Rutger Brouwer - Dissemin

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All papers authored by Rutger Brouwer

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2021 Erwin Brosens

ORCID

, Rutger W. W. Brouwer

ORCID

, Hannie Douben, Yolande van Bever, Alice S. Brooks, Rene M. H. Wijnen, Wilfred F. J. van IJcken, Dick Tibboel, Robbert J. Rottier

ORCID

, Annelies de Klein

Heritability and De Novo Mutations in Oesophageal Atresia and Tracheoesophageal Fistula Aetiology

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Marja W. Wessels, Marjon H. Cnossen

ORCID

, Thamar B. van Dijk, Nynke Gillemans, K. L. Juliëtte Schmidt, Kirsten van Lom, Divya S. Vinjamur

ORCID

, Steven Coyne, Ryo Kurita, Yukio Nakamura, Stella A. de Man

ORCID

ORCID

, Zakia Azmani, Rutger W. W. Brouwer

ORCID

, Daniel E. Bauer

ORCID

and 3 other authors

Molecular analysis of the erythroid phenotype of a patient with BCL11A haploinsufficiency

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C. Mircea S. Tesileanu, C. Mircea S. Tesileanu

ORCID

, Martin J. van den Bent

ORCID

ORCID

, Wolfgang Wick

ORCID

, Alba A. Brandes, Paul M. Clement, Sara C. Erridge, Michael A. Vogelbaum, Anna K. Nowak, Jean F. Baurain, Warren P. Mason, Helen Wheeler, Olivier L. Chinot, Sanjeev Gill and 24 other authors

Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma

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Mieke Veltman, Juan B. De Sanctis

ORCID

, Marta Stolarczyk, Nikolai Klymiuk, Andrea Bähr, Rutger W. Brouwer

ORCID

, Edwin Oole, Juhi Shah, Tomas Ozdian, Jie Liao, Carolina Martini, Danuta Radzioch, John W. Hanrahan, Bob J. Scholte

CFTR Correctors and Antioxidants Partially Normalize Lipid Imbalance but not Abnormal Basal Inflammatory Cytokine Profile in CF Bronchial Epithelial Cells

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Ilias Boltsis, Karol Nowosad, Rutger W. W. Brouwer

ORCID

, Przemko Tylzanowski, Wilfred F. J. van IJcken, Danny Huylebroeck, Frank Grosveld, Petros Kolovos

Low Input Targeted Chromatin Capture (Low-T2C)

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

J. C. Birkhoff, A. L. Korporaal, R. W. W. Brouwer

ORCID

, C. Milazzo, L. Mouratidou, M. C. G. N. van den Hout, W. F. J. van IJcken, D. Huylebroeck, A. Conidi

Zeb2 DNA-binding sites in ES cell derived neuroprogenitor cells reveal autoregulation and align with neurodevelopmental knockout mouse and disease phenotypes

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2020 Maaike R. Scheenstra, Patricia Martínez‐Botía, Andrea Acebes‐Huerta, Rutger W. W. Brouwer

ORCID

, Noemí Caballero‐Sánchez, Nynke Gillemans, Pieter De Bleser, Benjamin Nota, Iris M. De Cuyper, Vishal Salunkhe, Andrea M. Woltman, Lianne Laar, Erikjan Rijkers, Jeroen A. A. Demmers, Wilfred F. J. IJcken

ORCID

and 4 other authors

Comparison of the PU.1 transcriptional regulome and interactome in human and mouse inflammatory dendritic cells

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Nicolle H. R. Litjens, Amy C. L. van der List, Anton W. Langerak, Amy C. J. van der List, Mariska Klepper, Maaike de Bie, Zakia Azmani, Alexander T. den Dekker, Rutger W. W. Brouwer

ORCID

, Michiel G. H. Betjes, Wilfred F. J. Van IJcken

Validation of a Combined Transcriptome and T Cell Receptor Alpha/Beta (TRA/TRB) Repertoire Assay at the Single Cell Level for Paucicellular Samples

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Judith C. Birkhoff, Rutger W. W. Brouwer

ORCID

, Petros Kolovos, Anne L. Korporaal, Ana Bermejo-Santos, Ilias Boltsis, Karol Nowosad

ORCID

, Mirjam C. G. N. van den Hout, Frank G. Grosveld, Wilfred F. J. van IJcken, Danny Huylebroeck, Andrea Conidi

ORCID

Targeted chromatin conformation analysis identifies novel distal neural enhancers of ZEB2 in pluripotent stem cell differentiation

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Ilaria Parenti

ORCID

, Farah Diab, Sara Ruiz Gil, Eskeatnaf Mulugeta, Valentina Casa, Riccardo Berutti, Rutger W. W. Brouwer

