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    Results: 1 to 50 of 264

    1.

    The Role of Body Mass Index, Insulin, and Adiponectin in the Relation Between Fat Distribution and Bone Mineral Density.

    Zillikens MC, Uitterlinden AG, van Leeuwen JP, Berends AL, Henneman P, van Dijk KW, Oostra BA, van Duijn CM, Pols HA, Rivadeneira F.

    Calcif Tissue Int. 2009 Dec 3. [Epub ahead of print]PMID: 19957167 [PubMed - as supplied by publisher]Related articles

    2.

    The association of serum testosterone levels and ventricular repolarization.

    van Noord C, Dörr M, Sturkenboom MC, Straus SM, Reffelmann T, Felix SB, Hofman A, Kors JA, Haring R, de Jong FH, Nauck M, Uitterlinden AG, Wallaschofski H, Witteman JC, Völzke H, Stricker BH.

    Eur J Epidemiol. 2009 Dec 3. [Epub ahead of print]PMID: 19957021 [PubMed - as supplied by publisher]Related articles

    3.

    The PCLO gene and depressive disorders: replication in a population-based study.

    Hek K, Mulder CL, Luijendijk HJ, van Duijn CM, Hofman A, Uitterlinden AG, Tiemeier H.

    Hum Mol Genet. 2009 Nov 26. [Epub ahead of print]PMID: 19942622 [PubMed - as supplied by publisher]Related articles

    4.

    The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring.

    Vujkovic M, Steegers EA, van Meurs J, Yazdanpanah N, van Rooij IA, Uitterlinden AG, Steegers-Theunissen RP.

    Eur J Clin Nutr. 2009 Nov 25. [Epub ahead of print]PMID: 19935819 [PubMed - as supplied by publisher]Related articles

    5.

    Interaction between polymorphisms in the OCT1 and MATE1 transporter and metformin response.

    Becker ML, Visser LE, van Schaik RH, Hofman A, Uitterlinden AG, Stricker BH.

    Pharmacogenet Genomics. 2009 Nov 5. [Epub ahead of print]PMID: 19898263 [PubMed - as supplied by publisher]Related articles

    6.

    Common genetic variation in the ABCB1 gene is associated with the cholesterol-lowering effect of simvastatin in males.

    Becker ML, Visser LE, van Schaik RH, Hofman A, Uitterlinden AG, Stricker BH.

    Pharmacogenomics. 2009 Nov;10(11):1743-51.PMID: 19891551 [PubMed - in process]Related articles

    7.

    Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

    Ganesh SK, Zakai NA, van Rooij FJ, Soranzo N, Smith AV, Nalls MA, Chen MH, Kottgen A, Glazer NL, Dehghan A, Kuhnel B, Aspelund T, Yang Q, Tanaka T, Jaffe A, Bis JC, Verwoert GC, Teumer A, Fox CS, Guralnik JM, Ehret GB, Rice K, Felix JF, Rendon A, Eiriksdottir G, Levy D, Patel KV, Boerwinkle E, Rotter JI, Hofman A, Sambrook JG, Hernandez DG, Zheng G, Bandinelli S, Singleton AB, Coresh J, Lumley T, Uitterlinden AG, Vangils JM, Launer LJ, Cupples LA, Oostra BA, Zwaginga JJ, Ouwehand WH, Thein SL, Meisinger C, Deloukas P, Nauck M, Spector TD, Gieger C, Gudnason V, van Duijn CM, Psaty BM, Ferrucci L, Chakravarti A, Greinacher A, O'Donnell CJ, Witteman JC, Furth S, Cushman M, Harris TB, Lin JP.

    Nat Genet. 2009 Nov;41(11):1191-8. Epub 2009 Oct 11.PMID: 19862010 [PubMed - in process]Related articles

    8.

    Genetic association analysis of LARS2 with type 2 diabetes.

    Reiling E, Jafar-Mohammadi B, van 't Riet E, Weedon MN, van Vliet-Ostaptchouk JV, Hansen T, Saxena R, van Haeften TW, Arp PA, Das S, Nijpels G, Groenewoud MJ, van Hove EC, Uitterlinden AG, Smit JW, Morris AD, Doney AS, Palmer CN, Guiducci C, Hattersley AT, Frayling TM, Pedersen O, Slagboom PE, Altshuler DM, Groop L, Romijn JA, Maassen JA, Hofker MH, Dekker JM, McCarthy MI, 't Hart LM.

