124 related articles for article (PubMed ID: 27448670)
1. The rs12917707 polymorphism at the UMOD locus and glomerular filtration rate in individuals with type 2 diabetes: evidence of heterogeneity across two different European populations.
Prudente S; Di Paola R; Copetti M; Lucchesi D; Lamacchia O; Pezzilli S; Mercuri L; Alberico F; Giusti L; Garofolo M; Penno G; Cignarelli M; De Cosmo S; Trischitta V
Nephrol Dial Transplant; 2017 Oct; 32(10):1718-1722. PubMed ID: 27448670
[TBL] [Abstract][Full Text] [Related]
2. Investigation of known estimated glomerular filtration rate loci in patients with type 2 diabetes.
Deshmukh HA; Palmer CN; Morris AD; Colhoun HM
Diabet Med; 2013 Oct; 30(10):1230-5. PubMed ID: 23586973
[TBL] [Abstract][Full Text] [Related]
3. Next generation sequencing search for uromodulin gene variants related with impaired renal function.
Gómez J; Díaz-Corte C; Tranche S; Alvarez F; Iglesias S; Alonso B; Coto E
Mol Biol Rep; 2015 Sep; 42(9):1353-8. PubMed ID: 26040415
[TBL] [Abstract][Full Text] [Related]
4. Uromodulin rs4293393 T>C variation is associated with kidney disease in patients with type 2 diabetes.
Kumar V; Yadav AK; Kumar V; Bhansali A; Jha V
Indian J Med Res; 2017 Nov; 146(Suppol):S15-S21. PubMed ID: 29578190
[TBL] [Abstract][Full Text] [Related]
5. Uromodulin gene variant is associated with type 2 diabetic nephropathy.
Ahluwalia TS; Lindholm E; Groop L; Melander O
J Hypertens; 2011 Sep; 29(9):1731-4. PubMed ID: 21738052
[TBL] [Abstract][Full Text] [Related]
6. UMOD as a susceptibility gene for end-stage renal disease.
Reznichenko A; Böger CA; Snieder H; van den Born J; de Borst MH; Damman J; van Dijk MC; van Goor H; Hepkema BG; Hillebrands JL; Leuvenink HG; Niesing J; Bakker SJ; Seelen M; Navis G;
BMC Med Genet; 2012 Sep; 13():78. PubMed ID: 22947327
[TBL] [Abstract][Full Text] [Related]
7. UMOD polymorphism rs12917707 is not associated with severe or stable IgA nephropathy in a large Caucasian cohort.
Dinic M; Ghisdal L; Racapé J; Thibaudin L; Gatault P; Essig M; Le Meur Y; Noël C; Touchard G; Merville P; Ajarchouh Z; Mariat C; Abramowicz M; Abramowicz D; Alamartine E
BMC Nephrol; 2014 Aug; 15():138. PubMed ID: 25163389
[TBL] [Abstract][Full Text] [Related]
8. Uromodulin associates with cardiorenal function in patients with hypertension and cardiovascular disease.
Algharably EAH; Bolbrinker J; Lezius S; Reibis R; Wegscheider K; Völler H; Kreutz R
J Hypertens; 2017 Oct; 35(10):2053-2058. PubMed ID: 28598953
[TBL] [Abstract][Full Text] [Related]
9. Analysis of the association between rs12917707 and rs11864909 single nucleotide polymorphisms in the region of the uromoduline gene and chronic kidney disease - a family-based study.
Żywiec J; Kiliś-Pstrusińska K; Tomaszewski M; Grzeszczak W
Ann Agric Environ Med; 2017 Sep; 24(3):464-466. PubMed ID: 28954491
[TBL] [Abstract][Full Text] [Related]
10. Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.
Olden M; Corre T; Hayward C; Toniolo D; Ulivi S; Gasparini P; Pistis G; Hwang SJ; Bergmann S; Campbell H; Cocca M; Gandin I; Girotto G; Glaudemans B; Hastie ND; Loffing J; Polasek O; Rampoldi L; Rudan I; Sala C; Traglia M; Vollenweider P; Vuckovic D; Youhanna S; Weber J; Wright AF; Kutalik Z; Bochud M; Fox CS; Devuyst O
J Am Soc Nephrol; 2014 Aug; 25(8):1869-82. PubMed ID: 24578125
[TBL] [Abstract][Full Text] [Related]
11. A single nucleotide polymorphism in the UMOD promoter is associated with end stage renal disease.
Chen T; Wang Q; Li G; Wang L
BMC Med Genet; 2016 Dec; 17(1):95. PubMed ID: 27938332
[TBL] [Abstract][Full Text] [Related]
12. Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene.
Adam KM; Mohammed AM; Elamin AA
Medicine (Baltimore); 2020 Jan; 99(3):e18722. PubMed ID: 32011449
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.
