Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 65 Records) |
| Query Trace: Disease and UMOD[original query] |
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| Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland. Renal failure 2019 9 41 (1): 832-841. Cormican S, Connaughton D M, Kennedy C, Murray S, Živná M, Kmoch S, Fennelly N K, O'Kelly P, Benson K A, Conlon E T, Cavalleri G, Foley C, Doyle B, Dorman A, Little M A, Lavin P, Kidd K, Bleyer A J, Conlon P |
| Genetic Susceptibility to Chronic Kidney Disease - Some More Pieces for the Heritability Puzzle. Frontiers in genetics 2019 10 453. Cañadas-Garre Marisa, Anderson Kerry, Cappa Ruaidhri, Skelly Ryan, Smyth Laura Jane, McKnight Amy Jayne, Maxwell Alexander Pet |
| Urinary Uromodulin Levels and UMOD Variants in Black South Africans with Hypertension-Attributed Chronic Kidney Disease. International journal of nephrology 2019 2019 8094049. Nqebelele Nolubabalo Unati, Dickens Caroline, Dix-Peek Therese, Duarte Raquel, Naicker Saralade |
| A novel disease-causing mutation in the Renin gene in a Tunisian family with autosomal dominant tubulointerstitial kidney disease. The international journal of biochemistry & cell biology 2019 10 117 105625. Abdelwahed Mayssa, Chaabouni Yosr, Michel-Calemard Laurence, Chaabouni Khansa, Morel Yves, Hachicha Jamil, Makni Fatma Ayedi, Kamoun Hassen, Ammar-Keskes Leila, Belghith Nei |
| Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene. Medicine 2020 Jan 99 (3): e18722. Adam Khalid Mohamed, Mohammed Ali Mahmoud, Elamin Abubakr A |
| Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. Scientific reports 2020 Jan 10 (1): 144. Corredor Zuray, Filho Miguel Inácio da Silva, Rodríguez-Ribera Lara, Velázquez Antonia, Hernández Alba, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José, Vallés Prats Martí, Calabia Martínez Jordi, Försti Asta, Marcos Ricard, Pastor Susa |
| Auxiliary genetic analysis in a Chinese adolescent NPH family by single nucleotide polymorphism screening. Molecular medicine reports 2020 1 21 (3): 1115-1124. Tang Chunrong, Zhou Daoyuan, Tan Rongshao, Zhong Xiaoshi, Xiao Xiao, Qin Danping, Liu Yun, Hu Jianguang, Liu Y |
| Polymorphism in the GATM Locus Associated with Dialysis-Independent Chronic Kidney Disease but Not Dialysis-Dependent Kidney Failure. Genes 2021 May 12 (6): . Šalamon Špela, Bevc Sebastjan, Ekart Robert, Hojs Radovan, Poto?nik Ur |
| Study of Uromodulin Gene Polymorphism in Egyptian Patients with End-Stage Renal Disease. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 0 32 (1): 157-162. Abdelsalam Mostafa, Motawea Mohamad, Kyrillos Fadyazmy, Abdel-Razik Ahmed, Zaki Maysaa El Sayed, Abdel-Wahab Ahm |
| Familial juvenile hyperuricemia in early childhood in a boy with a novel gene mutation. CEN case reports 2021 2 10 (3): 426-430. Takemasa Yoichi, Hirano Daishi, Kawakami Yuhei, Tokunaga Ai, Umeda Chisato, Miwa Saori, Kakegawa Daisuke, Ito Akira, Ida Hiroyu |
| Autosomal dominant tubulointerstitial kidney disease genotype and phenotype correlation in a Chinese cohort. Scientific reports 2021 2 11 (1): 3615. Gong Kunjing, Xia Min, Wang Yaqin, Wang Na, Liu Ying, Zhang Victor Wei, Cheng Hong, Chen Yuqi |