    Diabetologia. 2009 Oct 22. [Epub ahead of print]PMID: 19847392 [PubMed - as supplied by publisher]Related articles

    9.

    Association of the exon 3 deleted/full-length GHR polymorphism with recombinant growth hormone dose in growth hormone-deficient adults.

    Meyer S, Schaefer S, Stolk L, Arp P, Uitterlinden AG, Plöckinger U, Stalla GK, Tuschy U, Weber MM, Weise A, Pfützner A, Kann PH.

    Pharmacogenomics. 2009 Oct;10(10):1599-608.PMID: 19842933 [PubMed - in process]Related articles

    10.

    Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture.

    Richards JB, Kavvoura FK, Rivadeneira F, Styrkársdóttir U, Estrada K, Halldórsson BV, Hsu YH, Zillikens MC, Wilson SG, Mullin BH, Amin N, Aulchenko YS, Cupples LA, Deloukas P, Demissie S, Hofman A, Kong A, Karasik D, van Meurs JB, Oostra BA, Pols HA, Sigurdsson G, Thorsteinsdottir U, Soranzo N, Williams FM, Zhou Y, Ralston SH, Thorleifsson G, van Duijn CM, Kiel DP, Stefansson K, Uitterlinden AG, Ioannidis JP, Spector TD; Genetic Factors for Osteoporosis Consortium.

    Ann Intern Med. 2009 Oct 20;151(8):528-37.PMID: 19841454 [PubMed - indexed for MEDLINE]Related articles

    11.

    Vascular endothelial growth factor polymorphisms are associated with endocardial cushion defects: a family based case-control study.

    Smedts HP, Isaacs A, de Costa D, Uitterlinden AG, van Duijn CM, Gittenberger-de Groot AC, Helbing WA, Steegers EA, Steegers-Theunissen RP.

    Pediatr Res. 2009 Sep 23. [Epub ahead of print]PMID: 19816237 [PubMed - as supplied by publisher]Related articles

    12.

    Genetic variation in the renin-angiotensin system and arterial stiffness. The Rotterdam study.

    Sie MP, Yazdanpanah M, Mattace-Raso FU, Uitterlinden AG, Hofman A, Hoeks AP, Reneman RS, Asmar R, Van Duijn CM, Witteman JC.

    Clin Exp Hypertens. 2009 Jul;31(5):389-99.PMID: 19811349 [PubMed - in process]Related articles

    13.

    Influence of genetic variation in CYP3A4 and ABCB1 on dose decrease or switching during simvastatin and atorvastatin therapy.

    Becker ML, Visser LE, van Schaik RH, Hofman A, Uitterlinden AG, Ch Stricker BH.

    Pharmacoepidemiol Drug Saf. 2009 Oct 2. [Epub ahead of print]PMID: 19802823 [PubMed - as supplied by publisher]Related articles

    14.

    Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.

    Rivadeneira F, Styrkársdottir U, Estrada K, Halldórsson BV, Hsu YH, Richards JB, Zillikens MC, Kavvoura FK, Amin N, Aulchenko YS, Cupples LA, Deloukas P, Demissie S, Grundberg E, Hofman A, Kong A, Karasik D, van Meurs JB, Oostra B, Pastinen T, Pols HA, Sigurdsson G, Soranzo N, Thorleifsson G, Thorsteinsdottir U, Williams FM, Wilson SG, Zhou Y, Ralston SH, van Duijn CM, Spector T, Kiel DP, Stefansson K, Ioannidis JP, Uitterlinden AG; Genetic Factors for Osteoporosis (GEFOS) Consortium.

    Nat Genet. 2009 Nov;41(11):1199-206. Epub 2009 Oct 4.PMID: 19801982 [PubMed - in process]Related articles

    15.

    Low prevalence of NOD2 SNPs in Behçet's disease suggests protective association in Caucasians.

