Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 62 Records) |
Query Trace: F12[original query] |
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Antihistamine-resistant angioedema in women with negative family history: estrogens and F12 gene mutations. The American journal of medicine 2013 Dec 126 (12): 12. Bork K, Wulff K, Witzke G, Stanger C, Lohse P, Hardt J |
Fluorescence resonance energy transfer-based real-time polymerase chain reaction method without DNA extraction for the genotyping of F5, F2, F12, MTHFR, and HFE. Journal of blood medicine 2014 5 99-106. Martinez-Serra Jordi, Robles Juan, Nicolàs Antoni, Gutierrez Antonio, Ros Teresa, Amat Juan Carlos, Alemany Regina, Vögler Oliver, Abelló Aina, Noguera Aina, Besalduch Jo |
Multilocus genetic risk scores for venous thromboembolism risk assessment. Journal of the American Heart Association 2014 Oct 3 (5): e001060. Soria José Manuel, Morange Pierre-Emmanuel, Vila Joan, Souto Juan Carlos, Moyano Manel, Trégouët David-Alexandre, Mateo José, Saut Noémi, Salas Eduardo, Elosua Rober |
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 |
Characterization of patients with angioedema without wheals: the importance of F12 gene screening. Clinical immunology (Orlando, Fla.) 2015 Apr 157 (2): 239-48. Firinu Davide, Bafunno Valeria, Vecchione Gennaro, Barca Maria Pina, Manconi Paolo Emilio, Santacroce Rosa, Margaglione Maurizio, Del Giacco Stefano |
A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study. Human molecular genetics 2015 Apr 24 (8): 2401-8. Weng Lu-Chen, Cushman Mary, Pankow James S, Basu Saonli, Boerwinkle Eric, Folsom Aaron R, Tang Weiho |
Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels.
Thrombosis and haemostasis 2016 Sep 116 (6): . Zhang Weihua, Jernerén Fredrik, Lehne Benjamin C, Chen Ming-Huei, Luben Robert N, Johnston Carole, Elshorbagy Amany, Eppinga Ruben N, Scott William R, Adeyeye Elizabeth, Scott James, Böger Rainer H, Khaw Kay-Tee, van der Harst Pim, Wareham Nicholas J, Vasan Ramachandran S, Chambers John C, Refsum Helga, Kooner Jaspal |
Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system. BMC medical genetics 2016 17 (1): 21. Biswas Nilima, Maihofer Adam X, Mir Saiful Anam, Rao Fangwen, Zhang Kuixing, Khandrika Srikrishna, Mahata Manjula, Friese Ryan S, Hightower C Makena, Mahata Sushil K, Baker Dewleen G, Nievergelt Caroline M, Vaingankar Sucheta M, O'Connor Daniel |
Identification of novel loci affecting circulating chromogranins and related peptides.
Human molecular genetics 2017 Jan 26 (1): 233-242. Benyamin Beben, Maihofer Adam X, Schork Andrew J, Hamilton Bruce A, Rao Fangwen, Schmid-Schönbein Geert W, Zhang Kuixing, Mahata Manjula, Stridsberg Mats, Schork Nicholas J, Biswas Nilima, Hook Vivian Y, Wei Zhiyun, Montgomery Grant W, Martin Nicholas G, Nievergelt Caroline M, Whitfield John B, O'Connor Daniel |
Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study. Human molecular genetics 2017 9 26 (17): 3442-3450. de Vries Paul S, Yu Bing, Feofanova Elena V, Metcalf Ginger A, Brown Michael R, Zeighami Atefeh L, Liu Xiaoming, Muzny Donna M, Gibbs Richard A, Boerwinkle Eric, Morrison Alanna |
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 |
Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families. The journal of allergy and clinical immunology. In practice 2017 11 6 (4): 1209-1216.e8. Veronez Camila Lopes, Moreno Adriana S, Constantino-Silva Rosemeire Navickas, Maia Luana S M, Ferriani Mariana P L, Castro Fábio F M, Valle Solange Rodrigues, Nakamura Victor Koji, Cagini Nathália, Gonçalves Rozana Fátima, Mansour Eli, Serpa Faradiba Sarquis, Coelho Dias Gabriela Andrade, Piccirillo Miguel Alberto, Toledo Eliana, de Souza Bernardes Marli, Cichon Sven, Stieber Christiane, Arruda L Karla, Pesquero João Bosco, Grumach Anete Sevciov |
Genetics of Obesity Traits: A Bivariate Genome-Wide Association Analysis.
