Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and SLC34A1[original query] |
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New loci associated with kidney function and chronic kidney disease.
Nature genetics 2010 May 42 (5): 376-84. Köttgen Anna, Pattaro Cristian, Böger Carsten A, Fuchsberger Christian, Olden Matthias, Glazer Nicole L, Parsa Afshin, Gao Xiaoyi, Yang Qiong, Smith Albert V, O'Connell Jeffrey R, Li Man, Schmidt Helena, Tanaka Toshiko, Isaacs Aaron, Ketkar Shamika, Hwang Shih-Jen, Johnson Andrew D, Dehghan Abbas, Teumer Alexander, Paré Guillaume, Atkinson Elizabeth J, Zeller Tanja, Lohman Kurt, Cornelis Marilyn C, Probst-Hensch Nicole M, Kronenberg Florian, Tönjes Anke, Hayward Caroline, Aspelund Thor, Eiriksdottir Gudny, Launer Lenore J, Harris Tamara B, Rampersaud Evadnie, Mitchell Braxton D, Arking Dan E, Boerwinkle Eric, Struchalin Maksim, Cavalieri Margherita, Singleton Andrew, Giallauria Francesco, Metter Jeffrey, de Boer Ian H, Haritunians Talin, Lumley Thomas, Siscovick David, Psaty Bruce M, Zillikens M Carola, Oostra Ben A, Feitosa Mary, Province Michael, de Andrade Mariza, Turner Stephen T, Schillert Arne, Ziegler Andreas, Wild Philipp S, Schnabel Renate B, Wilde Sandra, Munzel Thomas F, Leak Tennille S, Illig Thomas, Klopp Norman, Meisinger Christa, Wichmann H-Erich, Koenig Wolfgang, Zgaga Lina, Zemunik Tatijana, Kolcic Ivana, Minelli Cosetta, Hu Frank B, Johansson Asa, Igl Wilmar, Zaboli Ghazal, Wild Sarah H, Wright Alan F, Campbell Harry, Ellinghaus David, Schreiber Stefan, Aulchenko Yurii S, Felix Janine F, Rivadeneira Fernando, Uitterlinden Andre G, Hofman Albert, Imboden Medea, Nitsch Dorothea, Brandstätter Anita, Kollerits Barbara, Kedenko Lyudmyla, Mägi Reedik, Stumvoll Michael, Kovacs Peter, Boban Mladen, Campbell Susan, Endlich Karlhans, Völzke Henry, Kroemer Heyo K, Nauck Matthias, Völker Uwe, Polasek Ozren, Vitart Veronique, Badola Sunita, Parker Alexander N, Ridker Paul M, Kardia Sharon L R, Blankenberg Stefan, Liu Yongmei, Curhan Gary C, Franke Andre, Rochat Thierry, Paulweber Bernhard, Prokopenko Inga, Wang Wei, Gudnason Vilmundur, Shuldiner Alan R, Coresh Josef, Schmidt Reinhold, Ferrucci Luigi, Shlipak Michael G, van Duijn Cornelia M, Borecki Ingrid, Krämer Bernhard K, Rudan Igor, Gyllensten Ulf, Wilson James F, Witteman Jacqueline C, Pramstaller Peter P, Rettig Rainer, Hastie Nick, Chasman Daniel I, Kao W H, Heid Iris M, Fox Caroline |
| Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD. PLoS genetics 2011 Sep 7 (9): e1002292. Böger Carsten A, Gorski Mathias, Li Man, Hoffmann Michael M, Huang Chunmei, Yang Qiong, Teumer Alexander, Krane Vera, O'Seaghdha Conall M, Kutalik Zoltán, Wichmann H-Erich, Haak Thomas, Boes Eva, Coassin Stefan, Coresh Josef, Kollerits Barbara, Haun Margot, Paulweber Bernhard, Köttgen Anna, Li Guo, Shlipak Michael G, Powe Neil, Hwang Shih-Jen, Dehghan Abbas, Rivadeneira Fernando, Uitterlinden André, Hofman Albert, Beckmann Jacques S, Krämer Bernhard K, Witteman Jacqueline, Bochud Murielle, Siscovick David, Rettig Rainer, Kronenberg Florian, Wanner Christoph, Thadhani Ravi I, Heid Iris M, Fox Caroline S, Kao W H, |
| Common and rare variants associated with kidney stones and biochemical traits.
Nature communications 2015 6 7975. Oddsson Asmundur, Sulem Patrick, Helgason Hannes, Edvardsson Vidar O, Thorleifsson Gudmar, Sveinbjörnsson Gardar, Haraldsdottir Eik, Eyjolfsson Gudmundur I, Sigurdardottir Olof, Olafsson Isleifur, Masson Gisli, Holm Hilma, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Indridason Olafur S, Palsson Runolfur, Stefansson Ka |
| Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.
