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GRANTOMICS


Grant Database|Publication|PHGKB
Last data update: Mar 19, 2019. (Total: 54184 Records)
      HHS Only

Query Trace: Grant ID>>N01HC025195

Scientific literature funded by the grant(s) selected

11 publications from Genomics & Health Impact Scan Database.



433 publications from HuGE Literature Finder.

  • Validated SNPs for eGFR and their associations with albuminuria. External Web Site Icon
    Human molecular genetics 2012 Jul 21 (14): 3293-8.
    Ellis Jaclyn W, Chen Ming-Huei, Foster Meredith C, Liu Ching-Ti, Larson Martin G, de Boer Ian, Köttgen Anna, Parsa Afshin, Bochud Murielle, Böger Carsten A, Kao Linda, Fox Caroline S, O'Seaghdha Conall M, ,
  • The relationship of estrogen receptor-alpha and -beta genes with osteoarthritis of the hand. External Web Site Icon
    The Journal of rheumatology 2009 Dec 36 (12): 2772-9.
    Wise Barton L, Demissie Serkalem, Cupples L Adrienne, Felson David T, Yang Mei, Shearman Amanda M, Aliabadi Piran, Hunter David J
  • Multiple loci associated with indices of renal function and chronic kidney disease. External Web Site Icon
    Nature genetics 2009 Jun 41 (6): 712-7.
    Köttgen Anna, Glazer Nicole L, Dehghan Abbas, Hwang Shih-Jen, Katz Ronit, Li Man, Yang Qiong, Gudnason Vilmundur, Launer Lenore J, Harris Tamara B, Smith Albert V, Arking Dan E, Astor Brad C, Boerwinkle Eric, Ehret Georg B, Ruczinski Ingo, Scharpf Robert B, Chen Yii-Der Ida, de Boer Ian H, Haritunians Talin, Lumley Thomas, Sarnak Mark, Siscovick David, Benjamin Emelia J, Levy Daniel, Upadhyay Ashish, Aulchenko Yurii S, Hofman Albert, Rivadeneira Fernando, Uitterlinden André G, van Duijn Cornelia M, Chasman Daniel I, Paré Guillaume, Ridker Paul M, Kao W H Linda, Witteman Jacqueline C, Coresh Josef, Shlipak Michael G, Fox Caroline S
  • Variants in the CNR1 and the FAAH genes and adiposity traits in the community. External Web Site Icon
    Obesity (Silver Spring, Md.) 2009 Apr 17 (4): 755-60.
    Lieb Wolfgang, Manning Alisa K, Florez Jose C, Dupuis Josée, Cupples L Adrienne, McAteer Jarred B, Vasan Ramachandran S, Hoffmann Udo, O'Donnell Christopher J, Meigs James B, Fox Caroline S
  • Haplotypes and gene expression implicate the MAPT region for Parkinson disease. The GenePD Study. External Web Site Icon
    Neurology 2008 May .
    Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, Goldwurm S, Pezzoli G, Singer C, Saint-Hilaire MH, Hendricks AE, Williamson S, Nagle MW, Wilk JB, Massood T, Laramie JM, Destefano AL, Litvan I, Nicholson G, Corbett A, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Sherman S, Al-Hinti J, Drasby E, Nance M, Moller AT, Ostergaard K, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH,
  • Genome-wide association of sleep and circadian phenotypes. External Web Site Icon
    BMC medical genetics 2007 8 Suppl 1 S9.
    Gottlieb Daniel J, O'Connor George T, Wilk Jemma B

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