    Kappen JH, Wallace GR, Stolk L, Rivadeneira F, Uitterlinden AG, van Daele PL, Laman JD, Kuijpers RW, Baarsma GS, Stanford MR, Fortune F, Madanat W, van Hagen PM, van Laar JA.

    Rheumatology (Oxford). 2009 Nov;48(11):1375-7. Epub 2009 Sep 11.PMID: 19748964 [PubMed - in process]Related articles

    16.

    SIRT1 genetic variation is related to BMI and risk of obesity.

    Zillikens MC, van Meurs JB, Rivadeneira F, Amin N, Hofman A, Oostra BA, Sijbrands EJ, Witteman JC, Pols HA, van Duijn CM, Uitterlinden AG.

    Diabetes. 2009 Dec;58(12):2828-34. Epub 2009 Sep 9.PMID: 19741164 [PubMed - in process]Related articles

    17.

    Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.

    van Es MA, Veldink JH, Saris CG, Blauw HM, van Vught PW, Birve A, Lemmens R, Schelhaas HJ, Groen EJ, Huisman MH, van der Kooi AJ, de Visser M, Dahlberg C, Estrada K, Rivadeneira F, Hofman A, Zwarts MJ, van Doormaal PT, Rujescu D, Strengman E, Giegling I, Muglia P, Tomik B, Slowik A, Uitterlinden AG, Hendrich C, Waibel S, Meyer T, Ludolph AC, Glass JD, Purcell S, Cichon S, Nöthen MM, Wichmann HE, Schreiber S, Vermeulen SH, Kiemeney LA, Wokke JH, Cronin S, McLaughlin RL, Hardiman O, Fumoto K, Pasterkamp RJ, Meininger V, Melki J, Leigh PN, Shaw CE, Landers JE, Al-Chalabi A, Brown RH Jr, Robberecht W, Andersen PM, Ophoff RA, van den Berg LH.

    Nat Genet. 2009 Oct;41(10):1083-7. Epub 2009 Sep 6.PMID: 19734901 [PubMed - indexed for MEDLINE]Related articles

    18.

    The Rotterdam Study: 2010 objectives and design update.

    Hofman A, Breteler MM, van Duijn CM, Janssen HL, Krestin GP, Kuipers EJ, Stricker BH, Tiemeier H, Uitterlinden AG, Vingerling JR, Witteman JC.

    Eur J Epidemiol. 2009;24(9):553-72.PMID: 19728115 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    GRIMP: a web- and grid-based tool for high-speed analysis of large-scale genome-wide association using imputed data.

    Estrada K, Abuseiris A, Grosveld FG, Uitterlinden AG, Knoch TA, Rivadeneira F.

    Bioinformatics. 2009 Oct 15;25(20):2750-2. Epub 2009 Aug 21.PMID: 19700477 [PubMed - in process]Related articlesFree article

    20.

    Vitamin D status, bone mineral density, and the development of radiographic osteoarthritis of the knee: The Rotterdam Study.

    Bergink AP, Uitterlinden AG, Van Leeuwen JP, Buurman CJ, Hofman A, Verhaar JA, Pols HA.

    J Clin Rheumatol. 2009 Aug;15(5):230-7.PMID: 19654490 [PubMed - indexed for MEDLINE]Related articles

    21.

    Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.

    Eijgelsheim M, Newton-Cheh C, Aarnoudse AL, van Noord C, Witteman JC, Hofman A, Uitterlinden AG, Stricker BH.

    Hum Mol Genet. 2009 Nov 1;18(21):4213-8. Epub 2009 Jul 30.PMID: 19643915 [PubMed - in process]Related articles

    22.

    Evaluation of risk prediction updates from commercial genome-wide scans.

    Mihaescu R, van Hoek M, Sijbrands EJ, Uitterlinden AG, Witteman JC, Hofman A, van Duijn CM, Janssens AC.

    Genet Med. 2009 Aug;11(8):588-94.PMID: 19636253 [PubMed - in process]Related articles

    23.

    Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies.

    Mook-Kanamori DO, de Kort SW, van Duijn CM, Uitterlinden AG, Hofman A, Moll HA, Steegers EA, Hokken-Koelega AC, Jaddoe VW.

