Characterization of the ferret TRB locus guided by V, D, J, and C gene expression analysis

gan Gerritsen, Bram, Pandit, Aridaman, Zaaraoui-Boutahar, Fatiha, van den Hout, Mirjam C. G. N., van IJcken, Wilfred F. J., de Boer, Rob J., Andeweg, Arno C.
Cyhoeddwyd yn Immunogenetics (2019)

Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia

gan Papasavva, Thessalia, van IJcken, Wilfred F J, Kockx, Christel E M, van den Hout, Mirjam C G N, Kountouris, Petros, Kythreotis, Loukas, Kalogirou, Eleni, Grosveld, Frank G, Kleanthous, Marina
Cyhoeddwyd 2013

Deciphering the RNA landscape by RNAome sequencing

gan Derks, Kasper WJ, Misovic, Branislav, van den Hout, Mirjam CGN, Kockx, Christel EM, Payan Gomez, Cesar, Brouwer, Rutger WW, Vrieling, Harry, Hoeijmakers, Jan HJ, van IJcken, Wilfred FJ, Pothof, Joris
Cyhoeddwyd yn RNA Biol (2015)

Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer element

gan Zuin, Jessica, Casa, Valentina, Pozojevic, Jelena, Kolovos, Petros, van den Hout, Mirjam C. G. N., van Ijcken, Wilfred F. J., Parenti, Ilaria, Braunholz, Diana, Baron, Yorann, Watrin, Erwan, Kaiser, Frank J., Wendt, Kerstin S.
Cyhoeddwyd yn PLoS Genet (2017)

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

gan Vojinovic, Dina, Kavousi, Maryam, Ghanbari, Mohsen, Brouwer, Rutger W. W., van Rooij, Jeroen G. J., van den Hout, Mirjam C. G. N., Kraaij, Robert, van Ijcken, Wilfred F. J., Uitterlinden, Andre G., van Duijn, Cornelia M., Amin, Najaf
Cyhoeddwyd yn Front Genet (2018)

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

gan Birkhoff, Judith C, Brouwer, Rutger W W, Kolovos, Petros, Korporaal, Anne L, Bermejo-Santos, Ana, Boltsis, Ilias, Nowosad, Karol, van den Hout, Mirjam C G N, Grosveld, Frank G, van IJcken, Wilfred F J, Huylebroeck, Danny, Conidi, Andrea
Cyhoeddwyd yn Hum Mol Genet (2020)

Dynamic long-range chromatin interactions control Myb proto-oncogene transcription during erythroid development

gan Stadhouders, Ralph, Thongjuea, Supat, Andrieu-Soler, Charlotte, Palstra, Robert-Jan, Bryne, Jan Christian, van den Heuvel, Anita, Stevens, Mary, de Boer, Ernie, Kockx, Christel, van der Sloot, Antoine, van den Hout, Mirjam, van IJcken, Wilfred, Eick, Dirk, Lenhard, Boris, Grosveld, Frank, Soler, Eric
Cyhoeddwyd 2012

Whole-transcriptome analysis of endothelial to hematopoietic stem cell transition reveals a requirement for Gpr56 in HSC generation

gan Solaimani Kartalaei, Parham, Yamada-Inagawa, Tomoko, Vink, Chris S., de Pater, Emma, van der Linden, Reinier, Marks-Bluth, Jonathon, van der Sloot, Anthon, van den Hout, Mirjam, Yokomizo, Tomomasa, van Schaick-Solernó, M. Lucila, Delwel, Ruud, Pimanda, John E., van IJcken, Wilfred F.J., Dzierzak, Elaine
Cyhoeddwyd yn J Exp Med (2015)

Engram-specific transcriptome profiling of contextual memory consolidation

gan Rao-Ruiz, Priyanka, Couey, Jonathan J., Marcelo, Ivo M., Bouwkamp, Christian G., Slump, Denise E., Matos, Mariana R., van der Loo, Rolinka J., Martins, Gabriela J., van den Hout, Mirjam, van IJcken, Wilfred F., Costa, Rui M., van den Oever, Michel C., Kushner, Steven A.
Cyhoeddwyd yn Nat Commun (2019)

The dystrophin gene and cognitive function in the general population

gan Vojinovic, Dina, Adams, Hieab HH, van der Lee, Sven J, Ibrahim-Verbaas, Carla A, Brouwer, Rutger, van den Hout, Mirjam CGN, Oole, Edwin, van Rooij, Jeroen, Uitterlinden, Andre, Hofman, Albert, van IJcken, Wilfred FJ, Aartsma-Rus, Annemieke, van Ommen, GertJan B, Ikram, M Arfan, van Duijn, Cornelia M, Amin, Najaf
Cyhoeddwyd yn Eur J Hum Genet (2015)

