Research ExplorerScientific StaffUwe Kordes Publications

PD Dr. med. ID: 51028

Uwe Kordes

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Affiliations
ORCID: 0000-0001-6375-2320
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Publications

  1. 2023

  2. Rhabdoid tumors in patients conceived following ART: is there an association?

    Nemes, K., Benesch, M., Kolarova, J., Johann, P., Hasselblatt, M., Thomas, C., Bens, S., Glaser, S., Ammerpohl, O., Liaugaudiene, O., Sadeghipour, A., von der Weid, N., Schmid, I., Gidding, C., Erdreich-Epstein, A., Khurana, C., Ebetsberger-Dachs, G., Lemmer, A., Khatib, Z., Hernández Marqués, C., Pears, J., Quehenberger, F., Kordes, U., Vokuhl, C., Gerss, J., Schwarz, H., Bison, B., Biegel, J. A., Siebert, R. & Frühwald, M. C., 03.10.2023, In: HUM REPROD. 38, 10, p. 2028-2038 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  3. Clinical outcome of pediatric medulloblastoma patients with Li-Fraumeni syndrome

    Kolodziejczak, A. S., Guerrini-Rousseau, L., Planchon, J. M., Ecker, J., Selt, F., Mynarek, M., Obrecht, D., Sill, M., Autry, R. J., Zhao, E., Hirsch, S., Amouyal, E., Dufour, C., Ayrault, O., Torrejon, J., Waszak, S. M., Ramaswamy, V., Pentikainen, V., Demir, H. A., Clifford, S. C., Schwalbe, E. C., Massimi, L., Snuderl, M., Galbraith, K., Karajannis, M. A., Hill, K., Li, B. K., Walsh, M., White, C. L., Redmond, S., Loizos, L., Jakob, M., Kordes, U. R., Schmid, I., Hauer, J., Blattmann, C., Filippidou, M., Piccolo, G., Scheurlen, W., Farrag, A., Grund, K., Sutter, C., Pietsch, T., Frank, S., Schewe, D. M., Malkin, D., Ben-Arush, M., Sehested, A., Wong, T-T., Wu, K-S., Liu, Y-L., Carceller, F., Mueller, S., Stoller, S., Taylor, M. D., Tabori, U., Bouffet, E., Kool, M., Sahm, F., von Deimling, A., Korshunov, A., von Hoff, K., Kratz, C. P., Sturm, D., Jones, D. T. W., Rutkowski, S., van Tilburg, C. M., Witt, O., Bougeard, G., Pajtler, K. W., Pfister, S. M., Bourdeaut, F. & Milde, T., 28.06.2023, In: NEURO-ONCOLOGY.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  4. Generalized Infantile Myofibromatosis with Extensive Small Bowel Involvement in a Neonate

    Schubert, J. P., Wößmann, W., Königs, I., Clauditz, T., Kordes, U. & Reinshagen, K., 06.2023, In: Z GEBURTSH NEONATOL. 227, 3, p. 231-235 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  5. Germ Cell Maintenance and Sustained Testosterone and Precursor Hormone Production in Human Prepubertal Testis Organ Culture with Tissues from Boys 7 Years+ under Conditions from Adult Testicular Tissue

    Aden, N. L., Bleeke, M., Kordes, U., Brunne, B., Holstermann, B., Biemann, R., Ceglarek, U., Soave, A., Salzbrunn, A., Schneider, S. & Kopylow, K. V., 26.01.2023, In: CELLS-BASEL. 12, 3, 415.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  6. 2022

  7. Coping with Diffuse Intrinsic Pontine Glioma in Children - Findings from an Interview Study on Bereaved Parents

    Radlanski, K., Hartwig, M. & Kordes, U., 11.2022, In: KLIN PADIATR. 234, 6, p. 374-381 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  8. SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni Syndrome

    Hasselblatt, M., Thomas, C., Federico, A., Nemes, K., Johann, P. D., Bison, B., Bens, S., Dahlum, S., Kordes, U., Redlich, A., Lessel, L., Pajtler, K. W., Mawrin, C., Schüller, U., Nolte, K., Kramm, C. M., Hinz, F., Sahm, F., Giannini, C., Penkert, J., Kratz, C. P., Pfister, S. M., Siebert, R., Paulus, W., Kool, M. & Frühwald, M. C., 01.09.2022, In: AM J SURG PATHOL. 46, 9, p. 1277-1283 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  9. Genotype-phenotype associations within the Li-Fraumeni spectrum: a report from the German Registry

    Penkert, J., Strüwe, F. J., Dutzmann, C. M., Doergeloh, B. B., Montellier, E., Freycon, C., Keymling, M., Schlemmer, H-P., Sänger, B., Hoffmann, B., Gerasimov, T., Blattmann, C., Fetscher, S., Frühwald, M., Hettmer, S., Kordes, U., Ridola, V., Kroiss Benninger, S., Mastronuzzi, A., Schott, S., Nees, J., Prokop, A., Redlich, A., Seidel, M. G., Zimmermann, S., Pajtler, K. W., Pfister, S. M., Hainaut, P. & Kratz, C. P., 16.08.2022, In: J HEMATOL ONCOL. 15, 1, 107.