    BMC Med Genet. 2009 Jul 17;10:67.PMID: 19615048 [PubMed - indexed for MEDLINE]Related articlesFree article

    24.

    Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.

    Benjamin EJ, Rice KM, Arking DE, Pfeufer A, van Noord C, Smith AV, Schnabel RB, Bis JC, Boerwinkle E, Sinner MF, Dehghan A, Lubitz SA, D'Agostino RB Sr, Lumley T, Ehret GB, Heeringa J, Aspelund T, Newton-Cheh C, Larson MG, Marciante KD, Soliman EZ, Rivadeneira F, Wang TJ, Eiríksdottir G, Levy D, Psaty BM, Li M, Chamberlain AM, Hofman A, Vasan RS, Harris TB, Rotter JI, Kao WH, Agarwal SK, Stricker BH, Wang K, Launer LJ, Smith NL, Chakravarti A, Uitterlinden AG, Wolf PA, Sotoodehnia N, Köttgen A, van Duijn CM, Meitinger T, Mueller M, Perz S, Steinbeck G, Wichmann HE, Lunetta KL, Heckbert SR, Gudnason V, Alonso A, Kääb S, Ellinor PT, Witteman JC.

    Nat Genet. 2009 Aug;41(8):879-81. Epub 2009 Jul 13.PMID: 19597492 [PubMed - indexed for MEDLINE]Related articles

    25.

    A study of the SORL1 gene in Alzheimer's disease and cognitive function.

    Liu F, Ikram MA, Janssens AC, Schuur M, de Koning I, Isaacs A, Struchalin M, Uitterlinden AG, den Dunnen JT, Sleegers K, Bettens K, Van Broeckhoven C, van Swieten J, Hofman A, Oostra BA, Aulchenko YS, Breteler MM, van Duijn CM.

    J Alzheimers Dis. 2009;18(1):51-64.PMID: 19584446 [PubMed - in process]Related articles

    26.

    Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.

    Vasan RS, Glazer NL, Felix JF, Lieb W, Wild PS, Felix SB, Watzinger N, Larson MG, Smith NL, Dehghan A, Grosshennig A, Schillert A, Teumer A, Schmidt R, Kathiresan S, Lumley T, Aulchenko YS, König IR, Zeller T, Homuth G, Struchalin M, Aragam J, Bis JC, Rivadeneira F, Erdmann J, Schnabel RB, Dörr M, Zweiker R, Lind L, Rodeheffer RJ, Greiser KH, Levy D, Haritunians T, Deckers JW, Stritzke J, Lackner KJ, Völker U, Ingelsson E, Kullo I, Haerting J, O'Donnell CJ, Heckbert SR, Stricker BH, Ziegler A, Reffelmann T, Redfield MM, Werdan K, Mitchell GF, Rice K, Arnett DK, Hofman A, Gottdiener JS, Uitterlinden AG, Meitinger T, Blettner M, Friedrich N, Wang TJ, Psaty BM, van Duijn CM, Wichmann HE, Munzel TF, Kroemer HK, Benjamin EJ, Rotter JI, Witteman JC, Schunkert H, Schmidt H, Völzke H, Blankenberg S.

    JAMA. 2009 Jul 8;302(2):168-78.PMID: 19584346 [PubMed - indexed for MEDLINE]Related articles

    27.

    No modification of the beneficial effect of NSAIDs on colorectal cancer by CYP2C9 genotype.

    Siemes C, Eijgelsheim M, Dieleman JP, van Schaik RH, Uitterlinden AG, van Duijn CM, Hofman A, Coebergh JW, Stricker BH, Visser LE.

    Neth J Med. 2009 Apr;67(4):134-41.PMID: 19581657 [PubMed - in process]Related articlesFree article

    28.

    A genome-wide association study of acenocoumarol maintenance dosage.

    Teichert M, Eijgelsheim M, Rivadeneira F, Uitterlinden AG, van Schaik RH, Hofman A, De Smet PA, van Gelder T, Visser LE, Stricker BH.

    Hum Mol Genet. 2009 Oct 1;18(19):3758-68. Epub 2009 Jul 4.PMID: 19578179 [PubMed - indexed for MEDLINE]Related articles

    29.

