Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline von Granzow, M., Paramasivam, N., Hinderhofer, K., Fischer, C., Chotewutmontri, S., Kaufmann, L., Evers, C., Kotzaeridou, U., Rohrschneider, K., Schlesner, M., Sturm, M., Pinkert, S., Eils, R., Bartram, C.R., Bauer, P., Moog, U.

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Minimal residual disease-directed risk stratification using real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene rearrangements in the international multi... von Flohr, T, Schrauder, A, Cazzaniga, G, Panzer-Grümayer, R, van der Velden, V, Fischer, S, Stanulla, M, Basso, G, Niggli, F K, Schäfer, B W, Sutton, R, Koehler, R, Zimmermann, M, Valsecchi, M G, Gadner, H, Masera, G, Schrappe, M, van Dongen, J J M, Biondi, A, Bartram, C R

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ERG deletion is associated with CD2 and attenuates the negative impact of IKZF1 deletion in childhood acute lymphoblastic leukemia von Zaliova, M, Zimmermannova, O, Dörge, P, Eckert, C, Möricke, A, Zimmermann, M, Stuchly, J, Teigler-Schlegel, A, Meissner, B, Koehler, R, Bartram, C R, Karawajew, L, Rhein, P, Zuna, J, Schrappe, M, Cario, G, Stanulla, M

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Chromosomal aberrations in sporadic pituitary tumors von Trautmann, K., Thakker, R.V., Ellison, D.W., Ibrahim, A., Lees, P.D., Harding, B., Fischer, C., Popp, S., Bartram, C.R., Jauch, A.

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Eberhard Passarge zum 75. Geburtstag von Bartram, C.R.

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Very early early relapses of acute lymphoblastic leukemia show unexpected changes of clonal markers and high heterogeneity in response to initial and relapse treatment von Eckert, C, Flohr, T, Koehler, R, Hagedorn, N, Moericke, A, Stanulla, M, Kirschner-Schwabe, R, Cario, G, Stackelberg, Av, Bartram, C R, Henze, G, Schrappe, M, Schrauder, A

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Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients von Wesołowska-Andersen, A, Borst, L, Dalgaard, M D, Yadav, R, Rasmussen, K K, Wehner, P S, Rasmussen, M, Ørntoft, T F, Nordentoft, I, Koehler, R, Bartram, C R, Schrappe, M, Sicheritz-Ponten, T, Gautier, L, Marquart, H, Madsen, H O, Brunak, S, Stanulla, M, Gupta, R, Schmiegelow, K

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ERG deletion is associated with CD2 and attenuates the negative impact of IKZF1 deletion in childhood acute lymphoblastic leukemia von Zaliova, M, Zimmermannova, O, Dörge, P, Eckert, C, Möricke, A, Zimmermann, M, Stuchly, J, Teigler-Schlegel, A, Meissner, B, Koehler, R, Bartram, C R, Karawajew, L, Rhein, P, Zuna, J, Schrappe, M, Cario, G, Stanulla, M

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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia von Vijayakrishnan, J, Studd, J, Broderick, P, Kinnersley, B, Holroyd, A, Law, P.J, Kumar, R, Allan, J.M, Harrison, C.J, Moorman, A.V, Vora, A, Roman, E, Rachakonda, S, Kinsey, S.E, Sheridan, E, Thompson, P.D, Irving, J.A, Koehler, R, Hoffmann, P, Nöthen, M.M, Heilmann-Heimbach, S, Jöckel, K.H, Easton, D.F, Pharaoh, P.D.P, Dunning, A.M, Peto, J, Canzian, F, Swerdlow, A, Eeles, R.A, Kote-Jarai, Z, Muir, K, Pashayan, N, Greaves, M, Zimmerman, M, Bartram, C.R, Schrappe, M, Stanulla, M, Hemminki, K, Houlston, R.S, Henderson, B.E, Haiman, C.A, Benlloch, S, Schumacher, F.R, Olama, A.A.A, Berndt, S.I, Conti, D.V, Wiklund, F, Chanock, S, Stevens, V.L, Tangen, C.M, Batra, J, Clements, J, Gronberg, H, Schleutker, J, Albanes, D, Weinstein, S, Wolk, A, West, C, Mucci, L, Cancel-Tassin, G, Koutros, S, Sorensen, K.D, Maehle, L, Neal, D.E, Travis, R.C, Hamilton, R.J, Ingles, S.A, Rosenstein, B, Lu, Y.J, Giles, G.G, Kibel, A.S, Vega, A, Kogevinas, M, Penney, K.L, Park, J.Y, Stanford, J.L, The PRACTICAL Consortium

