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    Results: 1 to 50 of 79

    1.

    Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene.

    Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Floyd J, Hastie N, Knott S, Lauc G, Pichler I, Rotim K, Wild SH, Zorkoltseva IV, Wilson JF, Rudan I, Campbell H, Pattaro C, Pramstaller P, Oostra BA, Wright AF, van Duijn CM, Aulchenko YS, Gyllensten U; for the EUROSPAN Consortium.

    Obesity (Silver Spring). 2009 Oct 22. [Epub ahead of print]PMID: 19851299 [PubMed - as supplied by publisher]Related articles

    2.

    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

    3.

    Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.

    Hoppenbrouwers IA, Aulchenko YS, Janssens AC, Ramagopalan SV, Broer L, Kayser M, Ebers GC, Oostra BA, van Duijn CM, Hintzen RQ.

    J Hum Genet. 2009 Nov;54(11):676-80. Epub 2009 Oct 16.PMID: 19834503 [PubMed - in process]Related articles

    4.

    A powerful genome-wide feasible approach to detect parent-of-origin effects in studies of quantitative traits.

    Belonogova NM, Axenovich TI, Aulchenko YS.

    Eur J Hum Genet. 2009 Oct 7. [Epub ahead of print]PMID: 19809476 [PubMed - as supplied by publisher]Related articles

    5.

    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

    6.

    Novel strategy to identify genetic risk factors for COPD severity: a genetic isolate.

    van Diemen CC, Postma DS, Aulchenko YS, Snijders PJ, Oostra BA, van Duijn CM, Boezen HM.

    Eur Respir J. 2009 Sep 24. [Epub ahead of print]PMID: 19797132 [PubMed - as supplied by publisher]Related articles

    7.

    Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins.

    Kollerits B, Coassin S, Beckmann ND, Teumer A, Kiechl S, Döring A, Kavousi M, Hunt SC, Lamina C, Paulweber B, Kutalik Z, Nauck M, van Duijn CM, Heid IM, Willeit J, Brandstätter A, Adams TD, Mooser V, Aulchenko YS, Völzke H, Kronenberg F.

    Hum Mol Genet. 2009 Dec 1;18(23):4669-76. Epub 2009 Sep 3.PMID: 19729411 [PubMed - in process]Related articlesFree article

    8.

    Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease.

    Combarros O, van Duijn CM, Hammond N, Belbin O, Arias-Vásquez A, Cortina-Borja M, Lehmann MG, Aulchenko YS, Schuur M, Kölsch H, Heun R, Wilcock GK, Brown K, Kehoe PG, Harrison R, Coto E, Alvarez V, Deloukas P, Mateo I, Gwilliam R, Morgan K, Warden DR, Smith AD, Lehmann DJ.

    J Neuroinflammation. 2009 Aug 23;6:22.PMID: 19698145 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Shared genetic factors in the co-occurrence of symptoms of depression and cardiovascular risk factors.

    López-León S, Aulchenko YS, Tiemeier H, Oostra BA, van Duijn CM, Janssens AC.

    J Affect Disord. 2009 Aug 10. [Epub ahead of print]PMID: 19674795 [PubMed - as supplied by publisher]Related articles

    10.

    PedStr software for cutting large pedigrees for haplotyping, IBD computation and multipoint linkage analysis.

    Kirichenko AV, Belonogova NM, Aulchenko YS, Axenovich TI.

    Ann Hum Genet. 2009 Sep;73(Pt 5):527-31. Epub 2009 Jul 9.PMID: 19604226 [PubMed - in process]Related articles

    11.

    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

    12.

    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

    13.

    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

    14.

    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

    15.

    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

    16.

    Association of FGFR2 gene polymorphisms with the risk of breast cancer in population of West Siberia.

    Boyarskikh UA, Zarubina NA, Biltueva JA, Sinkina TV, Voronina EN, Lazarev AF, Petrova VD, Aulchenko YS, Filipenko ML.

    Eur J Hum Genet. 2009 Dec;17(12):1688-91. Epub 2009 Jun 17.PMID: 19536173 [PubMed - in process]Related articles

    17.

    Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated population.

    Axenovich TI, Zorkoltseva IV, Belonogova NM, Struchalin MV, Kirichenko AV, Kayser M, Oostra BA, van Duijn CM, Aulchenko YS.

    Hum Genet. 2009 Sep;126(3):457-71. Epub 2009 May 24.PMID: 19466457 [PubMed - indexed for MEDLINE]Related articles

    18.

