Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Disease and F12[original query] |
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| Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population. Stroke; a journal of cerebral circulation 2004 Aug 35 (8): 1795-9. Santamaría Amparo, Mateo José, Tirado Isabel, Oliver Arturo, Belvís Roberto, Martí-Fábregas Joan, Felices Rosa, Soria José Manuel, Souto Juan Carlos, Fontcuberta Jor |
| Homozygosity of the T allele of the 46 C-->T polymorphism in the F12 gene is a risk factor for acute coronary artery disease in the Spanish population. Haematologica 2004 Jul 89 (7): 878-9. Santamaría Amparo, Martínez-Rubio Antonio, Mateo José, Tirado Isabel, Soria José M, Fontcuberta Jor |
| Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis. Thrombosis and haemostasis 2004 May 91 (5): 899-904. Tirado Isabel, Soria José Manuel, Mateo José, Oliver Artur, Souto Juan Carlos, Santamaria Amparo, Felices Rosa, Borrell Montserrat, Fontcuberta Jor |
| Rapid detection of the 46C --> T polymorphism in the factor XII gene, a novel genetic risk factor for thrombosis, by melting peak analysis using fluorescence hybridization probes. Genetic testing 2003 7 (4): 295-301. Tirado I, Fontcuberta J, Soria JM |
| The functional promoter polymorphism of the coagulation factor XII gene is not associated with peripheral arterial disease. Angiology 2010 Feb 61 (2): 211-5. Yazdani-Biuki Babak, Krippl Peter, Brickmann Kerstin, Fuerst Florentine, Langsenlehner Uwe, Paulweber Bernhard, Pilger Ernst, Wascher Thomas C, Brezinschek Hans-Peter, Renner Wilfri |
| Rapid triplex asymmetric real-time PCR hybridization probe assay for the joint genotyping of F2, F5 and F12. Clinical biochemistry 2009 Aug 42 (12): 1317-24. Martínez-Serra J, Gutierrez A, Amat J C, Galmés B, Vila A, Julia M, López H, Bautista A M, Truyols C, Ros T, Navarro M, Canaro M, Díaz M, Besalduch |
| Factor XII 46C --> T gene polymorphism in Chilean subjects with coronary artery disease and controls. Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2009 18 (2): 137-42. Caamaño José, Jaramillo Priscilla C, Lanas Cecilia, Lanas Fernando, Salazar Luis |
| Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels. Human molecular genetics 2010 Feb 19 (3): 517-25. Calafell Francesc, Almasy Laura, Sabater-Lleal Maria, Buil Alfonso, Mordillo Carolina, Ramírez-Soriano Anna, Sikora Martin, Souto Juan Carlos, Blangero John, Fontcuberta Jordi, Soria José Manu |
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
American journal of human genetics 2012 Jul 91 (1): 152-62. Tang Weihong, Schwienbacher Christine, Lopez Lorna M, Ben-Shlomo Yoav, Oudot-Mellakh Tiphaine, Johnson Andrew D, Samani Nilesh J, Basu Saonli, Gögele Martin, Davies Gail, Lowe Gordon D O, Tregouet David-Alexandre, Tan Adrian, Pankow James S, Tenesa Albert, Levy Daniel, Volpato Claudia B, Rumley Ann, Gow Alan J, Minelli Cosetta, Yarnell John W G, Porteous David J, Starr John M, Gallacher John, Boerwinkle Eric, Visscher Peter M, Pramstaller Peter P, Cushman Mary, Emilsson Valur, Plump Andrew S, Matijevic Nena, Morange Pierre-Emmanuel, Deary Ian J, Hicks Andrew A, Folsom Aaron |
