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Works (8)

Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options

European Journal of Human Genetics
2024-11 | Journal article
DOI: 10.1038/s41431-024-01601-2
Contributors: Niels Vos; Lotte Kleinendorst; Liselot van der Laan; Jorrit van Uhm; Philip R. Jansen; Agnies M. van Eeghen; Saskia M. Maas; Marcel M.A.M. Mannens; Mieke M. van Haelst
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Crossref

Functional Insight into and Refinement of the Genomic Boundaries of the <i>JARID2</i>-Neurodevelopmental Disorder Episignature

International Journal of Molecular Sciences
2023-09 | Journal article | Author
DOI: 10.3390/ijms241814240
Contributors: Liselot van der Laan; Kathleen Rooney; Sadegheh Haghshenas; Ananília Silva; Haley McConkey; Raissa Relator; Michael A. Levy; Irene Valenzuela; Laura Trujillano; Amaia Lasa-Aranzasti et al.
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Multidisciplinary Digital Publishing Institute

Single-cell characterization of peripheral blood mononuclear cells from vedolizumab-treated patients with Crohn's disease identifies response-associated differences among the plasmacytoid dendritic cell and classical monocyte populations.

2023-06-29 | Preprint
DOI: 10.1101/2023.06.23.23291732
Contributors: Andrew Y.F. Li Yim; Ishtu L. Hageman; Vincent W. Joustra; Ahmed M.I.M. Elfiky; Mohammed Ghiboub; Evgeni Levin; Jan Verhoeff; Caroline Verseijden; Iris Admiraal-van den Berg; Marcel M.A.M. Mannens et al.
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Crossref

DNA methylation episignatures: insight into copy number variation

Epigenomics
2022-11 | Journal article
DOI: 10.2217/epi-2022-0287
Contributors: Liselot van der Laan; Kathleen Rooney; Tessa MA Trooster; Marcel MAM Mannens; Bekim Sadikovic; Peter Henneman
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Prenatal Neun+ Neurons of Down Syndrome Display Aberrant Integrative DNA Methylation and Gene Expression Profiles

Epigenomics
2022-04 | Journal article
DOI: 10.2217/epi-2021-0523
Contributors: Peter Henneman; Adri N Mul; Andrew YF Li Yim; Izabela M Krzyzewska; Mariëlle Alders; Adelia Adelia; Mark R Mizee; Marcel M Mannens
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Crossref

Screening for inborn errors of metabolism in psychotic patients using Next Generation Sequencing

Journal of Psychiatric Research
2021-06 | Journal article
DOI: 10.1016/j.jpsychires.2021.03.060
Contributors: Nikita van de Burgt; Silvana van Koningsbruggen; Leonie Behrens; Nicole Leibold; Pilar Martinez-Martinez; Marcel Mannens; Therese van Amelsvoort
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Whole-genome DNA methylation profiling of CD14+ monocytes reveals disease status and activity differences in Crohn’s disease patients

2020-03-12 | Other
DOI: 10.1101/2020.03.09.20033043
Contributors: Andrew Y.F. Li Yim; Nicolette W. Duijvis; Mohammed Ghiboub; Catriona Sharp; Enrico Ferrero; Marcel M.A.M. Mannens; Geert R. D’Haens; Wouter J. de Jonge; Anje A. te Velde; Peter Henneman
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Crossref

Defining tissue- and disease-associated macrophages using a transcriptome-based classification model

2019-01-29 | Other
DOI: 10.1101/532986
Contributors: Hung-Jen Chen; Andrew Y.F. Li Yim; Guillermo R. Griffith; Wouter J. de Jonge; Marcel M.A.M. Mannens; Enrico Ferrero; Peter Henneman; Menno P.J. de Winther
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