Publikationslista i omvänd kronologisk ordning

McBrayer, A., Camp, J.V., Tapp, R., Yamshchikov, V., Grimes, S., Noah, D., Jonsson, C.B., Bruder, C.E., Course of Seasonal Influenza A/Brisbane/59/07 H1N1 Infection in the Ferret. Virology Journal, Accepted for publication

Bruder, C.E., Yao, S., Larson, F., Camp, J., Tapp, R., McBrayer, A., Powers, N., Valdivia Granda, W., and Jonsson, C.B., Transcriptome sequencing and development of an expression microarray platform for the domestic ferret. BMC Genomics, 2010. 11(1): p. 251.

Sandgren, J., Diaz de Stahl, T., Andersson, R., Menzel, U., Piotrowski, A., Nord, H., Backdahl, M., Kiss, N., Brauckhoff, M., Komorowski, J., Dralle, H., Hessman, O., Larsson, C., Akerstrom, G., Bruder, C., Dumanski, J., and Westin, G., Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array-CGH analysis. Endocr Relat Cancer, 2010.

Poplawski, A.B., Jankowski, M., Erickson, S.W., Diaz de Stahl, T., Partridge, E.C., Crasto, C., Guo, J., Gibson, J., Menzel, U., Bruder, C.E., Kaczmarczyk, A., Benetkiewicz, M., Andersson, R., Sandgren, J., Zegarska, B., Bala, D., Srutek, E., Allison, D.B., Piotrowski, A., Zegarski, W., and Dumanski, J.P., Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression. Eur J Hum Genet, 2010. 18(5): p. 560-8.

Enjin, A., Rabe, N., Nakanishi, S.T., Vallstedt, A., Gezelius, H., Memic, F., Lind, M., Hjalt, T., Tourtellotte, W.G., Bruder, C.E., Eichele, G., Whelan, P.J., and Kullander, K., Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as markers for fast motor neurons and partition cells. Journal Comparative Neurology, 2010. 518 (12): p. 2284-2304.

Nord, H., Hartmann, C., Andersson, R., Menzel, U., Pfeifer, S., Piotrowski, A., Bogdan, A., Kloc, W., Sandgren, J., Olofsson, T., Hesselager, G., Blomquist, E., Komorowski, J., von Deimling, A., Bruder, C.E., Dumanski, J.P., and de Stahl, T.D., Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array. Neuro Oncol, 2009. 11(6): p. 803-18.

Wineinger, N.E., Kennedy, R.E., Erickson, S.W., Wojczynski, M.K., Bruder, C.E., and Tiwari, H.K., Statistical issues in the analysis of DNA Copy Number Variations. Int J Comput Biol Drug Des, 2008. 1(4): p. 368-95.

Piotrowski, A., Bruder, C.E., Andersson, R., de Stahl, T.D., Menzel, U., Sandgren, J., Poplawski, A., von Tell, D., Crasto, C., Bogdan, A., Bartoszewski, R., Bebok, Z., Krzyzanowski, M., Jankowski, Z., Partridge, E.C., Komorowski, J., and Dumanski, J.P., Somatic mosaicism for copy number variation in differentiated human tissues. Hum Mutat, 2008. 29(9): p. 1118-24.

Descartes, M., Franklin, J., de Stahl, T.D., Piotrowski, A., Bruder, C.E., Dumanski, J.P., Carroll, A.J., and Mikhail, F.M., Distal 22q11.2 microduplication encompassing the BCR gene. Am J Med Genet A, 2008. 146A(23): p. 3075-81.

de Stahl, T.D., Sandgren, J., Piotrowski, A., Nord, H., Andersson, R., Menzel, U., Bogdan, A., Thuresson, A.C., Poplawski, A., von Tell, D., Hansson, C.M., Elshafie, A.I., Elghazali, G., Imreh, S., Nordenskjold, M., Upadhyaya, M., Komorowski, J., Bruder, C.E., and Dumanski, J.P., Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array. Hum Mutat, 2008. 29(3): p. 398-408.

