Reed, M. W.; Camp, N. J. and Cox, A. (2011). Association of the TNFRSF10A and TNFRSF10B Gene Region on Chromosome 8 with Breast Cancer Risk. In: Journal of Medical Genetics, BMJ, 48 S41-S41.

2010

Rigas, S. H.; Parry, M.; Reed, M. W.; Camp, N. and Cox, A. (2010). Assessing the functional role of caspase-8 gene variants in breast cancer. In: Breast Cancer Research, 12(1 (Supp.)), article no. P24.

Abo, Ryan P.; Parry, Marina; Rigas, Sushila H.; Cox, Angela and Camp, Nicola J. (2010). Abstract 2844: Association of genetic variants in TNFRSF10B and breast cancer. In: Cancer Research, AACR, 70(8 Suppl), article no. 2844.

2009

Shephard, Neil Duncan; Abo, Ryan; Rigas, Sushila Harkisandas; Frank, Bernd; Lin, Wei-Yu; Brock, Ian Wallace; Shippen, Adam; Balasubramanian, Sabapathy Prakash; Reed, Malcolm Walter Ronald; Bartram, Claus Rainer; Meindl, Alfons; Schmutzler, Rita Katharina; Engel, Christopher; Burwinkel, Barbara; Cannon-Albright, Lisa Anne; Allen-Brady, Kristina; Camp, Nicola Jane and Cox, Angela (2009). A Breast Cancer Risk Haplotype in the Caspase-8 Gene. Cancer Research, 69(7) pp. 2724–2728.

Cox, Angela; Lin, Wei-Yu; Elliott, Graeme; Rigas, Sushila; Bishop, D Timothy; Cannon-Albright, Lisa; Cai, Zheng; Camp, Nicola; Neal, David; Donovan, Jenny and Hamdy, Freddie (2009). Abstract# 2556: An investigation of the role of the caspase-8 gene in prostate and colon cancer susceptibility using a SNP-tagging approach. In: Proc Am Assoc Cancer Res; 2009, Abstract nr 2556, AACR.

Rigas, Sushila H.; Parry, Marina; Reed, Malcolm W. and Cox, Angela (2009). The functional Role of CASP8 D302H and Other Apoptosis Gene Variants In Breast Cancer. In: Journal of Medical Genetics, BMJ, 46 S108.

2008

Frank, Bernd; Rigas, Sushila H.; Bermejo, Justo Lorenzo; Wiestler, Miriam; Wagner, Kerstin; Hemminki, Kari; Reed, Malcolm W.; Sutter, Christian; Wappenschmidt, Barbara; Balasubramanian, Sabapathy P.; Meindl, Alfons; Kiechle, Marion; Bugert, Peter; Schmutzler, Rita K.; Bartram, Claus R.; Justenhoven, Christina; Ko, Yon-Dschun; Brüning, Thomas; Brauch, Hiltrud; Hamann, Ute; Pharoah, Paul P. D.; Dunning, Alison M.; Pooley, Karen A.; Easton, Douglas F.; Cox, Angela and Burwinkel, Barbara (2008). The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study. Breast Cancer Research and Treatment, 111(1) pp. 139–144.

Freedberg, Daniel E.; Rigas, Sushila H.; Russak, Julie; Gai, Weiming; Kaplow, Margarita; Osman, Iman; Turner, Faye; Randerson-Moor, Juliette A.; Houghton, Alan; Busam, Klaus; Bishop, D. Timothy; Bastian, Boris C.; Newton-Bishop, Julia A. and Polsky, David (2008). Frequent p16-Independent Inactivation of p14ARF in Human Melanoma. Journal of the National Cancer Institute, 100(11) pp. 784–795.

2007

Goldstein, Alisa M.; Chan, May; Harland, Mark; Hayward, Nicholas K.; Demenais, Florence; Bishop, D. Timothy; Azizi, Esther; Bergman, Wilma; Bianchi-Scarra, Giovanna; Bruno, William; Calista, Donata; Cannon Albright, Lisa A.; Chaudru, Valerie; Chompret, Agnes; Cuellar, Francisco; Elder, David E.; Ghiorzo, Paola; Gillanders, Elizabeth M.; Gruis, Nelleke A.; Hansson, Johan; Hogg, David; Holland, Elizabeth A.; Kanetsky, Peter A.; Kefford, Richard F.; Landi, Maria Teresa; Lang, Julie; Leachman, Sancy A.; MacKie, Rona M.; Magnusson, Veronica; Mann, Graham J.; Newton Bishop, Julia; Palmer, Jane M.; Puig, Susana; Puig-Butille, Joan A.; Stark, Mitchell; Tsao, Hensin; Tucker, Margaret A.; Whitaker, Linda; Yakobson, Emanuel; The Lund Melanoma Study Group and The Melanoma Genetics Consortium (GenoMEL) (2007). Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. Journal of Medical Genetics, 44(2) pp. 99–106.

2006

Rigas, Sushila; Rafii, S; Shippen, AL; MacPherson, G; Balasubramanian, S; Reed, MW and Cox, A (2006). Role of CASP8 D302H and Other Apoptosis Gene Variants in Breast Cancer. In: Breast Cancer Research, 8(Suppl 2). file

Goldstein, Alisa M.; Chan, May; Harland, Mark; Gillanders, Elizabeth M.; Hayward, Nicholas K.; Avril, Marie-Francoise; Azizi, Esther; Bianchi-Scarra, Giovanna; Bishop, D. Timothy; Bressac-de Paillerets, Brigitte; Bruno, William; Calista, Donato; Cannon Albright, Lisa A.; Demenais, Florence; Elder, David E.; Ghiorzo, Paola; Gruis, Nelleke A.; Hansson, Johan; Hogg, David; Holland, Elizabeth A.; Kanetsky, Peter A.; Kefford, Richard F.; Landi, Maria Teresa; Lang, Julie; Leachman, Sancy A.; MacKie, Rona M.; Magnusson, Veronica; Mann, Graham J.; Niendorf, Kristin; Newton Bishop, Julia; Palmer, Jane M.; Puig, Susana; Puig-Butille, Joan A.; de Snoo, Femke A.; Stark, Mitchell; Tsao, Hensin; Tucker, Margaret A.; Whitaker, Linda; Yakobson, Emanuel; The Lund Melanoma Study Group and The Melanoma Genetics Consortium (GenoMEL) (2006). High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL. Cancer Research, 66(20) pp. 9818–9828.

2005

Mistry, Sushila H.; Taylor, Claire; Randerson-Moor, Juliette A.; Harland, Mark; Turner, Faye; Barrett, Jennifer H.; Whitaker, Linda; Jenkins, Robert B.; Knowles, Margaret A.; Newton Bishop, Julia A. and Bishop, D. Timothy (2005). Prevalence of 9p21 Deletions in UK Melanoma Families. Genes, Chromosomes & Cancer, 44(3) pp. 292–300.

2004

Mistry, Sushilaben Harkisandas (2004). The Role Of p14ARF In Familial And Sporadic Melanoma. PhD thesis University of Leeds.

2001

Harland, Mark; Mistry, Sushila; Bishop, D. Timothy and Newton Bishop, Julia A. (2001). A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees. Human Molecular Genetics, 10(23) pp. 2679–2686.

This list was generated on Fri Aug 23 14:35:50 2019 BST.

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