Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: RYK[original query] |
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Angiotensin-converting enzyme (ACE) insertion/deletion polymorphism and survival in a cohort of chronic hemodialysis patients. Clinical nephrology 2002 Nov 58 (5): 370-5. Higashiuesato Y, Tana T, Tozawa M, Iseki C, Iseki K, Fukiyama K, Takishita |
Influence of common XPD and XRCC1 variant alleles on p53 mutations in lung tumors. Environmental and molecular mutagenesis 2003 41 (1): 37-42. Hou Sai-Mei, Ryk Charlotta, Kannio Annamaria, Angelini Sabrina, Fält Susann, Nyberg Fredrik, Husgafvel-Pursiainen Kirs |
UGT1A1 variation and gallstone formation in sickle cell disease. Blood 2005 Feb 105 (3): 968-72. Haverfield Eden V, McKenzie Colin A, Forrester Terrence, Bouzekri Nourdine, Harding Rosalind, Serjeant Graham, Walker Thomas, Peto Tim E A, Ward Ryk, Weatherall David |
Association between evolutionary history of angiotensinogen haplotypes and plasma levels. Human genetics 2004 Sep 115 (4): 310-8. Fejerman Laura, Bouzekri Nourdine, Wu Xiaodong, Adeyemo Adebowale, Luke Amy, Zhu Xiaofeng, Ward Ryk, Cooper Richard |
Influence of GSTM1, GSTT1, GSTP1 and NAT2 genotypes on the p53 mutational spectrum in bladder tumours. International journal of cancer. Journal international du cancer 2005 Feb 113 (5): 761-8. Ryk Charlotta, Berggren Petra, Kumar Rajiv, Hemminki Kari, Larsson Per, Steineck Gunnar, Lambert Bo, Hou Sai-M |
Influence of polymorphism in DNA repair and defence genes on p53 mutations in bladder tumours. Cancer letters 2006 Sep 241 (1): 142-9. Ryk Charlotta, Kumar Rajiv, Sanyal Somali, de Verdier Petra J Berggren, Hemminki Kari, Larsson Per, Steineck Gunnar, Hou Sai-M |
A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2006 May 43 (3): 310-6. Watanabe Akira, Akita Sadanori, Tin Nguyen Thi Duc, Natsume Nagato, Nakano Yoko, Niikawa Norio, Uchiyama Takeshi, Yoshiura Koh-ichi |
Polymorphisms in the DNA repair genes XRCC1, APEX1, XRCC3 and NBS1, and the risk for lung cancer in never- and ever-smokers. Lung cancer (Amsterdam, Netherlands) 2006 Dec 54 (3): 285-92. Ryk Charlotta, Kumar Rajiv, Thirumaran Ranjit K, Hou Sai-M |
Polymorphisms in NQO1 and the clinical course of urinary bladder neoplasms. Scandinavian journal of urology and nephrology 2007 41 (3): 182-90. Sanyal Somali, Ryk Charlotta, De Verdier Petra J, Steineck Gunnar, Larsson Per, Onelöv Erik, Hemminki Kari, Kumar Raj |
Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.
Nature genetics 2008 Nov 40 (11): 1307-12. Kiemeney Lambertus A, Thorlacius Steinunn, Sulem Patrick, Geller Frank, Aben Katja K H, Stacey Simon N, Gudmundsson Julius, Jakobsdottir Margret, Bergthorsson Jon T, Sigurdsson Asgeir, Blondal Thorarinn, Witjes J Alfred, Vermeulen Sita H, Hulsbergen-van de Kaa Christina A, Swinkels Dorine W, Ploeg Martine, Cornel Erik B, Vergunst Henk, Thorgeirsson Thorgeir E, Gudbjartsson Daniel, Gudjonsson Sigurjon A, Thorleifsson Gudmar, Kristinsson Kari T, Mouy Magali, Snorradottir Steinunn, Placidi Donatella, Campagna Marcello, Arici Cecilia, Koppova Kvetoslava, Gurzau Eugene, Rudnai Peter, Kellen Eliane, Polidoro Silvia, Guarrera Simonetta, Sacerdote Carlotta, Sanchez Manuel, Saez Berta, Valdivia Gabriel, Ryk Charlotta, de Verdier Petra, Lindblom Annika, Golka Klaus, Bishop D Timothy, Knowles Margaret A, Nikulasson Sigfus, Petursdottir Vigdis, Jonsson Eirikur, Geirsson Gudmundur, Kristjansson Baldvin, Mayordomo Jose I, Steineck Gunnar, Porru Stefano, Buntinx Frank, Zeegers Maurice P, Fletcher Tony, Kumar Rajiv, Matullo Giuseppe, Vineis Paolo, Kiltie Anne E, Gulcher Jeffrey R, Thorsteinsdottir Unnur, Kong Augustine, Rafnar Thorunn, Stefansson Ka |
Influence of DNA repair gene polymorphisms on the initial repair of MMS-induced DNA damage in human lymphocytes as measured by the alkaline comet assay. Environmental and molecular mutagenesis 2008 Dec 49 (9): 669-75. Ryk Charlotta, Routledge Michael N, Allan James M, Wild Christopher P, Kumar Rajiv, Lambert Bo, Hou Saim |
Testing reported associations of genetic risk factors for oral clefts in a large Irish study population. Birth defects research. Part A, Clinical and molecular teratology 2010 Feb 88 (2): 84-93. Carter Tonia C, Molloy Anne M, Pangilinan Faith, Troendle James F, Kirke Peadar N, Conley Mary R, Orr David J A, Earley Michael, McKiernan Eamon, Lynn Ena C, Doyle Anne, Scott John M, Brody Lawrence C, Mills James |
The (CCTTT)n microsatellite polymorphism in the nitric oxide synthase 2 gene may influence bladder cancer pathogenesis. The Journal of urology 2010 Nov 184 (5): 2150-7. Ryk Charlotta, Steineck Gunnar, Wiklund N Peter, Nyberg Tommy, de Verdier Petra |
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.
