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    Results: 1 to 20 of 87

    2.

    Emerging trends in the search for genetic variants predisposing to human obesity.

    Swarbrick MM, Vaisse C.

    Curr Opin Clin Nutr Metab Care. 2003 Jul;6(4):369-75. Review.

    PMID:
    12806208
    [PubMed - indexed for MEDLINE]
    3.

    Towards a complete resolution of the genetic architecture of disease.

    Singleton AB, Hardy J, Traynor BJ, Houlden H.

    Trends Genet. 2010 Oct;26(10):438-42.

    PMID:
    20813421
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    Hundreds of variants clustered in genomic loci and biological pathways affect human height.

    Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segrè AV, Speliotes EK, Wheeler E, Soranzo N, Park JH, Yang J, Gudbjartsson D, Heard-Costa NL, Randall JC, Qi L, Vernon Smith A, Mägi R, Pastinen T, Liang L, Heid IM, Luan J, Thorleifsson G, Winkler TW, Goddard ME, Sin Lo K, Palmer C, Workalemahu T, Aulchenko YS, Johansson A, Zillikens MC, Feitosa MF, Esko T, Johnson T, Ketkar S, Kraft P, Mangino M, Prokopenko I, Absher D, Albrecht E, Ernst F, Glazer NL, Hayward C, Hottenga JJ, Jacobs KB, Knowles JW, Kutalik Z, Monda KL, Polasek O, Preuss M, Rayner NW, Robertson NR, Steinthorsdottir V, Tyrer JP, Voight BF, Wiklund F, Xu J, Zhao JH, Nyholt DR, Pellikka N, Perola M, Perry JR, Surakka I, Tammesoo ML, Altmaier EL, Amin N, Aspelund T, Bhangale T, Boucher G, Chasman DI, Chen C, Coin L, Cooper MN, Dixon AL, Gibson Q, Grundberg E, Hao K, Juhani Junttila M, Kaplan LM, Kettunen J, König IR, Kwan T, Lawrence RW, Levinson DF, Lorentzon M, McKnight B, Morris AP, Müller M, Suh Ngwa J, Purcell S, Rafelt S, Salem RM, Salvi E, Sanna S, Shi J, Sovio U, Thompson JR, Turchin MC, Vandenput L, Verlaan DJ, Vitart V, White CC, Ziegler A, Almgren P, Balmforth AJ, Campbell H, Citterio L, De Grandi A, Dominiczak A, Duan J, Elliott P, Elosua R, Eriksson JG, Freimer NB, Geus EJ, Glorioso N, Haiqing S, Hartikainen AL, Havulinna AS, Hicks AA, Hui J, Igl W, Illig T, Jula A, Kajantie E, Kilpeläinen TO, Koiranen M, Kolcic I, Koskinen S, Kovacs P, Laitinen J, Liu J, Lokki ML, Marusic A, Maschio A, Meitinger T, Mulas A, Paré G, Parker AN, Peden JF, Petersmann A, Pichler I, Pietiläinen KH, Pouta A, Ridderstråle M, Rotter JI, Sambrook JG, Sanders AR, Schmidt CO, Sinisalo J, Smit JH, Stringham HM, Bragi Walters G, Widen E, Wild SH, Willemsen G, Zagato L, Zgaga L, Zitting P, Alavere H, Farrall M, McArdle WL, Nelis M, Peters MJ, Ripatti S, van Meurs JB, Aben KK, Ardlie KG, Beckmann JS, Beilby JP, Bergman RN, Bergmann S, Collins FS, Cusi D, den Heijer M, Eiriksdottir G, Gejman PV, Hall AS, Hamsten A, Huikuri HV, Iribarren C, Kähönen M, Kaprio J, Kathiresan S, Kiemeney L, Kocher T, Launer LJ, Lehtimäki T, Melander O, Mosley TH Jr, Musk AW, Nieminen MS, O'Donnell CJ, Ohlsson C, Oostra B, Palmer LJ, Raitakari O, Ridker PM, Rioux JD, Rissanen A, Rivolta C, Schunkert H, Shuldiner AR, Siscovick DS, Stumvoll M, Tönjes A, Tuomilehto J, van Ommen GJ, Viikari J, Heath AC, Martin NG, Montgomery GW, Province MA, Kayser M, Arnold AM, Atwood LD, Boerwinkle E, Chanock SJ, Deloukas P, Gieger C, Grönberg H, Hall P, Hattersley AT, Hengstenberg C, Hoffman W, Lathrop GM, Salomaa V, Schreiber S, Uda M, Waterworth D, Wright AF, Assimes TL, Barroso I, Hofman A, Mohlke KL, Boomsma DI, Caulfield MJ, Cupples LA, Erdmann J, Fox CS, Gudnason V, Gyllensten U, Harris TB, Hayes RB, Jarvelin MR, Mooser V, Munroe PB, Ouwehand WH, Penninx BW, Pramstaller PP, Quertermous T, Rudan I, Samani NJ, Spector TD, Völzke H, Watkins H, Wilson JF, Groop LC, Haritunians T, Hu FB, Kaplan RC, Metspalu A, North KE, Schlessinger D, Wareham NJ, Hunter DJ, O'Connell JR, Strachan DP, Wichmann HE, Borecki IB, van Duijn CM, Schadt EE, Thorsteinsdottir U, Peltonen L, Uitterlinden AG, Visscher PM, Chatterjee N, Loos RJ, Boehnke M, McCarthy MI, Ingelsson E, Lindgren CM, Abecasis GR, Stefansson K, Frayling TM, Hirschhorn JN.

