Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH von Mantripragada, K K, Thuresson, A-C, Piotrowski, A, Díaz de Ståhl, T, Menzel, U, Grigelionis, G, Ferner, R E, Griffiths, S, Bolund, L, Mautner, V, Nordling, M, Legius, E, Vetrie, D, Dahl, N, Messiaen, L, Upadhyaya, M, Bruder, C E G, Dumanski, J P

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High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH von BRUDER, Carl E. G, HIRVELÄ, Carina, ZUCMAN-ROSSI, Jessica, HERGERSBERG, Martin, BOLTSHAUSER, Eugene, PAPI, Laura, ROULEAU, Guy A, POPTODOROV, George, JORDANOVA, Albena, RASK-ANDERSEN, Helge, KLUWE, Lan, MAUTNER, Victor, TAPIA-PAEZ, Isabel, SAINIO, Markku, HUNG, Gene, MATHIESEN, Tiit, MÖLLER, Claes, PULST, Stefan M, HARDER, Henrik, HEIBERG, Arvid, HONDA, Mariko, NIIMURA, Michihito, SAHLEN, Sigrid, FRANSSON, Ingegerd, BLENNOW, Elisabeth, ALBERTSON, Donna G, PINKEL, Daniel, DUMANSKI, Jan P, SEGRAVES, Richard, HAMILTON, Greg, XIAO XIAO ZHANG, EVANS, D. Gareth, WALLACE, Andrew J, BASER, Michael E

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Premature ageing in mice expressing defective mitochondrial DNA polymerase von Larsson, Nils-Göran, Trifunovic, Aleksandra, Wredenberg, Anna, Falkenberg, Maria, Spelbrink, Johannes N, Rovio, Anja T, Bruder, Carl E, Bohlooly-Y, Mohammad, Gidlöf, Sebastian, Oldfors, Anders, Wibom, Rolf, Törnell, Jan, Jacobs, Howard T

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The mouse ortholog of the human SMARCB1 gene encodes two splice forms von Bruder, C E, Dumanski, J P, Kedra, D

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Fine mapping of the constitutional translocation t(11;22)(q23;q11) von TAPIA-PAEZ, I, O'BRIEN, K. P, BLENNOW, E, DUMANSKI, J. P, KOST-ALIMOVA, M, SAHLEN, S, KEDRA, D, BRUDER, C. E. G, ANDERSSON, B, ROE, B. A, PING HU, IMREH, S

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Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: Possible localization of a neurofibromatosis type 2 modifier gene? von Bruder, Carl E.G., Ichimura, Koichi, Blennow, Elisabeth, Ikeuchi, Tatsuro, Yamaguchi, Takekane, Yuasa, Yasuhito, Collins, V. Peter, Dumanski, Jan P.

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A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene von Bruder, C E, Ichimura, K, Tingby, O, Hirakawa, K, Komatsuzaki, A, Tamura, A, Yuasa, Y, Collins, V P, Dumanski, J P

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De-novo transcriptome sequencing of a normalized cDNA pool from influenza infected ferrets von Camp, Jeremy V, Svensson, Thomas L, McBrayer, Alexis, Jonsson, Colleen B, Liljeström, Peter, Bruder, Carl E

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Host gene expression signatures discriminate between ferrets infected with genetically similar H1N1 strains von Ljungberg, Karl, McBrayer, Alexis, Camp, Jeremy V, Chu, Yong-Kyu, Tapp, Ronald, Noah, Diana L, Grimes, Sheila, Proctor, Mary L, Liljeström, Peter, Jonsson, Colleen B, Bruder, Carl E

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Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret von McBrayer, Alexis, Camp, Jeremy V, Tapp, Ron, Yamshchikov, Vladimir, Grimes, Sheila, Noah, Diana L, Jonsson, Colleen B, Bruder, Carl E

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Strong conservation of the human NF2 locus based on sequence comparison in five species von Hansson, Caisa M, Ali, Haider, Bruder, Carl E G, Fransson, Ingegerd, Kluge, Sindy, Andersson, Björn, Roe, Bruce A, Menzel, Uwe, Dumanski, Jan P