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Eberhard Passarge zum 75. Geburtstag von Bartram, C.R.

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Disruption of the RanBP17/Hox11L2 region by recombination with the TCRδ locus in acute lymphoblastic leukemias with t(5;14)(q34;q11) von HANSEN-HAGGE, T. E, SCHÄFER, M, KIYOI, H, MORRIS, S. W, WHITLOCK, J. A, KOCH, P, BOHLMANN, I, MAHOTKA, C, BARTRAM, C. R, JANSSEN, J. W. G

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Humangenetische Diagnostik: Wissenschaftliche Grundlagen Und Gesellschaftliche Konsequenzen von Uhl, D, Bartram, C.R, Beckmann, J.P, Breyer, F, Fey, G, Fonatsch, C, Irrgang, B, Taupitz, J, Seel, K.-M, Thiele, F

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Detection of chimeric BCR-ABL genes in acute lymphoblastic leukaemia by the polymerase chain reaction von Maurer, J., Thiel, E., Ludwig, W.-D., Janssen, J.W.G., Bartram, C.R., Heinze, B., van Denderen, J., Aydemir, U., Fonatsch, C., Harbott, J., Reiter, A., Riehm, H., Hoelzer, D.

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Germline mutation of the p27/Kip1 gene in childhood acute lymphoblastic leukemia von Takeuchi, C, Takeuchi, S, Ikezoe, T, Bartram, C R, Taguchi, H, Koeffler, H P

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RAS Gene Mutations in Acute and Chronic Myelocytic Leukemias, Chronic Myeloproliferative Disorders, and Myelodysplastic Syndromes von Johannes W. G. Janssen, Ada C. M. Steenvoorden, Lyons, John, Anger, Bernd, Böhlke, Jörg U., Bos, Johannes L., Seliger, Hartmut, Bartram, Claus R.

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Primary Pulmonary Hypertension Is Predominantly a Hereditary Disease von Grünig, E., Mereles, D., Arnold, K., Benz, A., Olschewski, Horst, Miltenberger-Miltenyi, G., Borst, M.M., Abushi, A., Seeger, W., Winkler, J., Höper, M.M., Bartram, C.R., Kübler, W., Janssen, B.

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93 Risk adapted treatment for childhood ALL: the BFM experience von Schrappe, M., Schrauder, A., Flohr, T., Bartram, C.R., Zimmermann, M.

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POLYMERASE CHAIN REACTION FOR DETECTION OF RESIDUAL LEUKAEMIA von Morgan, G.J., Janssen, J.W.G., Guo, Ai-Pu, Wiedemann, L.M., Hughes, T., Gow, J., Goldman, J.M., Bartram, C.R.

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C‐abl and bcr are rearranged in a Ph1‐negative CML patient von Bartram, C.R., Kleihauer, E., Klein, A., Grosveld, G., Teyssier, J.R., Heisterkamp, N., Groffen, J.

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False-positive results with PCR to detect leukaemia-specific transcript von Hughes, Timothy, Janssen, J.W.G, Morgan, Gareth, Martiat, Philippe, Saglio, Guiseppe, Pignon, J.M, Pignatti, FrancoPier, Mills, Ken, Keating, Armand, Gluckman, Eliane, Bartram, C.R, Goldman, J.M

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