Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: F13B[original query] |
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[Analysis of Alu-polymorphism in Buryat populations]. Genetika 2001 Nov 37 (11): 1553-8. Khitrinskaia I Iu, Stepanov V A, Pyzyrev V |
An interactive association of common sequence variants in the neuropeptide Y gene with susceptibility to ischemic stroke. Stroke; a journal of cerebral circulation 2007 Oct 38 (10): 2663-9. Lee Chaeyoung, Kong Minyou |
Coagulation factor XIII gene variation, oral contraceptives, and risk of ischemic stroke. Blood 2008 Feb 111 (3): 1282-6. Pruissen D Martijn O, Slooter Arjen J C, Rosendaal Frits R, van der Graaf Yolanda, Algra A |
Prothrombotic gene variation in patients with large and small vessel disease. Neuroepidemiology 2008 31 (2): 89-92. Pruissen D Martijn O, Kappelle L Jaap, Rosendaal Frits R, Algra Ale, |
The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration. BMC medical genetics 2008 9 (1): 51. Zhang Hong, Morrison Margaux A, Dewan Andy, Adams Scott, Andreoli Michael, Huynh Nancy, Regan Maureen, Brown Alison, Miller Joan W, Kim Ivana K, Hoh Josephine, Deangelis Margaret |
Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degeneration. Human genomics 2011 Jul 5 (5): 420-40. Hageman Gregory S, Gehrs Karen, Lejnine Serguei, Bansal Aruna T, Deangelis Margaret M, Guymer Robyn H, Baird Paul N, Allikmets Rando, Deciu Cosmin, Oeth Paul, Perlee Lorah |
Prothrombotic gene variants and mortality after cerebral ischemia of arterial origin. Neuroepidemiology 2011 37 (2): 109-13. Pruissen D Martijn O, Rosendaal Frits R, Frijns Catharina J M, Kappelle L Jaap, Vos Hans L, Algra Ale, |
Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration. PloS one 2012 7 (4): e35255. Cantsilieris Stuart, White Stefan J, Richardson Andrea J, Guymer Robyn H, Baird Paul |
Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth. Human genetics 2013 Aug 132 (8): 935-42. McElroy Jude J, Gutman Courtney E, Shaffer Christian M, Busch Tamara D, Puttonen Hilkka, Teramo Kari, Murray Jeffrey C, Hallman Mikko, Muglia Louis |
Genetic influences on the outcome of anti-vascular endothelial growth factor treatment in neovascular age-related macular degeneration. Ophthalmology 2013 Aug 120 (8): 1641-8. Abedi Farshad, Wickremasinghe Sanjeewa, Richardson Andrea J, Islam Amirul F M, Guymer Robyn H, Baird Paul |
Inclusion of genotype with fundus phenotype improves accuracy of predicting choroidal neovascularization and geographic atrophy. Ophthalmology 2013 Sep 120 (9): 1880-92. Perlee Lorah T, Bansal Aruna T, Gehrs Karen, Heier Jeffrey S, Csaky Karl, Allikmets Rando, Oeth Paul, Paladino Toni, Farkas Daniel H, Rawlings P Lyle, Hageman Gregory |
A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population. Annals of hematology 2013 Jul 92 (7): 975-9. Ivaskevicius Vytautas, Biswas Arijit, Thomas Anne, Lyonga Sophie, Rott Hannelore, Halimeh Susan, Kappert Guenther, Klammroth Robert, Scholz Ute, Eberl Wolfgang, Harbrecht Ursula, Gnida Christine, Hertfelder Hans-Joerg, Marquardt Natascha, Oldenburg Johann |
Assessment of Proteins Associated With Complement Activation and Inflammation in Maculae of Human Donors Homozygous Risk at Chromosome 1 CFH-to-F13B. Investigative ophthalmology & visual science 2015 Jul 56 (8): 4870-9. Keenan Tiarnan D L, Toso Marc, Pappas Chris, Nichols Lisa, Bishop Paul N, Hageman Gregory |
Factor XIII B subunit polymorphisms and the risk of coronary artery disease. International journal of molecular sciences 2015 16 (1): 1143-59. Mezei Zoltán A, Bereczky Zsuzsanna, Katona Éva, Gindele Réka, Balogh Emília, Fiatal Szilvia, Balogh László, Czuriga István, Ádány Róza, Édes István, Muszbek Lász |
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 |
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- Page last updated:Apr 22, 2024
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