Frontiers in genetics 2018 9 179. Wu Yili, Duan Haiping, Tian Xiaocao, Xu Chunsheng, Wang Weijing, Jiang Wenjie, Pang Zengchang, Zhang Dongfeng, Tan Qih |
The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis. BMC medical genetics 2018 Mar 19 (1): 50. Wu Xi, Ding Qiulan, Wang Xuefeng, Dai Jing, Wu Wenm |
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 |
Assessment of two contact activation reagents for the diagnosis of congenital factor XI deficiency. Thrombosis research 2018 Jan 163 64-70. Salloum-Asfar Salam, de la Morena-Barrio María E, Esteban Julio, Miñano Antonia, Aroca Cristina, Vicente Vicente, Roldán Vanessa, Corral Javi |
[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 |
Angiotensin-Converting Enzyme Inhibitor-Associated Angioedema: From Bed to Bench. Journal of investigational allergology & clinical immunology 2019 10 30 (4): 272-280. Carucci L, Bova M, Petraroli A, Ferrara A L, Sutic A, de Crescenzo G, Cordisco G, Margaglione M, Gambardella J, Spadaro G, Genovese A, Loffredo |
Double Heterozygous Mutations (Cys247Tyr and 252delAsn) Cause Factor XII Deficiency in a Chinese Family. Hamostaseologie 2020 9 40 (5): 650-654. Wang Yu, Zhang Haiyue, Liu Siqi, Ye Jiaj |
Study of angiopoietin and plasminogen genes in hereditary angioedema. Revista da Associacao Medica Brasileira (1992) 2020 6 66 (4): 502-506. Kruk Tatielly, Chong-Neto Herberto José, Dias Marina Mendonça, Campos Wagner Narciso, Moreno Adriana Santos, Mikami Liya Regina, Ferrari Lilian Pereira, Arruda Luísa Karla de Paula, Rosário Filho Nels |
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 |
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes. Frontiers in genetics 2022 8 13 914376. Mathey Carina M, Maj Carlo, Scheer Annika B, Fazaal Julia, Wedi Bettina, Wieczorek Dorothea, Amann Philipp M, Löffler Harald, Koch Lukas, Schöffl Clemens, Dickel Heinrich, Ganjuur Nomun, Hornung Thorsten, Forkel Susann, Greve Jens, Wurpts Gerda, Hallberg Pär, Bygum Anette, Von Buchwald Christian, Karawajczyk Malgorzata, Steffens Michael, Stingl Julia, Hoffmann Per, Heilmann-Heimbach Stefanie, Mangold Elisabeth, Ludwig Kerstin U, Rasmussen Eva R, Wadelius Mia, Sachs Bernhardt, Nöthen Markus M, Forstner Andreas |
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 |
Identification of tumor antigens and immune subtypes of hepatocellular carcinoma for mRNA vaccine development. World journal of gastrointestinal oncology 2023 11 15 (10): 1717-1738. Tai-Liang Lu, Cheng-Long Li, Yong-Qiang Gong, Fu-Tao Hou, Chao-Wu Ch |
Screening and identifying a novel M-MDSCs-related gene signature for predicting prognostic risk and immunotherapeutic responses in patients with lung adenocarcinoma. Frontiers in genetics 2023 1 13 989141. Wang Geng-Chong, Zhou Mi, Zhang Yan, Cai Hua-Man, Chiang Seok-Theng, Chen Qi, Han Tian-Zhen, Li Rong-X |
Factor XII deficiency: a clinical and molecular genetic study. International journal of hematology 2023 1 . Demidova Ekaterina, Salomashkina Valentina, Pshenichnikova Olesya, Selivanova Daria, Yakovleva Elena, Zozulya Nadezda, Gorgidze Lana, Surin Vad |
The breast cancer coagulome in the tumor microenvironment and its role in prognosis and treatment response to chemotherapy. Journal of thrombosis and haemostasis : JTH 2024 1 . Mari Tinholt, Xavier Tekpli, Lilly Anne Torland, Andliena Tahiri, Jürgen Geisler, Vessela Kristensen, Per Morten Sandset, Nina Ivers |
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