Currently browsing: Items authored or edited by Sushila Rigas https://orcid.org/0000-0002-0401-7681

Khokhar, Fahad; Pereira Dias, Joana; Mylona, Elli; Keane, Jacqueline; Chattaway, Marie; MacQueen, Hilary; Rigas, Sushila; Baker, Stephen and Holmes, Mark (2023). Transcriptional activity of XDR Salmonella Typhi after exposure to subinhibitory antibiotic concentrations. In: 33rd European Congress of Clinical Microbiology and Infectious Diseases (ECCMID), 15-18 Apr 2023, Copenhagen, Denmark.

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Khokhar, Fahad; Pickard, Derek; Dyson, Zoe; Iqbal, Junaid; Pragasam, Agila; John, Jobin Jacob; Veeraraghavan, Balaji; Qamar, Farah; Dougan, Gordon; MacQueen, Hilary; Rigas, Sushila; Holmes, Mark and Mutreja, Ankur (2022). Multiplex PCR assay to detect high risk lineages of Salmonella Typhi and Paratyphi A. PLOS ONE, 17(7), article no. e0267805.

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Khokhar, F.; Pickard, D.; Dyson, Z.; Jacob John, J.; Pragasam, A.; Veeraraghavan, B.; Iqbal, J.; Qamar, F.; Dougan, G.; MacQueen, H.; Rigas, S.; Holmes, M. and Mutreja, A. (2022). Multiplex PCR Assay to Detect High Risk Lineages of Salmonella Typhi. In: 13th International Meeting on Microbial Epidemiological Markers (IMMEM XIII), 14-17 Sep 2022, Bath, UK.

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Latarani, Maryam; Pucci, Perla; Roig-Carles, David; Eccleston, Mark; Xue, Hui; Hawkes, Cheryl; Rigas, Sushila; Wang, Yuzhuo and Crea, Francesco (2020). EZH2 as a therapeutic target for aggressive prostate cancer. In: Crick Cancer Research Symposium, iPoster, 5-6 Oct 2020, The Francis Crick Institute and Virtual.

Pucci, Perla; Crea, Francesco; Alborelli, Ilaria; Quagliata, Luca; Bootman, Martin; Rigas, Sushilaben; Romero, Ignacio and Wang, Yuzhuo (2020). Long non-coding RNAs are key players in Prostate cancer tumorigenesis and drug resistance. In: 27th Annual PCF Scientific Retreat Virtual Poster Session, 20-23 Oct 2020, Virtual, Morressier.

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Pucci, Perla; Venalainen, Erik; Alborelli, Ilaria; Quagliata, Luca; Hawkes, Cheryl; Mather, Rebecca; Romero, Ignacio A; Rigas, Sushila; Wang, Yuzhuo and Crea, Francesco (2020). LncRNA HORAS5 promotes taxane resistance in castration-resistant prostate cancer via a BCL2A1-dependent mechanism. Epigenomics, 12(13) pp. 1123–1138.

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Pucci, P.; Venalainen, E.; Alborelli, I.; Quagliata, L.; Mather, R.; Rigas, S.; Romero, I.; Wang, Y. and Crea, F. (2019). HORAS5 promotes cabazitaxel resistance in castration resistant prostate cancer via a BCL2A1-dependent survival mechanism. Annals of Oncology, 30(5) v798.

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, 79(13) pp. 1580–1586.

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Chandler, Stephen; Gangadharannambiar, Priyadarsini; Crea, Francesco; Hirst, Mark; Cox, Angela and Rigas, Sushila (2019). Discovery of candidate hub genes in breast cancer. In: New Developments in Breast Cancer Research - From the Lab to the Clinic, 2019 BACR Special Conference, 9-11 Oct 2019, The Sage, Newcastle Gateshead, UK.

Chandler, Stephen; Gangadharannambiar, Priyadarsini; Crea, Francesco; Hirst, Mark; Cox, Angela and Rigas, Sushila (2019). Discovery of candidate long non-coding RNAs as biomarkers and treatment targets for prostate cancer. In: NEPC 2019. Treatment-emergent neuroendocrine prostate cancer: clinical relevance and molecular pathogenesis., 25 Jun 2019, The Open University, Milton Keynes, UK.

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.

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.

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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.

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.

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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.

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.

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.

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.

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.

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 p14^ARF in Human Melanoma. Journal of the National Cancer Institute, 100(11) pp. 784–795.

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.

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).

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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.

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.

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

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.