Padmanabhan S; Melander O; Johnson T; Di Blasio AM; Lee WK; Gentilini D; Hastie CE; Menni C; Monti MC; Delles C; Laing S; Corso B; Navis G; Kwakernaak AJ; van der Harst P; Bochud M; Maillard M; Burnier M; Hedner T; Kjeldsen S; Wahlstrand B; Sjögren M; Fava C; Montagnana M; Danese E; Torffvit O; Hedblad B; Snieder H; Connell JM; Brown M; Samani NJ; Farrall M; Cesana G; Mancia G; Signorini S; Grassi G; Eyheramendy S; Wichmann HE; Laan M; Strachan DP; Sever P; Shields DC; Stanton A; Vollenweider P; Teumer A; Völzke H; Rettig R; Newton-Cheh C; Arora P; Zhang F; Soranzo N; Spector TD; Lucas G; Kathiresan S; Siscovick DS; Luan J; Loos RJ; Wareham NJ; Penninx BW; Nolte IM; McBride M; Miller WH; Nicklin SA; Baker AH; Graham D; McDonald RA; Pell JP; Sattar N; Welsh P; ; Munroe P; Caulfield MJ; Zanchetti A; Dominiczak AF
PLoS Genet; 2010 Oct; 6(10):e1001177. PubMed ID: 21082022
[TBL] [Abstract][Full Text] [Related]
14. Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations.
Bollée G; Dahan K; Flamant M; Morinière V; Pawtowski A; Heidet L; Lacombe D; Devuyst O; Pirson Y; Antignac C; Knebelmann B
Clin J Am Soc Nephrol; 2011 Oct; 6(10):2429-38. PubMed ID: 21868615
[TBL] [Abstract][Full Text] [Related]
15. Association of the Q121 variant of ENPP1 gene with decreased kidney function among patients with type 2 diabetes.
De Cosmo S; Minenna A; Zhang YY; Thompson R; Miscio G; Vedovato M; Rauseo A; Saller A; Mastroianno S; Pellegrini F; Trevisan R; Fioretto P; Doria A; Trischitta V
Am J Kidney Dis; 2009 Feb; 53(2):273-80. PubMed ID: 18950909
[TBL] [Abstract][Full Text] [Related]
16. Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans.
Guan M; Ma J; Keaton JM; Dimitrov L; Mudgal P; Stromberg M; Bonomo JA; Hicks PJ; Freedman BI; Bowden DW; Ng MC
Hum Genet; 2016 Nov; 135(11):1251-1262. PubMed ID: 27461219
[TBL] [Abstract][Full Text] [Related]
17. A comparison of type 2 diabetes risk allele load between African Americans and European Americans.
Keaton JM; Cooke Bailey JN; Palmer ND; Freedman BI; Langefeld CD; Ng MC; Bowden DW
Hum Genet; 2014 Dec; 133(12):1487-95. PubMed ID: 25273842
[TBL] [Abstract][Full Text] [Related]
18.
Wang J; Liu L; He K; Gao B; Wang F; Zhao M; Zhang L; On Behalf Of The Chinese Cohort Study Of Chronic Kidney Disease C-Stride
Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828293
[TBL] [Abstract][Full Text] [Related]
19. Association of estimated glomerular filtration rate and urinary uromodulin concentrations with rare variants identified by UMOD gene region sequencing.
Köttgen A; Yang Q; Shimmin LC; Tin A; Schaeffer C; Coresh J; Liu X; Rampoldi L; Hwang SJ; Boerwinkle E; Hixson JE; Kao WH; Fox CS
PLoS One; 2012; 7(5):e38311. PubMed ID: 22693617
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide association study of kidney function decline in individuals of European descent.
Gorski M; Tin A; Garnaas M; McMahon GM; Chu AY; Tayo BO; Pattaro C; Teumer A; Chasman DI; Chalmers J; Hamet P; Tremblay J; Woodward M; Aspelund T; Eiriksdottir G; Gudnason V; Harris TB; Launer LJ; Smith AV; Mitchell BD; O'Connell JR; Shuldiner AR; Coresh J; Li M; Freudenberger P; Hofer E; Schmidt H; Schmidt R; Holliday EG; Mitchell P; Wang JJ; de Boer IH; Li G; Siscovick DS; Kutalik Z; Corre T; Vollenweider P; Waeber G; Gupta J; Kanetsky PA; Hwang SJ; Olden M; Yang Q; de Andrade M; Atkinson EJ; Kardia SL; Turner ST; Stafford JM; Ding J; Liu Y; Barlassina C; Cusi D; Salvi E; Staessen JA; Ridker PM; Grallert H; Meisinger C; Müller-Nurasyid M; Krämer BK; Kramer H; Rosas SE; Nolte IM; Penninx BW; Snieder H; Fabiola Del Greco M; Franke A; Nöthlings U; Lieb W; Bakker SJ; Gansevoort RT; van der Harst P; Dehghan A; Franco OH; Hofman A; Rivadeneira F; Sedaghat S; Uitterlinden AG; Coassin S; Haun M; Kollerits B; Kronenberg F; Paulweber B; Aumann N; Endlich K; Pietzner M; Völker U; Rettig R; Chouraki V; Helmer C; Lambert JC; Metzger M; Stengel B; Lehtimäki T; Lyytikäinen LP; Raitakari O; Johnson A; Parsa A; Bochud M; Heid IM; Goessling W; Köttgen A; Kao WH; Fox CS; Böger CA
Kidney Int; 2015 May; 87(5):1017-29. PubMed ID: 25493955
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
