Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 301 Records) |
| Query Trace: Disease and CFH[original query] |
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| Clinicopathologic Implications of Complement Genetic Variants in Kidney Transplantation. Frontiers in medicine 2021 12 8 775280. Ren Zhen, Perkins Stephen J, Love-Gregory Latisha, Atkinson John P, Java Anu |
| C3 glomerulopathy associated with monoclonal gammopathy: impact of chronic histologic lesions and beneficial effects of clone-targeted therapies. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2021 Oct . Caravaca-Fontán Fernando, Lucientes Laura, Serra Núria, Cavero Teresa, Rodado Raquel, Ramos Natalia, Gonzalez Fayna, Shabaka Amir, Cabello Virginia, Huerta Ana, Pampa-Saico Saúl, Gutiérrez Eduardo, Quintana Luis F, López-Rubio Maria Esperanza, Draibe Juliana, Alonso Titos Juana, Fernández-Juárez Gema, Goicoechea de Jorge Elena, Praga Manu |
| Complement factor H variants are associated with microangiopathy lesions in IgA nephropathy. International immunopharmacology 2022 Sep 112 109234. Hou Wanyin, Shi Sufang, Zhou Xujie, Wang Suxia, Cai Qingqing, Chen Pei, Liu Lijun, Zhu Li, Lv Jicheng, Zhang Ho |
| Phenotypic Expression of CFH Rare Variants in Age-Related Macular Degeneration Patients in the Coimbra Eye Study. Investigative ophthalmology & visual science 2022 8 63 (9): 5. Farinha Cláudia, Barreto Patrícia, Coimbra Rita, Iutis Adela, Cachulo Maria Luz, Cunha-Vaz José, Lechanteur Yara T E, Hoyng Carel B, Silva Rufi |
| Common and rare genetic risk variants in age-related macular degeneration and genetic risk score in the Coimbra eye study. Acta ophthalmologica 2022 Aug . Farinha Cláudia, Barreto Patricia, Coimbra Rita, Cachulo Maria Luz, Melo Joana Barbosa, Cunha-Vaz José, Lechanteur Yara, Hoyng Carel B, Silva Rufi |
| Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations. American journal of human genetics 2022 8 109 (9): 1680-1691. Kumar Vikrant, Pouw Richard B, Autio Matias I, Sagmeister Manfred G, Phua Zai Yang, Borghini Lisa, Wright Victoria J, Hoggart Clive, Pan Bangfen, Tan Antson Kiat Yee, Binder Alexander, Brouwer Mieke C, Pinnock Ellie, De Groot Ronald, Hazelzet Jan, Emonts Marieke, Van Der Flier Michiel, Reiter Karl, Nöthen Markus M, Hoffmann Per, , Schlapbach Luregn J, Bellos Evangelos, Anderson Suzanne, Secka Fatou, Martinón-Torres Federico, Salas Antonio, Fink Colin, Carrol Enitan D, Pollard Andrew J, Coin Lachlan J, Zenz Werner, Wouters Diana, Ang Lay Teng, Hibberd Martin L, Levin Michael, Kuijpers Taco W, Davila Son |
| Inflammasome Activation in Retinal Pigment Epithelium from Human Donors with Age-Related Macular Degeneration. Cells 2022 7 11 (13): . Ebeling Mara C, Fisher Cody R, Kapphahn Rebecca J, Stahl Madilyn R, Shen Shichen, Qu Jun, Montezuma Sandra R, Ferrington Deborah |
| Correlation between genetic and environmental risk factors for age-related macular degeneration in Brazilian patients. PloS one 2022 6 17 (6): e0268795. Rim Priscila H H, de Vasconcellos José Paulo C, de Melo Mônica B, Medina Flavio M C, Sacconi Daniela P D, Lana Tamires P, Hirata Fabio E, Magna Luis A, Marques-de-Faria Antonia |
| SUBRETINAL DRUSENOID DEPOSITS AND SOFT DRUSEN: Are They Markers for Distinct Retinal Diseases? Retina (Philadelphia, Pa.) 2022 2 42 (7): 1311-1318. Thomson Robert J, Chazaro Joshua, Otero-Marquez Oscar, Ledesma-Gil Gerardo, Tong Yuehong, Coughlin Arielle C, Teibel Zachary R, Alauddin Sharmina, Tai Katy, Lloyd Harriet, Scolaro Maria, Govindaiah Arun, Bhuiyan Alauddin, Dhamoon Mandip S, Deobhakta Avnish, Narula Jagat, Rosen Richard B, Yannuzzi Lawrence A, Freund K Bailey, Smith R Theodo |
| Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritis. Frontiers in immunology 2022 10 13 960068. Gouda Heba R, Talaat Iman M, Bouzid Amal, El-Assi Hoda, Nabil Amira, Venkatachalam Thenmozhi, Manasa Bhamidimarri Poorna, Wohlers Inken, Mahdami Amena, El-Gendi Saba, ElKoraie Ahmed, Busch Hauke, Saber-Ayad Maha, Hamoudi Rifat, Baddour Nah |
| Associations of Single-Nucleotide Polymorphisms in Slovenian Patients with Acute Central Serous Chorioretinopathy. Genes 2021 12 13 (1): . Kiraly Peter, Zupan Andrej, Matjaši? Alenka, Mekjavi? Polona Ja |
| Exogenous CFH Modulates Levels of Pro-Inflammatory Mediators to Prevent Oxidative Damage of Retinal Pigment Epithelial Cells with the At-Risk CFH Y402H Variant. Antioxidants (Basel, Switzerland) 2023 8 12 (8): . Henry Velazquez-Soto, Sergio Groman-Lupa, Marisa Cruz-Aguilar, Alberto L Salazar, Juan C Zenteno, Maria C Jimenez-Martin |
| 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 |
