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Whole-Genome DNA Methylation Profiling of CD14+ Monocytes Reveals Disease Status and Activity Differences in Crohn's Disease Patients.
Published in:
Journal of Clinical Medicine, 2020, v. 9, n. 4, p. 1055, doi. 10.3390/jcm9041055
By:
- Li Yim, Andrew Y.F.;
- Duijvis, Nicolette W.;
- Ghiboub, Mohammed;
- Sharp, Catriona;
- Ferrero, Enrico;
- Mannens, Marcel M.A.M.;
- D'Haens, Geert R.;
- de Jonge, Wouter J.;
- te Velde, Anje A.;
- Henneman, Peter
Publication type:
Article
Cardiac conduction defects associate with mutations in SCN5A.
Published in:
Nature Genetics, 1999, v. 23, n. 1, p. 20, doi. 10.1038/12618
By:
- Schott, Jean-Jacques;
- Alshinawi, Connie;
- Kyndt, Florence;
- Probst, Vincent;
- Hoorntje, Theo M.;
- Hulsbeek, Miriam;
- Wilde, Arthur A.M.;
- Escande, Denis;
- Mannens, Marcel M.A.M.;
- Le Marec, Hervé
Publication type:
Article
Genome-wide DNA methylation analysis on C-reactive protein among Ghanaians suggests molecular links to the emerging risk of cardiovascular diseases.
Published in:
NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00213-9
By:
- Chilunga, Felix P.;
- Henneman, Peter;
- Venema, Andrea;
- Meeks, Karlijn A. C.;
- Requena-Méndez, Ana;
- Beune, Erik;
- Mockenhaupt, Frank P.;
- Smeeth, Liam;
- Bahendeka, Silver;
- Danquah, Ina;
- Klipstein-Grobusch, Kerstin;
- Adeyemo, Adebowale;
- Mannens, Marcel M.A.M;
- Agyemang, Charles
Publication type:
Article
A Novel Early Onset Lethal Form of Catecholaminergic Polymorphic Ventricular Tachycardia Maps to Chromosome 7p14-p22.
Published in:
Journal of Cardiovascular Electrophysiology, 2007, v. 18, n. 10, p. 1060, doi. 10.1111/j.1540-8167.2007.00913.x
By:
- BHUIYAN, ZAHURUL A.;
- HAMDAN, MOHAMED A.;
- SHAMSI, EMAN T.A.;
- POSTMA, ALEX V.;
- MANNENS, MARCEL M.A.M.;
- WILDE, ARTHUR A. M.;
- AL‐GAZALI, LIHADH
Publication type:
Article
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.
Published in:
European Heart Journal, 2011, v. 32, n. 9, p. 1161, doi. 10.1093/eurheartj/ehr092
By:
- Christiaans, Imke;
- Birnie, Erwin;
- Bonsel, Gouke J.;
- Mannens, Marcel M.A.M.;
- Michels, Michelle;
- Majoor-Krakauer, Daniëlle;
- Dooijes, Dennis;
- van Tintelen, J. Peter;
- van den Berg, Maarten P.;
- Volders, Paul G.A.;
- Arens, Yvonne H.;
- van den Wijngaard, Arthur;
- Atsma, Douwe E.;
- Helderman-van den Enden, Apollonia T.J.M.;
- Houweling, Arjan C.;
- de Boer, Karin;
- van der Smagt, Jasper J.;
- Hauer, Richard N.W.;
- Marcelis, Carlo L.M.;
- Timmermans, Janneke
Publication type:
Article
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?
Published in:
European Heart Journal, 2007, v. 28, n. 5, p. 575
By:
- Hofman, Nynke;
- Wilde, Arthur A.M.;
- Kääb, Stefan;
- van Langen, Irene M.;
- Tanck, Michael W.T.;
- Mannens, Marcel M.A.M.;
- Hinterseer, Martin;
- Beckmann, Britt-Maria;
- Tan, Hanno L.
