Exploring the Influence of Alcohol Industry Funding in Observational Studies on Moderate Alcohol Consumption and Health von Vos, Moniek, van Soest, Annick P M, van Wingerden, Tim, Janse, Marion L, Dijk, Rick M, Brouwer, Rutger J, de Koning, Iris, Feskens, Edith J M, Sierksma, Aafje

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Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells von Zuin, Jessica, Dixon, Jesse R., van der Reijden, Michael I. J. A., Ye, Zhen, Kolovos, Petros, Brouwer, Rutger W. W., van de Corput, Mariëtte P. C., van de Werken, Harmen J. G., Knoch, Tobias A., van IJcken, Wilfred F. J., Grosveld, Frank G., Ren, Bing, Wendt, Kerstin S.

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In vitro capture and characterization of embryonic rosette-stage pluripotency between naive and primed states von Neagu, Alex, van Genderen, Emiel, Escudero, Irene, Verwegen, Lucas, Kurek, Dorota, Lehmann, Johannes, Stel, Jente, Dirks, René A. M., van Mierlo, Guido, Maas, Alex, Eleveld, Cindy, Ge, Yang, den Dekker, Alexander. T., Brouwer, Rutger W. W., van IJcken, Wilfred F. J., Modic, Miha, Drukker, Micha, Jansen, Joop H., Rivron, Nicolas C., Baart, Esther B., Marks, Hendrik, ten Berge, Derk

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Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model von Alves, Maria M., Sribudiani, Yunia, Brouwer, Rutger W.W., Amiel, Jeanne, Antiñolo, Guillermo, Borrego, Salud, Ceccherini, Isabella, Chakravarti, Aravinda, Fernández, Raquel M., Garcia-Barcelo, Maria-Mercè, Griseri, Paola, Lyonnet, Stanislas, Tam, Paul K., van IJcken, Wilfred F.J., Eggen, Bart J.L., te Meerman, Gerard J., Hofstra, Robert M.W.

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Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice von Halim, Danny, Wilson, Michael P., Oliver, Daniel, Brosens, Erwin, Verheij, Joke B. G. M., Han, Yu, Nanda, Vivek, Lyu, Qing, Doukas, Michael, Stoop, Hans, Brouwer, Rutger W. W., van IJcken, Wilfred F. J., Slivano, Orazio J., Burns, Alan J., Christie, Christine K., de Mesy Bentley, Karen L., Brooks, Alice S., Tibboel, Dick, Xu, Suowen, Jin, Zheng Gen, Djuwantono, Tono, Yan, Wei, Alves, Maria M., Hofstra, Robert M. W., Miano, Joseph M.

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Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma von Koopmans, Anna E, Verdijk, Robert M, Brouwer, Rutger W W, van den Bosch, Thierry P P, van den Berg, Mike M P, Vaarwater, Jolanda, Kockx, Christel E M, Paridaens, Dion, Naus, Nicole C, Nellist, Mark, van IJcken, Wilfred F J, Kiliç, Emine, de Klein, Annelies

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Clinical lymph node staging in colorectal cancer; a flip of the coin? von Brouwer, Nelleke P.M., Stijns, Rutger C.H., Lemmens, Valery E.P.P., Nagtegaal, Iris D., Beets-Tan, Regina G.H., Fütterer, Jurgen J., Tanis, Pieter J., Verhoeven, Rob H.A., de Wilt, Johannes H.W.

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Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts von Heshusius, Steven, Grech, Laura, Gillemans, Nynke, Brouwer, Rutger W. W., den Dekker, Xander T., van IJcken, Wilfred F. J., Nota, Benjamin, Felice, Alex E., van Dijk, Thamar B., von Lindern, Marieke, Borg, Joseph, van den Akker, Emile, Philipsen, Sjaak

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Identification of candidate enhancers controlling the transcriptome during the formation of interphalangeal joints von Nowosad, Karol, Brouwer, Rutger W. W., Odrzywolski, Adrian, Korporaal, Anne L., Gielniewski, Bartłomiej, Wojtaś, Bartosz, van IJcken, Wilfred F. J., Grosveld, Frank, Huylebroeck, Danny, Tylzanowski, Przemko

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Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome von Halim, Danny, Brosens, Erwin, Muller, Françoise, Wangler, Michael F., Beaudet, Arthur L., Lupski, James R., Akdemir, Zeynep H. Coban, Doukas, Michael, Stoop, Hans J., de Graaf, Bianca M., Brouwer, Rutger W.W., van Ijcken, Wilfred F.J., Oury, Jean-François, Rosenblatt, Jonathan, Burns, Alan J., Tibboel, Dick, Hofstra, Robert M.W., Alves, Maria M.