    Birth size, postnatal growth and growth during growth hormone treatment in small-for-gestational-age children: associations with IGF1 gene polymorphisms and haplotypes?

    Ester WA, van Meurs JB, Arends NJ, Uitterlinden AG, de Ridder MA, Hokken-Koelega AC.

    Horm Res. 2009;72(1):15-24. Epub 2009 Jun 30.PMID: 19571555 [PubMed - indexed for MEDLINE]Related articles

    30.

    A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.

    Estrada K, Krawczak M, Schreiber S, van Duijn K, Stolk L, van Meurs JB, Liu F, Penninx BW, Smit JH, Vogelzangs N, Hottenga JJ, Willemsen G, de Geus EJ, Lorentzon M, von Eller-Eberstein H, Lips P, Schoor N, Pop V, de Keijzer J, Hofman A, Aulchenko YS, Oostra BA, Ohlsson C, Boomsma DI, Uitterlinden AG, van Duijn CM, Rivadeneira F, Kayser M.

    Hum Mol Genet. 2009 Sep 15;18(18):3516-24. Epub 2009 Jul 1.PMID: 19570815 [PubMed - in process]Related articlesFree article

    31.

    Variation at the ANP32A gene is associated with risk of hip osteoarthritis in women.

    Valdes AM, Lories RJ, van Meurs JB, Kerkhof H, Doherty S, Hofman A, Hart DJ, Zhang F, Luyten FP, Uitterlinden AG, Doherty M, Spector TD.

    Arthritis Rheum. 2009 Jul;60(7):2046-54.PMID: 19565487 [PubMed - indexed for MEDLINE]Related articles

    32.

    NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.

    Heard-Costa NL, Zillikens MC, Monda KL, Johansson A, Harris TB, Fu M, Haritunians T, Feitosa MF, Aspelund T, Eiriksdottir G, Garcia M, Launer LJ, Smith AV, Mitchell BD, McArdle PF, Shuldiner AR, Bielinski SJ, Boerwinkle E, Brancati F, Demerath EW, Pankow JS, Arnold AM, Chen YD, Glazer NL, McKnight B, Psaty BM, Rotter JI, Amin N, Campbell H, Gyllensten U, Pattaro C, Pramstaller PP, Rudan I, Struchalin M, Vitart V, Gao X, Kraja A, Province MA, Zhang Q, Atwood LD, Dupuis J, Hirschhorn JN, Jaquish CE, O'Donnell CJ, Vasan RS, White CC, Aulchenko YS, Estrada K, Hofman A, Rivadeneira F, Uitterlinden AG, Witteman JC, Oostra BA, Kaplan RC, Gudnason V, O'Connell JR, Borecki IB, van Duijn CM, Cupples LA, Fox CS, North KE.

    PLoS Genet. 2009 Jun;5(6):e1000539. Epub 2009 Jun 26.PMID: 19557197 [PubMed - indexed for MEDLINE]Related articlesFree article

    33.

    Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.

