Mirjam C G N van den Hout (Mirjam van den Hout)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Topics

Gene Expression

Genome Wide Association Study

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Danny Noack, Anouk van Haperen, Mirjam C G N van den Hout, Eleanor M Marshall, Rosanne W Koutstaal, Vincent van Duinen, Lisa Bauer, Anton Jan van Zonneveld, Wilfred F J Van IJcken, Marion P G Koopmans, Barry Rockx
A three-dimensional vessel-on-chip model to study Puumala orthohantavirus pathogenesis. Lab on a chip (2024)
Bastian V H Hornung, Zakia Azmani, Alexander T den Dekker, Edwin Oole, Zeliha Ozgur, Rutger W W Brouwer, Mirjam C G N van den Hout, Wilfred F J Van IJcken
Comparison of Single Cell Transcriptome Sequencing Methods: Of Mice and Men. Genes 14 (12) (2023)
Bastian V H Hornung, Zakia Azmani, Alexander T den Dekker, Edwin Oole, Zeliha Ozgur, Rutger W W Brouwer, Mirjam C G N van den Hout, Wilfred F J Van IJcken
Comparison of Single Cell Transcriptome Sequencing Methods: Of Mice and Men. Genes 14 (12) (2023)
Judith C Birkhoff, Anne L Korporaal, Rutger W W Brouwer, Karol Nowosad, Claudia Milazzo, Lidia Mouratidou, Mirjam C G N van den Hout, Wilfred F J Van IJcken, Danny Huylebroeck, Andrea Conidi
Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome. Genes 14 (3) (2023)
Bastian V H Hornung, Zakia Azmani, Alexander T den Dekker, Edwin Oole, Zeliha Ozgur, Rutger W W Brouwer, Mirjam C G N van den Hout, Wilfred F J Van IJcken
Comparison of Single Cell Transcriptome Sequencing Methods: Of Mice and Men. Genes 14 (12) (2023)
Judith C Birkhoff, Anne L Korporaal, Rutger W W Brouwer, Karol Nowosad, Claudia Milazzo, Lidia Mouratidou, Mirjam C G N van den Hout, Wilfred F J Van IJcken, Danny Huylebroeck, Andrea Conidi
Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome. Genes 14 (3) (2023)
Judith C Birkhoff, Anne L Korporaal, Rutger W W Brouwer, Karol Nowosad, Claudia Milazzo, Lidia Mouratidou, Mirjam C G N van den Hout, Wilfred F J Van IJcken, Danny Huylebroeck, Andrea Conidi
Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome. Genes 14 (3) (2023)
Widia Soochit, Frank Sleutels, Grégoire Stik, Marek Bartkuhn, Sreya Basu, Silvia C Hernandez, Sarra Merzouk, Enrique Vidal, Ruben G Boers, Joachim Boers, Michael van der Reijden, Bart Geverts, Wiggert A van Cappellen, Mirjam C G N van den Hout, Zeliha Ozgur, Wilfred F J Van IJcken, Joost Gribnau, Rainer Renkawitz, Thomas Graf, Adriaan Houtsmuller, Frank Grosveld, Ralph Stadhouders, Niels Galjart
CTCF chromatin residence time controls three-dimensional genome organization, gene expression and DNA methylation in pluripotent cells. Nature cell biology 23 (8) (2021)
Marja W Wessels, Marjon H Cnossen, Thamar B van Dijk, Nynke Gillemans, K L Juliëtte Schmidt, Kirsten van Lom, Divya S Vinjamur, Steven Coyne, Ryo Kurita, Yukio Nakamura, Stella A de Man, Rolph Pfundt, Zakia Azmani, Rutger W W Brouwer, Daniel E Bauer, Mirjam C G N van den Hout, Wilfred F J Van IJcken, Sjaak Philipsen
Molecular analysis of the erythroid phenotype of a patient with BCL11A haploinsufficiency. Blood advances 5 (9) (2021)
Bram Gerritsen, Aridaman Pandit, Fatiha Zaaraoui-Boutahar, Mirjam C G N van den Hout, Wilfred F J Van IJcken, Rob J De Boer, Arno C Andeweg
Characterization of the ferret TRB locus guided by V, D, J, and C gene expression analysis. Immunogenetics 72 (1-2) (2019)
Priyanka Rao-Ruiz, Jonathan J Couey, Ivo M Marcelo, Christian G Bouwkamp, Denise E Slump, Mariana R Matos, Rolinka J van der Loo, Gabriela J Martins, Mirjam C G N van den Hout, Wilfred F J Van IJcken, Rui M Costa, Michel C van den Oever, Steven A Kushner
Engram-specific transcriptome profiling of contextual memory consolidation. Nature communications 10 (1) (2019)
Mohsen Ghanbari, Shashini T Munshi, Buyun Ma, Bas Lendemeijer, Sakshi Bansal, Hieab H Adams, Wenshi Wang, Kerstin Goth, Denise E Slump, Mirjam C G N van den Hout, Wilfred F J Van IJcken, Saverio Bellusci, Maikel P Peppelenbosch, Stefan J Erkeland, Femke M S de Vrij, Steven A Kushner, Mohammad Arfan Ikram
A functional variant in the miR-142 promoter modulating its expression and conferring risk of Alzheimer disease. Human mutation 40 (11) (2019)