    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

    19.

    Genome-wide linkage analysis of serum creatinine in three isolated European populations.

    Pattaro C, Aulchenko YS, Isaacs A, Vitart V, Hayward C, Franklin CS, Polasek O, Kolcic I, Biloglav Z, Campbell S, Hastie N, Lauc G, Meitinger T, Oostra BA, Gyllensten U, Wilson JF, Pichler I, Hicks AA, Campbell H, Wright AF, Rudan I, van Duijn CM, Riegler P, Marroni F, Pramstaller PP; EUROSPAN Consortium.

    Kidney Int. 2009 Aug;76(3):297-306. Epub 2009 Apr 22.PMID: 19387472 [PubMed - in process]Related articles

    20.

    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.

    N Engl J Med. 2009 Apr 23;360(17):1718-28. Epub 2009 Apr 15.PMID: 19369658 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    Genetic factors influence the clustering of depression among individuals with lower socioeconomic status.

    López-León S, Choy WC, Aulchenko YS, Claes SJ, Oostra BA, Mackenbach JP, van Duijn CM, Janssens AC.

    PLoS One. 2009;4(3):e5069. Epub 2009 Mar 31.PMID: 19333388 [PubMed - indexed for MEDLINE]Related articlesFree article

    22.

    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

    23.

    Predicting human height by Victorian and genomic methods.

    Aulchenko YS, Struchalin MV, Belonogova NM, Axenovich TI, Weedon MN, Hofman A, Uitterlinden AG, Kayser M, Oostra BA, van Duijn CM, Janssens AC, Borodin PM.

    Eur J Hum Genet. 2009 Aug;17(8):1070-5. Epub 2009 Feb 18.PMID: 19223933 [PubMed - indexed for MEDLINE]Related articles

    24.

    Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population.

    Amin N, Aulchenko YS, Dekker MC, Ferdinand RF, van Spreeken A, Temmink AH, Verhulst FC, Oostra BA, van Duijn CM.

    Eur J Hum Genet. 2009 Jul;17(7):958-66. Epub 2009 Jan 21.PMID: 19156173 [PubMed - indexed for MEDLINE]Related articles

    25.

    Role of shared genetic and environmental factors in symptoms of depression and body composition.

    Choy WC, López-León S, Aulchenko YS, Mackenbach JP, Oostra BA, van Duijn CM, Janssens AC.

    Psychiatr Genet. 2009 Feb;19(1):32-8.PMID: 19125106 [PubMed - indexed for MEDLINE]Related articles

    26.

    Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.

    Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Penninx BW, Janssens AC, Wilson JF, Spector T, Martin NG, Pedersen NL, Kyvik KO, Kaprio J, Hofman A, Freimer NB, Jarvelin MR, Gyllensten U, Campbell H, Rudan I, Johansson A, Marroni F, Hayward C, Vitart V, Jonasson I, Pattaro C, Wright A, Hastie N, Pichler I, Hicks AA, Falchi M, Willemsen G, Hottenga JJ, de Geus EJ, Montgomery GW, Whitfield J, Magnusson P, Saharinen J, Perola M, Silander K, Isaacs A, Sijbrands EJ, Uitterlinden AG, Witteman JC, Oostra BA, Elliott P, Ruokonen A, Sabatti C, Gieger C, Meitinger T, Kronenberg F, Döring A, Wichmann HE, Smit JH, McCarthy MI, van Duijn CM, Peltonen L; ENGAGE Consortium.

    Nat Genet. 2009 Jan;41(1):47-55. Epub 2008 Dec 7.PMID: 19060911 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    The apolipoprotein E gene and its age-specific effects on cognitive function.

    Liu F, Pardo LM, Schuur M, Sanchez-Juan P, Isaacs A, Sleegers K, de Koning I, Zorkoltseva IV, Axenovich TI, Witteman JC, Janssens AC, van Swieten JC, Aulchenko YS, Oostra BA, van Duijn CM.

    Neurobiol Aging. 2008 Nov 10. [Epub ahead of print]PMID: 19004527 [PubMed - as supplied by publisher]Related articles

    28.

    Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.

    Aulchenko YS, Hoppenbrouwers IA, Ramagopalan SV, Broer L, Jafari N, Hillert J, Link J, Lundström W, Greiner E, Dessa Sadovnick A, Goossens D, Van Broeckhoven C, Del-Favero J, Ebers GC, Oostra BA, van Duijn CM, Hintzen RQ.

