These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 26272126)

  • 21. Calcium kidney stones are associated with a haplotype of the calcium-sensing receptor gene regulatory region.
    Vezzoli G; Terranegra A; Arcidiacono T; Gambaro G; Milanesi L; Mosca E; Soldati L;
    Nephrol Dial Transplant; 2010 Jul; 25(7):2245-52. PubMed ID: 20067903
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Temporal trends in the incidence of kidney stone disease.
    Edvardsson VO; Indridason OS; Haraldsson G; Kjartansson O; Palsson R
    Kidney Int; 2013 Jan; 83(1):146-52. PubMed ID: 22992468
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Stones: Gene variants associated with formation.
    Stone L
    Nat Rev Urol; 2015 Oct; 12(10):536. PubMed ID: 26334086
    [No Abstract]   [Full Text] [Related]  

  • 24. Association between calcium-sensing receptor gene polymorphisms and recurrent calcium kidney stone disease: a comprehensive gene analysis.
    Shakhssalim N; Kazemi B; Basiri A; Houshmand M; Pakmanesh H; Golestan B; Eilanjegh AF; Kashi AH; Kilani M; Azadvari M
    Scand J Urol Nephrol; 2010 Dec; 44(6):406-12. PubMed ID: 20602573
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Association between metabolic syndrome and the presence of kidney stones in a screened population.
    Jeong IG; Kang T; Bang JK; Park J; Kim W; Hwang SS; Kim HK; Park HK
    Am J Kidney Dis; 2011 Sep; 58(3):383-8. PubMed ID: 21620546
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetics of kidney stone disease-Polygenic meets monogenic.
    Halbritter J
    Nephrol Ther; 2021 Apr; 17S():S88-S94. PubMed ID: 33910705
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association of urokinase gene 3'-UTR polymorphism with calcium oxalate nephrolithiasis.
    Mittal RD; Bid HK; Kumar A; Bhandari M
    J Endourol; 2006 Feb; 20(2):157-60. PubMed ID: 16509805
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Antioxidants and self-reported history of kidney stones: the National Health and Nutrition Examination Survey.
    Holoch PA; Tracy CR
    J Endourol; 2011 Dec; 25(12):1903-8. PubMed ID: 21864023
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genome-wide association studies: potential next steps on a genetic journey.
    McCarthy MI; Hirschhorn JN
    Hum Mol Genet; 2008 Oct; 17(R2):R156-65. PubMed ID: 18852205
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Diversity in non-repetitive human sequences not found in the reference genome.
    Kehr B; Helgadottir A; Melsted P; Jonsson H; Helgason H; Jonasdottir A; Jonasdottir A; Sigurdsson A; Gylfason A; Halldorsson GH; Kristmundsdottir S; Thorgeirsson G; Olafsson I; Holm H; Thorsteinsdottir U; Sulem P; Helgason A; Gudbjartsson DF; Halldorsson BV; Stefansson K
    Nat Genet; 2017 Apr; 49(4):588-593. PubMed ID: 28250455
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Weighting sequence variants based on their annotation increases power of whole-genome association studies.
    Sveinbjornsson G; Albrechtsen A; Zink F; Gudjonsson SA; Oddson A; Másson G; Holm H; Kong A; Thorsteinsdottir U; Sulem P; Gudbjartsson DF; Stefansson K
    Nat Genet; 2016 Mar; 48(3):314-7. PubMed ID: 26854916
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Past, present and future of genomics for kidney stone disease.
    Jahrreiss V; Özsoy M; Seitz C; Somani B
    Curr Opin Urol; 2023 Mar; 33(2):73-76. PubMed ID: 36710592
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
    Sigurdsson S; Alexandersson KF; Sulem P; Feenstra B; Gudmundsdottir S; Halldorsson GH; Olafsson S; Sigurdsson A; Rafnar T; Thorgeirsson T; Sørensen E; Nordholm-Carstensen A; Burcharth J; Andersen J; Jørgensen HS; Possfelt-Møller E; Ullum H; Thorleifsson G; Masson G; Thorsteinsdottir U; Melbye M; Gudbjartsson DF; Stefansson T; Jonsdottir I; Stefansson K
    Nat Commun; 2017 Jun; 8():15789. PubMed ID: 28585551
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of sequence variants influencing immunoglobulin levels.