    Nature. 2010 Oct 14;467(7317):832-8. Epub 2010 Sep 29.

    PMID:
    20881960
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    5.

    Replication strategies for rare variant complex trait association studies via next-generation sequencing.

    Liu DJ, Leal SM.

    Am J Hum Genet. 2010 Dec 10;87(6):790-801.

    PMID:
    21129725
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    Final Report on Carcinogens Background Document for Styrene.

    National Toxicology Program.

    Rep Carcinog Backgr Doc. 2008 Sep;(8-5978):i-398.

    PMID:
    20737009
    [PubMed - as supplied by publisher]
    7.

    An evaluation of statistical approaches to rare variant analysis in genetic association studies.

    Morris AP, Zeggini E.

    Genet Epidemiol. 2010 Feb;34(2):188-93.

    PMID:
    19810025
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    [Development of antituberculous drugs: current status and future prospects].

    Tomioka H, Namba K.

    Kekkaku. 2006 Dec;81(12):753-74. Review. Japanese.

    PMID:
    17240921
    [PubMed - indexed for MEDLINE]
    9.

    The allelic architecture of human disease genes: common disease-common variant...or not?

    Pritchard JK, Cox NJ.

    Hum Mol Genet. 2002 Oct 1;11(20):2417-23. Review.

    PMID:
    12351577
    [PubMed - indexed for MEDLINE]
    Free Article
    10.

    Identification of causal sequence variants of disease in the next generation sequencing era.

    Kingsley CB.

    Methods Mol Biol. 2011;700:37-46. Review.

    PMID:
    21204025
    [PubMed - indexed for MEDLINE]
    11.

    Health-related disparities: influence of environmental factors.

    Olden K, White SL.

    Med Clin North Am. 2005 Jul;89(4):721-38. Review.

    PMID:
    15925646
    [PubMed - indexed for MEDLINE]
    12.

    The genetic basis of complex traits: rare variants or "common gene, common disease"?

    Iyengar SK, Elston RC.

    Methods Mol Biol. 2007;376:71-84.

    PMID:
    17984539
    [PubMed - indexed for MEDLINE]
    13.

    The relative importance of common and rare genetic variants in the development of hypertriglyceridemia.

    Evans D, Aberle J, Beil FU.

    Expert Rev Cardiovasc Ther. 2011 May;9(5):637-44. Review.

    PMID:
    21615327
    [PubMed - indexed for MEDLINE]
    14.

    From genomic advances to public health benefits: the unbearable lightness of being stuck.

    Rudan I, Rudan P.

    Coll Antropol. 2004 Dec;28(2):483-507.

    PMID:
    15666582
    [PubMed - indexed for MEDLINE]
    15.

    Genetic association studies of complex traits: design and analysis issues.

    Newton-Cheh C, Hirschhorn JN.

    Mutat Res. 2005 Jun 3;573(1-2):54-69. Review.

    PMID:
    15829237
    [PubMed - indexed for MEDLINE]
    16.

    Finding the missing heritability of complex diseases.

    Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, Rotimi CN, Slatkin M, Valle D, Whittemore AS, Boehnke M, Clark AG, Eichler EE, Gibson G, Haines JL, Mackay TF, McCarroll SA, Visscher PM.

    Nature. 2009 Oct 8;461(7265):747-53. Review.

    PMID:
    19812666
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    Genome-wide association studies for complex traits: consensus, uncertainty and challenges.

    McCarthy MI, Abecasis GR, Cardon LR, Goldstein DB, Little J, Ioannidis JP, Hirschhorn JN.

    Nat Rev Genet. 2008 May;9(5):356-69. Review.

    PMID:
    18398418
    [PubMed - indexed for MEDLINE]
    18.

    Uncovering the roles of rare variants in common disease through whole-genome sequencing.

    Cirulli ET, Goldstein DB.

    Nat Rev Genet. 2010 Jun;11(6):415-25. Review.

    PMID:
    20479773
    [PubMed - indexed for MEDLINE]
    19.

    Molecular genetics of human intracranial aneurysms.

    Zhang J, Claterbuck RE.

    Int J Stroke. 2008 Nov;3(4):272-87. Review.

    PMID:
    18811744
    [PubMed - indexed for MEDLINE]
    20.

    Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

    Visscher PM, Goddard ME, Derks EM, Wray NR.

    Mol Psychiatry. 2011 Jun 14. doi: 10.1038/mp.2011.65. [Epub ahead of print]

    PMID:
    21670730
    [PubMed - as supplied by publisher]

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