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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

European heart journal, 2021-05, Vol.42 (20), p.2000-2011

2021

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MethDB--a public database for DNA methylation data

Nucleic acids research, 2001-01, Vol.29 (1), p.270

2001

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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

European heart journal, 2021-05, Vol.42 (20), p.2000-2011

2021

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A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

European heart journal, 2011-05, Vol.32 (9), p.1065-1076

2011

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Global analysis of DNA methylation and transcription of human repetitive sequences

Epigenetics, 2009-07, Vol.4 (5), p.339-350

2009

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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

BMC genomics, 2010-03, Vol.11 (1), p.195-195, Article 195

2010

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DNA Methylation Database “MethDB”: a User Guide

The Journal of nutrition, 2002-08, Vol.132 (8), p.2435S-2439S

2002

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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

European heart journal, 2021-05, Vol.42 (20), p.2000-2011

2021

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Prognosis and Guideline-Adherent Antithrombotic Treatment in Patients With Atrial Fibrillation and Atrial Flutter

Chest, 2011-10, Vol.140 (4), p.911-917

2011

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Recombination across the centromere of disjoined and non-disjoined chromosome 21

Human molecular genetics, 2003-09, Vol.12 (17), p.2229-2239

2003

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Risk Scores in ST-Segment Elevation Myocardial Infarction Patients with Refractory Cardiogenic Shock and Veno-Arterial Extracorporeal Membrane Oxygenation

Journal of clinical medicine, 2021-03, Vol.10 (5), p.956

2021

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Human centromeric alphoid domains are periodically homogenized so that they vary substantially between homologues. Mechanism and implications for centromere functioning

Nucleic acids research, 2006-01, Vol.34 (6), p.1912

Roizès, Gérard

2006

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Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy

European journal of human genetics : EJHG, 2003-09, Vol.11 (9), p.659-664

2003

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A compositional map of the cen-q21 region of human chromosome 21

Gene, 1997-07, Vol.194 (1), p.107-113

1997

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BAGE genes generated by juxtacentromeric reshuffling in the hominidae lineage are under selective pressure

Genomics (San Diego, Calif.), 2003-04, Vol.81 (4), p.391-399

2003

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Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

Journal of molecular and cellular cardiology, 1999-05, Vol.31 (5), p.1025-1032

1999

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Polymorphism at VNTR Locus 3′ to the apolipoprotein B gene in a tunisian population: Difference from other ethnic groups

Genetic epidemiology, 1995, Vol.12 (4), p.381-389

1995

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Hypothesis: for the worst and for the best, L1Hs retrotransposons actively participate in the evolution of the human centromeric alphoid sequences

Chromosome research, 1999-06, Vol.7 (4), p.305-317

1999

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Characterization of the human tubulin tyrosine ligase-like 1 gene ( TTLL1) mapping to 22q13.1

Gene, 2000-10, Vol.257 (1), p.109-117

2000

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Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes

Prenatal diagnosis, 1995-03, Vol.15 (3), p.237-248

1995

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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

Gene, 2002-02, Vol.284 (1-2), p.73-81

2002

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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

Human genetics, 2000-08, Vol.107 (2), p.127-131

2000

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Lack of association between polymorphisms of eight candidate genes and Idiopathic dilated cardiomyopathy : The CARDIGENE study

Journal of the American College of Cardiology, 2000, Vol.35 (1), p.29-35

2000

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Analysis of pericentromeric chromosome 21 specific YAC clones by FISH : identification of new markers for molecular-cytogenetic application

Human genetics, 1995-03, Vol.95 (3), p.287-292

1995

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Recognition sequence of restriction endonuclease III from Hemophilus influenzae

Journal of molecular biology, 1975-02, Vol.92 (2), p.331,IN13,337-336,IN13,339

1975

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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

MethDB--a public database for DNA methylation data

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

Global analysis of DNA methylation and transcription of human repetitive sequences

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

DNA Methylation Database “MethDB”: a User Guide

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

Prognosis and Guideline-Adherent Antithrombotic Treatment in Patients With Atrial Fibrillation and Atrial Flutter

Recombination across the centromere of disjoined and non-disjoined chromosome 21

Risk Scores in ST-Segment Elevation Myocardial Infarction Patients with Refractory Cardiogenic Shock and Veno-Arterial Extracorporeal Membrane Oxygenation

Human centromeric alphoid domains are periodically homogenized so that they vary substantially between homologues. Mechanism and implications for centromere functioning

Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy

A compositional map of the cen-q21 region of human chromosome 21

BAGE genes generated by juxtacentromeric reshuffling in the hominidae lineage are under selective pressure

Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

Polymorphism at VNTR Locus 3′ to the apolipoprotein B gene in a tunisian population: Difference from other ethnic groups

Hypothesis: for the worst and for the best, L1Hs retrotransposons actively participate in the evolution of the human centromeric alphoid sequences

Characterization of the human tubulin tyrosine ligase-like 1 gene ( TTLL1) mapping to 22q13.1

Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes

MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia

Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21

Lack of association between polymorphisms of eight candidate genes and Idiopathic dilated cardiomyopathy : The CARDIGENE study

Analysis of pericentromeric chromosome 21 specific YAC clones by FISH : identification of new markers for molecular-cytogenetic application

Recognition sequence of restriction endonuclease III from Hemophilus influenzae

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