    Lindgren CM, Heid IM, Randall JC, Lamina C, Steinthorsdottir V, Qi L, Speliotes EK, Thorleifsson G, Willer CJ, Herrera BM, Jackson AU, Lim N, Scheet P, Soranzo N, Amin N, Aulchenko YS, Chambers JC, Drong A, Luan J, Lyon HN, Rivadeneira F, Sanna S, Timpson NJ, Zillikens MC, Zhao JH, Almgren P, Bandinelli S, Bennett AJ, Bergman RN, Bonnycastle LL, Bumpstead SJ, Chanock SJ, Cherkas L, Chines P, Coin L, Cooper C, Crawford G, Doering A, Dominiczak A, Doney AS, Ebrahim S, Elliott P, Erdos MR, Estrada K, Ferrucci L, Fischer G, Forouhi NG, Gieger C, Grallert H, Groves CJ, Grundy S, Guiducci C, Hadley D, Hamsten A, Havulinna AS, Hofman A, Holle R, Holloway JW, Illig T, Isomaa B, Jacobs LC, Jameson K, Jousilahti P, Karpe F, Kuusisto J, Laitinen J, Lathrop GM, Lawlor DA, Mangino M, McArdle WL, Meitinger T, Morken MA, Morris AP, Munroe P, Narisu N, Nordström A, Nordström P, Oostra BA, Palmer CN, Payne F, Peden JF, Prokopenko I, Renström F, Ruokonen A, Salomaa V, Sandhu MS, Scott LJ, Scuteri A, Silander K, Song K, Yuan X, Stringham HM, Swift AJ, Tuomi T, Uda M, Vollenweider P, Waeber G, Wallace C, Walters GB, Weedon MN; Wellcome Trust Case Control Consortium, Witteman JC, Zhang C, Zhang W, Caulfield MJ, Collins FS, Davey Smith G, Day IN, Franks PW, Hattersley AT, Hu FB, Jarvelin MR, Kong A, Kooner JS, Laakso M, Lakatta E, Mooser V, Morris AD, Peltonen L, Samani NJ, Spector TD, Strachan DP, Tanaka T, Tuomilehto J, Uitterlinden AG, van Duijn CM, Wareham NJ, Hugh Watkins; Procardis Consortia, Waterworth DM, Boehnke M, Deloukas P, Groop L, Hunter DJ, Thorsteinsdottir U, Schlessinger D, Wichmann HE, Frayling TM, Abecasis GR, Hirschhorn JN, Loos RJ, Stefansson K, Mohlke KL, Barroso I, McCarthy MI; Giant Consortium.

    PLoS Genet. 2009 Jun;5(6):e1000508. Epub 2009 Jun 26. Erratum in: PLoS Genet. 2009 Jul;5(7). doi: 10.1371/annotation/b6e8f9f6-2496-4a40-b0e3-e1d1390c1928. PMID: 19557161 [PubMed - indexed for MEDLINE]Related articlesFree article

    34.

    Vitamin D binding protein genotype and osteoporosis.

    Fang Y, van Meurs JB, Arp P, van Leeuwen JP, Hofman A, Pols HA, Uitterlinden AG.

    Calcif Tissue Int. 2009 Aug;85(2):85-93. Epub 2009 Jun 2.PMID: 19488670 [PubMed - indexed for MEDLINE]Related articlesFree article

    35.

    Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand.

    Evangelou E, Chapman K, Meulenbelt I, Karassa FB, Loughlin J, Carr A, Doherty M, Doherty S, Gómez-Reino JJ, Gonzalez A, Halldorsson BV, Hauksson VB, Hofman A, Hart DJ, Ikegawa S, Ingvarsson T, Jiang Q, Jonsdottir I, Jonsson H, Kerkhof HJ, Kloppenburg M, Lane NE, Li J, Lories RJ, van Meurs JB, Näkki A, Nevitt MC, Rodriguez-Lopez J, Shi D, Slagboom PE, Stefansson K, Tsezou A, Wallis GA, Watson CM, Spector TD, Uitterlinden AG, Valdes AM, Ioannidis JP.

    Arthritis Rheum. 2009 Jun;60(6):1710-21.PMID: 19479880 [PubMed - indexed for MEDLINE]Related articles

    36.

    Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.

    Perry JR, Stolk L, Franceschini N, Lunetta KL, Zhai G, McArdle PF, Smith AV, Aspelund T, Bandinelli S, Boerwinkle E, Cherkas L, Eiriksdottir G, Estrada K, Ferrucci L, Folsom AR, Garcia M, Gudnason V, Hofman A, Karasik D, Kiel DP, Launer LJ, van Meurs J, Nalls MA, Rivadeneira F, Shuldiner AR, Singleton A, Soranzo N, Tanaka T, Visser JA, Weedon MN, Wilson SG, Zhuang V, Streeten EA, Harris TB, Murray A, Spector TD, Demerath EW, Uitterlinden AG, Murabito JM.

    Nat Genet. 2009 May 17. [Epub ahead of print]PMID: 19448620 [PubMed - as supplied by publisher]Related articles

    37.

    Loci at chromosomes 13, 19 and 20 influence age at natural menopause.

    Stolk L, Zhai G, van Meurs JB, Verbiest MM, Visser JA, Estrada K, Rivadeneira F, Williams FM, Cherkas L, Deloukas P, Soranzo N, de Keyzer JJ, Pop VJ, Lips P, Lebrun CE, van der Schouw YT, Grobbee DE, Witteman J, Hofman A, Pols HA, Laven JS, Spector TD, Uitterlinden AG.

