Not logged in Share Save
Crosstalk Between NK Cell Receptors and Tumor Membrane Hsp70-Derived Peptide: A Combined Computational and Experimental Study Yazdi, Mina; Kafshgari, Morteza Hasanzadeh; Moghadam, Fatemeh Khademi; Zarezade, Vahid; Oellinger, Rupert; Khosravi, Mohammad; Haas, Stefan; Hoch, Cosima C.; Pockley, Alan Graham; Wagner, Ernst; Wollenberg, Barbara; Multhoff, Gabriele; Dezfouli, Ali Bashiri Share Save
Induction of kidney-related gene programs through co-option of SALL1 in mole ovotestes Schindler, Magdalena; Osterwalder, Marco; Harabula, Izabela; Wittler, Lars; Tzika, Athanasia C.; Dechmann, Dina K. N.; Vingron, Martin; Visel, Axel; Haas, Stefan A.; Real, Francisca M. Share Save
Share Save
Preformed chromatin topology assists transcriptional robustness of Shh during limb development Paliou, Christina; Guckelberger, Philine; Schoepflin, Robert; Heinrich, Verena; Esposito, Andrea; Chiariello, Andrea M.; Bianco, Simona; Annunziatella, Carlo; Helmuth, Johannes; Haas, Stefan; Jerkovic, Ivana; Brieske, Norbert; Wittler, Lars; Timmermann, Bernd; Nicodemi, Mario; Vingron, Martin; Mundlos, Stefan; Andrey, Guillaume Share Save
Mutation p.R356Q in the Collybistin Phosphoinositide Binding Site Is Associated With Mild Intellectual Disability Chiou, Tzu-Ting; Long, Philip; Schumann-Gillett, Alexandra; Kanamarlapudi, Venkateswarlu; Haas, Stefan A.; Harvey, Kirsten; O'Mara, Megan L.; De Blasi, Angel L.; Kalscheuer, Vera M.; Harvey, Robert J. Share Save
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder Frints, Suzanna G. M.; Ozanturk, Aysegul; Rodriguez Criado, German; Grasshoff, Ute; de Hoon, Bas; Field, Michael; Manouvrier-Hanu, Sylvie; Hickey, Scott E.; Kammoun, Molka; Gripp, Karen W.; Bauer, Claudia; Schroeder, Christopher; Toutain, Annick; Mosher, Theresa Mihalic; Kelly, Benjamin J.; White, Peter; Dufke, Andreas; Rentmeester, Eveline; Moon, Sungjin; Koboldt, Daniel C.; van Roozendaal, Kees E. P.; Hu, Hao; Haas, Stefan A.; Ropers, Hans-Hilger; Murray, Lucinda; Haan, Eric; Shaw, Marie; Carroll, Renee; Friend, Kathryn; Liebelt, Jan; Hobson, Lynne; De Rademaeker, Marjan; Geraedts, Joep; Fryns, Jean-Pierre; Vermeesch, Joris; Raynaud, Martine; Riess, Olaf; Gribnau, Joost; Katsanis, Nicholas; Devriendt, Koen; Bauer, Peter; Gecz, Jozef; Golzio, Christelle; Gontan, Cristina; Kalscheuer, Vera M. Share Save
Genomic and Functional Fidelity of Small Cell Lung Cancer Patient-Derived Xenografts Drapkin, Benjamin J.; George, Julie; Christensen, Camilla L.; Mino-Kenudson, Mari; Dries, Ruben; Sundaresan, Tilak; Phat, Sarah; Myers, David T.; Zhong, Jun; Igo, Peter; Hazar-Rethinam, Mehlika H.; Licausi, Joseph A.; Gomez-Caraballo, Maria; Kem, Marina; Jani, Kandarp N.; Azimi, Roxana; Abedpour, Nima; Menon, Roopika; Lakis, Sotirios; Heist, Rebecca S.; Buettner, Reinhard; Haas, Stefan; Sequist, Lecia V.; Shaw, Alice T.; Wong, Kwok-Kin; Hata, Aaron N.; Toner, Mehmet; Maheswaran, Shyamala; Haber, Daniel A.; Peifer, Martin; Dyson, Nicholas; Thomas, Roman K.; Farago, Anna F. Share Save
Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors George, Julie; Walter, Vonn; Peifer, Martin; Alexandrov, Ludmil B.; Seidel, Danila; Leenders, Frauke; Maas, Lukas; Mueller, Christian; Dahmen, Ilona; Delhomme, Tiffany M.; Ardin, Maude; Leblay, Noemie; Byrnes, Graham; Sun, Ruping; De Reynies, Aurelien; McLeer-Florin, Anne; Bosco, Graziella; Malchers, Florian; Menon, Roopika; Altmuller, Janine; Becker, Christian; Nurnberg, Peter; Achter, Viktor; Lang, Ulrich; Schneider, Peter M.; Bogus, Magdalena; Soloway, Matthew G.; Wilkerson, Matthew D.; Cun, Yupeng; McKay, James D.; Moro-Sibilot, Denis; Brambilla, Christian G.; Lantuejoul, Sylvie; Lemaitre, Nicolas; Soltermann, Alex; Weder, Walter; Tischler, Verena; Brustugun, Odd Terje; Lund-Iversen, Marius; Helland, Aslaug; Solberg, Steinar; Ansen, Sascha; Wright, Gavin; Solomon, Benjamin; Roz, Luca; Pastorino, Ugo; Petersen, Iver; Clement, Joachim H.; Saenger, Jorg; Wolf, Jurgen; Vingron, Martin; Zander, Thomas; Perner, Sven; Travis, William D.; Haas, Stefan A.; Olivier, Magali; Foll, Matthieu; Buettner, Reinhard; Hayes, David Neil; Brambilla, Elisabeth; Fernandez-Cuesta, Lynnette; Thomas, Roman K. Share Save
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features Niturad, Cristina Elena; Lev, Dorit; Kalscheuer, Vera M.; Charzewska, Agnieszka; Schubert, Julian; Lerman-Sagie, Tally; Kroes, Hester Y.; Oegema, Renske; Traverso, Monica; Specchio, Nicola; Lassota, Maria; Chelly, Jamel; Bennett-Back, Odeya; Carmi, Nirit; Koffler-Brill, Tal; Iacomino, Michele; Trivisano, Marina; Capovilla, Giuseppe; Striano, Pasquale; Nawara, Magdalena; Rzonca, Sylwia; Fischer, Ute; Bienek, Melanie; Jensen, Corinna; Hu, Hao; Thiele, Holger; Altmuller, Janine; Krause, Roland; May, Patrick; Becker, Felicitas; Balling, Rudi; Biskup, Saskia; Haas, Stefan A.; Nuernberg, Peter; van Gassen, Koen L. I.; Lerche, Holger; Zara, Federico; Maljevic, Snezana; Leshinsky-Silver, Esther Share Save
Haplotype-resolved sweet potato genome traces back its hexaploidization history Yang, Jun; Moeinzadeh, M-Hossein; Kuhl, Heiner; Helmuth, Johannes; Xiao, Peng; Haas, Stefan; Liu, Guiling; Zheng, Jianli; Sun, Zhe; Fan, Weijuan; Deng, Gaifang; Wang, Hongxia; Hu, Fenhong; Zhao, Shanshan; Fernie, Alisdair R.; Boerno, Stefan; Timmermann, Bernd; Zhang, Peng; Vingron, Martin Share Save
EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO Skopkova, Martina; Hennig, Friederike; Shin, Byung-Sik; Turner, Clesson E.; Stanikova, Daniela; Brennerova, Katarina; Stanik, Juraj; Fischer, Ute; Henden, Lyndal; Mueller, Ulrich; Steinberger, Daniela; Leshinsky-Silver, Esther; Bottani, Armand; Kurdiova, Timea; Ukropec, Jozef; Nyitrayova, Olga; Kolnikova, Miriam; Klimes, Iwar; Borck, Guntram; Bahlo, Melanie; Haas, Stefan A.; Kim, Joo-Ran; Lotspeich-Cole, Leda E.; Gasperikova, Daniela; Dever, Thomas E.; Kalscheuer, Vera M. Share Save
