Human Genome Epidemiology Literature Finder
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Records 1 - 26 (of 26 Records) |
| Query Trace: Disease and C9[original query] |
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| Genetic analysis of complement component 9 (C9) polymorphisms with clearance of hepatitis B virus infection. Digestive diseases and sciences 2011 Sep 56 (9): 2735-41. Bae Joon Seol, Pasaje Charisse Flerida A, Park Byung Lae, Cheong Hyun Sub, Kim Jeong-Hyun, Park Tae Joon, Kim Jason Yongha, Lee Jin Sol, Koh In Song, Lee Hyo-Suk, Kim Yoon Jun, Shin Hyoung D |
| Coding polymorphisms in the genes of the alternative complement pathway and abdominal aortic aneurysm. International journal of immunogenetics 2011 Jun 38 (3): 243-8. Bradley D T, Badger S A, Bown M J, Sayers R D, Hughes A |
| Homeobox C9 is not potentially related to congenital heart disease in Chinese patients. Genetic testing and molecular biomarkers 2012 May 16 (5): 439-41. Sun Lei, Cheng Longfei, Li Congmin, Gao Bingren, Wang Binbin, Wang Jing, Wang Xiaochen, Huang Tianchu, Li Hui, Ma |
| Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration. Nature genetics 2013 Nov 45 (11): 1366-70. Seddon Johanna M, Yu Yi, Miller Elizabeth C, Reynolds Robyn, Tan Perciliz L, Gowrisankar Sivakumar, Goldstein Jacqueline I, Triebwasser Michael, Anderson Holly E, Zerbib Jennyfer, Kavanagh David, Souied Eric, Katsanis Nicholas, Daly Mark J, Atkinson John P, Raychaudhuri Soum |
| Epistasis analysis links immune cascades and cerebral amyloidosis. Journal of neuroinflammation 2015 12 (1): 227. Benedet Andréa L, Labbe Aurélie, Lemay Philippe, Zimmer Eduardo R, Pascoal Tharick A, Leuzy Antoine, Mathotaarachchi Sulantha, Mohades Sara, Shin Monica, Dionne-Laporte Alexandre, Beaudry Thomas, Picard Cynthia, Gauthier Serge, Poirier Judes, Rouleau Guy, Rosa-Neto Pedro, |
| Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration†. Human molecular genetics 2016 Dec . Yu Yi, Wagner Erin K, Souied Eric H, Seitsonen Sanna, Immonen Ilkka J, Häppölä Paavo, Raychaudhuri Soumya, Daly Mark J, Seddon Johanna |
| Rare Genetic Variants Associated With Development of Age-Related Macular Degeneration. JAMA ophthalmology 2016 Jan 1-8. Saksens Nicole T M, Geerlings Maartje J, Bakker Bjorn, Schick Tina, Daha Mohamed R, Fauser Sascha, Boon Camiel J F, de Jong Eiko K, Hoyng Carel B, den Hollander Anneke |
Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms.
PloS one 2016 4 11 (4): e0153672. Yet Idil, Menni Cristina, Shin So-Youn, Mangino Massimo, Soranzo Nicole, Adamski Jerzy, Suhre Karsten, Spector Tim D, Kastenmüller Gabi, Bell Jordana |
| Neuroimaging patterns along the ALS-FTD spectrum: a multiparametric imaging study. Amyotrophic lateral sclerosis & frontotemporal degeneration 2017 May 1-13. Omer Taha, Finegan Eoin, Hutchinson Siobhan, Doherty Mark, Vajda Alice, McLaughlin Russell L, Pender Niall, Hardiman Orla, Bede Pet |
| Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population. Human molecular genetics 2016 Nov 25 (22): 5027-5034. Momozawa Yukihide, Akiyama Masato, Kamatani Yoichiro, Arakawa Satoshi, Yasuda Miho, Yoshida Shigeo, Oshima Yuji, Mori Ryusaburo, Tanaka Koji, Mori Keisuke, Inoue Satoshi, Terasaki Hiroko, Yasuma Tetsuhiro, Honda Shigeru, Miki Akiko, Inoue Maiko, Fujisawa Kimihiko, Takahashi Kanji, Yasukawa Tsutomu, Yanagi Yasuo, Kadonosono Kazuaki, Sonoda Koh-Hei, Ishibashi Tatsuro, Takahashi Atsushi, Kubo Michia |
| Sparking Fire Under the Skin? Answers From the Association of Complement Genes With Pemphigus Foliaceus. Frontiers in immunology 2018 9 695. Bumiller-Bini Valéria, Cipolla Gabriel Adelman, de Almeida Rodrigo Coutinho, Petzl-Erler Maria Luiza, Augusto Danillo Gardenal, Boldt Angelica Beate Wint |
| Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study. Annals of neurology 2019 6 86 (2): 158-167. Querin Giorgia, Bede Peter, El Mendili Mohamed Mounir, Li Menghan, Pélégrini-Issac Mélanie, Rinaldi Daisy, Catala Martin, Saracino Dario, Salachas François, Camuzat Agnes, Marchand-Pauvert Véronique, Cohen-Adad Julien, Colliot Olivier, Le Ber Isabelle, Pradat Pierre-François, |
| Increased prevalence of granulovacuolar degeneration in C9orf72 mutation. Acta neuropathologica 2019 5 138 (5): 783-793. Riku Yuichi, Duyckaerts Charles, Boluda Susana, Plu Isabelle, Le Ber Isabelle, Millecamps Stéphanie, Salachas François, , Yoshida Mari, Ando Takashi, Katsuno Masahisa, Sobue Gen, Seilhean Daniel |