Exome-Wide Meta-Analysis Identifies Rare 3′-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea

gan van der Spek, Ashley, Luik, Annemarie I., Kocevska, Desana, Liu, Chunyu, Brouwer, Rutger W. W., van Rooij, Jeroen G. J., van den Hout, Mirjam C. G. N., Kraaij, Robert, Hofman, Albert, Uitterlinden, André G., van IJcken, Wilfred F. J., Gottlieb, Daniel J., Tiemeier, Henning, van Duijn, Cornelia M., Amin, Najaf
Cyhoeddwyd yn Front Genet (2017)

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

gan Wessels, Marja W., Cnossen, Marjon H., van Dijk, Thamar B., Gillemans, Nynke, Schmidt, K. L. Juliëtte, van Lom, Kirsten, Vinjamur, Divya S., Coyne, Steven, Kurita, Ryo, Nakamura, Yukio, de Man, Stella A., Pfundt, Rolph, Azmani, Zakia, Brouwer, Rutger W. W., Bauer, Daniel E., van den Hout, Mirjam C. G. N., van IJcken, Wilfred F. J., Philipsen, Sjaak
Cyhoeddwyd yn Blood Adv (2021)

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

gan van der Spek, Ashley, Warner, Sophie C., Broer, Linda, Nelson, Christopher P., Vojinovic, Dina, Ahmad, Shahzad, Arp, Pascal P., Brouwer, Rutger W. W., Denniff, Matthew, van den Hout, Mirjam C. G. N., van Rooij, Jeroen G. J., Kraaij, Robert, van IJcken, Wilfred F. J., Samani, Nilesh J., Ikram, M. Arfan, Uitterlinden, André G., Codd, Veryan, Amin, Najaf, van Duijn, Cornelia M.
Cyhoeddwyd yn Front Genet (2020)

PLD3-variants in population studies

gan van der Lee, Sven J., Holstege, Henne, Wong, Tsz Hang, Jakobsdottir, Johanna, Bis, Joshua C., Chouraki, Vincent, van Rooij, Jeroen G.J., Grove, Megan L., Smith, Albert V., Amin, Najaf, Choi, Seung-Hoan, Beiser, Alexa S., Garcia, Melissa E., van IJcken, Wilfred F.J., Pijnenburg, Yolande A.L., Louwersheimer, Eva, Brouwer, Rutger W.W., van den Hout, Mirjam C.G.N., Oole, Edwin, Eirkisdottir, Gudny, Levy, Daniel, Rotter, Jerome I., Emilsson, Valur, O’Donnell, Christopher J., Aspelund, Thor, Uitterlinden, Andre G., Launer, Lenore J., Hofman, Albert, Boerwinkle, Eric, Psaty, Bruce M., DeStefano, Anita L., Scheltens, Philip, Seshadri, Sudha, van Swieten, John C., Gudnason, Vilmundur, van der Flier, Wiesje M., Ikram, M. Arfan, van Duijn, Cornelia M.
Cyhoeddwyd yn Nature (2015)

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

gan Gui, Hongsheng, Schriemer, Duco, Cheng, William W., Chauhan, Rajendra K., Antiňolo, Guillermo, Berrios, Courtney, Bleda, Marta, Brooks, Alice S., Brouwer, Rutger W. W., Burns, Alan J., Cherny, Stacey S., Dopazo, Joaquin, Eggen, Bart J. L., Griseri, Paola, Jalloh, Binta, Le, Thuy-Linh, Lui, Vincent C. H., Luzón-Toro, Berta, Matera, Ivana, Ngan, Elly S. W., Pelet, Anna, Ruiz-Ferrer, Macarena, Sham, Pak C., Shepherd, Iain T., So, Man-Ting, Sribudiani, Yunia, Tang, Clara S. M., van den Hout, Mirjam C. G. N., van der Linde, Herma C., van Ham, Tjakko J., van IJcken, Wilfred F. J., Verheij, Joke B. G. M., Amiel, Jeanne, Borrego, Salud, Ceccherini, Isabella, Chakravarti, Aravinda, Lyonnet, Stanislas, Tam, Paul K. H., Garcia-Barceló, Maria-Mercè, Hofstra, Robert M. W.
Cyhoeddwyd yn Genome Biol (2017)