Publication type:
Article
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome
Published in:
Cardiovascular Research, 2005, v. 68, n. 3, p. 441, doi. 10.1016/j.cardiores.2005.06.027
By:
- Verkerk, Arie O.;
- Wilders, Ronald;
- Schulze-Bahr, Eric;
- Beekman, Leander;
- Bhuiyan, Zahurul A.;
- Bertrand, Jessica;
- Eckardt, Lars;
- Lin, Dongxin;
- Borggrefe, Martin;
- Breithardt, Günter;
- Mannens, Marcel M.A.M.;
- Tan, Hanno L.;
- Wilde, Arthur A.M.;
- Bezzina, Connie R.
Publication type:
Article
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization
Published in:
Cardiovascular Research, 2003, v. 59, n. 1, p. 27, doi. 10.1016/S0008-6363(03)00342-0
By:
- Bezzina, Connie R.;
- Verkerk, Arie O.;
- Busjahn, Andreas;
- Jeron, Andreas;
- Erdmann, Jeanette;
- Koopmann, Tamara T.;
- Bhuiyan, Zahurul A.;
- Wilders, Ronald;
- Mannens, Marcel M.A.M.;
- Tan, Hanno L.;
- Luft, Friedrich C.;
- Schunkert, Heribert;
- Wilde, Arthur A.M.
Publication type:
Article
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics
Published in:
Cardiovascular Research, 2003, v. 57, n. 4, p. 1072, doi. 10.1016/S0008-6363(02)00838-6
By:
- Groenewegen, W. Antoinette;
- Bezzina, Connie R.;
- van Tintelen, J. Peter;
- Hoorntje, Theo M.;
- Mannens, Marcel M.A.M.;
- Wilde, Arthur A.M.;
- Jongsma, Habo. J.;
- Rook, Martin B.
Publication type:
Article
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome*.
Published in:
Cardiovascular Research, 1999, v. 44, n. 3, p. 507, doi. 10.1016/S0008-6363(99)00350-8
By:
- Rook, Martin B.;
- Bezzina Alshinawi, Connie;
- Groenewegen, W.Antoinette;
- van Gelder, Isabelle C.;
- van Ginneken, Antoni C.G.;
- Jongsma, Habo J.;
- Mannens, Marcel M.A.M.;
- Wilde, Arthur A.M.
Publication type:
Article
Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy.
Published in:
2017
By:
- Jansweijer, Joeri A.;
- Nieuwhof, Karin;
- Russo, Francesco;
- Hoorntje, Edgar T.;
- Jongbloed, Jan D.H.;
- Lekanne Deprez, Ronald H.;
- Postma, Alex V.;
- Bronk, Marieke;
- van Rijsingen, Ingrid A.W.;
- de Haij, Simone;
- Biagini, Elena;
- van Haelst, Paul L.;
- van Wijngaarden, Jan;
- van den Berg, Maarten P.;
- Wilde, Arthur A.M.;
- Mannens, Marcel M.A.M.;
- de Boer, Rudolf A.;
- van Spaendonck-Zwarts, Karin Y.;
- van Tintelen, J. Peter;
- Pinto, Yigal M.
Publication type:
journal article
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.
Published in:
Human Molecular Genetics, 2001, v. 10, n. 5, p. 467, doi. 10.1093/hmg/10.5.467
By:
- Bliek, Jet;
- Maas, Saskia M.;
- Ruijter, Jan M.;
- Hennekam, Raoul C.M.;
- Alders, Marielle;
- Westerveld, Andries;
- Mannens, Marcel M.A.M.
Publication type:
Article
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: Determination of the molecular basis.
Published in:
Human Mutation, 2000, v. 16, n. 1, p. 18, doi. 10.1002/1098-1004(200007)16:1<18::AID-HUMU4>3.0.CO;2-N
By:
- Aalfs, Cora M.;
- Salieb-Beugelaar, Georgette B.;
- Wanders, Ronald J.A.;
- Mannens, Marcel M.A.M.;
- Wijburg, Frits A.
Publication type:
Article

Found: 13