    Research output: SCORING: Contribution to journal › Letter › Research

  10. ALK inhibition as a salvage therapy for a relapsed unclassifiable sarcomatous CNS tumor with EML4/ALK fusion in an infant

    Holsten, T., Bronsema, A., Sturm, D., Sahm, F., Rutkowski, S., Ulrich, S., Wößmann, W. & Kordes, U. R., 08.2022, In: PEDIATR BLOOD CANCER. 69, 8, e29594.

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  11. ATRT-SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance

    Federico, A., Thomas, C., Miskiewicz, K., Woltering, N., Zin, F., Nemes, K., Bison, B., Johann, P. D., Hawes, D., Bens, S., Kordes, U., Albrecht, S., Dohmen, H., Hauser, P., Keyvani, K., van Landeghem, F. K. H., Lund, E. L., Scheie, D., Mawrin, C., Monoranu, C-M., Parm Ulhøi, B., Pietsch, T., Reinhard, H., Riemenschneider, M. J., Sehested, A., Sumerauer, D., Siebert, R., Paulus, W., Frühwald, M. C., Kool, M. & Hasselblatt, M., 06.2022, In: ACTA NEUROPATHOL. 143, 6, p. 697-711 15 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  12. Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC

    Hasselblatt, M., Thomas, C., Federico, A., Bens, S., Hellström, M., Casar-Borota, O., Kordes, U., Neumann, J. E., Dottermusch, M., Rodriguez, F. J., Lo, A. C., Cheng, S., Hendson, G., Hukin, J., Hartmann, C., Koch, A., Capper, D., Siebert, R., Paulus, W., Nemes, K., Johann, P. D., Frühwald, M. C. & Kool, M., 06.2022, In: NEUROPATH APPL NEURO. 48, 4, p. e12797 e12797.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  13. Infants and Newborns with Atypical Teratoid Rhabdoid Tumors (ATRT) and Extracranial Malignant Rhabdoid Tumors (eMRT) in the EU-RHAB Registry: A Unique and Challenging Population

    Nemes, K., Johann, P. D., Steinbügl, M., Gruhle, M., Bens, S., Kachanov, D., Teleshova, M., Hauser, P., Simon, T., Tippelt, S., Eberl, W., Chada, M., Lopez, V. S-M., Grigull, L., Hernáiz-Driever, P., Eyrich, M., Pears, J., Milde, T., Reinhard, H., Leipold, A., van de Wetering, M., Gil-da-Costa, M. J., Ebetsberger-Dachs, G., Kerl, K., Lemmer, A., Boztug, H., Furtwängler, R., Kordes, U., Vokuhl, C., Hasselblatt, M., Bison, B., Kröncke, T., Melchior, P., Timmermann, B., Gerss, J., Siebert, R. & Frühwald, M. C., 27.04.2022, In: CANCERS. 14, 9, 2185.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  14. Spatial molecular profiling of a central nervous system low-grade diffusely infiltrative tumour with INI1 deficiency featuring a high-grade atypical teratoid/rhabdoid tumour component

    Dottermusch, M., Schumann, Y., Kordes, U., Hasselblatt, M. & Neumann, J. E., 04.2022, In: NEUROPATH APPL NEURO. 48, 3, p. e12777 e12777.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  15. Final results of the Choroid Plexus Tumor study CPT-SIOP-2000

    Wolff, J. E., Van Gool, S. W., Kutluk, T., Diez, B., Kebudi, R., Timmermann, B., Garami, M., Sterba, J., Fuller, G. N., Bison, B. & Kordes, U. R., 02.2022, In: J NEURO-ONCOL. 156, 3, p. 599-613 15 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  16. 2021

  17. Ex vivo testis explant culture of human testicular tissue

    Aden, N. L., Soave, A., Kordes, U., Bleeke, M., Salzbrunn, A. & von Kopylow, K., 05.12.2021, In: J Reprodmed Endokrinol. 2020, 17 (Supplementum 1), 39-40

    Research output: SCORING: Contribution to journal › Conference abstract in journal › Research

  18. Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group

    Frühwald, M. C., Nemes, K., Boztug, H., Cornips, M. C. A., Evans, D. G., Farah, R., Glentis, S., Jorgensen, M., Katsibardi, K., Hirsch, S., Jahnukainen, K., Kventsel, I., Kerl, K., Kratz, C. P., Pajtler, K. W., Kordes, U., Ridola, V., Stutz, E. & Bourdeaut, F., 10.2021, In: FAM CANCER. 20, 4, p. 305-316 12 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  19. Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6

    Kordes, U., Mautner, V-F., Oyen, F., Hagel, C., Hartmann, C., Heuser, M., Frühwald, M., Hasselblatt, M., Oehl-Huber, K., Siebert, R., Schneppenheim, R. & Schüller, U., 10.2021, In: PEDIATR BLOOD CANCER. 68, 10, p. e29185

