Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and CLDN14[original query] |
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Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.
Nature genetics 2009 Aug 41 (8): 926-30. Thorleifsson Gudmar, Holm Hilma, Edvardsson Vidar, Walters G Bragi, Styrkarsdottir Unnur, Gudbjartsson Daniel F, Sulem Patrick, Halldorsson Bjarni V, de Vegt Femmie, d'Ancona Frank C H, den Heijer Martin, Franzson Leifur, Christiansen Claus, Alexandersen Peter, Rafnar Thorunn, Kristjansson Kristleifur, Sigurdsson Gunnar, Kiemeney Lambertus A, Bodvarsson Magnus, Indridason Olafur S, Palsson Runolfur, Kong Augustine, Thorsteinsdottir Unnur, Stefansson Ka |
| Polymorphisms in CaSR and CLDN14 Genes Associated with Increased Risk of Kidney Stone Disease in Patients from the Eastern Part of India. PloS one 2015 10 (6): e0130790. Guha Manalee, Bankura Biswabandhu, Ghosh Sudakshina, Pattanayak Arup Kumar, Ghosh Saurabh, Pal Dilip Kumar, Puri Anurag, Kundu Anup Kumar, Das Madhusud |
| A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density. Scientific reports 2016 Feb 6 19877. Tang Ruqi, Wei Yiran, Li Zhiqiang, Chen Haoyan, Miao Qi, Bian Zhaolian, Zhang Haiyan, Wang Qixia, Wang Zhaoyue, Lian Min, Yang Fan, Jiang Xiang, Yang Yue, Li Enling, Seldin Michael F, Gershwin M Eric, Liao Wilson, Shi Yongyong, Ma Xio |
| Genetic Variants Associated with Circulating Parathyroid Hormone.
Journal of the American Society of Nephrology : JASN 2016 Dec . Robinson-Cohen Cassianne, Lutsey Pamela L, Kleber Marcus E, Nielson Carrie M, Mitchell Braxton D, Bis Joshua C, Eny Karen M, Portas Laura, Eriksson Joel, Lorentzon Mattias, Koller Daniel L, Milaneschi Yuri, Teumer Alexander, Pilz Stefan, Nethander Maria, Selvin Elizabeth, Tang Weihong, Weng Lu-Chen, Wong Hoi Suen, Lai Dongbing, Peacock Munro, Hannemann Anke, Völker Uwe, Homuth Georg, Nauk Matthias, Murgia Federico, Pattee Jack W, Orwoll Eric, Zmuda Joseph M, Riancho Jose Antonio, Wolf Myles, Williams Frances, Penninx Brenda, Econs Michael J, Ryan Kathleen A, Ohlsson Claes, Paterson Andrew D, Psaty Bruce M, Siscovick David S, Rotter Jerome I, Pirastu Mario, Streeten Elizabeth, März Winfried, Fox Caroline, Coresh Josef, Wallaschofski Henri, Pankow James S, de Boer Ian H, Kestenbaum Bry |
| A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect. Human genetics 2016 Nov . Pater Justin A, Benteau Tammy, Griffin Anne, Penney Cindy, Stanton Susan G, Predham Sarah, Kielley Bernadine, Squires Jessica, Zhou Jiayi, Li Quan, Abdelfatah Nelly, O'Rielly Darren D, Young Terry-Ly |
| Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease. Frontiers in genetics 2019 10 76. Gallego-Martinez Alvaro, Requena Teresa, Roman-Naranjo Pablo, Lopez-Escamez Jose |
| 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 |
| 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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