| Alzheimer's disease-associated complement gene variants influence plasma complement protein levels. Journal of neuroinflammation 2023 7 20 (1): 169. Aurora Veteleanu, Joshua Stevenson-Hoare, Samuel Keat, Nikoleta Daskoulidou, Henrik Zetterberg, Amanda Heslegrave, Valentina Escott-Price, Julie Williams, Rebecca Sims, Wioleta M Zelek, Sarah M Carpanini, Bryan Paul Morg |
| The prognostic role of gene polymorphisms in patients with indolent non-Hodgkin lymphomas and mantle-cell lymphoma receiving bendamustine and rituximab: results of the 5-year follow-up study. Leukemia & lymphoma 2023 7 1-9. Emanuele Cencini, Anna Sicuranza, Alberto Fabbri, Cristina Marzano, Paola Pacelli, Federico Caroni, Donatella Raspadori, Monica Bocch |
| Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa. Frontiers in aging neuroscience 2023 6 15 1114810. Wided Boukhalfa, Haifa Jmel, Nadia Kheriji, Ismail Gouiza, Hamza Dallali, Mariem Hechmi, Rym Ke |
| Ultra-rare complement factor 8 coding variants in families with age-related macular degeneration. iScience 2023 5 26 (4): 106417. Lina Zelinger, Tammy M Martin, Jayshree Advani, Laura Campello, Milton A English, Alan Kwong, Claire Weber, Jennifer Maykoski, Yuri V Sergeev, Robert Fariss, Emily Y Chew, Michael L Klein, Anand Swaro |
| Association of C-reactive protein and complement factor H gene polymorphisms with risk of lupus nephritis in Chinese population. World journal of clinical cases 2023 5 11 (13): 2934-2944. Qiu-Yu Li, Jian-Min Lv, Xiao-Ling Liu, Hai-Yun Li, Feng |
| CRISPR editing demonstrates rs10490924 raised oxidative stress in iPSC-derived retinal cells from patients with ARMS2/HTRA1-related AMD. Proceedings of the National Academy of Sciences of the United States of America 2023 5 120 (19): e2215005120. Ya-Ju Chang, Laura A Jenny, Yong-Shi Li, Xuan Cui, Yang Kong, Yao Li, Janet R Sparrow, Stephen H Tsa |
| Pentosan polysulfate sodium (Elmiron) maculopathy: a genetic perspective. Retina (Philadelphia, Pa.) 2023 3 . Kalaw Fritz Gerald P, Ignacio John Carlos I, Wu Chris Y, Ferreyra Henry, Nudleman Eric, Baxter Sally L, Freeman William R, Borooah Shyaman |
| Influence of Clinical and Genetic Factors on the Progression of Age-Related Macular Degeneration: A 3-Year Follow-Up. Journal of clinical medicine 2023 3 12 (5): . Krytkowska El?bieta, Ula?czyk Zofia, Grabowicz Aleksandra, Safranow Krzysztof, Kawa Mi?osz Piotr, Pa?ucha Andrzej, W?sowska Anna, Matczy?ska Ewa, Boguszewska-Chachulska Anna, Machali?ska An |
| 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 |
| Citrullinated and MMP-degraded vimentin is associated with chronic pulmonary diseases and genetic variants in PADI3/PADI4 and CFH in postmenopausal women. Scientific reports 2023 12 13 (1): 23039. Cecilie Liv Bager, Joseph P M Blair, Man-Hung Eric Tang, Joachim Høg Mortensen, Anne-Christine Bay-Jensen, Peder Frederiksen, Diana Leeming, Claus Christiansen, Morten Asser Karsd |
| 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 |
| 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 |
| 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, |
| Analysis of Complement Factor H gene polymorphisms and their association with clinical manifestations ofleptospirosis. Immunogenetics 2024 11 77 (1): 4. Lazara Elena Santiesteban-Lores, Leonardo Moura Midon, ThirsaAlvares Franco, Luciano Marcondes de Oliveira, Sumire Hibi, Yosena Chiani, GdayllonCavalcante Meneses, Elizabeth De Francesco Daher, Denise Moraes Fonseca, Alessandra Pontillo, Lourdes Isa |
| Genetic Risk of Reticular Pseudodrusen in Age-Related Macular Degeneration: HTRA1 /lncRNA BX842242.1 dominates, with no evidence for Complement Cascade involvement. medRxiv : the preprint server for health sciences 2024 10 . Samaneh Farashi, Carla J Abbott, Brendan Re Ansell, Zhichao Wu, Lebriz Altay, Ella Arnon, Louis Arnould, Yelena Bagdasarova, Konstantinos Balaskas, Fred K Chen, Emily Chew, Itay Chowers, Steven Clarke, Catherine Cukras, Cécile Delcourt, Marie-Noëlle Delyfer, Anneke I den Hollander, Sascha Fauser, Robert P Finger, Pierre-Henry Gabrielle, Jiru Han, Lauren Ab Hodgson, Ruth Hogg, Frank G Holz, Carel Hoyng, Himeesh Kumar, Eleonora M Lad, Aaron Lee, Ulrich Fo Luhmann, Matthias M Mauschitz, Amy J McKnight, Samuel McLenachan, Aniket Mishra, Ismail Moghul, Luz D Orozco, Danuta M Sampson, Liam W Scott, Vasilena Sitnilska, Scott Song, Amy Stockwell, Anand Swaroop, Jan H Terheyden, Liran Tiosano, Adnan Tufail, Brian L Yaspan, , , Alice Pébay, Erica L Fletcher, Robyn H Guymer, Melanie Bah |
- Page last reviewed:Feb 1, 2024
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