Marcel Mannens
机构: Hoogleraar genoomdiagnostiek in het bijzonder epigenetica van ziekten
主页: google.com
每年引用次数
引用次数
引用: 17,590
H-指数: 72
I10-指数 : 169
出版物: 330
Sudden death in young men due to arrhythmogenic right ventricular dysplasia
Wilde Aa , Van Langen Im , Mannens Ma
Nederlands Tijdschrift voor Geneeskunde 142 ( 13) 739
1998
Iatrogene collaps; is die te voorkomen?
M. M. Mannens , A. A. Wilde
Nederlands Tijdschrift voor Geneeskunde 141 ( 16) 796 -797
1997
Clinical implications of epigenetic changes
Mannens Mmam
Nederlands Tijdschrift voor Geneeskunde 163
2019
The idiopathic preterm delivery methylation profile in umbilical cord blood DNA
Febilla Fernando , Remco Keijser , Peter Henneman , Anne-Marie F. van der Kevie-Kersemaekers
BMC Genomics 16 ( 1) 736 -736
31
2015
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.
Ruud van den Bogaard , Cees AP Fijen , Mariëtte GJ Schipper , Louis de Galan
European Journal of Human Genetics 8 ( 7) 513 -518
25
2000
Novel tools for extraction and validation of disease-related mutations applied to Fabry disease.
Remko Kuipers , Tom van den Bergh , Henk-Jan Joosten , Ronald H. Lekanne dit Deprez
Human Mutation 31 ( 9) 1026 -1032
21
2010
DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes
Jan Maarten Cobben , Izabela M Krzyzewska , Andrea Venema , Adri N Mul
Epigenomics 11 ( 7) 767 -785
30
2019
Lessons from BWS twins: Complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells
Jet Bliek , Marielle Alders , Saskia M Maas , Roelof-Jan Oostra
European Journal of Human Genetics 17 ( 12) 1625 -1634
79
2009
Prevalence and determinants of type 2 diabetes among lean African migrants and non-migrants : the RODAM study
Felix P Chilunga , Peter Henneman , Karlijn AC Meeks , Erik Beune
Journal of Global Health 9 ( 2) 020426
6
2019
Comprehensive open reading frame mutational analysis of the RYR2-encoded ryanodine receptor/calcium channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome
Argelia Medeiros-Domingo , Zahurul A Bhuiyan , David J Tester , Nynke Hofman
Journal of the American College of Cardiology 54 ( 22) 2065
16
2009
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Henne Holstege , Marc Hulsman , Camille Charbonnier , Benjamin Grenier-Boley
Nature genetics 54 ( 12) 1786 -1794
75
2022
Summary statistics for" Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's Disease"
Holger Hummerich , Margaret A Pericak-Vance , Rachel Raybould , Erik Sistermans
Zenodo
2
2022
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as novel risk factors for Alzheimers Disease
Henne Holstege , Marc Hulsman , Camille Charbonnier , Benjamin Grenier-Boley
1
2020
Genome-wide DNA methylation analysis on C-reactive protein among Ghanaians suggests molecular links to the emerging risk of cardiovascular diseases
Felix P Chilunga , Peter Henneman , Andrea Venema , Karlijn AC Meeks
NPJ genomic medicine 6 ( 1) 46 -46
7
2021
The contribution of body composition to ethnic differences in type 2 diabetes
Karlijn AC Meeks , Karien Stronks , Erik JAJ Beune , Adebowale Adeyemo
Epidemiology and epigenetics of type 2 diabetes among African migrants in Europe 110 ( 2) 97 -97
2015
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics
W Antoinette Groenewegen , Connie R Bezzina , J Peter van Tintelen , Theo M Hoorntje
Cardiovascular Research 57 ( 4) 1072 -1078
21
2003
A knockout may not always be a knockout-Response
Arthur AM Wilde , Marcel MAM Mannens , Marielle Alders , K van der Lip
Circulation 102 ( 18) E122 -E122
2000
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?
Nynke Hofman , Arthur AM Wilde , Stefan Kääb , Irene M Van Langen
European Heart Journal 28 ( 11) 1399 -1399
2007
Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders
Michael A Levy , Raissa Relator , Haley McConkey , Erinija Pranckeviciene
Human mutation 43 ( 11) 1609 -1628
33
2022
Genome-wide DNA methylation differences and their relationship with neural abnormalities in youth with and without posttraumatic stress disorder
Judith Ensink , Taylor J Keding , Peter Henneman , Jasper Zantvoord
European Neuropsychopharmacology 29 1163 -1164
2019
Irene van Langen J. Peter van Tintelen Dr AV Postma Prof. Charles Agyemang C. Heyting Veronica van Heyningen Karlijn A.C. Meeks Andrew P. Feinberg Liam Smeeth Ronald Wilders Andrew Li Yim Adebowale Adeyemo Ellis Owusu-Dabo Wouter de Jonge lihadh al-gazali van der wal allard c Matthias B. Schulze Joachim Spranger