| Gene panels to help identify subgroups at high and low risk of coronary heart disease among those randomized to antihypertensive treatment: the GenHAT study. Pharmacogenetics and genomics 2012 May 22 (5): 355-66. Lynch Amy I, Eckfeldt John H, Davis Barry R, Ford Charles E, Boerwinkle Eric, Leiendecker-Foster Catherine, Arnett Donna |
| Prevalence of thrombosis-related DNA polymorphisms in a healthy Greek population. In vivo (Athens, Greece) 0 26 (6): 1095-101. Yapijakis Christos, Serefoglou Zoe, Nixon Alexander M, Vylliotis Antonis, Ragos Vassilis, Vairaktaris Eleftheri |
| F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema. Allergy 2015 Aug . Speletas M, Szilágyi Á, Csuka D, Koutsostathis N, Psarros F, Moldovan D, Magerl M, Kompoti M, Varga L, Maurer M, Farkas H, Germenis A |
| Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset. International archives of allergy and immunology 2017 11 174 (3-4): 200-204. Gianni Panagiota, Loules Gedeon, Zamanakou Maria, Kompoti Maria, Csuka Dorottya, Psarros Fotis, Magerl Markus, Moldovan Dimitru, Maurer Marcus, Speletas Matthaios G, Farkas Henriette, Germenis Anastasios |
| Genetic determinants of activity and antigen levels of contact system factors. Journal of thrombosis and haemostasis : JTH 2018 Oct . Rohmann J L, de Haan H G, Algra A, Vossen C Y, Rosendaal F R, Siegerink |
| [A clinical and genetic analysis of risk factors for the development of acute and chronic cerebral ischemia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (3. Vyp. 2): 62-67. Anisimova A V, Gunchenko A S, Ikonnikova A Yu, Galkin S S, Avdonina M A, Nasedkina T |
| Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor. Journal of clinical medicine 2020 10 9 (11): . Loules Gedeon, Parsopoulou Faidra, Zamanakou Maria, Csuka Dorottya, Bova Maria, González-Quevedo Teresa, Psarros Fotis, Porebski Gregor, Speletas Matthaios, Firinu Davide, Del Giacco Stefano, Suffritti Chiara, Makris Michael, Vatsiou Sofia, Zanichelli Andrea, Farkas Henriette, Germenis Anastasios |
| Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
| In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency. Clinical reviews in allergy & immunology 2021 1 61 (1): 1-14. Loli-Ausejo David, López-Lera Alberto, Drouet Christian, Lluncor Marina, Phillips-Anglés Elsa, Pedrosa María, Cabañas Rosario, Caballero Tere |
| Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE). Frontiers in allergy 2022 7 3 868185. Parsopoulou Faidra, Loules Gedeon, Zamanakou Maria, Csuka Dorottya, Szilagyi Agnes, Kompoti Maria, Porebski Grzegorz, Psarros Fotis, Magerl Markus, Valerieva Anna, Staevska Maria, Obtulowicz Krystyna, Maurer Marcus, Speletas Matthaios, Farkas Henriette, Germenis Anastasios |
| [Analysis of A Pedigree with Hereditary Coagulation Factor ? Deficiency Caused by Compound Heterozygous Mutations]. Zhongguo shi yan xue ye xue za zhi 2022 4 30 (2): 571-576. Chen Jing, Li Yun-Xia, Zhong Fan, Li Ren-Hua, Yang Ji-Yun, Zhou Wen-Ji |
| Discovery and prioritization of genetic determinants of kidney function in 297,355 individuals from Taiwan and Japan. Nature communications 2024 10 15 (1): 9317. Hung-Lin Chen, Hsiu-Yin Chiang, David Ray Chang, Chi-Fung Cheng, Charles C N Wang, Tzu-Pin Lu, Chien-Yueh Lee, Amrita Chattopadhyay, Yu-Ting Lin, Che-Chen Lin, Pei-Tzu Yu, Chien-Fong Huang, Chieh-Hua Lin, Hung-Chieh Yeh, I-Wen Ting, Huai-Kuang Tsai, Eric Y Chuang, Adrienne Tin, Fuu-Jen Tsai, Chin-Chi K |
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