    Jonsson S; Sveinbjornsson G; de Lapuente Portilla AL; Swaminathan B; Plomp R; Dekkers G; Ajore R; Ali M; Bentlage AEH; Elmér E; Eyjolfsson GI; Gudjonsson SA; Gullberg U; Gylfason A; Halldorsson BV; Hansson M; Holm H; Johansson Å; Johnsson E; Jonasdottir A; Ludviksson BR; Oddsson A; Olafsson I; Olafsson S; Sigurdardottir O; Sigurdsson A; Stefansdottir L; Masson G; Sulem P; Wuhrer M; Wihlborg AK; Thorleifsson G; Gudbjartsson DF; Thorsteinsdottir U; Vidarsson G; Jonsdottir I; Nilsson B; Stefansson K
    Nat Genet; 2017 Aug; 49(8):1182-1191. PubMed ID: 28628107
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.
    Styrkarsdottir U; Thorleifsson G; Helgadottir HT; Bomer N; Metrustry S; Bierma-Zeinstra S; Strijbosch AM; Evangelou E; Hart D; Beekman M; Jonasdottir A; Sigurdsson A; Eiriksson FF; Thorsteinsdottir M; Frigge ML; Kong A; Gudjonsson SA; Magnusson OT; Masson G; ; ; Hofman A; Arden NK; Ingvarsson T; Lohmander S; Kloppenburg M; Rivadeneira F; Nelissen RG; Spector T; Uitterlinden A; Slagboom PE; Thorsteinsdottir U; Jonsdottir I; Valdes AM; Meulenbelt I; van Meurs J; Jonsson H; Stefansson K
    Nat Genet; 2014 May; 46(5):498-502. PubMed ID: 24728293
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sequence variants associating with urinary biomarkers.
    Benonisdottir S; Kristjansson RP; Oddsson A; Steinthorsdottir V; Mikaelsdottir E; Kehr B; Jensson BO; Arnadottir GA; Sulem G; Sveinbjornsson G; Kristmundsdottir S; Ivarsdottir EV; Tragante V; Gunnarsson B; Runolfsdottir HL; Arthur JG; Deaton AM; Eyjolfsson GI; Davidsson OB; Asselbergs FW; Hreidarsson AB; Rafnar T; Thorleifsson G; Edvardsson V; Sigurdsson G; Helgadottir A; Halldorsson BV; Masson G; Holm H; Onundarson PT; Indridason OS; Benediktsson R; Palsson R; Gudbjartsson DF; Olafsson I; Thorsteinsdottir U; Sulem P; Stefansson K
    Hum Mol Genet; 2019 Apr; 28(7):1199-1211. PubMed ID: 30476138
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.
    Ivarsdottir EV; Holm H; Benonisdottir S; Olafsdottir T; Sveinbjornsson G; Thorleifsson G; Eggertsson HP; Halldorsson GH; Hjorleifsson KE; Melsted P; Gylfason A; Arnadottir GA; Oddsson A; Jensson BO; Jonasdottir A; Jonasdottir A; Juliusdottir T; Stefansdottir L; Tragante V; Halldorsson BV; Petersen H; Thorgeirsson G; Thorsteinsdottir U; Sulem P; Hinriksdottir I; Jonsdottir I; Gudbjartsson DF; Stefansson K
    Commun Biol; 2021 Jun; 4(1):706. PubMed ID: 34108613
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Joint mouse-human phenome-wide association to test gene function and disease risk.
    Wang X; Pandey AK; Mulligan MK; Williams EG; Mozhui K; Li Z; Jovaisaite V; Quarles LD; Xiao Z; Huang J; Capra JA; Chen Z; Taylor WL; Bastarache L; Niu X; Pollard KS; Ciobanu DC; Reznik AO; Tishkov AV; Zhulin IB; Peng J; Nelson SF; Denny JC; Auwerx J; Lu L; Williams RW
    Nat Commun; 2016 Feb; 7():10464. PubMed ID: 26833085
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic polymorphisms in CLDN14 (rs219780) and ALP (rs1256328) genes are associated with risk of nephrolithiasis in Egyptian children.
    Elshamaa MF; Fadel FI; Kamel S; Farouk H; Alahmady M; Ramadan Y
    Turk J Urol; 2021 Jan; 47(1):73-80. PubMed ID: 33052825
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Association of
    Litvinova MM; Khafizov K; Korchagin VI; Speranskaya AS; Asanov AY; Matsvay AD; Kiselev DA; Svetlichnaya DV; Nuralieva SZ; Moskalev AA; Filippova TV
    Front Genet; 2021; 12():621049. PubMed ID: 34054913
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.