Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 306 Records) |
| Query Trace: Disease and C3[original query] |
|---|
| Causal Associations between Vitamin D Levels and Psoriasis, Atopic Dermatitis, and Vitiligo: A Bidirectional Two-Sample Mendelian Randomization Analysis. Nutrients 2022 12 14 (24): . Ren Yunqing, Liu Jipeng, Li Wei, Zheng Huiwen, Dai Huatuo, Qiu Guiying, Yu Dianhe, Yao Dianyi, Yin Xianyo |
| Serum interleukin 40: an innovative diagnostic biomarker for patients with systemic lupus erythematosus. The Medical journal of Malaysia 2023 9 78 (5): 609-615. A M Al Rubaye, I K Sharquie, F I Gori |
| Polygenic Risk Score and Rare Variant Burden Identified by Targeted Sequencing in a Group of Patients with Pigment Epithelial Detachment in Age-Related Macular Degeneration. Genes 2023 9 14 (9): . Anna W?sowska, Adam Sendecki, Anna Boguszewska-Chachulska, S?awomir Tep |
| Genetic investigation of Nordic patients with complement-mediated kidney diseases. Frontiers in immunology 2023 9 14 1254759. Viktor Rydberg, Sigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Naila Svitacheva, Diana Karpm |
| Mesangial C3 Deposition, Complement-Associated Variant, and Disease Progression in IgA Nephropathy. Clinical journal of the American Society of Nephrology : CJASN 2023 8 . Yuqi Kang, Boyang Xu, Sufang Shi, Xujie Zhou, Pei Chen, Lijun Liu, Yebei Li, Yueqi Leng, Jicheng Lv, Li Zhu, Hong Zha |
| Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis. Clinical journal of the American Society of Nephrology : CJASN 2023 8 . Marie Sophie Meuleman, Paula Vieira Martins, Carine El Sissy, Vincent Audard, Véronique Baudouin, Dominique Bertrand, Frank Bridoux, Férielle Louillet, Claire Dossier, Vincent Esnault, Noémie Jourde-Chiche, Alexandre Karras, Marie-Pascale Morin, François Provot, Philippe Remy, David Ribes, Caroline Rousset-Rouviere, Aude Servais, Eric Thervet, Leila Tricot, Mohamad Zaidan, Alain Wynckel, Julien Zuber, Moglie Le Quintrec, Véronique Frémeaux-Bacchi, Sophie Chauv |
| Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers. Journal of cardiovascular translational research 2023 6 . Mark Jansen, A F Schmidt, J J M Jans, I Christiaans, S N van der Crabben, Y M Hoedemaekers, D Dooijes, J D H Jongbloed, L G Boven, R H Lekanne Deprez, A A M Wilde, J van der Velden, R A de Boer, J P van Tintelen, F W Asselbergs, A F Ba |
| Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease. Current developments in nutrition 2023 6 7 (4): 100051. Reina Yamamoto, Yumie Takeshita, Hiromasa Tsujiguchi, Takayuki Kannon, Takehiro Sato, Kazuyoshi Hosomichi, Keita Suzuki, Yuki Kita, Takeo Tanaka, Hisanori Goto, Yujiro Nakano, Tatsuya Yamashita, Shuichi Kaneko, Atsushi Tajima, Hiroyuki Nakamura, Toshinari Takamu |
| ITGAM rs1143679 Variant in Systemic Lupus Erythematosus Is Associated with Increased Serum Calcification Propensity. Genes 2023 5 14 (5): . Matthieu Halfon, Li Zhang, Driss Ehirchiou, Vishnuprabu Durairaj Pandian, Suzan Dahdal, Uyen Huynh-Do, Andreas Pasch, Camillo Ribi, Nathalie Bus |
| Influence of Genetics on the Response to Omalizumab in Patients with Severe Uncontrolled Asthma with an Allergic Phenotype. International journal of molecular sciences 2023 4 24 (8): . Susana Rojo-Tolosa, José Antonio Sánchez-Martínez, Laura Elena Pineda-Lancheros, José María Gálvez-Navas, María Victoria González-Gutiérrez, Gonzalo Jiménez-Gálvez, Cristina Pérez-Ramírez, Concepción Morales-García, Alberto Jiménez-Moral |