Bruder, C.E., Piotrowski, A., Gijsbers, A.A., Andersson, R., Erickson, S., de Stahl, T.D., Menzel, U., Sandgren, J., von Tell, D., Poplawski, A., Crowley, M., Crasto, C., Partridge, E.C., Tiwari, H., Allison, D.B., Komorowski, J., van Ommen, G.J., Boomsma, D.I., Pedersen, N.L., den Dunnen, J.T., Wirdefeldt, K., and Dumanski, J.P., Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles. Am J Hum Genet, 2008. 82(3): p. 763-71.

Ardesjo, B., Hansson, C.M., Bruder, C.E., Rorsman, F., Betterle, C., Dumanski, J.P., Kampe, O., and Ekwall, O., Autoantibodies to glutathione S-transferase theta 1 in patients with primary sclerosing cholangitis and other autoimmune diseases. J Autoimmun, 2008. 30(4): p. 273-82.

Andersson, R., Bruder, C.E., Piotrowski, A., Menzel, U., Nord, H., Sandgren, J., Hvidsten, T.R., Diaz de Stahl, T., Dumanski, J.P., and Komorowski, J., A segmental maximum a posteriori approach to genome-wide copy number profiling. Bioinformatics, 2008. 24(6): p. 751-8.

Mikhail, F.M., Sathienkijkanchai, A., Robin, N.H., Prucka, S., Biggerstaff, J.S., Komorowski, J., Andersson, R., Bruder, C.E., Piotrowski, A., de Stahl, T.D., Dumanski, J.P., and Carroll, A.J., Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter). Am J Med Genet A, 2007. 143A(15): p. 1760-6.

Mikhail, F.M., Descartes, M., Piotrowski, A., Andersson, R., de Stahl, T.D., Komorowski, J., Bruder, C.E., Dumanski, J.P., and Carroll, A.J., A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene. Am J Med Genet A, 2007. 143A(18): p. 2178-84.

Erickson, R.P., de Stahl, T.D., Bruder, C.E., and Dumanski, J.P., A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients. Am J Med Genet A, 2007. 143A(24): p. 3302-8.

Mantripragada, K.K., Thuresson, A.C., Piotrowski, A., Diaz de Stahl, 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., and Dumanski, J.P., Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH. J Med Genet, 2006. 43(1): p. 28-38.

Bohlooly, Y.M., Olsson, B., Bruder, C.E., Linden, D., Sjogren, K., Bjursell, M., Egecioglu, E., Svensson, L., Brodin, P., Waterton, J.C., Isaksson, O.G., Sundler, F., Ahren, B., Ohlsson, C., Oscarsson, J., and Tornell, J., Growth hormone overexpression in the central nervous system results in hyperphagia-induced obesity associated with insulin resistance and dyslipidemia. Diabetes, 2005. 54(1): p. 51-62.

Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J.N., Rovio, A.T., Bruder, C.E., Bohlooly, Y.M., Gidlof, S., Oldfors, A., Wibom, R., Tornell, J., Jacobs, H.T., and Larsson, N.G., Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature, 2004. 429(6990): p. 417-23.

Lindmark, H., Rosengren, B., Hurt-Camejo, E., and Bruder, C.E., Gene expression profiling shows that macrophages derived from mouse embryonic stem cells is an improved in vitro model for studies of vascular disease. Exp Cell Res, 2004. 300(2): p. 335-44.

von Tell, D., Bruder, C.E., Anderson, L.V., Anvret, M., and Ahlberg, G., Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus. Neurogenetics, 2003. 4(4): p. 173-7.

Szijan, I., Rochefort, D., Bruder, C., Surace, E., Machiavelli, G., Dalamon, V., Cotignola, J., Ferreiro, V., Campero, A., Basso, A., Dumanski, J.P., and Rouleau, G.A., NF2 tumor suppressor gene: a comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGH. Neuromolecular Med, 2003. 3(1): p. 41-52.

Mantripragada, K.K., Buckley, P.G., Benetkiewicz, M., De Bustos, C., Hirvela, C., Jarbo, C., Bruder, C.E., Wensman, H., Mathiesen, T., Nyberg, G., Papi, L., Collins, V.P., Ichimura, K., Evans, G., and Dumanski, J.P., High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH. Int J Oncol, 2003. 22(3): p. 615-22.