    Nat Genet. 2008 Dec;40(12):1402-3. Epub 2008 Nov 9.PMID: 18997785 [PubMed - indexed for MEDLINE]Related articles

    29.

    Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.

    Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Dunlop MG, Floyd J, Hastie N, Hofman A, Knott S, Kolcic I, Pichler I, Polasek O, Rivadeneira F, Tenesa A, Uitterlinden AG, Wild SH, Zorkoltseva IV, Meitinger T, Wilson JF, Rudan I, Campbell H, Pattaro C, Pramstaller P, Oostra BA, Wright AF, van Duijn CM, Aulchenko YS, Gyllensten U; EUROSPAN Consortium.

    Hum Mol Genet. 2009 Jan 15;18(2):373-80. Epub 2008 Oct 24.PMID: 18952825 [PubMed - indexed for MEDLINE]Related articles

    30.

    Sex-specific genetic effects influence variation in body composition.

    Zillikens MC, Yazdanpanah M, Pardo LM, Rivadeneira F, Aulchenko YS, Oostra BA, Uitterlinden AG, Pols HA, van Duijn CM.

    Diabetologia. 2008 Dec;51(12):2233-41. Epub 2008 Oct 7.PMID: 18839131 [PubMed - indexed for MEDLINE]Related articles

    31.

    Angiotensinogen M235T polymorphism and symptoms of depression in a population-based study and a family-based study.

    López-León S, Janssens AC, Tiemeier H, Hofman A, Aulchenko YS, Snijders PJ, Claes S, Oostra BA, van Duijn CM.

    Psychiatr Genet. 2008 Aug;18(4):162-6.PMID: 18628677 [PubMed - indexed for MEDLINE]Related articles

    32.

    Familial aggregation of preeclampsia and intrauterine growth restriction in a genetically isolated population in The Netherlands.

    Berends AL, Steegers EA, Isaacs A, Aulchenko YS, Liu F, de Groot CJ, Oostra BA, van Duijn CM.

    Eur J Hum Genet. 2008 Dec;16(12):1437-42. Epub 2008 Jul 9.PMID: 18612323 [PubMed - indexed for MEDLINE]Related articles

    33.

    Prevalence and heritability of the metabolic syndrome and its individual components in a Dutch isolate: the Erasmus Rucphen Family study.

    Henneman P, Aulchenko YS, Frants RR, van Dijk KW, Oostra BA, van Duijn CM.

    J Med Genet. 2008 Sep;45(9):572-7. Epub 2008 Jun 11.PMID: 18550697 [PubMed - indexed for MEDLINE]Related articles

    34.

    Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.

    Franke L, de Kovel CG, Aulchenko YS, Trynka G, Zhernakova A, Hunt KA, Blauw HM, van den Berg LH, Ophoff R, Deloukas P, van Heel DA, Wijmenga C.

    Am J Hum Genet. 2008 Jun;82(6):1316-33.PMID: 18519066 [PubMed - indexed for MEDLINE]Related articlesFree article

    35.

    Rapid and robust association mapping of expression quantitative trait loci.

    Lam AC, Schouten M, Aulchenko YS, Haley CS, de Koning DJ.

    BMC Proc. 2007;1 Suppl 1:S144. Epub 2007 Dec 18.PMID: 18466488 [PubMed - in process]Related articlesFree article

    36.

    EVI5 is a risk gene for multiple sclerosis.

    Hoppenbrouwers IA, Aulchenko YS, Ebers GC, Ramagopalan SV, Oostra BA, van Duijn CM, Hintzen RQ.

    Genes Immun. 2008 Jun;9(4):334-7. Epub 2008 Apr 10.PMID: 18401352 [PubMed - indexed for MEDLINE]Related articles

    37.

    Cyclin-dependent kinase 5 is associated with risk for Alzheimer's disease in a Dutch population-based study.

    Arias-Vásquez A, Aulchenko YS, Isaacs A, van Oosterhout A, Sleegers K, Hofman A, van Broeckhoven C, Oostra BA, Breteler M, van Duijn CM.

    J Neurol. 2008 May;255(5):655-62. Epub 2008 Mar 20.PMID: 18350355 [PubMed - indexed for MEDLINE]Related articles

    38.

    Maternal transmission of multiple sclerosis in a dutch population.

    Hoppenbrouwers IA, Liu F, Aulchenko YS, Ebers GC, Oostra BA, van Duijn CM, Hintzen RQ.

