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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
Garnier S, Harakalova M, Weiss S, Mokry M, Regitz-Zagrosek V, Hengstenberg C, Cappola TP, Isnard R, Arbustini E, Cook SA, van Setten J, Calis JJA, Hakonarson H, Morley MP, Stark K, Prasad SK, Li J, O'Regan DP, Grasso M, [...] Charron P
Eur Heart J, 42(20):2000-2011, 01 May 2021
Cited by: 28 articles | PMID: 33677556 | PMCID: PMC8139853
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Genome wide association analysis in dilated cardiomyopathy reveals two new key players in systolic heart failure on chromosome 3p25.1 and 22q11.23
Garnier S, Harakalova M, Weiss S, Mokry M, Regitz-Zagrosek V, Hengstenberg C, Cappola TP, Isnard R, Arbustini E, Cook SA, van Setten J, Callis J, Hakonarson H, Morley MP, Stark K, Prasad SK, Li J, O’Regan DP, Grasso M, [...] On behalf of GENMED consortium
bioRxiv, 28 Feb 2020
Cited by: 0 articles | PPR: PPR115194
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A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
Villard E, Perret C, Gary F, Proust C, Dilanian G, Hengstenberg C, Ruppert V, Arbustini E, Wichter T, Germain M, Dubourg O, Tavazzi L, Aumont MC, DeGroote P, Fauchier L, Trochu JN, Gibelin P, Aupetit JF, Stark K, [...] Cambien F
Eur Heart J, 32(9):1065-1076, 01 Apr 2011
Cited by: 208 articles | PMID: 21459883 | PMCID: PMC3086901
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Molecular and evolutionary characteristics of the fraction of human alpha satellite DNA associated with CENP-A at the centromeres of chromosomes 1, 5, 19, and 21.
Pironon N, Puechberty J, Roizès G
BMC Genomics, 11:195, 23 Mar 2010
Cited by: 17 articles | PMID: 20331851 | PMCID: PMC2853522
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Global analysis of DNA methylation and transcription of human repetitive sequences.
Horard B, Eymery A, Fourel G, Vassetzky N, Puechberty J, Roizes G, Lebrigand K, Barbry P, Laugraud A, Gautier C, Simon EB, Devaux F, Magdinier F, Vourc'h C, Gilson E
Epigenetics, 4(5):339-350, 17 Jul 2009
Cited by: 19 articles | PMID: 19633427
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Human centromeric alphoid domains are periodically homogenized so that they vary substantially between homologues. Mechanism and implications for centromere functioning.
Roizès G
Nucleic Acids Res, 34(6):1912-1924, 05 Apr 2006
Cited by: 27 articles | PMID: 16598075 | PMCID: PMC1447651
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Centromeres and neocentromeres.
Roizés G, Grunau C, Buard J, De Sario A, Puechberty J
Methods Mol Biol, 240:77-104, 01 Jan 2004
Cited by: 0 articles | PMID: 14970406
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BAGE genes generated by juxtacentromeric reshuffling in the Hominidae lineage are under selective pressure.
Ruault M, Ventura M, Galtier N, Brun ME, Archidiacono N, Roizès G, De Sario A
Genomics, 81(4):391-399, 01 Apr 2003
Cited by: 16 articles | PMID: 12676563
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Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy.
Poirier O, Nicaud V, McDonagh T, Dargie HJ, Desnos M, Dorent R, Roizès G, Schwartz K, Tiret L, Komajda M, Cambien F
Eur J Hum Genet, 11(9):659-664, 01 Sep 2003
Cited by: 16 articles | PMID: 12939651
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Recombination across the centromere of disjoined and non-disjoined chromosome 21.
Laurent AM, Li M, Sherman S, Roizès G, Buard J
Hum Mol Genet, 12(17):2229-2239, 08 Jul 2003
Cited by: 9 articles | PMID: 12915463
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Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms.
Brun ME, Ruault M, Ventura M, Roizès G, De Sario A
Gene, 312:41-50, 01 Jul 2003
Cited by: 21 articles | PMID: 12909339
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New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile.