| UMOD Polymorphisms Associated with Kidney Function, Serum Uromodulin and Risk of Mortality among Patients with Chronic Kidney Disease, Results from the C-STRIDE Study. Genes 2021 Oct 12 (11): . Wang Jinwei, Liu Lili, He Kevin, Gao Bixia, Wang Fang, Zhao Minghui, Zhang Luxia, On Behalf Of The Chinese Cohort Study Of Chronic Kidney Disease C-Strid |
| ASSOCIATION OF GENETIC POLYMORPHISM AND EXPRESSION OF UMOD GENE AND CHRONIC KIDNEY DISEASE. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2021 74 (9 cz 2): 2297-2300. Hasan Farah Thamer, Mohey Mahmood Ahm |
| Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease. Kidney international 2021 Oct . Ponte Belen, Sadler Marie C, Olinger Eric, Vollenweider Peter, Bochud Murielle, Padmanabhan Sandosh, Hayward Caroline, Kutalik Zoltán, Devuyst Olivi |
| An intermediate-effect size variant in UMOD confers risk for chronic kidney disease. Proceedings of the National Academy of Sciences of the United States of America 2022 8 119 (33): e2114734119. Olinger Eric, Schaeffer Céline, Kidd Kendrah, Elhassan Elhussein A E, Cheng Yurong, Dufour Inès, Schiano Guglielmo, Mabillard Holly, Pasqualetto Elena, Hofmann Patrick, Fuster Daniel G, Kistler Andreas D, Wilson Ian J, Kmoch Stanislav, Raymond Laure, Robert Thomas, , Eckardt Kai-Uwe, Bleyer Anthony J, Köttgen Anna, Conlon Peter J, Wiesener Michael, Sayer John A, Rampoldi Luca, Devuyst Olivi |
| UMOD and the architecture of kidney disease. Pflugers Archiv : European journal of physiology 2022 7 474 (8): 771-781. Devuyst Olivier, Bochud Murielle, Olinger Er |
| Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies. Kidney international 2022 Jun . Gorski Mathias, Rasheed Humaira, Teumer Alexander, Thomas Laurent F, Graham Sarah E, Sveinbjornsson Gardar, Winkler Thomas W, Günther Felix, Stark Klaus J, Chai Jin-Fang, Tayo Bamidele O, Wuttke Matthias, Li Yong, Tin Adrienne, Ahluwalia Tarunveer S, Ärnlöv Johan, Åsvold Bjørn Olav, Bakker Stephan J L, Banas Bernhard, Bansal Nisha, Biggs Mary L, Biino Ginevra, Böhnke Michael, Boerwinkle Eric, Bottinger Erwin P, Brenner Hermann, Brumpton Ben, Carroll Robert J, Chaker Layal, Chalmers John, Chee Miao-Li, Chee Miao-Ling, Cheng Ching-Yu, Chu Audrey Y, Ciullo Marina, Cocca Massimiliano, Cook James P, Coresh Josef, Cusi Daniele, de Borst Martin H, Degenhardt Frauke, Eckardt Kai-Uwe, Endlich Karlhans, Evans Michele K, Feitosa Mary F, Franke Andre, Freitag-Wolf Sandra, Fuchsberger Christian, Gampawar Piyush, Gansevoort Ron T, Ghanbari Mohsen, Ghasemi Sahar, Giedraitis Vilmantas, Gieger Christian, Gudbjartsson Daniel F, Hallan Stein, Hamet Pavel, Hishida Asahi, Ho Kevin, Hofer Edith, Holleczek Bernd, Holm Hilma, Hoppmann Anselm, Horn Katrin, Hutri-Kähönen Nina, Hveem Kristian, Hwang Shih-Jen, Ikram M Arfan, Josyula Navya Shilpa, Jung Bettina, Kähönen Mika, Karabegovi? Irma, Khor Chiea-Chuen, Koenig Wolfgang, Kramer Holly, Krämer Bernhard K, Kühnel Brigitte, Kuusisto Johanna, Laakso Markku, Lange Leslie A, Lehtimäki Terho, Li Man, Lieb Wolfgang, , Lind Lars, Lindgren Cecilia M, Loos Ruth J F, Lukas Mary Ann, Lyytikäinen Leo-Pekka, Mahajan Anubha, Matias-Garcia Pamela R, Meisinger Christa, Meitinger Thomas, Melander Olle, Milaneschi Yuri, Mishra Pashupati P, Mononen Nina, Morris Andrew P, Mychaleckyj Josyf C, Nadkarni Girish N, Naito Mariko, Nakatochi Masahiro, Nalls Mike A, Nauck Matthias, Nikus