Validation of a Combined Transcriptome and T Cell Receptor Alpha/Beta (TRA/TRB) Repertoire Assay at the Single Cell Level for Paucicellular Samples by Nicolle H. R. Litjens, Anton W. Langerak, Amy C. J. van der List, Mariska Klepper, Maaike de Bie, Zakia Azmani, Zakia Azmani, Alexander T. den Dekker, Alexander T. den Dekker, Rutger W. W. Brouwer, Rutger W. W. Brouwer, Michiel G. H. Betjes, Wilfred F. J. Van IJcken, Wilfred F. J. Van IJcken

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

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Effect of bovine milk fat-based infant formulae on microbiota, metabolites and stool parameters in healthy term infants in a randomized, crossover, placebo-controlled trial by Ellen Looijesteijn, Rutger W. W. Brouwer, Ruud J. W. Schoemaker, Laurien H. Ulfman, Stephanie L. Ham, Prescilla Jeurink, Eva Karaglani, Wilfred F. J. van IJcken, Yannis Manios

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

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Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge by Erwin Brosens, Nina C. J. Peters, Kim S. van Weelden, Kim S. van Weelden, Kim S. van Weelden, Charlotte Bendixen, Rutger W. W. Brouwer, Rutger W. W. Brouwer, Frank Sleutels, Hennie T. Bruggenwirth, Wilfred F. J. van Ijcken, Wilfred F. J. van Ijcken, Danielle C. M. Veenma, Danielle C. M. Veenma, Suzan C. M. Cochius-Den Otter, Rene M. H. Wijnen, Alex J. Eggink, Marieke F. van Dooren, Heiko Martin Reutter, Heiko Martin Reutter, Robbert J. Rottier, Robbert J. Rottier, J. Marco Schnater, Dick Tibboel, Annelies de Klein

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

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Exome-Wide Meta-Analysis Identifies Rare 3′-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea by Ashley van der Spek, Annemarie I. Luik, Desana Kocevska, Chunyu Liu, Chunyu Liu, Chunyu Liu, Rutger W. W. Brouwer, Jeroen G. J. van Rooij, Jeroen G. J. van Rooij, Jeroen G. J. van Rooij, Mirjam C. G. N. van den Hout, Robert Kraaij, Robert Kraaij, Robert Kraaij, Albert Hofman, Albert Hofman, André G. Uitterlinden, André G. Uitterlinden, André G. Uitterlinden, Wilfred F. J. van IJcken, Daniel J. Gottlieb, Daniel J. Gottlieb, Daniel J. Gottlieb, Henning Tiemeier, Henning Tiemeier, Cornelia M. van Duijn, Najaf Amin

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Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length by Ashley van der Spek, Ashley van der Spek, Sophie C. Warner, Linda Broer, Christopher P. Nelson, Christopher P. Nelson, Dina Vojinovic, Shahzad Ahmad, Pascal P. Arp, Rutger W. W. Brouwer, Matthew Denniff, Mirjam C. G. N. van den Hout, Jeroen G. J. van Rooij, Jeroen G. J. van Rooij, Robert Kraaij, Wilfred F. J. van IJcken, Nilesh J. Samani, Nilesh J. Samani, M. Arfan Ikram, André G. Uitterlinden, André G. Uitterlinden, Veryan Codd, Veryan Codd, Najaf Amin, Najaf Amin, Cornelia M. van Duijn, Cornelia M. van Duijn

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