American journal of human genetics 2016 Sep 99 (3): 636-46. Mahajan Anubha, Rodan Aylin R, Le Thu H, Gaulton Kyle J, Haessler Jeffrey, Stilp Adrienne M, Kamatani Yoichiro, Zhu Gu, Sofer Tamar, Puri Sanjana, Schellinger Jeffrey N, Chu Pei-Lun, Cechova Sylvia, van Zuydam Natalie, , , Arnlov Johan, Flessner Michael F, Giedraitis Vilmantas, Heath Andrew C, Kubo Michiaki, Larsson Anders, Lindgren Cecilia M, Madden Pamela A F, Montgomery Grant W, Papanicolaou George J, Reiner Alex P, Sundström Johan, Thornton Timothy A, Lind Lars, Ingelsson Erik, Cai Jianwen, Martin Nicholas G, Kooperberg Charles, Matsuda Koichi, Whitfield John B, Okada Yukinori, Laurie Cathy C, Morris Andrew P, Franceschini No |
| Renal phosphate handling and inherited disorders of phosphate reabsorption: an update. Pediatric nephrology (Berlin, Germany) 2017 12 34 (4): 549-559. Wagner Carsten A, Rubio-Aliaga Isabel, Hernando Na |
| Clinical aspects of the phosphate transporters NaPi-IIa and NaPi-IIb: mutations and disease associations. Pflugers Archiv : European journal of physiology 2018 12 471 (1): 137-148. Lederer Eleanor, Wagner Carsten |
| Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis. Human genetics 2019 Feb . Amar Ali, Majmundar Amar J, Ullah Ihsan, Afzal Ayesha, Braun Daniela A, Shril Shirlee, Daga Ankana, Jobst-Schwan Tilman, Ahmad Mumtaz, Sayer John A, Gee Heon Yung, Halbritter Jan, Knöpfel Thomas, Hernando Nati, Werner Andreas, Wagner Carsten, Khaliq Shagufta, Hildebrandt Friedhe |
| Association of CASR, CALCR, and ORAI1 Genes Polymorphisms With the Calcium Urolithiasis Development in Russian Population. Frontiers in genetics 2021 12 621049. Litvinova Maria M, Khafizov Kamil, Korchagin Vitaly I, Speranskaya Anna S, Asanov Aliy Yu, Matsvay Alina D, Kiselev Daniil A, Svetlichnaya Diana V, Nuralieva Sevda Z, Moskalev Alexey A, Filippova Tamara |
| Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. Frontiers in endocrinology 2021 11 12 736240. Molin Arnaud, Lemoine Sandrine, Kaufmann Martin, Breton Pierre, Nowoczyn Marie, Ballandonne Céline, Coudray Nadia, Mittre Hervé, Richard Nicolas, Ryckwaert Amélie, Lavillaureix Alinoe, Jones Glenville, Bacchetta Justine, Kottler Marie-Lau |
| Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
| Systematic assessment of monogenic etiology in adult-onset kidney stone formers undergoing urological intervention-evidence for genetic pretest probability. American journal of medical genetics. Part C, Seminars in medical genetics 2022 8 190 (3): 279-288. Schönauer Ria, Scherer Lotte, Nemitz-Kliemchen Melanie, Hagemann Tobias, Hantmann Elena, Seidel Anna, Müller Luise, Kehr Stephanie, Voigt Cornelia, Stolzenburg Jens-Uwe, Halbritter J |
| Metabolic and Genetic Evaluation in Children with Nephrolithiasis. Indian journal of pediatrics 2022 Jul . Mandal Anita, Khandelwal Priyanka, Geetha Thenral S, Murugan Sakthivel, Meena Jitendra, Jana Manisha, Sinha Aditi, Kumar Rajeev, Seth Amlesh, Hari Pankaj, Bagga Arvi |
| Single nucleotide polymorphisms in the GFR-related gene and the SNP-SNP interactions on the risk of diabetic kidney disease in Chinese Han population. Acta diabetologica 2022 11 60 (1): 115-125. Liu Yanxiu, Chen Yan, Yang Qiwei, Shen Dihan, Du Zhenwu, Zhang Guizh |
| Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c. Kidney international 2024 10 . Max Brunkhorst, Lena Brunkhorst, Helge Martens, Svetlana Papizh, Martine Besouw, Corinna Grasemann, Serap Turan, Przemyslaw Sikora, Milan Chromek, Elisabeth Cornelissen, Marc Fila, Marc Lilien, Jeremy Allgrove, Thomas J Neuhaus, Mehmet Eltan, Laura Espinosa, Dirk Schnabel, Ibrahim Gokce, Juan David González-Rodríguez, Priyanka Khandelwal, Mandy G Keijzer-Veen, Felix Lechner, Maria Szczepa?ska, Marcin Zaniew, Justine Bacchetta, Francesco Emma, Dieter Haffn |
| CASR, CLDN 14, ALPL & SLC34A1 genes are associated with the risk of nephrolithiasis in Egyptian children. Journal of pediatric urology 2025 1 . Fatina I Fadel, Manal F Elshamaa, Mervat Ismail, Alaa Rashad, Ashraf Galal, Solaf Kamel, Eman Awadallah, Rasha Nazeeh, Eman Mahmoud, Yasmin Ramad |
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