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NOXA expression drives synthetic lethality to RUNX1 inhibition in pancreatic cancer von Doffo, Josefina, Bamopoulos, Stefanos A, Köse, Hazal, Orben, Felix, Zang, Chuanbing, Pons, Miriam, den Dekker, Alexander T, Brouwer, Rutger W W, Baluapuri, Apoorva, Habringer, Stefan, Reichert, Maximillian, Illendula, Anuradha, Krämer, Oliver H, Schick, Markus, Wolf, Elmar, van IJcken, Wilfred F J, Esposito, Irene, Keller, Ulrich, Schneider, Günter, Wirth, Matthias

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MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome von Parenti, Ilaria, Diab, Farah, Gil, Sara Ruiz, Mulugeta, Eskeatnaf, Casa, Valentina, Berutti, Riccardo, Brouwer, Rutger W.W., Dupé, Valerie, Eckhold, Juliane, Graf, Elisabeth, Puisac, Beatriz, Ramos, Feliciano, Schwarzmayr, Thomas, Gines, Macarena Moronta, van Staveren, Thomas, van IJcken, Wilfred F.J., Strom, Tim M., Pié, Juan, Watrin, Erwan, Kaiser, Frank J., Wendt, Kerstin S.

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The tumor suppressor MIR139 is silenced by POLR2M to promote AML oncogenesis von Stavast, Christiaan J., van Zuijen, Iris, Karkoulia, Elena, Özçelik, Arman, van Hoven-Beijen, Antoinette, Leon, Leticia G., Voerman, Jane S. A., Janssen, George M. C., van Veelen, Peter A., Burocziova, Monika, Brouwer, Rutger W. W., van IJcken, Wilfred F. J., Maas, Alex, Bindels, Eric M., van der Velden, Vincent H. J., Schliehe, Christopher, Katsikis, Peter D., Alberich-Jorda, Meritxell, Erkeland, Stefan J.

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Single-Cell RNA Sequencing of Donor-Reactive T Cells Reveals Role of Apoptosis in Donor-Specific Hyporesponsiveness of Kidney Transplant Recipients von van der List, Amy C. J., Litjens, Nicolle H. R., Brouwer, Rutger W. W., Klepper, Mariska, den Dekker, Alexander T., van Ijcken, Wilfred F. J., Betjes, Michiel G. H.

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PTRHD1 Loss‐of‐function mutation in an african family with juvenile‐onset Parkinsonism and intellectual disability von Kuipers, Demy J.S., Carr, Jonathan, Bardien, Soraya, Thomas, Pearl, Sebate, Boiketlo, Breedveld, Guido J., van Minkelen, Rick, Brouwer, Rutger W.W., van Ijcken, Wilfred F.J., van Slegtenhorst, Marjon A., Bonifati, Vincenzo, Quadri, Marialuisa

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BMP4 and Temozolomide Synergize in the Majority of Patient-Derived Glioblastoma Cultures von Verploegh, Iris S C, Conidi, Andrea, El Hassnaoui, Hoesna, Verhoeven, Floor A M, Korporaal, Anne L, Ntafoulis, Ioannis, van den Hout, Mirjam C G N, Brouwer, Rutger W W, Lamfers, Martine L M, van IJcken, Wilfred F J, Huylebroeck, Danny, Leenstra, Sieger

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A systematic review and meta-analysis of hyperbaric oxygen therapy for diabetic foot ulcers with arterial insufficiency von Brouwer, Robin J., Lalieu, Rutger C., Hoencamp, Rigo, van Hulst, Rob A., Ubbink, Dirk T.

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Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations von Nellist, Mark, Brouwer, Rutger W W, Kockx, Christel E M, van Veghel-Plandsoen, Monique, Withagen-Hermans, Caroline, Prins-Bakker, Lida, Hoogeveen-Westerveld, Marianne, Mrsic, Alan, van den Berg, Mike M P, Koopmans, Anna E, de Wit, Marie-Claire, Jansen, Floor E, Maat-Kievit, Anneke J A, van den Ouweland, Ans, Halley, Dicky, de Klein, Annelies, van IJcken, Wilfred F J

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Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study von Van Opstal, Diane, van Maarle, Merel C, Lichtenbelt, Klaske, Weiss, Marjan M, Schuring-Blom, Heleen, Bhola, Shama L, Hoffer, Mariette J V, Huijsdens-van Amsterdam, Karin, Macville, Merryn V, Kooper, Angelique J A, Faas, Brigitte H W, Govaerts, Lutgarde, Tan-Sindhunata, Gita M, den Hollander, Nicolette, Feenstra, Ilse, Galjaard, Robert-Jan H, Oepkes, Dick, Ghesquiere, Stijn, Brouwer, Rutger W W, Beulen, Lean, Bollen, Sander, Elferink, Martin G, Straver, Roy, Henneman, Lidewij, Page-Christiaens, Godelieve C, Sistermans, Erik A

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Comparative single-cell RNA-sequencing profiling of BMP4-treated primary glioma cultures reveals therapeutic markers von Verploegh, Iris S C, Conidi, Andrea, Brouwer, Rutger W W, Balcioglu, Hayri E, Karras, Panagiotis, Makhzami, Samira, Korporaal, Anne, Marine, Jean-Christophe, Lamfers, Martine, Van IJcken, Wilfred F J, Leenstra, Sieger, Huylebroeck, Danny

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