Genome-Wide Binding of Posterior HOXA/D Transcription Factors Reveals Subgrouping and Association with CTCF Jerkovic, Ivana; Ibrahim, Daniel M.; Andrey, Guillaume; Haas, Stefan; Hansen, Peter; Janetzki, Catrin; Navarrete, Irene Gonzalez; Robinson, Peter N.; Hecht, Jochen; Mundlos, Stefan Share Save
Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding Andrey, Guillaume; Schoeflin, Robert; Jerkovic, Ivana; Heinrich, Verena; Ibrahim, Daniel M.; Paliou, Christina; Hochradel, Myriam; Timmermann, Bernd; Haas, Stefan; Vingron, Martin; Mundlos, Stefan Share Save
Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family Kalscheuer, Vera M.; James, Victoria M.; Himelright, Miranda L.; Long, Philip; Oegema, Renske; Jensen, Corinna; Bienek, Melanie; Hu, Hao; Haas, Stefan A.; Topf, Maya; Hoogeboom, A. Jeannette M.; Harvey, Kirsten; Walikonis, Randall; Harvey, Robert J. Share Save
Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems Kumar, Raman; Corbett, Mark A.; Van Bon, Bregje W. M.; Gardner, Alison; Woenig, Joshua A.; Jolly, Lachlan A.; Douglas, Evelyn; Friend, Kathryn; Tan, Chuan; Van Esch, Hilde; Holvoet, Maureen; Raynaud, Martine; Field, Michael; Leffler, Melanie; Budny, Bartlomiej; Wisniewska, Marzena; Badura-Stronka, Magdalena; Latos-Bielenska, Anna; Batanian, Jacqueline; Rosenfeld, Jill A.; Basel-Vanagaite, Lina; Jensen, Corinna; Bienek, Melanie; Froyen, Guy; Ullmann, Reinhard; Hu, Hao; Love, Michael I.; Haas, Stefan A.; Stankiewicz, Pawel; Cheung, Sau Wai; Baxendale, Anne; Nicholl, Jillian; Thompson, Elizabeth M.; Haan, Eric; Kalscheuer, Vera M.; Gecz, Jozef Share Save
A Novel Mutation in RPL10(Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia Zanni, Ginevra; Kalscheuer, Vera M.; Friedrich, Andreas; Barresi, Sabina; Alfieri, Paolo; Di Capua, Matteo; Haas, Stefan A.; Piccini, Giorgia; Karl, Thomas; Klauck, Sabine M.; Bellacchio, Emanuele; Emma, Francesco; Cappa, Marco; Bertini, Enrico; Breitenbach-Koller, Lore Share Save
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling Blok, Lot Snijders; Madsen, Erik; Juusola, Jane; Gilissen, Christian; Baralle, Diana; Reijnders, Margot R. F.; Venselaar, Hanka; Helsmoorte, Celine; Cho, Megan T.; Hoischen, Alexander; Vissers, Lisenka E. L. M.; Koemans, Tom S.; Wissink-Lindhout, Willemijn; Eichler, Evan E.; Romano, Corrado; Van Esch, Hilde; Stumpel, Connie; Vreeburg, Maaike; Smeets, Eric; Obemdorff, Karin; van Bon, Bregje W. M.; Shaw, Marie; Gecz, Jozef; Haan, Eric; Bienek, Melanie; Jensen, Corinna; Loeys, Bart L.; Van Diick, Anke; Innes, A. Micheil; Racher, Hilary; Vermeer, Sascha; Di Donato, Nataliya; Rump, Andreas; Tatton-Brown, Katrina; Parker, Michael