    Arch Neurol. 2008 Mar;65(3):345-8.PMID: 18332246 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    An approach for cutting large and complex pedigrees for linkage analysis.

    Liu F, Kirichenko A, Axenovich TI, van Duijn CM, Aulchenko YS.

    Eur J Hum Genet. 2008 Jul;16(7):854-60. Epub 2008 Feb 27.PMID: 18301450 [PubMed - indexed for MEDLINE]Related articlesFree article

    40.

    Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.

    Kayser M, Liu F, Janssens AC, Rivadeneira F, Lao O, van Duijn K, Vermeulen M, Arp P, Jhamai MM, van Ijcken WF, den Dunnen JT, Heath S, Zelenika D, Despriet DD, Klaver CC, Vingerling JR, de Jong PT, Hofman A, Aulchenko YS, Uitterlinden AG, Oostra BA, van Duijn CM.

    Am J Hum Genet. 2008 Feb;82(2):411-23. Epub 2008 Jan 25. Erratum in: Am J Hum Genet. 2008 Mar;82(3):801. PMID: 18252221 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

    A genomic background based method for association analysis in related individuals.

    Amin N, van Duijn CM, Aulchenko YS.

    PLoS One. 2007 Dec 5;2(12):e1274.PMID: 18060068 [PubMed - indexed for MEDLINE]Related articlesFree article

    42.

    Breaking loops in large complex pedigrees.

    Axenovich TI, Zorkoltseva IV, Liu F, Kirichenko AV, Aulchenko YS.

    Hum Hered. 2008;65(2):57-65. Epub 2007 Sep 26. Review.PMID: 17898536 [PubMed - indexed for MEDLINE]Related articlesFree article

    43.

    LPIN2 is associated with type 2 diabetes, glucose metabolism, and body composition.

    Aulchenko YS, Pullen J, Kloosterman WP, Yazdanpanah M, Hofman A, Vaessen N, Snijders PJ, Zubakov D, Mackay I, Olavesen M, Sidhu B, Smith VE, Carey A, Berezikov E, Uitterlinden AG, Plasterk RH, Oostra BA, van Duijn CM.

    Diabetes. 2007 Dec;56(12):3020-6. Epub 2007 Sep 5.PMID: 17804763 [PubMed - indexed for MEDLINE]Related articlesFree article

    44.

    Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis.

    Aulchenko YS, de Koning DJ, Haley C.

    Genetics. 2007 Sep;177(1):577-85. Epub 2007 Jul 29.PMID: 17660554 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    Genetic contributions to glaucoma: heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphology.

    van Koolwijk LM, Despriet DD, van Duijn CM, Pardo Cortes LM, Vingerling JR, Aulchenko YS, Oostra BA, Klaver CC, Lemij HG.

    Invest Ophthalmol Vis Sci. 2007 Aug;48(8):3669-76.PMID: 17652737 [PubMed - indexed for MEDLINE]Related articlesFree article

    46.

    A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.

    Liu F, Arias-Vásquez A, Sleegers K, Aulchenko YS, Kayser M, Sanchez-Juan P, Feng BJ, Bertoli-Avella AM, van Swieten J, Axenovich TI, Heutink P, van Broeckhoven C, Oostra BA, van Duijn CM.

    Am J Hum Genet. 2007 Jul;81(1):17-31. Epub 2007 May 29.PMID: 17564960 [PubMed - indexed for MEDLINE]Related articlesFree article

    47.

    The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer's disease.

    Arias-Vásquez A, Isaacs A, Aulchenko YS, Hofman A, Oostra BA, Breteler M, van Duijn CM.

    Neurogenetics. 2007 Aug;8(3):189-93. Epub 2007 May 15.PMID: 17503098 [PubMed - indexed for MEDLINE]Related articles

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    Effects of the renin-angiotensin system genes and salt sensitivity genes on blood pressure and atherosclerosis in the total population and patients with type 2 diabetes.

    Yazdanpanah M, Aulchenko YS, Hofman A, Janssen JA, Sayed-Tabatabaei FA, van Schaik RH, Klungel OH, Stricker BH, Pols HA, Witteman JC, Lamberts SW, Oostra BA, van Duijn CM.

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    Epistatic effect of cholesteryl ester transfer protein and hepatic lipase on serum high-density lipoprotein cholesterol levels.

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    GenABEL: an R library for genome-wide association analysis.

    Aulchenko YS, Ripke S, Isaacs A, van Duijn CM.

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