Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Disease and SERPING1[original query] |
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| Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study. Lancet (London, England) 2008 Nov 372 (9652): 1828-34. Ennis Sarah, Jomary Catherine, Mullins Robert, Cree Angela, Chen Xiaoli, Macleod Alex, Jones Stephen, Collins Andrew, Stone Edwin, Lotery Andr |
| Common variation in the SERPING1 gene is not associated with age-related macular degeneration in two independent groups of subjects. Molecular vision 2009 15 200-7. Park Kyu Hyung, Ryu Euijung, Tosakulwong Nirubol, Wu Yanhong, Edwards Albert |
| Determination of a gene and environment risk model for age-related macular degeneration. The British journal of ophthalmology 2010 Oct 94 (10): 1382-7. Gibson Jane, Cree Angela, Collins Andrew, Lotery Andrew, Ennis Sar |
| Variation in complement component C1 inhibitor in age-related macular degeneration. Immunobiology 2012 Feb 217 (2): 251-5. Gibson J, Hakobyan S, Cree A J, Collins A, Harris C L, Ennis S, Morgan B P, Lotery A |
| No evidence for linkage between the hereditary angiooedema clinical phenotype and the BDKR1, BDKR2, ACE or MBL2 gene. Scandinavian journal of immunology 2011 Jul 74 (1): 100-6. Freiberger T, Grombi?íková H, Rav?uková B, Jarkovský J, Kuklínek P, Kryšt?fková O, Hanzlíková J, Da?ková E, Kopecký O, Zachová R, Lahodná M, Vašáková M, Grodecká L, Litzman |
| Analysis of SERPING1 expression on hereditary angioedema patients: quantitative analysis of full-length and exon 3 splicing variants. Immunology letters 2012 Jan 141 (2): 158-64. de la Cruz Rocío Mena, López-Lera Alberto, López-Trascasa Margari |
| Mutations analysis of C1 inhibitor coding sequence gene among Portuguese patients with hereditary angioedema. Molecular immunology 2013 Apr 53 (4): 431-4. Martinho A, Mendes J, Simões O, Nunes R, Gomes J, Dias Castro E, Leiria-Pinto P, Ferreira M B, Pereira C, Castel-Branco M G, Pais |
| 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 |
| Discovery of coding genetic variants influencing diabetes-related serum biomarkers and their impact on risk of type 2 diabetes. The Journal of clinical endocrinology and metabolism 2015 Apr 100 (4): E664-71. Ahluwalia Tarunveer Singh, Allin Kristine Højgaard, Sandholt Camilla Helene, Sparsø Thomas Hempel, Jørgensen Marit Eika, Rowe Michael, Christensen Cramer, Brandslund Ivan, Lauritzen Torsten, Linneberg Allan, Husemoen Lise Lotte, Jørgensen Torben, Hansen Torben, Grarup Niels, Pedersen Ol |
| Genetic Investigation of Complement Pathway Genes in Type 2 Diabetic Retinopathy: An Inflammatory Perspective. Mediators of inflammation 2016 2016 1313027. Yang Ming Ming, Wang Jun, Ren Hong, Sun Yun Duan, Fan Jiao Jie, Teng Yan, Li Yan |
| First Analysis of SERPING1 Gene in Patients with Hereditary Angioedema in Colombia Reveals Two Genotypic Variants in a Highly Symptomatic Individual. Journal of clinical immunology 2018 Apr . Rodríguez Jairo A, Narváez Carlos |
| Exome sequencing in large, multiplex bipolar disorder families from Cuba. PloS one 2018 13 (10): e0205895. Maaser Anna, Forstner Andreas J, Strohmaier Jana, Hecker Julian, Ludwig Kerstin U, Sivalingam Sugirthan, Streit Fabian, Degenhardt Franziska, Witt Stephanie H, Reinbold Céline S, Koller Anna C, Raff Ruth, Heilmann-Heimbach Stefanie, Fischer Sascha B, , Herms Stefan, Hoffmann Per, Thiele Holger, Nürnberg Peter, Löhlein Fier Heide, Orozco-Díaz Guillermo, Carmenate-Naranjo Deinys, Proenza-Barzaga Niurka, Auburger Georg W J, Andlauer Till F M, Cichon Sven, Marcheco-Teruel Beatriz, Mors Ole, Rietschel Marcella, Nöthen Markus |
| Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations). Immunological investigations 2020 9 51 (1): 170-181. Nabilou Susan, Pak Fatemeh, Alizadeh Zahra, Fazlollahi Mohammad Reza, Houshmand Masoud, Ayazi Maryam, Mohammadzadeh Iraj, Bemanian Mohammad Hasan, Fayezi Abbas, Nabavi Mohammad, Saghafi Shiva, Mohammadian Sajedeh, Kokhaei Parviz, Moin Mostafa, Pourpak Zah |
| CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in immunology 2021 3 12 608723. Yang Ming Ming, Sun Hong Yan, Meng Ting, Qiu Shan Hu, Zeng Qi Qiao, Ng Tsz Kin, Jiang Li, Deng Ting Ming, Zeng Ai Neng, Wang Jun, Luo Xiao Li |
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 |
| Mutation update of SERPING1 related to hereditary angioedema in the Chinese population. Hereditas 2022 Jul 159 (1): 28. Wang Xue, Lei Shubin, Xu Yingyang, Liu Shuang, Zhi Yuxia |
| High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of personalized medicine 2022 10 12 (10): . Tesolin Paola, Bertinetto Francesca Eleonora, Sonaglia Arianna, Cappellani Stefania, Concas Maria Pina, Morgan Anna, Ferrero Norma Maria, Zabotti Alen, Gasparini Paolo, Amoroso Antonio, Quartuccio Luca, Girotto Giorg |
| Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort. Journal of clinical immunology 2023 8 . Hana Grombirikova, Viktor Bily, Premysl Soucek, Michal Kramarek, Roman Hakl, Lucie Ballonova, Barbora Ravcukova, Dita Ricna, Karolina Kozena, Lucie Kratochvilova, Marta Sobotkova, Radana Zachova, Pavel Kuklinek, Pavlina Kralickova, Irena Krcmova, Jana Hanzlikova, Martina Vachova, Olga Krystufkova, Eva Dankova, Milos Jesenak, Martina Novackova, Michal Svoboda, Jiri Litzman, Tomas Freiberg |
| Screening for type II hereditary angioedema-the "poor man's c1-inhibitor function". The journal of allergy and clinical immunology. Global 2023 11 3 (1): 100179. Ankur Kumar Jindal, Valerie Chiang, Prabal Barman, Archan Sil, Sanchi Chawla, Elaine Y L Au, Amit Rawat, Philip H |
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