| Clinical characteristics of early-onset paediatric systemic lupus erythematosus in a single centre in China. Rheumatology (Oxford, England) 2023 2 . Hou Yipei, Wang Li, Luo Chong, Tang Wenjing, Dai Rongxin, An Yunfei, Tang Xuem |
| The bi-directional association between bipolar disorder and obesity: Evidence from Meta and bioinformatics analysis. International journal of obesity (2005) 2023 2 . Kambey Piniel Alphayo, Kodzo Lalit Dzifa, Serojane Fattimah, Oluwasola Bolorunduro Jan |
| Targeted genotyping of COVID-19 patients reveals a signature of complement C3 and factor B coding SNPs associated with severe infection. Immunobiology 2023 2 228 (2): 152351. Tsiftsoglou Stefanos A, Gavriilaki Eleni, Touloumenidou Tasoula, Koravou Evaggelia-Evdoxia, Koutra Maria, Papayanni Penelope Georgia, Karali Vassiliki, Papalexandri Apostolia, Varelas Christos, Chatzopoulou Fani, Chatzidimitriou Maria, Chatzidimitriou Dimitrios, Veleni Anastasia, Rapti Evdoxia, Kioumis Ioannis, Kaimakamis Evaggelos, Bitzani Milly, Boumpas Dimitrios T, Tsantes Argyris, Sotiropoulos Damianos, Papadopoulou Anastasia, Sakellari Ioanna, Kokoris Styliani, Anagnostopoulos Achill |
| Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil? Pediatric nephrology (Berlin, Germany) 2023 12 . Neslihan Günay, ?smail Dursun, ?brahim Gökçe, Mehtap Akbal?k Kara, Demet Tekcan, Neslihan Çiçek, Meral Torun Bayram, Mustafa Koyun, Nida Dinçel, Hasan Dursun, Seha Sayg?l?, Zeynep Nagehan Yürük Y?ld?r?m, Selçuk Yüksel, Osman Dönmez, Sibel Yel, Beltinge Demircio?lu K?l?ç, Özlem Aydo?, Bahriye Atm??, Aysun Çalt?k Y?lmaz, Sevcan A Bakkalo?lu, Mehmet Baha Aytaç, Mehmet Ta?demir, Belde Kasap Demir, Alper Soylu, Elif Çomak, Asl? Kantar Öz?ahin, Alper Kaçar, Nur Canpolat, Alev Y?lmaz, ?lknur Giri?gen, Kadirye Betül Akkoyunlu, Harika Alpay, Hakan M Poyrazo? |
| Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration. Human molecular genetics 2023 11 . Alan Kwong, Matthew Zawistowski, Lars G Fritsche, Xiaowei Zhan, Jennifer Bragg-Gresham, Kari E Branham, Jayshree Advani, Mohammad Othman, Rinki Ratnapriya, Tanya M Teslovich, Dwight Stambolian, Emily Y Chew, Gonçalo R Abecasis, Anand Swaro |
| Association of elevated levels of peripheral complement components with cortical thinning and impaired logical memory in drug-naïve patients with first-episode schizophrenia. Schizophrenia (Heidelberg, Germany) 2023 11 9 (1): 79. Hua Yu, Peiyan Ni, Yang Tian, Liansheng Zhao, Mingli Li, Xiaojing Li, Wei Wei, Jinxue Wei, Qiang Wang, Wanjun Guo, Wei Deng, Xiaohong Ma, Jeremy Coid, Tao |
| Complement alternative pathway determines disease susceptibility and severity in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Kidney international 2023 11 . Laura Lucientes-Continente, Gema Fernández-Juárez, Bárbara Márquez-Tirado, Laura Jiménez-Villegas, Mercedes Acevedo, Teresa Cavero, Luís Sánchez Cámara, Juliana Draibe, Paula Anton-Pampols, Fernando Caravaca-Fontán, Manuel Praga, Javier Villacorta, Elena Goicoechea de Jor |
| Low C3 in a 4-month-old baby: is it a problem? Pediatric nephrology (Berlin, Germany) 2023 11 . Gül?ah Kaya Aksoy, Mustafa Gökhan Ertosun, Mustafa Koyun, Elif Çomak, Sema Akm |
