Overexpression of Full-Length ETV1 Transcripts in Clinical Prostate Cancer Due to Gene Translocation

Por Gasi, Delila, van der Korput, Hetty A., Douben, Hannie C., de Klein, Annelies, de Ridder, Corrina M., van Weerden, Wytske M., Trapman, Jan
Publicado em 2011

MN1 affects expression of genes involved in hematopoiesis and can enhance as well as inhibit RAR/RXR-induced gene expression

Por Meester-Smoor, Magda A., Janssen, Marjolein J.F.W., Grosveld, Gerard C., de Klein, Annelies, van IJcken, Wilfred F.J., Douben, Hannie, Zwarthoff, Ellen C.
Publicado em 2008

Comparable Low-Level Mosaicism in Affected and Non Affected Tissue of a Complex CDH Patient

Por Veenma, Danielle, Beurskens, Niels, Douben, Hannie, Eussen, Bert, Noomen, Petra, Govaerts, Lutgarde, Grijseels, Els, Lequin, Maarten, de Krijger, Ronald, Tibboel, Dick, de Klein, Annelies, Van Opstal, Dian
Publicado em 2010

Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts

Por Veenma, Danielle, Brosens, Erwin, de Jong, Elisabeth, van de Ven, Cees, Meeussen, Connie, Cohen-Overbeek, Titia, Boter, Marjan, Eussen, Hubertus, Douben, Hannie, Tibboel, Dick, de Klein, Annelies
Publicado em 2012

Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies

Por van der Veken, Lars T, Dieleman, Marianne MJ, Douben, Hannie, van de Brug, Judith C, van de Graaf, Raoul, Hoogeboom, A Jeannette M, Poddighe, Pino J, de Klein, Annelies
Publicado em 2010

5q11.2 deletion in a patient with tracheal agenesis

Por de Jong, Elisabeth M, Douben, Hannie, Eussen, Bert H, Felix, Janine F, Wessels, Marja W, Poddighe, Pino J, Nikkels, Peter G J, de Krijger, Ronald R, Tibboel, Dick, de Klein, Annelies
Publicado em 2010

Stable X Chromosome Reactivation in Female Human Induced Pluripotent Stem Cells

Por Barakat, Tahsin Stefan, Ghazvini, Mehrnaz, de Hoon, Bas, Li, Tracy, Eussen, Bert, Douben, Hannie, van der Linden, Reinier, van der Stap, Nathalie, Boter, Marjan, Laven, Joop S., Galjaard, Robert-Jan, Grootegoed, J. Anton, de Klein, Annelies, Gribnau, Joost
Publicado no Stem Cell Reports (2015)

Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation

Por de Esch, Celine E.F., Ghazvini, Mehrnaz, Loos, Friedemann, Schelling-Kazaryan, Nune, Widagdo, W., Munshi, Shashini T., van der Wal, Erik, Douben, Hannie, Gunhanlar, Nilhan, Kushner, Steven A., Pijnappel, W.W.M. Pim, de Vrij, Femke M.S., Geijsen, Niels, Gribnau, Joost, Willemsen, Rob
Publicado no Stem Cell Reports (2014)

Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice

Por Beck, Tyler F., Veenma, Danielle, Shchelochkov, Oleg A., Yu, Zhiyin, Kim, Bum Jun, Zaveri, Hitisha P., van Bever, Yolande, Choi, Sunju, Douben, Hannie, Bertin, Terry K., Patel, Pragna I., Lee, Brendan, Tibboel, Dick, de Klein, Annelies, Stockton, David W., Justice, Monica J., Scott, Daryl A.
Publicado em 2013

Unbalanced der(5)t(5;20) translocation associated with Megalencephaly, perisylvian Polymicrogyria, Polydactyly and Hydrocephalus

Por Verkerk, Annemieke J.M.H., Schot, Rachel, van Waterschoot, Laura, Douben, Hannie, Poddighe, Pino J., Lequin, Maarten H., de Vries, Linda S., Terhal, Paulien, Hahnemann, Johanne M.D., de Coo, Irenaeus F.M., de Wit, Marie-Claire Y., Wafelman, Leontien S., Garavelli, Livia, Dobyns, William B., Van der Spek, Peter J., de Klein, Annelies, Mancini, Grazia M.S.
Publicado em 2010

Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula

Por Brosens, Erwin, Marsch, Florian, de Jong, Elisabeth M, Zaveri, Hitisha P, Hilger, Alina C, Choinitzki, Vera Gisela, Hölscher, Alice, Hoffmann, Per, Herms, Stefan, Boemers, Thomas M, Ure, Benno M, Lacher, Martin, Ludwig, Michael, Eussen, Bert H, van der Helm, Robert M, Douben, Hannie, Van Opstal, Diane, Wijnen, Rene M H, Beverloo, H Berna, van Bever, Yolande, Brooks, Alice S, IJsselstijn, Hanneke, Scott, Daryl A, Schumacher, Johannes, Tibboel, Dick, Reutter, Heiko, de Klein, Annelies
Publicado no Eur J Hum Genet (2016)