ORCID

, Valerie Dupé, Juliane Eckhold, Elisabeth Graf, Beatriz Puisac, Feliciano Ramos, Thomas Schwarzmayr, Macarena Moronta Gines, Thomas van Staveren and 6 other authors

MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome

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Alex Neagu, Emiel van Genderen, Irene Escudero, Lucas Verwegen, Dorota Kurek, Johannes Lehmann, Jente Stel, René A. M. Dirks

ORCID

, Guido van Mierlo

ORCID

, Alex Maas, Cindy Eleveld, Yang Ge

ORCID

, Alexander T. den Dekker, Rutger W. W. Brouwer

ORCID

, Wilfred F. J. van IJcken

ORCID

and 7 other authors

In vitro capture and characterization of embryonic rosette-stage pluripotency between naive and primed states

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Ashley van der Spek, Sophie C. Warner, Linda Broer, Christopher P. Nelson, Dina Vojinovic, Shahzad Ahmad, Pascal P. Arp, Rutger W. W. Brouwer

ORCID

, Matthew Denniff, Mirjam C. G. N. van den Hout, Jeroen G. J. van Rooij, Robert Kraaij, Wilfred F. J. van IJcken, Nilesh J. Samani, M. Arfan Ikram and 4 other authors

Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length

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Chantal A. Kate

ORCID

, Rutger W. W. Brouwer

ORCID

, Yolande Bever, Vera K. Martens, Tom Brands, Nicole W. G. Beelen, Alice S. Brooks, Daphne Huigh, Robert M. Helm, Bert H. F. M. M. Eussen, Wilfred F. J. IJcken, Hanneke IJsselstijn, Dick Tibboel, Rene M. H. Wijnen, Annelies Klein and 2 other authors

Infantile hypertrophic pyloric stenosis in patients with esophageal atresia

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2019 Hui Liu

ORCID

, Ann L. B. Seynhaeve, Rutger W. W. Brouwer

ORCID

, Wilfred F. J. van IJcken

ORCID

, Liu Yang, Yinyin Wang, Zhijie Chang, Timo L. M. ten Hagen

CREPT Promotes Melanoma Progression Through Accelerated Proliferation and Enhanced Migration by RhoA-Mediated Actin Filaments and Focal Adhesion Formation

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C. A. ten Kate, R. W. W. Brouwer

ORCID

, Y. van Bever, V. K. Martens, T. Brands, N. W. G. van Beelen, A. S. Brooks, D. Huigh, B. J. Eussen, W. F. J. van IJcken, H. IJsselstijn, D. Tibboel, R. M. H. Wijnen, A. de Klein, R. M. W. Hofstra and 1 other authors

Models for infantile hypertrophic pyloric stenosis development in patients with esophageal atresia

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2018 Demy J. S. Kuipers, Jonathan Carr, Soraya Bardien, Pearl Thomas, Boiketlo Sebate, Guido J. Breedveld, Rick van Minkelen, Rutger W. W. Brouwer

ORCID

, Wilfred F. J. van Ijcken, Marjon A. van Slegtenhorst, Vincenzo Bonifati, Marialuisa Quadri

PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability

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Dina Vojinovic, Maryam Kavousi

ORCID

, Mohsen Ghanbari, Rutger W. W. Brouwer

ORCID

, Jeroen G. J. van Rooij, Mirjam C. G. N. van den Hout, Robert Kraaij, Wilfred F. J. van Ijcken, Andre G. Uitterlinden, Cornelia M. van Duijn, Najaf Amin

Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness

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S. C. Doebar, N. M. Krol, R. van Marion, R. W. W. Brouwer

ORCID

, W. F. J. van Ijcken, J. M. Martens, W. N. M. Dinjens, C. H. M. van Deurzen

Progression of ductal carcinoma in situ to invasive breast cancer: comparative genomic sequencing

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Marialuisa Quadri, Wim Mandemakers, Martyna M. Grochowska, Roy Masius, Hanneke Geut, Edito Fabrizio, Guido J. Breedveld, Demy Kuipers, Michelle Minneboo, Leonie J. M. Vergouw, Ana Carreras Mascaro, Ekaterina Yonova-Doing, Erik Simons, Tianna Zhao, Alessio B. Di Fonzo

ORCID

and 82 other authors

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

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Yunia Sribudiani, Rajendra K. Chauhan, Maria M. Alves, Lucy Petrova, Erwin Brosens

ORCID

, Colin Harrison, Tara Wabbersen, Bianca M. de Graaf, Tim Rügenbrink, Grzegorz Burzynski, Rutger W. W. Brouwer

ORCID

, Wilfred F. J. van IJcken, Saskia M. Maas, Annelies de Klein, Jan Osinga and 5 other authors

Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease

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