Kjell, Ning Boting, Nolte Ilja M, Nutile Teresa, O'Donoghue Michelle L, O'Connell Jeffrey, Olafsson Isleifur, Orho-Melander Marju, Parsa Afshin, Pendergrass Sarah A, Penninx Brenda W J H, Pirastu Mario, Preuss Michael H, Psaty Bruce M, Raffield Laura M, Raitakari Olli T, Rheinberger Myriam, Rice Kenneth M, Rizzi Federica, Rosenkranz Alexander R, Rossing Peter, Rotter Jerome I, Ruggiero Daniela, Ryan Kathleen A, Sabanayagam Charumathi, Salvi Erika, Schmidt Helena, Schmidt Reinhold, Scholz Markus, Schöttker Ben, Schulz Christina-Alexandra, Sedaghat Sanaz, Shaffer Christian M, Sieber Karsten B, Sim Xueling, Sims Mario, Snieder Harold, Stanzick Kira J, Thorsteinsdottir Unnur, Stocker Hannah, Strauch Konstantin, Stringham Heather M, Sulem Patrick, Szymczak Silke, Taylor Kent D, Thio Chris H L, Tremblay Johanne, Vaccargiu Simona, van der Harst Pim, van der Most Peter J, Verweij Niek, Völker Uwe, Wakai Kenji, Waldenberger Melanie, Wallentin Lars, Wallner Stefan, Wang Judy, Waterworth Dawn M, White Harvey D, Willer Cristen J, Wong Tien-Yin, Woodward Mark, Yang Qiong, Yerges-Armstrong Laura M, Zimmermann Martina, Zonderman Alan B, Bergler Tobias, Stefansson Kari, Böger Carsten A, Pattaro Cristian, Köttgen Anna, Kronenberg Florian, Heid Iris |
| Vignette-Based Reflections to Inform Genetic Testing Policies in Living Kidney Donors. Genes 2022 4 13 (4): . Singh Gurmukteshwar, Gohh Reginald, Clark Dinah, Kalra Kartik, Das Manoj, Bradauskaite Gitana, Bleyer Anthony J, Tanriover Bekir, Chang Alex R, Anand Prince |
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.
Journal of the American Society of Nephrology : JASN 2022 3 33 (3): 511-529. Joseph Christina B, Mariniello Marta, Yoshifuji Ayumi, Schiano Guglielmo, Lake Jennifer, Marten Jonathan, Richmond Anne, Huffman Jennifer E, Campbell Archie, Harris Sarah E, Troyanov Stephan, Cocca Massimiliano, Robino Antonietta, Thériault Sébastien, Eckardt Kai-Uwe, Wuttke Matthias, Cheng Yurong, Corre Tanguy, Kolcic Ivana, Black Corrinda, Bruat Vanessa, Concas Maria Pina, Sala Cinzia, Aeschbacher Stefanie, Schaefer Franz, Bergmann Sven, Campbell Harry, Olden Matthias, Polasek Ozren, Porteous David J, Deary Ian J, Madore Francois, Awadalla Philip, Girotto Giorgia, Ulivi Sheila, Conen David, Wuehl Elke, Olinger Eric, Wilson James F, Bochud Murielle, Köttgen Anna, Hayward Caroline, Devuyst Olivi |
| Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases.
JCI insight 2022 4 7 (10): . Li Yong, Cheng Yurong, Consolato Francesco, Schiano Guglielmo, Chong Michael R, Pietzner Maik, Nguyen Ngoc Quynh H, Scherer Nora, Biggs Mary L, Kleber Marcus E, Haug Stefan, Göçmen Burulça, Pigeyre Marie, Sekula Peggy, Steinbrenner Inga, Schlosser Pascal, Joseph Christina B, Brody Jennifer A, Grams Morgan E, Hayward Caroline, Schultheiss Ulla T, Krämer Bernhard K, Kronenberg Florian, Peters Annette, Seissler Jochen, Steubl Dominik, Then Cornelia, Wuttke Matthias, März Winfried, Eckardt Kai-Uwe, Gieger Christian, Boerwinkle Eric, Psaty Bruce M, Coresh Josef, Oefner Peter J, Pare Guillaume, Langenberg Claudia, Scherberich Jürgen E, Yu Bing, Akilesh Shreeram, Devuyst Olivier, Rampoldi Luca, Köttgen An |
| Nidogen-1 could play a role in diabetic kidney disease development in type 2 diabetes: a genome-wide association meta-analysis.