J.; Henderson, Alex; Lynch, Sally A.; Fryer, Alan; Ross, Alison; Vasudevan, Pradeep; Kini, Usha; Newbury-Ecob, Ruth; Chandler, Kate; Male, Alison; Dijkstra, Sybe; Schieving, Jolanda; Giltay, Jacques; Van Gassen, Koen L. I.; Schuurs-Hoeijmakers, Janneke; Tan, Perciliz L.; Pediaditakis, Igor; Haas, Stefan A.; Retterer, Kyle; Reed, Patrick; Monaghan, Kristin G.; Haverfield, Eden; Natowicz, Marvin; Myers, Angela; Kruer, Michael C.; Stein, Quinn; Strauss, Kevin A.; Brigatti, Karlla W.; Keating, Katherine; Burton, Barbara K.; Kim, Katherine H.; Charrow, Joel; Norman, Jennifer; Foster-Barber, Audrey; Kline, Antonie D.; Kimball, Amy; Zackai, Elaine; Harr, Margaret; Fox, Joyce; McLaughlin, Julie; Lindstrom, Kristin; Haude, Katrina M.; van Roozendaal, Kees; Brunner, Han; Chung, Wendy K.; Kooy, R. Frank; Pfundt, Rolph; Kalscheuer, Vera; Mehta, Sarju G.; Katsanis, Nicholas; Kleefstra, Tjitske Share Save
THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability Kumar, Raman; Corbett, Mark A.; van Bon, Bregje W. M.; Woenig, Joshua A.; Weir, Lloyd; Douglas, Evelyn; Friend, Kathryn L.; Gardner, Alison; Shaw, Marie; Jolly, Lachlan A.; Tan, Chuan; Hunter, Matthew F.; Hackett, Anna; Field, Michael; Palmer, Elizabeth E.; Leffler, Melanie; Rogers, Carolyn; Boyle, Jackie; Bienek, Melanie; Jensen, Corinna; Van Buggenhout, Griet; Van Esch, Hilde; Hoffmann, Katrin; Raynaud, Martine; Zhao, Huiying; Reed, Robin; Hu, Hao; Haas, Stefan A.; Haan, Eric; Kalscheuer, Vera M.; Gecz, Jozef Share Save
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes Hu, H.; Haas, S. A.; Chelly, J.; Van Esch, H.; Raynaud, M.; de Brouwer, A. P. M.; Weinert, S.; Froyen, G.; Frints, S. G. M.; Laumonnier, F.; Zemojtel, T.; Love, M. I.; Richard, H.; Emde, A-K; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; Wissink-Lindhout, W.; Lebrun, N.; Castelnau, L.; Rucci, J.; Montjean, R.; Dorseuil, O.; Billuart, P.; Stuhlmann, T.; Shaw, M.; Corbett, M. A.; Gardner, A.; Willis-Owen, S.; Tan, C.; Friend, K. L.; Belet, S.; van Roozendaal, K. E. P.; Jimenez-Pocquet, M.; Moizard, M-P; Ronce, N.; Sun, R.; O'Keeffe, S.; Chenna, R.; Van Boemmel, A.; Goeke, J.; Hackett, A.; Field, M.; Christie, L.; Boyle, J.; Haan, E.; Nelson, J.; Turner, G.; Baynam, G.; Gillessen-Kaesbach, G.; Mueller, U.; Steinberger, D.; Budny, B.; Badura-Stronka, M.; Latos-Bielenska, A.; Ousager, L. B.; Wieacker, P.; Criado, G. Rodriguez; Bondeson, M-L; Anneren, G.; Dufke, A.; Cohen, M.; Van Maldergem, L.; Vincent-Delorme, C.; Echenne, B.; Simon-Bouy, B.; Kleefstra, T.; Willemsen, M.; Fryns, J-P; Devriendt, K.; Ullmann, R.; Vingron, M.; Wrogemann, K.; Wienker, T. F.; Tzschach, A.; van Bokhoven, H.; Gecz, J.; Jentsch, T. J.; Chen, W.; Ropers, H-H; Kalscheuer, V. M. Share Save
.png){kind=icon}
.png){kind=icon}
Not logged in.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
