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

द्वारा 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.
में प्रकाशित Immunogenetics (2019)

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

द्वारा 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
प्रकाशित 2013

Deciphering the RNA landscape by RNAome sequencing

द्वारा 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
में प्रकाशित RNA Biol (2015)

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

द्वारा 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.
में प्रकाशित PLoS Genet (2017)

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

द्वारा 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
में प्रकाशित Front Genet (2018)

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

द्वारा 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
में प्रकाशित Hum Mol Genet (2020)

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

द्वारा 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
प्रकाशित 2012

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

द्वारा 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
में प्रकाशित J Exp Med (2015)

Engram-specific transcriptome profiling of contextual memory consolidation

द्वारा 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.
में प्रकाशित Nat Commun (2019)

The dystrophin gene and cognitive function in the general population

द्वारा 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
में प्रकाशित Eur J Hum Genet (2015)

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

द्वारा 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
में प्रकाशित Front Genet (2017)

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

द्वारा 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
में प्रकाशित Blood Adv (2021)

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

द्वारा 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.
में प्रकाशित Front Genet (2020)

PLD3-variants in population studies

द्वारा 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.
में प्रकाशित Nature (2015)

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

द्वारा 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.
में प्रकाशित Genome Biol (2017)

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

द्वारा 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
में प्रकाशित Eur J Hum Genet (2015)

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

द्वारा 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
में प्रकाशित Eur J Hum Genet (2015)

Genetic variants in RBFOX3 are associated with sleep latency

द्वारा 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
में प्रकाशित Eur J Hum Genet (2016)