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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 7, 2023. (Total: 217722Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Gout and UMOD[original query]
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. GWAS Catalog
PLoS genetics 2010 Jul 6 (7): e1001039.
Gudbjartsson Daniel F, Holm Hilma, Indridason Olafur S, Thorleifsson Gudmar, Edvardsson Vidar, Sulem Patrick, de Vegt Femmie, d'Ancona Frank C H, den Heijer Martin, Wetzels Jack F M, Franzson Leifur, Rafnar Thorunn, Kristjansson Kristleifur, Bjornsdottir Unnur S, Eyjolfsson Gudmundur I, Kiemeney Lambertus A, Kong Augustine, Palsson Runolfur, Thorsteinsdottir Unnur, Stefansson Ka
Association between genotype and phenotype in uromodulin-associated kidney disease.
Clinical journal of the American Society of Nephrology : CJASN 2013 Aug 8 (8): 1349-57.
Moskowitz Jonathan L, Piret Sian E, Lhotta Karl, Kitzler Thomas M, Tashman Adam P, Velez Erin, Thakker Rajesh V, Kotanko Pet
Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2018 5 72 (3): 411-418.
Ayasreh Nadia, Bullich Gemma, Miquel Rosa, Furlano Mónica, Ruiz Patricia, Lorente Laura, Valero Oliver, García-González Miguel Angel, Arhda Nisrine, Garin Intza, Martínez Víctor, Pérez-Gómez Vanessa, Fulladosa Xavier, Arroyo David, Martínez-Vea Alberto, Espinosa Mario, Ballarín Jose, Ars Elisabet, Torra Ros
Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease.
BMC nephrology 2018 10 19 (1): 301.
Gast Christine, Marinaki Anthony, Arenas-Hernandez Monica, Campbell Sara, Seaby Eleanor G, Pengelly Reuben J, Gale Daniel P, Connor Thomas M, Bunyan David J, Hoda?ová Kate?ina, Živná Martina, Kmoch Stanislav, Ennis Sarah, Venkat-Raman
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
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
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