Nature genetics 2010 May 42 (5): 415-9. Kiemeney Lambertus A, Sulem Patrick, Besenbacher Soren, Vermeulen Sita H, Sigurdsson Asgeir, Thorleifsson Gudmar, Gudbjartsson Daniel F, Stacey Simon N, Gudmundsson Julius, Zanon Carlo, Kostic Jelena, Masson Gisli, Bjarnason Hjordis, Palsson Stefan T, Skarphedinsson Oskar B, Gudjonsson Sigurjon A, Witjes J Alfred, Grotenhuis Anne J, Verhaegh Gerald W, Bishop D Timothy, Sak Sei Chung, Choudhury Ananya, Elliott Faye, Barrett Jennifer H, Hurst Carolyn D, de Verdier Petra J, Ryk Charlotta, Rudnai Peter, Gurzau Eugene, Koppova Kvetoslava, Vineis Paolo, Polidoro Silvia, Guarrera Simonetta, Sacerdote Carlotta, Campagna Marcello, Placidi Donatella, Arici Cecilia, Zeegers Maurice P, Kellen Eliane, Gutierrez Berta Saez, Sanz-Velez José I, Sanchez-Zalabardo Manuel, Valdivia Gabriel, Garcia-Prats Maria D, Hengstler Jan G, Blaszkewicz Meinolf, Dietrich Holger, Ophoff Roel A, van den Berg Leonard H, Alexiusdottir Kristin, Kristjansson Kristleifur, Geirsson Gudmundur, Nikulasson Sigfus, Petursdottir Vigdis, Kong Augustine, Thorgeirsson Thorgeir, Mungan N Aydin, Lindblom Annika, van Es Michael A, Porru Stefano, Buntinx Frank, Golka Klaus, Mayordomo José I, Kumar Rajiv, Matullo Giuseppe, Steineck Gunnar, Kiltie Anne E, Aben Katja K H, Jonsson Eirikur, Thorsteinsdottir Unnur, Knowles Margaret A, Rafnar Thorunn, Stefansson Ka |
European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.
Human molecular genetics 2011 Nov 20 (21): 4268-81. Rafnar Thorunn, Vermeulen Sita H, Sulem Patrick, Thorleifsson Gudmar, Aben Katja K, Witjes J Alfred, Grotenhuis Anne J, Verhaegh Gerald W, Hulsbergen-van de Kaa Christina A, Besenbacher Soren, Gudbjartsson Daniel, Stacey Simon N, Gudmundsson Julius, Johannsdottir Hrefna, Bjarnason Hjordis, Zanon Carlo, Helgadottir Hafdis, Jonasson Jon Gunnlaugur, Tryggvadottir Laufey, Jonsson Eirikur, Geirsson Gudmundur, Nikulasson Sigfus, Petursdottir Vigdis, Bishop D Timothy, Chung-Sak Sei, Choudhury Ananya, Elliott Faye, Barrett Jennifer H, Knowles Margaret A, de Verdier Petra J, Ryk Charlotta, Lindblom Annika, Rudnai Peter, Gurzau Eugene, Koppova Kvetoslava, Vineis Paolo, Polidoro Silvia, Guarrera Simonetta, Sacerdote Carlotta, Panadero Angeles, Sanz-Velez José I, Sanchez Manuel, Valdivia Gabriel, Garcia-Prats Maria D, Hengstler Jan G, Selinski Silvia, Gerullis Holger, Ovsiannikov Daniel, Khezri Abdolaziz, Aminsharifi Alireza, Malekzadeh Mahyar, van den Berg Leonard H, Ophoff Roel A, Veldink Jan H, Zeegers Maurice P, Kellen Eliane, Fostinelli Jacopo, Andreoli Daniele, Arici Cecilia, Porru Stefano, Buntinx Frank, Ghaderi Abbas, Golka Klaus, Mayordomo José I, Matullo Giuseppe, Kumar Rajiv, Steineck Gunnar, Kiltie Anne E, Kong Augustine, Thorsteinsdottir Unnur, Stefansson Kari, Kiemeney Lambertus |
Polymorphisms in nitric-oxide synthase 3 may influence the risk of urinary-bladder cancer. Nitric oxide : biology and chemistry / official journal of the Nitric Oxide Society 2011 Oct 25 (3): 338-43. Ryk Charlotta, Wiklund N Peter, Nyberg Tommy, de Verdier Petra |
Ser608Leu polymorphisms in the nitric oxide synthase-2 gene may influence urinary bladder cancer pathogenesis. Scandinavian journal of urology and nephrology 2011 Nov 45 (5): 319-25. Ryk Charlotta, Wiklund N Peter, Nyberg Tommy, De Verdier Petra |
