A segmental maximum a posteriori approach to genome-wide copy number profiling von Andersson, Robin, Bruder, Carl E. G., Piotrowski, Arkadiusz, Menzel, Uwe, Nord, Helena, Sandgren, Johanna, Hvidsten, Torgeir R., Diaz de Ståhl, Teresita, Dumanski, Jan P., Komorowski, Jan

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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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Transcriptome sequencing and development of an expression microarray platform for the domestic ferret von Bruder, Carl E, Yao, Suxia, Larson, Francis, Camp, Jeremy V, Tapp, Ronald, McBrayer, Alexis, Powers, Nicholas, Granda, Willy Valdivia, Jonsson, Colleen B

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Premature ageing in mice expressing defective mitochondrial DNA polymerase von 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., Larsson, Nils-Göran

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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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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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Somatic mosaicism for copy number variation in differentiated human tissues von Piotrowski, Arkadiusz, Bruder, Carl E.G, Andersson, Robin, de Ståhl, Teresita Diaz, Menzel, Uwe, Sandgren, Johanna, Poplawski, Andrzej, von Tell, Desiree, Crasto, Chiquito, Bogdan, Adam, Bartoszewski, Rafal, Bebok, Zsuzsa, Krzyzanowski, Maciej, Jankowski, Zbigniew, Partridge, E. Christopher, Komorowski, Jan, Dumanski, Jan P

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Growth Hormone Overexpression in the Central Nervous System Results in Hyperphagia-Induced Obesity Associated With Insulin Resistance and Dyslipidemia von BOLDOOLY, Mohammad, OLSSON, Bob, ISAKSSON, Olle G. P, SUNDLER, Frank, AHREN, Bo, OHLSSON, Claes, OSCARSSON, Jan, TÖRNELL, Jan, BRUDER, Carl E. G, LINDEN, Daniel, SJÖGREN, Klara, BJURSELL, Mikael, EGECIOGLU, Emit, SVENSSON, Lennart, BRODIN, Peter, WATERTON, John C

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Autoantibodies to glutathione S-transferase theta 1 in patients with primary sclerosing cholangitis and other autoimmune diseases von Ardesjö, Brita, Hansson, Caisa M, Bruder, Carl E.G, Rorsman, Fredrik, Betterle, Corrado, Dumanski, Jan P, Kämpe, Olle, Ekwall, Olov

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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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Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression von Popławski, Andrzej B, Jankowski, Michał, Erickson, Stephen W, Díaz de Ståhl, Teresita, Partridge, E Christopher, Crasto, Chiquito, Guo, Jingyu, Gibson, John, Menzel, Uwe, Bruder, Carl EG, Kaczmarczyk, Aneta, Benetkiewicz, Magdalena, Andersson, Robin, Sandgren, Johanna, Zegarska, Barbara, Bała, Dariusz, Śrutek, Ewa, Allison, David B, Piotrowski, Arkadiusz, Zegarski, Wojciech, Dumanski, Jan P

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Overlapping phenotype of Wolf–Hirschhorn and Beckwith–Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter) von Mikhail, Fady M., Sathienkijkanchai, Achara, Robin, Nathaniel H., Prucka, Sandra, Biggerstaff, Julie Sanford, Komorowski, Jan, Andersson, Robin, Bruder, Carl E.G., Piotrowski, Arkadiusz, de Ståhl, Teresita Diaz, Dumanski, Jan P., Carroll, Andrew J.

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Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array von Nord, Helena, Hartmann, Christian, Andersson, Robin, Menzel, Uwe, Pfeifer, Susan, Piotrowski, Arkadiusz, Bogdan, Adam, Kloc, Wojciech, Sandgren, Johanna, Olofsson, Tommie, Hesselager, Göran, Blomquist, Erik, Komorowski, Jan, von Deimling, Andreas, Bruder, Carl E G, Dumanski, Jan P, Díaz de Ståhl, Teresita

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Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array von de Ståhl, Teresita Díaz, Sandgren, Johanna, Piotrowski, Arkadiusz, Nord, Helena, Andersson, Robin, Menzel, Uwe, Bogdan, Adam, Thuresson, Ann-Charlotte, Poplawski, Andrzej, von Tell, Desiree, Hansson, Caisa M, Elshafie, Amir I, ElGhazali, Gehad, Imreh, Stephan, Nordenskjöld, Magnus, Upadhyaya, Meena, Komorowski, Jan, Bruder, Carl E.G, Dumanski, Jan P

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Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus von VON TELL, Désirée, BRUDER, Carl E. G, ANDERSON, Louise V. B, ANVRET, Maria, AHLBERG, Gabrielle

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Distal 22q11.2 microduplication encompassing the BCR gene von Descartes, Maria, Franklin, Judy, de Ståhl, Teresita Diaz, Piotrowski, Arkadiusz, Bruder, Carl E.G., Dumanski, Jan P., Carroll, Andrew J., Mikhail, Fady M.

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A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene von Mikhail, Fady M., Descartes, Maria, Piotrowski, Arkadiusz, Andersson, Robin, Diaz de Ståhl, Teresita, Komorowski, Jan, Bruder, Carl E.G., Dumanski, Jan P., Carroll, Andrew J.

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A patient with 22q11.2 deletion and Opitz syndrome‐like phenotype has the same deletion as velocardiofacial patients von Erickson, Robert P., de Ståhl, Teresita Díaz, Bruder, Carl E.G., Dumanski, Jan P.

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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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A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications von Buckley, Patrick G., Mantripragada, Kiran K., Benetkiewicz, Magdalena, Tapia-Páez, Isabel, Diaz de Ståhl, Teresita, Rosenquist, Magnus, Ali, Haider, Jarbo, Caroline, de Bustos, Cecilía, Hirvelä, Carina, Sinder Wilén, Birgitta, Fransson, Ingegerd, Thyr, Charlotte, Johnsson, Britt-Inger, Bruder, Carl E.G., Menzel, Uwe, Hergersberg, Martin, Mandahl, Nils, Blennow, Elisabeth, Wedell, Anna, Beare, David M., Collins, John E., Dunham, Ian, Albertson, Donna, Pinkel, Daniel, Bastian, Boris C., Faruqi, A. Fawad, Lasken, Roger S., Ichimura, Koichi, Collins, V. Peter, Dumanski, Jan P.

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