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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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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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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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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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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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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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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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 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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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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Gene expression profiling shows that macrophages derived from mouse embryonic stem cells is an improved in vitro model for studies of vascular disease von Lindmark, Helena, Rosengren, Birgitta, Hurt-Camejo, Eva, Bruder, Carl E.G.

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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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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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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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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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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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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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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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