Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and C7[original query] |
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| Association of HLA-C3 and smoking with vasculitis in patients with rheumatoid arthritis. Arthritis and rheumatism 2006 Sep 54 (9): 2776-83. Turesson Carl, Schaid Daniel J, Weyand Cornelia M, Jacobsson Lennart T, Goronzy Jörg J, Petersson Ingemar F, Dechant Sonja A, Nyähll-Wåhlin Britt-Marie, Truedsson Lennart, Sturfelt Gunnar, Matteson Eric |
| Evidence for association between multiple complement pathway genes and AMD. Genetic epidemiology 2007 Apr 31 (3): 224-37. Dinu Valentin, Miller Perry L, Zhao Hong |
| [Association of genetic factors with clinical peculiarities of hypertensive disease in patients with burdened familial anamnesis]. Kardiologiia 2009 49 (2): 38-46. Minushkina L O, Brazhnik V A, Nosikov V V, Sidorenko B A, Zate?shchikov D |
| Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS. Human molecular genetics 2009 May 18 (9): 1670-83. Kallio Suvi P, Jakkula Eveliina, Purcell Shaun, Suvela Minna, Koivisto Keijo, Tienari Pentti J, Elovaara Irina, Pirttilä Tuula, Reunanen Mauri, Bronnikov Denis, Viander Markku, Meri Seppo, Hillert Jan, Lundmark Frida, Harbo Hanne F, Lorentzen Aslaug R, De Jager Philip L, Daly Mark J, Hafler David A, Palotie Aarno, Peltonen Leena, Saarela Jan |
| 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 |
| Analysis of HLA-A, -B, -C, -DR, -DQ polymorphisms in the South Tunisian population and a comparison with other populations. Annals of human biology 2013 Jan 40 (1): 41-7. Mahfoudh Nadia, Ayadi Imen, Kamoun Arwa, Ammar Radhia, Mallek Bakhta, Maalej Leila, Hakim Faiza, Gaddour Lilia, Rebai Ahmed, Makni Hafe |
A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci.
PloS one 2013 8 (3): e58657. Scheetz Todd E, Fingert John H, Wang Kai, Kuehn Markus H, Knudtson Kevin L, Alward Wallace L M, Boldt H Culver, Russell Stephen R, Folk James C, Casavant Thomas L, Braun Terry A, Clark Abbot F, Stone Edwin M, Sheffield Val |
| Analysis of genome-wide variants through bulked segregant RNA sequencing reveals a major gene for resistance to Plasmodiophora brassicae in Brassica oleracea. Scientific reports 2018 12 8 (1): 17657. Dakouri Abdulsalam, Zhang Xingguo, Peng Gary, Falk Kevin C, Gossen Bruce D, Strelkov Stephen E, Yu Fengq |
| Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese. National science review 2019 4 6 (2): 257-274. Zhang Deng-Feng, Fan Yu, Xu Min, Wang Guihong, Wang Dong, Li Jin, Kong Li-Li, Zhou Hejiang, Luo Rongcan, Bi Rui, Wu Yong, Li Guo-Dong, , Li Ming, Luo Xiong-Jian, Jiang Hong-Yan, Tan Liwen, Zhong Chunjiu, Fang Yiru, Zhang Chen, Sheng Nengyin, Jiang Tianzi, Yao Yong-Ga |
| Dermal Phospho-Alpha-Synuclein Deposition in Patients With Parkinson's Disease and Mutation of the Glucocerebrosidase Gene. Frontiers in neurology 2019 1 9 1094. Doppler Kathrin, Brockmann Kathrin, Sedghi Annahita, Wurster Isabel, Volkmann Jens, Oertel Wolfgang H, Sommer Claud |
| Systems-level differential gene expression analysis reveals new genetic variants of oral cancer. Scientific reports 2020 9 10 (1): 14667. Abbas Syeda Zahra, Qadir Muhammad Imran, Muhammad Syed A |
| Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease. Movement disorders : official journal of the Movement Disorder Society 2020 10 36 (2): 449-459. Shadrin Alexey A, Mucha Sören, Ellinghaus David, Makarious Mary B, Blauwendraat Cornelis, Sreelatha Ashwin A K, Heras-Garvin Antonio, Ding Jinhui, Hammer Monia, Foubert-Samier Alexandra, Meissner Wassilios G, Rascol Olivier, Pavy-Le Traon Anne, Frei Oleksandr, O'Connell Kevin S, Bahrami Shahram, Schreiber Stefan, Lieb Wolfgang, Müller-Nurasyid Martina, Schminke Ulf, Homuth Georg, Schmidt Carsten O, Nöthen Markus M, Hoffmann Per, Gieger Christian, Wenning Gregor, , Gibbs J Raphael, Franke Andre, Hardy John, Stefanova Nadia, Gasser Thomas, Singleton Andrew, Houlden Henry, Scholz Sonja W, Andreassen Ole A, Sharma Ma |
| ICBP90 Regulates MIF Expression, Glucocorticoid Sensitivity, and Apoptosis at the MIF Immune Susceptibility Locus. Arthritis & rheumatology (Hoboken, N.J.) 2021 4 73 (10): 1931-1942. Yao Jie, Leng Lin, Fu Weiling, Li Jia, Bronner Christian, Bucala Richa |
| The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease. The Turkish journal of pediatrics 2021 63 (1): 118-125. Balamtekin Necati, Baysoy Gökhan, Tan Ça?man, K?z?lkan Nuray Uslu, Demir Hülya, Salt?k-Temizel ?nci Nur, Özen Hasan, Yüce Aysel, Tezcan ?lhan, Gürakan Fig |
| HLA-DQB1*05:02, *05:03, and *03:01 alleles as risk factors for myasthenia gravis in a Spanish cohort. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 May . Salvado Maria, Caro Jose Luis, Garcia Cecilia, Rudilla Francesc, Zalba-Jadraque Laura, Lopez Eva, Sanjuan Elia, Gamez Josep, Vidal-Taboada Jose Manu |
| Rare DNAJC7 Variants May Play a Minor Role in Chinese Patients with ALS. Molecular neurobiology 2023 10 . Shichan Wang, Xiaoting Zheng, Qianqian Wei, Junyu Lin, Tianmi Yang, Yi Xiao, Qirui Jiang, Chunyu Li, Huifang Sha |
| Peripheral cutaneous synucleinopathy characteristics in genetic Parkinson's disease. Frontiers in neurology 2024 5 15 1404492. Yanpeng Yuan, Yangyang Wang, Minglei Liu, Haiyang Luo, Xiaojing Liu, Lanjun Li, Chengyuan Mao, Ting Yang, Shuo Li, Xiaoyun Zhang, Yuan Gao, Yuming Xu, Jing Ya |
| Functional Genotype-Phenotype Associations in Recessive Dystrophic Epidermolysis Bullosa. Journal of the American Academy of Dermatology 2024 5 . Jodi Y So, Jaron Nazaroff, Vamsi K Yenamandra, Emily S Gorell, Nicki Harris, Shivali Fulchand, Edward Eid, John A Dolorito, M Peter Marinkovich, Jean Y Ta |
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