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High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH von Bruder, C E G, Hirvelä, Carina, Segraves, Richard, Wallace, Andrew J, Boltshauser, Eugene, Jordanova, Albena, Sainio, Markku, Harder, Henrik, Blennow, Elisabeth, Tapia-Paez, Isabel, Hamilton, Greg, Baser, Michael E, Papi, Laura, Rask-Andersen, Helge, Hung, Gene, Heiberg, Arvid, Albertson, Donna G, Fransson, Ingegerd, Zhang, Xiao Xiao, Zucman-Rossi6, Jessica, Rouleau, Guy A, Kluwe, Lan, Mathiesen, Tiit, Honda, Mariko, Pinkel, Daniel, Dumanski, Jan P, Evans, D Gareth, Hergersberg, Martin, Poptodorov, George

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A group of schwannomas with interstitial deletions on 22q located outside the NF2 iocus shows no detectable mutations in the NF2 gene von BRUDER, C. E. G, ICHIMURA, K, TINGBY, O, HIRAKAWA, K, KOMATSUZAKI, A, TAMURA, A, YUASA, Y, COLLINS, V. P, DUMANSKI, J. P

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Emotion recognition deficits as predictors of transition in individuals at clinical high risk for schizophrenia: a neurodevelopmental perspective von Corcoran, C. M., Keilp, J. G., Kayser, J., Klim, C., Butler, P. D., Bruder, G. E., Gur, R. C., Javitt, D. C.

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Harnessing heterologous and endogenous CRISPR-Cas machineries for efficient markerless genome editing in Clostridium von Pyne, Michael E., Bruder, Mark R., Moo-Young, Murray, Chung, Duane A., Chou, C. Perry

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The London Classification of gastrointestinal neuromuscular pathology: report on behalf of the Gastro 2009 International Working Group von Knowles, Charles H, De Giorgio, Roberto, Kapur, Raj P, Bruder, Elisabeth, Farrugia, Gianrico, Geboes, Karel, Lindberg, Greger, Martin, Joanne E, Meier-Ruge, William A, Milla, Peter J, Smith, Virpi V, Vandervinden, Jean Marie, Veress, Béla, Wedel, Thilo

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Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles von Bruder, Carl E.G., Piotrowski, Arkadiusz, Gijsbers, Antoinet A.C.J., Andersson, Robin, Erickson, Stephen, Diaz de Ståhl, Teresita, Menzel, Uwe, Sandgren, Johanna, von Tell, Desiree, Poplawski, Andrzej, Crowley, Michael, Crasto, Chiquito, Partridge, E. Christopher, Tiwari, Hemant, Allison, David B., Komorowski, Jan, van Ommen, Gert-Jan B., Boomsma, Dorret I., Pedersen, Nancy L., den Dunnen, Johan T., Wirdefeldt, Karin, Dumanski, Jan P.

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Neuronal generators of posterior EEG alpha reflect individual differences in prioritizing personal spirituality von Tenke, C.E., Kayser, J., Miller, L., Warner, V., Wickramaratne, P., Weissman, M.M., Bruder, G.E.

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Extending CRISPR-Cas9 Technology from Genome Editing to Transcriptional Engineering in the Genus Clostridium von Bruder, Mark R, Pyne, Michael E, Moo-Young, Murray, Chung, Duane A, Chou, C Perry

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Consequences of biodiversity loss for litter decomposition across biomes von Handa, I. Tanya, Aerts, Rien, Berendse, Frank, Berg, Matty P., Bruder, Andreas, Butenschoen, Olaf, Chauvet, Eric, Gessner, Mark O., Jabiol, Jérémy, Makkonen, Marika, McKie, Brendan G., Malmqvist, Björn, Peeters, Edwin T. H. M., Scheu, Stefan, Schmid, Bernhard, van Ruijven, Jasper, Vos, Veronique C. A., Hättenschwiler, Stephan

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