| CYP2 C9 polymorphism among patients with oral squamous cell carcinoma and its role in altering the metabolism of benzo[a]pyrene. Oral surgery, oral medicine, oral pathology and oral radiology 2020 Jul . R Hannah, Ramani Pratibha, Ramanathan Arvind, R Jancy Merlin, S Gheena, Ramasubramanian Abilasha, K Moni |
| Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle East. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Jul . Squitieri Ferdinando, Mazza Tommaso, Maffi Sabrina, De Luca Alessandro, AlSalmi Qasem, AlHarasi Salma, Collins Jennifer A, Kay Chris, Baine-Savanhu Fiona, Landwhermeyer Bernard G, Sabatini Umberto, Hayden Michael |
| Structural MRI Signatures in Genetic Presentations of the Frontotemporal Dementia/Motor Neuron Disease Spectrum. Neurology 2021 9 97 (16): e1594-e1607. Spinelli Edoardo Gioele, Ghirelli Alma, Basaia Silvia, Cividini Camilla, Riva Nilo, Canu Elisa, Castelnovo Veronica, Domi Teuta, Magnani Giuseppe, Caso Francesca, Caroppo Paola, Prioni Sara, Rossi Giacomina, Tremolizzo Lucio, Appollonio Ildebrando, Silani Vincenzo, Carrera Paola, Filippi Massimo, Agosta Federi |
| Associations between lifestyle and amyotrophic lateral sclerosis stratified by C9orf72 genotype: a longitudinal, population-based, case-control study. The Lancet. Neurology 2021 05 20 (5): 373-384. Westeneng Henk-Jan, van Veenhuijzen Kevin, van der Spek Rick A, Peters Susan, Visser Anne E, van Rheenen Wouter, Veldink Jan H, van den Berg Leonard |
| The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascade. Human molecular genetics 2021 3 30 (13): 1188-1199. McMahon O, Hallam T M, Patel S, Harris C L, Menny A, Zelek W M, Widjajahakim R, Java A, Cox T E, Tzoumas N, Steel D H W, Shuttleworth V G, Smith-Jackson K, Brocklebank V, Griffiths H, Cree A J, Atkinson J P, Lotery A J, Bubeck D, Morgan B P, Marchbank K J, Seddon J M, Kavanagh |
| Fibrinogen and hemoglobin predict near future cardiovascular events in asymptomatic individuals. Scientific reports 2021 2 11 (1): 4605. Lassé Moritz, Pilbrow Anna P, Kleffmann Torsten, Andersson Överström Elin, von Zychlinski Anne, Frampton Christopher M A, Poppe Katrina K, Troughton Richard W, Lewis Lynley K, Prickett Timothy C R, Pemberton Christopher J, Richards Arthur M, Cameron Vicky |
| Evaluating the Occurrence of Rare Variants in the Complement Factor H Gene in Patients With Early-Onset Drusen Maculopathy. JAMA ophthalmology 2021 Oct . de Breuk Anita, Heesterbeek Thomas J, Bakker Bjorn, Verzijden Timo, Lechanteur Yara T E, Klaver Caroline C W, den Hollander Anneke I, Hoyng Carel |
| Complement dysregulation and Alzheimer's disease in Down syndrome. Alzheimer's & dementia : the journal of the Alzheimer's Association 2022 Sep . Veteleanu Aurora, Pape Sarah, Davies Kate, Kodosaki Eleftheria, Hye Abdul, Zelek Wioleta M, Strydom Andre, Morgan B Pa |
| Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation. Frontiers in immunology 2023 9 14 1249958. Lilli Leimi, Jessica R Koski, Outi Kilpivaara, Kim Vettenranta, A Inkeri Lokki, Seppo Me |
| Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies. Neurology. Genetics 2023 6 9 (4): e200079. John Dou, Kelly Bakulski, Kai Guo, Junguk Hur, Lili Zhao, Sara Saez-Atienzar, Ali Stark, Ruth Chia, Alberto García-Redondo, Ricardo Rojas-Garcia, Juan Francisco Vázquez Costa, Ruben Fernandez Santiago, Sara Bandres-Ciga, Pilar Gómez-Garre, Maria Teresa Periñán, Pablo Mir, Jordi Pérez-Tur, Fernando Cardona, Manuel Menendez-Gonzalez, Javier Riancho, Daniel Borrego-Hernández, Lucia Galán-Dávila, Jon Infante Ceberio, Pau Pastor, Carmen Paradas, Oriol Dols-Icardo, Bryan J Traynor, Eva L Feldman, Stephen A Goutman, |
| Endo-lysosomal protein concentrations in CSF from patients with frontotemporal dementia caused by CHMP2B mutation. Alzheimer's & dementia (Amsterdam, Netherlands) 2023 2 15 (1): e12402. Toft Anders, Sjödin Simon, Simonsen Anja Hviid, Ejlerskov Patrick, Roos Peter, Musaeus Christian Sandøe, Henriksen Emil Elbæk, Nielsen Troels Tolstrup, Brinkmalm Ann, Blennow Kaj, Zetterberg Henrik, Nielsen Jørgen Er |
| Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis. Journal of neurology 2023 11 . Teuta Domi, Paride Schito, Giacomo Sferruzza, Tommaso Russo, Laura Pozzi, Federica Agosta, Paola Carrera, Nilo Riva, Massimo Filippi, Angelo Quattrini, Yuri Matteo Falzo |
| T2DM/CKD genetic risk scores and the progression of diabetic kidney disease in T2DM subjects. Gene 2024 6 927 148724. David Galuška, Lukáš Pácal, Katarína Chalásová, Petra Divácká, Jitka ?eho?ová, Jan Svojanovský, Jaroslav A Hubá?ek, V?ra Lánská, Kate?ina Ka?ko |
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