Ruault M, van der Bruggen P, Brun ME, Boyle S, Roizès G, De Sario A
Eur J Hum Genet, 10(12):833-840, 01 Dec 2002
Cited by: 23 articles | PMID: 12461691
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Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
Vorsanova SG, Yurov YB, Brusquant D, Carles E, Roizes G
Tsitol Genet, 36(1):46-49, 01 Jan 2002
Cited by: 2 articles | PMID: 12012596
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DNA Methylation Database "MethDB": a user guide.
Grunau C, Renault E, Roizes G
J Nutr, 132(8 suppl):2435S-2439S, 01 Aug 2002
Cited by: 3 articles | PMID: 12163707
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Idiopathic dilated cardiomyopathy: lack of association with haemochromatosis gene in the CARDIGENE study.
Hetet G, Grandchamp B, Bouchier C, Nicaud V, Tiret L, Roizès G, Desnos M, Schwartz K, Dorent R, Komajda M, CARDIGENE Group
Heart, 86(6):702-703, 01 Dec 2001
Cited by: 6 articles | PMID: 11711473 | PMCID: PMC1729998
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MethDB--a public database for DNA methylation data.
Grunau C, Renault E, Rosenthal A, Roizes G
Nucleic Acids Res, 29(1):270-274, 01 Jan 2001
Cited by: 55 articles | PMID: 11125109 | PMCID: PMC29842
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Characterization of the human tubulin tyrosine ligase-like 1 gene (TTLL1) mapping to 22q13.1.
Trichet V, Ruault M, Roizès G, De Sario A
Gene, 257(1):109-117, 01 Oct 2000
Cited by: 6 articles | PMID: 11054573
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MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia.
Ruault M, Brun ME, Ventura M, Roizès G, De Sario A
Gene, 284(1-2):73-81, 01 Feb 2002
Cited by: 76 articles | PMID: 11891048
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Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy: the CARDIGENE study.
Tiret L, Mallet C, Poirier O, Nicaud V, Millaire A, Bouhour JB, Roizès G, Desnos M, Dorent R, Schwartz K, Cambien F, Komajda M
J Am Coll Cardiol, 35(1):29-35, 01 Jan 2000
Cited by: 56 articles | PMID: 10636255
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Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21.
Guipponi M, Yaspo ML, Riesselman L, Chen H, De Sario A, Roizès G, Antonarakis SE
Hum Genet, 107(2):127-131, 01 Aug 2000
Cited by: 18 articles | PMID: 11030409
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Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group.
Tesson F, Charron P, Peuchmaurd M, Nicaud V, Cambien F, Tiret L, Poirier O, Desnos M, Jullières Y, Amouyel P, Roizès G, Dorent R, Schwartz K, Komajda M
J Mol Cell Cardiol, 31(5):1025-1032, 01 May 1999
Cited by: 77 articles | PMID: 10336842
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Genetic and physical analyses of the centromeric and pericentromeric regions of human chromosome 5: recombination across 5cen.
Puechberty J, Laurent AM, Gimenez S, Billault A, Brun-Laurent ME, Calenda A, Marçais B, Prades C, Ioannou P, Yurov Y, Roizès G
Genomics, 56(3):274-287, 01 Mar 1999
Cited by: 26 articles | PMID: 10087194
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Analysis of alphoid DNA variation and kinetochore size in human chromosome 21: evidence against pathological significance of alphoid satellite DNA diminutions.
Marzais B, Vorsanova SG, Roizes G, Yurov YB
Tsitol Genet, 33(1):25-31, 01 Jan 1999
Cited by: 6 articles | PMID: 10330695
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Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE group.
Charron P, Tesson F, Poirier O, Nicaud V, Peuchmaurd M, Tiret L, Cambien F, Amouyel P, Dubourg O, Bouhour J, Millaire A, Juilliere Y, Bareiss P, André-Fouët X, Pouillart F, Arveiler D, Ferrières J, Dorent R, Roizès G, [...] Komajda M
Eur Heart J, 20(21):1587-1591, 01 Nov 1999
Cited by: 31 articles | PMID: 10529327
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[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].
Solov'ev IV, Iurov IuB, Vorsanova SG, Marcais B, Rogaev EI, Kapanadze BI, Brodianskiĭ VM, Iankovskiĭ NK, Roizes G
Genetika, 34(11):1470-1479, 01 Nov 1998
Cited by: 1 article | PMID: 10096024
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