Publications by authors named "Adri Mul"

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Discovery of a DNA methylation episignature as a molecular biomarker for fetal alcohol syndrome.
Liselot van der Laan, Raissa Relator, Irene Valenzuela, Adri N Mul, Mariëlle Alders

Genet Med· December 2025

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Expression Quantitative Trait Methylation Analysis Identifies Whole Blood Molecular Footprint in Fetal Alcohol Spectrum Disorder (FASD).
Izabela M Krzyzewska, Peter Lauffer, Adri N Mul, Liselot van der Laan, Andrew Y F Li Yim

Int J Mol Sci· April 2023

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Prenatal NeuN+ neurons of Down syndrome display aberrant integrative DNA methylation and gene expression profiles.
Peter Henneman, Adri N Mul, Andrew Yf Li Yim, Izabela M Krzyzewska, Mariëlle Alders

Epigenomics· April 2022

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DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes.
Jan Maarten Cobben, Izabela M Krzyzewska, Andrea Venema, Adri N Mul, Abeltje Polstra

Epigenomics· May 2019

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Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates.
Peter Henneman, Arjan Bouman, Adri Mul, Lia Knegt, Anne-Marie van der Kevie-Kersemaekers

PLoS One· July 2018

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Genetic variant in CACNA1C is associated with PTSD in traumatized police officers.
Izabela M Krzyzewska, Judith B M Ensink, Laura Nawijn, Adri N Mul, Saskia B Koch

Eur J Hum Genet· February 2018

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Peripheral blood methylation profiling of female Crohn's disease patients.
Andrew Y F Li Yim, Nicolette W Duijvis, Jing Zhao, Wouter J de Jonge, Geert R A M D'Haens, Adri N P M Mul

Clin Epigenetics· December 2016

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Cow's milk allergy in Dutch children: an epigenetic pilot survey.
Nicole C M Petrus, Peter Henneman, Andrea Venema, Adri Mul, Femke van Sinderen

Clin Transl Allergy· May 2016

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Radioprotection of IDH1-Mutated Cancer Cells by the IDH1-Mutant Inhibitor AGI-5198.
Remco J Molenaar, Dennis Botman, Myrthe A Smits, Vashendriya V Hira, Sanne A van Lith, Adri N Mul

Cancer Res· November 2015

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Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity.
André B P van Kuilenburg, Judith Meijer, Adri N P M Mul, Rutger Meinsma, Veronika Schmid

Hum Genet· November 2010

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Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3).
André B P van Kuilenburg, Judith Meijer, Adri N P M Mul, Raoul C M Hennekam, Jan M N Hoovers, Christine E M de Die-Smulders

Hum Genet· June 2009

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Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: a recognizable syndrome.
Inge B Mathijssen, Jan M N Hoovers, Adri N P M Mul, Hai-Yen Man, Jan L Ket

Am J Med Genet A· July 2005

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Dissection of transient oxidative stress response in Saccharomyces cerevisiae by using DNA microarrays.
Marian Groot Koerkamp, Martijn Rep, Harmen J Bussemaker, Guy P M A Hardy, Adri Mul

Mol Biol Cell· August 2002

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