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects

gan Vrijenhoek, Terry, Kraaijeveld, Ken, Elferink, Martin, de Ligt, Joep, Kranendonk, Elcke, Santen, Gijs, Nijman, Isaac J, Butler, Derek, Claes, Godelieve, Costessi, Adalberto, Dorlijn, Wim, van Eyndhoven, Winfried, Halley, Dicky JJ, van den Hout, Mirjam CGN, van Hove, Steven, Johansson, Lennart F, Jongbloed, Jan DH, Kamps, Rick, Kockx, Christel EM, de Koning, Bart, Kriek, Marjolein, Deprez, Ronald Lekanne dit, Lunstroo, Hans, Mannens, Marcel, Mook, Olaf R, Nelen, Marcel, Ploem, Corrette, Rijnen, Marco, Saris, Jasper J, Sinke, Richard, Sistermans, Erik, van Slegtenhorst, Marjon, Sleutels, Frank, van der Stoep, Nienke, van Tienhoven, Marianne, Vermaat, Martijn, Vogel, Maartje, Waisfisz, Quinten, Weiss, Janneke Marjan, van den Wijngaard, Arthur, van Workum, Wilbert, Ijntema, Helger, van der Zwaag, Bert, van IJcken, Wilfred FJ, den Dunnen, Johan T, Veltman, Joris A, Hennekam, Raoul, Cuppen, Edwin
Cyhoeddwyd yn Eur J Hum Genet (2015)

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects

gan Vrijenhoek, Terry, Kraaijeveld, Ken, Elferink, Martin, de Ligt, Joep, Kranendonk, Elcke, Santen, Gijs, Nijman, Isaac J, Butler, Derek, Claes, Godelieve, Costessi, Adalberto, Dorlijn, Wim, van Eyndhoven, Winfried, Halley, Dicky J J, van den Hout, Mirjam C G N, van Hove, Steven, Johansson, Lennart F, Jongbloed, Jan D H, Kamps, Rick, Kockx, Christel E M, de Koning, Bart, Kriek, Marjolein, Lekanne dit Deprez, Ronald, Lunstroo, Hans, Mannens, Marcel, Mook, Olaf R, Nelen, Marcel, Ploem, Corrette, Rijnen, Marco, Saris, Jasper J, Sinke, Richard, Sistermans, Erik, van Slegtenhorst, Marjon, Sleutels, Frank, van der Stoep, Nienke, van Tienhoven, Marianne, Vermaat, Martijn, Vogel, Maartje, Waisfisz, Quinten, Marjan Weiss, Janneke, van den Wijngaard, Arthur, van Workum, Wilbert, Ijntema, Helger, van der Zwaag, Bert, van IJcken, Wilfred FJ, den Dunnen, Johan, Veltman, Joris A, Hennekam, Raoul, Cuppen, Edwin
Cyhoeddwyd yn Eur J Hum Genet (2015)

Genetic variants in RBFOX3 are associated with sleep latency

gan Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G, Mbarek, Hamdi, Watson, Nathaniel F, Melville, Scott A, Del Greco, Fabiola M, Byrne, Enda M, Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S, Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A, Zgaga, Lina, Mihailov, Evelin, Stone, Katie L, Campbell, Harry, Brouwer, Rutger WW, Demirkan, Ayse, Isaacs, Aaron, Dogas, Zoran, Marciante, Kristin D, Campbell, Susan, Borovecki, Fran, Luik, Annemarie I, Li, Man, Hottenga, Jouke Jan, Huffman, Jennifer E, van den Hout, Mirjam CGN, Cummings, Steven R, Aulchenko, Yurii S, Gehrman, Philip R, Uitterlinden, André G, Wichmann, Heinz-Erich, Müller-Nurasyid, Martina, Fehrmann, Rudolf SN, Montgomery, Grant W, Hofman, Albert, Kao, Wen Hong Linda, Oostra, Ben A, Wright, Alan F, Vink, Jacqueline M, Wilson, James F, Pramstaller, Peter P, Hicks, Andrew A, Polasek, Ozren, Punjabi, Naresh M, Redline, Susan, Psaty, Bruce M, Heath, Andrew C, Merrow, Martha, Tranah, Gregory J, Gottlieb, Daniel J, Boomsma, Dorret I, Martin, Nicholas G, Rudan, Igor, Tiemeier, Henning, van IJcken, Wilfred FJ, Penninx, Brenda W, Metspalu, Andres, Meitinger, Thomas, Franke, Lude, Roenneberg, Till, van Duijn, Cornelia M
Cyhoeddwyd yn Eur J Hum Genet (2016)