Hansson, C.M., Ali, H., Bruder, C.E., Fransson, I., Kluge, S., Andersson, B., Roe, B.A., Menzel, U., and Dumanski, J.P., Strong conservation of the human NF2 locus based on sequence comparison in five species. Mamm Genome, 2003. 14(8): p. 526-36.

Buckley, P.G., Mantripragada, K.K., Benetkiewicz, M., Tapia-Paez, I., Diaz De Stahl, T., Rosenquist, M., Ali, H., Jarbo, C., De Bustos, C., Hirvela, C., Sinder Wilen, B., Fransson, I., Thyr, C., Johnsson, B.I., Bruder, C.E., Menzel, U., Hergersberg, M., Mandahl, N., Blennow, E., Wedell, A., Beare, D.M., Collins, J.E., Dunham, I., Albertson, D., Pinkel, D., Bastian, B.C., Faruqi, A.F., Lasken, R.S., Ichimura, K., Collins, V.P., and Dumanski, J.P., A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications. Hum Mol Genet, 2002. 11(25): p. 3221-9.

Bruder, C.E., Hirvela, C., Tapia-Paez, I., Fransson, I., Segraves, R., Hamilton, G., Zhang, X.X., Evans, D.G., Wallace, A.J., Baser, M.E., Zucman-Rossi, J., Hergersberg, M., Boltshauser, E., Papi, L., Rouleau, G.A., Poptodorov, G., Jordanova, A., Rask-Andersen, H., Kluwe, L., Mautner, V., Sainio, M., Hung, G., Mathiesen, T., Moller, C., Pulst, S.M., Harder, H., Heiberg, A., Honda, M., Niimura, M., Sahlen, S., Blennow, E., Albertson, D.G., Pinkel, D., and Dumanski, J.P., High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH. Hum Mol Genet, 2001. 10(3): p. 271-82.

Tapia-Paez, I., O'Brien, K.P., Kost-Alimova, M., Sahlen, S., Kedra, D., Bruder, C.E., Andersson, B., Roe, B.A., Hu, P., Imreh, S., Blennow, E., and Dumanski, J.P., Fine mapping of the constitutional translocation t(11;22)(q23;q11). Hum Genet, 2000. 106(5): p. 506-16.

Dunham, I., Shimizu, N., Roe, B.A., Chissoe, S., Hunt, A.R., Collins, J.E., Bruskiewich, R., Beare, D.M., Clamp, M., Smink, L.J., Ainscough, R., Almeida, J.P., Babbage, A., Bagguley, C., Bailey, J., Barlow, K., Bates, K.N., Beasley, O., Bird, C.P., Blakey, S., Bridgeman, A.M., Buck, D., Burgess, J., Burrill, W.D., Bruder, C.E., O'Brien, K.P., and et al., The DNA sequence of human chromosome 22. Nature, 1999. 402(6761): p. 489-95.

Bruder, C.E., Ichimura, K., Tingby, O., Hirakawa, K., Komatsuzaki, A., Tamura, A., Yuasa, Y., Collins, V.P., and Dumanski, J.P., A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene. Hum Genet, 1999. 104(5): p. 418-24.

Bruder, C.E., Ichimura, K., Blennow, E., Ikeuchi, T., Yamaguchi, T., Yuasa, Y., Collins, V.P., and Dumanski, J.P., 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? Genes Chromosomes Cancer, 1999. 25(2): p. 184-90.

Bruder, C.E., Dumanski, J.P., and Kedra, D., The mouse ortholog of the human SMARCB1 gene encodes two splice forms. Biochem Biophys Res Commun, 1999. 257(3): p. 886-90.

Sulman, E.P., Dumanski, J.P., White, P.S., Zhao, H., Maris, J.M., Mathiesen, T., Bruder, C., Cnaan, A., and Brodeur, G.M., Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity. Cancer Res, 1998. 58(15): p. 3226-30.

Carlson, K.M., Bruder, C., Nordenskjold, M., and Dumanski, J.P., 1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization. Genes Chromosomes Cancer, 1997. 20(4): p. 419-24.