| Integration of exome-seq and mRNA-seq using DawnRank, identified genes involved in innate immunity as drivers of breast cancer in the Indian cohort. PeerJ 2023 10 11 e16033. Snehal Nirgude, Sagar Desai, Vartika Khanchandani, Vidhyavathy Nagarajan, Jayanti Thumsi, Bibha Choudha |
| Identification of an APOE ?4-specific blood-based molecular pathway for Alzheimer's disease risk. Alzheimer's & dementia (Amsterdam, Netherlands) 2023 10 15 (4): e12490. Qiushan Tao, Chao Zhang, Gustavo Mercier, Kathryn Lunetta, Ting Fang Alvin Ang, Samia Akhter-Khan, Zhengrong Zhang, Andrew Taylor, Ronald J Killiany, Michael Alosco, Jesse Mez, Rhoda Au, Xiaoling Zhang, Lindsay A Farrer, Wendy Wei Qiao Qiu, |
| FGF4L2 retrogene copy number is associated with intervertebral disc calcification and vertebral geometry in Nova Scotia Duck Tolling Retrievers. American journal of veterinary research 2023 1 84 (3): . Bianchi Catarina A, Marcellin-Little Denis J, Dickinson Peter J, Garcia Tanya C, Li Chai-Fei, Batcher Kevin, Bannasch Danika |
| Genetic Polymorphisms and Genetic Risk Scores Contribute to the Risk of Coronary Artery Disease (CAD) in a North Indian Population. International journal of molecular sciences 2024 8 25 (15): . Sarabjit Mastana, Kushni Charisma Halai, Liz Akam, David John Hunter, Puneetpal Sin |
| Roles of Single Nucleotide Polymorphisms of C3 Gene in Patients with Coronary Artery Disease. Reviews in cardiovascular medicine 2024 7 25 (4): 147. Shajidan Abudureyimu, Chunhui He, Dilihumaer Abulaiti, Wei Xie, Halisha Airikenjiang, Haitang Qiu, Mengjia Liu, Yan Cao, Hui Li, Jian Zhang, Ying G |
| Clinical outcomes of patients with mut-type methylmalonic acidemia identified through expanded newborn screening in China. Human genomics 2024 7 18 (1): 84. Shiying Ling, Shengnan Wu, Ruixue Shuai, Yue Yu, Wenjuan Qiu, Haiyan Wei, Chiju Yang, Peng Xu, Hui Zou, Jizhen Feng, Tingting Niu, Haili Hu, Huiwen Zhang, Lili Liang, Yu Wang, Ting Chen, Feng Xu, Xuefan Gu, Lianshu H |
| A cross sectional study assessing steatotic liver disease in patients with systemic lupus erythematosus. Scientific reports 2024 6 14 (1): 14275. Armando Antonio Baeza-Zapata, Ashuin Kammar-García, Ana Barrera-Vargas, Javier Merayo-Chalico, Sophia Eugenia Martínez-Vázquez, Carlos Moctezuma-Velazqu |
| Clinical Application of Polygenic Risk Score in IgA Nephropathy. Phenomics (Cham, Switzerland) 2024 6 4 (2): 146-157. Linlin Xu, Ting Gan, Pei Chen, Yang Liu, Shu Qu, Sufang Shi, Lijun Liu, Xujie Zhou, Jicheng Lv, Hong Zha |
| Role of interleukin 6 polymorphism and inflammatory markers in outcome of pediatric Covid- 19 patients. BMC pediatrics 2024 10 24 (1): 625. Reem A AbdelAziz, Samir Tamer Abd-Allah, Hend M Moness, Ahmed M Anwar, Zamzam Hassan Moham |
| Anti-factor B antibodies in atypical hemolytic uremic syndrome. Pediatric nephrology (Berlin, Germany) 2024 1 . Priyanka Khandelwal, Shreesha Nambiar, Rahul Saini, Savita Saini, Poonam Coshic, Aditi Sinha, Pankaj Hari, Jayanth Kumar Palanichamy, Arvind Bag |
| Clinical characteristics of bullous pemphigoid patients of different ages and the possible mechanism. The Journal of dermatology 2025 1 . Xinyi Chen, Bingjie Zhang, Xuming Mao, Yiman Wang, Yuyan Yang, Yangchun Liu, Fangyuan Chen, Li |
| Whole-Exome Sequencing: Discovering Genetic Causes of Granulomatous Mastitis. International journal of molecular sciences 2025 1 26 (1): . Beyza Ozcinar, Zeynep Ocak, Deryanaz Billur, Baris Ertugrul, Ozlem Timirci-Kahram |
- Page last reviewed:Feb 1, 2024
- Content source: