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DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes.
Epigenomics. 2019 May;11(7):767-785. doi: 10.2217/epi-2018-0221. Epub 2019 Mar 15.
Epigenomics. 2019.
PMID: 30873861
Free article.
Genetic variant in CACNA1C is associated with PTSD in traumatized police officers.
Krzyzewska IM, Ensink JBM, Nawijn L, Mul AN, Koch SB, Venema A, Shankar V, Frijling JL, Veltman DJ, Lindauer RJL, Olff M, Mannens MMAM, van Zuiden M, Henneman P.
Krzyzewska IM, et al.
Eur J Hum Genet. 2018 Feb;26(2):247-257. doi: 10.1038/s41431-017-0059-1. Epub 2018 Jan 23.
Eur J Hum Genet. 2018.
PMID: 29362489
Free PMC article.
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Oxytocin receptor gene methylation in male and female PTSD patients and trauma-exposed controls.
Nawijn L, Krzyzewska IM, van Zuiden M, Henneman P, Koch SBJ, Mul AN, Frijling JL, Veltman DJ, Mannens MMAM, Olff M.
Nawijn L, et al. Among authors: krzyzewska im.
Eur Neuropsychopharmacol. 2019 Jan;29(1):147-155. doi: 10.1016/j.euroneuro.2018.10.006. Epub 2018 Nov 8.
Eur Neuropsychopharmacol. 2019.
PMID: 30415783
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Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics.
Krzyzewska IM, Alders M, Maas SM, Bliek J, Venema A, Henneman P, Rezwan FI, Lip KVD, Mul AN, Mackay DJG, Mannens MMAM.
Krzyzewska IM, et al.
Clin Epigenetics. 2019 Mar 21;11(1):53. doi: 10.1186/s13148-019-0649-6.
Clin Epigenetics. 2019.
PMID: 30898153
Free PMC article.
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A genome-wide DNA methylation signature for SETD1B-related syndrome.
Krzyzewska IM, Maas SM, Henneman P, Lip KVD, Venema A, Baranano K, Chassevent A, Aref-Eshghi E, van Essen AJ, Fukuda T, Ikeda H, Jacquemont M, Kim HG, Labalme A, Lewis SME, Lesca G, Madrigal I, Mahida S, Matsumoto N, Rabionet R, Rajcan-Separovic E, Qiao Y, Sadikovic B, Saitsu H, Sweetser DA, Alders M, Mannens MMAM.
Krzyzewska IM, et al.
Clin Epigenetics. 2019 Nov 4;11(1):156. doi: 10.1186/s13148-019-0749-3.
Clin Epigenetics. 2019.
PMID: 31685013
Free PMC article.
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Prenatal NeuN+ neurons of Down syndrome display aberrant integrative DNA methylation and gene expression profiles.
Henneman P, Mul AN, Li Yim AY, Krzyzewska IM, Alders M, Adelia A, Mizee MR, Mannens MM.
Henneman P, et al. Among authors: krzyzewska im.
Epigenomics. 2022 Apr;14(7):375-390. doi: 10.2217/epi-2021-0523. Epub 2022 Mar 2.
Epigenomics. 2022.
PMID: 35232286
Free article.
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Expression Quantitative Trait Methylation Analysis Identifies Whole Blood Molecular Footprint in Fetal Alcohol Spectrum Disorder (FASD).
Krzyzewska IM, Lauffer P, Mul AN, van der Laan L, Yim AYFL, Cobben JM, Niklinski J, Chomczyk MA, Smigiel R, Mannens MMAM, Henneman P.
Krzyzewska IM, et al.
Int J Mol Sci. 2023 Apr 1;24(7):6601. doi: 10.3390/ijms24076601.
Int J Mol Sci. 2023.
PMID: 37047575
Free PMC article.
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Should testing for mosaic genome-wide paternal uniparental disomy in Beckwith-Wiedemann spectrum (BWSp) be implemented in diagnostic testing?
Maas SM, Krzyzewska IM, Lombardi MPR, Mannens MMA, Vos N, Bliek J.
Maas SM, et al. Among authors: krzyzewska im.
Eur J Hum Genet. 2023 Jun;31(6):615-616. doi: 10.1038/s41431-023-01354-4. Epub 2023 Apr 3.
Eur J Hum Genet. 2023.
PMID: 37012326
No abstract available.
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