Human genomics 2022 10 16 (1): 47. Khattab Ahmed, Torkamani A |
| Genome-Wide Association Study of Chronic Kidney Disease Progression. Journal of the American Society of Nephrology : JASN 2023 6 . C Robinson-Cohen, J L Triozzi, B Rowan, J He, H C Chen, N S Zheng, W Q Wei, O D Wilson, J N Hellwege, P S Tsao, J M Gaziano, A Bick, M E Matheny, C P Chung, L Lipworth, E D Siew, T A Ikizler, R Tao, A M Hu |
| Investigating polymorphisms related to chronic kidney disease and the effect of health and nursing education on self-management ability and quality of life in hemodialysis patients. Cellular and molecular biology (Noisy-le-Grand, France) 2023 5 69 (1): 25-29. Xiaoxiao Qu, Peng Sh |
| SPP1 and UMOD gene variants are synergistically associated with risk of renal stone disease. Gene 2023 2 863 147264. Patel Yash P, Patel Samir G, Patel Sandip B, Parikh Aditya, Soni Shailesh, Srivastava Ratika, Raval Chintal, Raval Manan A, Nand Pandey Sachchida, Ganpule Arvind P, Desai Mahesh |
| Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study. Scientific reports 2024 8 14 (1): 18281. Marco Luigetti, Francesca Vitali, Angela Romano, Maria Ausilia Sciarrone, Valeria Guglielmino, Michelangelo Ardito, Andrea Sabino, Serenella Servidei, Geny Piro, Carmine Carbone, Francesca Graziani, Rosa Lillo, Pietro Manuel Ferraro, Guido Primia |
| Evaluation of Genetic Associations with Clinical Phenotypes of Kidney Stone Disease. European urology open science 2024 8 67 38-44. Ryan S Hsi, Siwei Zhang, Jefferson L Triozzi, Adriana M Hung, Yaomin Xu, Cosmin A Bej |
| Uromodulin and progression of IgA nephropathy. Clinical kidney journal 2024 8 17 (8): sfae209. Zijin Chen, Lin-Lin Xu, Wen Du, Yan Ouyang, Xiangchen Gu, Zhengying Fang, Xialian Yu, Junru Li, Lin Xie, Yuanmeng Jin, Jun Ma, Zhaohui Wang, Xiaoxia Pan, Wen Zhang, Hong Ren, Weiming Wang, Xiaonong Chen, Xu-Jie Zhou, Hong Zhang, Nan Chen, Jingyuan X |
| Eight-Fold Increased COVID-19 Mortality in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations: An Observational Study. medRxiv : the preprint server for health sciences 2024 7 . Kendrah O Kidd, Adrienne H Williams, Abbigail Taylor, Lauren Martin, Victoria Robins, John A Sayer, Eric Olinger, Holly R Mabillard, Gregory Papagregoriou, Constantinos Deltas, Christoforos Stavrou, Peter J Conlon, Richard Edmund Hogan, Elhussein A E Elhassan, Drahomíra Springer, Tomáš Zima, Claudia Izzi, Alena Vrbacká, Lenka Piherová, Michal Pohludka, Martin Radina, Petr Vylet'al, Katerina Hodanova, Martina Zivna, Stanislav Kmoch, Anthony J Bley |
| UMOD Genotype and Determinants of Urinary Uromodulin in African Populations. Kidney international reports 2024 12 9 (12): 3477-3489. Michél Strauss-Kruger, Eric Olinger, Patrick Hofmann, Ian J Wilson, Carina Mels, Ruan Kruger, Lebo F Gafane-Matemane, John A Sayer, Cristian Ricci, Aletta E Schutte, Olivier Devuy |
| Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational study. BMC nephrology 2024 12 25 (1): 449. Kendrah O Kidd, Adrienne H Williams, Abbigail Taylor, Lauren Martin, Victoria Robins, John A Sayer, Eric Olinger, Holly R Mabillard, Gregory Papagregoriou, Constantinos Deltas, Christoforos Stavrou, Peter J Conlon, Richard Edmund Hogan, Elhussein A E Elhassan, Drahomíra Springer, Tomáš Zima, Claudia Izzi, Alena Vrbacká, Lenka Piherová, Michal Pohludka, Martin Radina, Petr Vylet'al, Katerina Hodanova, Martina Zivna, Stanislav Kmoch, Anthony J Bley |
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