    Nat Genet. 2009 May 17. [Epub ahead of print]PMID: 19448619 [PubMed - as supplied by publisher]Related articles

    38.

    Multiple loci associated with indices of renal function and chronic kidney disease.

    Köttgen A, Glazer NL, Dehghan A, Hwang SJ, Katz R, Li M, Yang Q, Gudnason V, Launer LJ, Harris TB, Smith AV, Arking DE, Astor BC, Boerwinkle E, Ehret GB, Ruczinski I, Scharpf RB, Ida Chen YD, de Boer IH, Haritunians T, Lumley T, Sarnak M, Siscovick D, Benjamin EJ, Levy D, Upadhyay A, Aulchenko YS, Hofman A, Rivadeneira F, Uitterlinden AG, van Duijn CM, Chasman DI, Paré G, Ridker PM, Kao WH, Witteman JC, Coresh J, Shlipak MG, Fox CS.

    Nat Genet. 2009 May 10. [Epub ahead of print]PMID: 19430482 [PubMed - as supplied by publisher]Related articles

    39.

    Genome-wide association study of blood pressure and hypertension.

    Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Köttgen A, Vasan RS, Rivadeneira F, Eiriksdottir G, Guo X, Arking DE, Mitchell GF, Mattace-Raso FU, Smith AV, Taylor K, Scharpf RB, Hwang SJ, Sijbrands EJ, Bis J, Harris TB, Ganesh SK, O'Donnell CJ, Hofman A, Rotter JI, Coresh J, Benjamin EJ, Uitterlinden AG, Heiss G, Fox CS, Witteman JC, Boerwinkle E, Wang TJ, Gudnason V, Larson MG, Chakravarti A, Psaty BM, van Duijn CM.

    Nat Genet. 2009 May 10. [Epub ahead of print]PMID: 19430479 [PubMed - as supplied by publisher]Related articles

    40.

    Genome-wide association meta-analysis for total serum bilirubin levels.

    Johnson AD, Kavousi M, Smith AV, Chen MH, Dehghan A, Aspelund T, Lin JP, van Duijn CM, Harris TB, Cupples LA, Uitterlinden AG, Launer L, Hofman A, Rivadeneira F, Stricker B, Yang Q, O'Donnell CJ, Gudnason V, Witteman JC.

    Hum Mol Genet. 2009 Jul 15;18(14):2700-10. Epub 2009 May 4.PMID: 19414484 [PubMed - indexed for MEDLINE]Related articles

    41.

    BclI glucocorticoid receptor polymorphism and smoking in the general population.

    Siiskonen SJ, Visser LE, Tiemeier H, Hofman A, Lamberts SW, Uitterlinden AG, Stricker BH.

    Addict Biol. 2009 Jul;14(3):349-55. Epub 2009 Apr 28.PMID: 19413563 [PubMed - indexed for MEDLINE]Related articles

    42.

    Genetic variation in the fibrinogen-alpha and fibrinogen-gamma genes in relation to arterial stiffness: the Rotterdam Study.

    Sie MP, Isaacs A, de Maat MP, Mattace-Raso FU, Uitterlinden AG, Kardys I, Hofman A, Hoeks AP, Reneman RS, van Duijn CM, Witteman JC.

    J Hypertens. 2009 Jul;27(7):1392-8.PMID: 19412134 [PubMed - indexed for MEDLINE]Related articles

    43.

    Genetic polymorphisms of GnRH and gonadotrophic hormone receptors affect the phenotype of polycystic ovary syndrome.

    Valkenburg O, Uitterlinden AG, Piersma D, Hofman A, Themmen AP, de Jong FH, Fauser BC, Laven JS.

    Hum Reprod. 2009 Aug;24(8):2014-22. Epub 2009 Apr 29.PMID: 19403562 [PubMed - indexed for MEDLINE]Related articles

    44.

    Genetic variation in the organic cation transporter 1 is associated with metformin response in patients with diabetes mellitus.