TERT promoter mutations in bladder cancer affect patient survival and disease recurrence through modification by a common polymorphism. Proceedings of the National Academy of Sciences of the United States of America 2013 Oct 110 (43): 17426-31. Rachakonda P Sivaramakrishna, Hosen Ismail, de Verdier Petra J, Fallah Mahdi, Heidenreich Barbara, Ryk Charlotta, Wiklund N Peter, Steineck Gunnar, Schadendorf Dirk, Hemminki Kari, Kumar Raj |
The (CCTTT)n microsatellite polymorphism in the NOS2 gene may influence lung cancer risk and long-term survival, especially in non-smokers. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 May 35 (5): 4425-34. Ryk Charlotta, Hou Sai-Mei, Pershagen Göran, Wiklund N Peter, Nyberg Fredrik, de Verdier Petra |
Outcome after BCG treatment for urinary bladder cancer may be influenced by polymorphisms in the NOS2 and NOS3 genes. Redox biology 2015 Aug 6 272-277. Ryk Charlotta, Koskela Lotta Renström, Thiel Tomas, Wiklund N Peter, Steineck Gunnar, Schumacher Martin C, de Verdier Petra |
Mutations in TERT promoter and FGFR3 and telomere length in bladder cancer. International journal of cancer. Journal international du cancer 2015 Oct 137 (7): 1621-9. Hosen Ismail, Rachakonda P Sivaramakrishna, Heidenreich Barbara, de Verdier Petra J, Ryk Charlotta, Steineck Gunnar, Hemminki Kari, Kumar Raj |
A targeted approach to genome-wide studies reveals new genetic associations with central corneal thickness. Molecular vision 2017 23 952-962. Benson Matthew D, Khor Chiea C, Gage Philip J, Lehmann Ordan |
The impact of single nucleotide polymorphisms in ADORA2A and ADORA3 genes on the early response to methotrexate and presence of therapy side effects in children with juvenile idiopathic arthritis: Results of a preliminary study. International journal of rheumatic diseases 2020 9 23 (11): 1505-1513. Roszkiewicz Justyna, Micha?ek Dominika, Ryk Aleksandra, Swacha Zbigniew, Szmyd Bartosz, Smolewska El?bie |
SLCO1B1 variants as predictors of methotrexate-related toxicity in children with juvenile idiopathic arthritis. Scandinavian journal of rheumatology 2020 10 50 (3): 213-217. Roszkiewicz J, Micha?ek D, Ryk A, Swacha Z, Szmyd B, Smolewska |
Novel Genome-Wide Interactions Mediated via BOLL and EDNRA Polymorphisms in Intracranial Aneurysm. Journal of Korean Neurosurgical Society 2022 Oct . Hong Eun Pyo, Youn Dong Hyuk, Kim Bong Jun, Lee Jae Jun, Nam Sehyeon, Yoo Hyojong, Kim Heung Cheol, Rhim Jong Kook, Park Jeong Jin, Jeon Jin Pyeo |
The impact of single nucleotide polymorphisms in MTHFR and MTRR genes on disease activity and the presence of methotrexate treatment side effects in children with juvenile idiopathic arthritis. Archives of medical science : AMS 2023 6 19 (3): 810-813. Justyna Roszkiewicz, Dominika Micha?ek, Aleksandra Ryk, Bartosz Szmyd, El?bieta Smolews |
RYK Gene Expression Associated with Drug Response Variation of Temozolomide and Clinical Outcomes in Glioma Patients. Pharmaceuticals (Basel, Switzerland) 2023 5 16 (5): . Ricardo D Gonzalez, George W Small, Adrian J Green, Farida S Akhtari, Tammy M Havener, Julia C F Quintanilha, Amber B Cipriani, David M Reif, Howard L McLeod, Alison A Motsinger-Reif, Tim Wiltshi |
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- Page last updated:Apr 22, 2024
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