    Becker ML, Visser LE, van Schaik RH, Hofman A, Uitterlinden AG, Stricker BH.

    Pharmacogenomics J. 2009 Aug;9(4):242-7. Epub 2009 Apr 21.PMID: 19381165 [PubMed - indexed for MEDLINE]Related articles

    45.

    Genomewide association studies of stroke.

    Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, Debette S, Lumley T, Folsom AR, van den Herik EG, Bos MJ, Beiser A, Cushman M, Launer LJ, Shahar E, Struchalin M, Du Y, Glazer NL, Rosamond WD, Rivadeneira F, Kelly-Hayes M, Lopez OL, Coresh J, Hofman A, DeCarli C, Heckbert SR, Koudstaal PJ, Yang Q, Smith NL, Kase CS, Rice K, Haritunians T, Roks G, de Kort PL, Taylor KD, de Lau LM, Oostra BA, Uitterlinden AG, Rotter JI, Boerwinkle E, Psaty BM, Mosley TH, van Duijn CM, Breteler MM, Longstreth WT Jr, Wolf PA.

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    46.

    Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.

    Soranzo N, Rivadeneira F, Chinappen-Horsley U, Malkina I, Richards JB, Hammond N, Stolk L, Nica A, Inouye M, Hofman A, Stephens J, Wheeler E, Arp P, Gwilliam R, Jhamai PM, Potter S, Chaney A, Ghori MJ, Ravindrarajah R, Ermakov S, Estrada K, Pols HA, Williams FM, McArdle WL, van Meurs JB, Loos RJ, Dermitzakis ET, Ahmadi KR, Hart DJ, Ouwehand WH, Wareham NJ, Barroso I, Sandhu MS, Strachan DP, Livshits G, Spector TD, Uitterlinden AG, Deloukas P.

    PLoS Genet. 2009 Apr;5(4):e1000445. Epub 2009 Apr 3.PMID: 19343178 [PubMed - indexed for MEDLINE]Related articlesFree article

    47.

    Common variants at ten loci influence QT interval duration in the QTGEN Study.

    Newton-Cheh C, Eijgelsheim M, Rice KM, de Bakker PI, Yin X, Estrada K, Bis JC, Marciante K, Rivadeneira F, Noseworthy PA, Sotoodehnia N, Smith NL, Rotter JI, Kors JA, Witteman JC, Hofman A, Heckbert SR, O'Donnell CJ, Uitterlinden AG, Psaty BM, Lumley T, Larson MG, Stricker BH.

    Nat Genet. 2009 Apr;41(4):399-406. Epub 2009 Mar 22.PMID: 19305408 [PubMed - indexed for MEDLINE]Related articlesFree article

    48.

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    Liu F, van Duijn K, Vingerling JR, Hofman A, Uitterlinden AG, Janssens AC, Kayser M.

    Curr Biol. 2009 Mar 10;19(5):R192-3. No abstract available. PMID: 19278628 [PubMed - indexed for MEDLINE]Related articles

    49.

    Genome-wide association study of smoking initiation and current smoking.

    Vink JM, Smit AB, de Geus EJ, Sullivan P, Willemsen G, Hottenga JJ, Smit JH, Hoogendijk WJ, Zitman FG, Peltonen L, Kaprio J, Pedersen NL, Magnusson PK, Spector TD, Kyvik KO, Morley KI, Heath AC, Martin NG, Westendorp RG, Slagboom PE, Tiemeier H, Hofman A, Uitterlinden AG, Aulchenko YS, Amin N, van Duijn C, Penninx BW, Boomsma DI.

    Am J Hum Genet. 2009 Mar;84(3):367-79. Epub 2009 Mar 5.PMID: 19268276 [PubMed - indexed for MEDLINE]Related articlesFree article

    50.

    Genetic variation in the multidrug and toxin extrusion 1 transporter protein influences the glucose-lowering effect of metformin in patients with diabetes: a preliminary study.

    Becker ML, Visser LE, van Schaik RH, Hofman A, Uitterlinden AG, Stricker BH.

    Diabetes. 2009 Mar;58(3):745-9. Epub 2009 Feb 19.PMID: 19228809 [PubMed - indexed for MEDLINE]Related articlesFree article

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