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  20. Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group

    Hettmer, S., Dachy, G., Seitz, G., Agaimy, A., Duncan, C., Jongmans, M., Hirsch, S., Kventsel, I., Kordes, U., de Krijger, R. R., Metzler, M., Michaeli, O., Nemes, K., Poluha, A., Ripperger, T., Russo, A., Smetsers, S., Sparber-Sauer, M., Stutz, E., Bourdeaut, F., Kratz, C. P. & Demoulin, J-B., 10.2021, In: FAM CANCER. 20, 4, p. 327-336 10 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  21. Atypical Teratoid/Rhabdoid Tumor (AT/RT) With Molecular Features of Pleomorphic Xanthoastrocytoma

    Thomas, C., Federico, A., Sill, M., Bens, S., Oyen, F., Nemes, K., Johann, P. D., Hartmann, C., Hartmann, W., Sumerauer, D., Paterno, V., Samii, A., Kordes, U., Siebert, R., Frühwald, M. C., Paulus, W., Kool, M. & Hasselblatt, M., 01.09.2021, In: AM J SURG PATHOL. 45, 9, p. 1228-1234 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  22. Malignant gliomas with H3F3A G34R mutation or MYCN amplification in pediatric patients with Li Fraumeni syndrome

    Schoof, M., Kordes, U., Volk, A. E., Al-Kershi, S., Kresbach, C. & Schüller, U., 09.2021, In: ACTA NEUROPATHOL. 142, 3, p. 591-593 3 p.

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  23. SMARCA4-deficient rhabdoid tumours show intermediate molecular features between SMARCB1-deficient rhabdoid tumours and small cell carcinomas of the ovary, hypercalcaemic type

    Andrianteranagna, M., Cyrta, J., Masliah-Planchon, J., Nemes, K., Corsia, A., Leruste, A., Holdhof, D., Kordes, U., Orbach, D., Corradini, N., Entz-Werle, N., Pierron, G., Castex, M-P., Brouchet, A., Weingertner, N., Ranchère, D., Fréneaux, P., Delattre, O., Bush, J., Leary, A., Frühwald, M. C., Schüller, U., Servant, N. & Bourdeaut, F., 09.2021, In: J PATHOL. 255, 1, p. 1-15 15 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  24. Inhibition of nuclear export restores nuclear localization and residual tumor suppressor function of truncated SMARCB1/INI1 protein in a molecular subset of atypical teratoid/rhabdoid tumors

    Pathak, R., Zin, F., Thomas, C., Bens, S., Gayden, T., Karamchandani, J., Dudley, R. W., Nemes, K., Johann, P. D., Oyen, F., Kordes, U., Jabado, N., Siebert, R., Paulus, W., Kool, M., Frühwald, M. C., Albrecht, S., Kalpana, G. V. & Hasselblatt, M., 08.2021, In: ACTA NEUROPATHOL. 142, 2, p. 361-374 14 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  25. Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor

    Thomas, C., Oehl-Huber, K., Bens, S., Soschinski, P., Koch, A., Nemes, K., Oyen, F., Kordes, U., Kool, M., Frühwald, M. C., Hasselblatt, M. & Siebert, R., 08.2021, In: GENE CHROMOSOME CANC. 60, 8, p. 586-590 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  26. The genetic landscape of choroid plexus tumors in children and adults

    Thomas, C., Soschinski, P., Zwaig, M., Oikonomopoulos, S., Okonechnikov, K., Pajtler, K. W., Sill, M., Schweizer, L., Koch, A., Neumann, J., Schüller, U., Sahm, F., Rauschenbach, L., Keyvani, K., Proescholdt, M., Riemenschneider, M. J., Segewiß, J., Ruckert, C., Grauer, O., Monoranu, C-M., Lamszus, K., Patrizi, A., Kordes, U., Siebert, R., Kool, M., Ragoussis, J., Foulkes, W. D., Paulus, W., Rivera, B. & Hasselblatt, M., 12.04.2021, In: NEURO-ONCOLOGY. 23, 4, p. 650-660 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  27. Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases

    Holdhof, D., Johann, P. D., Spohn, M., Bockmayr, M., Safaei, S., Joshi, P., Masliah-Planchon, J., Ho, B., Andrianteranagna, M., Bourdeaut, F., Huang, A., Kool, M., Upadhyaya, S. A., Bendel, A. E., Indenbirken, D., Foulkes, W. D., Bush, J. W., Creytens, D., Kordes, U., Frühwald, M. C., Hasselblatt, M. & Schüller, U., 02.2021, In: ACTA NEUROPATHOL. 141, 2, p. 291-301 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  28. Clinical and genetic risk factors define two risk groups of extracranial malignant rhabdoid tumours (eMRT/RTK)

    Nemes, K., Bens, S., Kachanov, D., Teleshova, M., Hauser, P., Simon, T., Tippelt, S., Woessmann, W., Beck, O., Flotho, C., Grigull, L., Driever, P. H., Schlegel, P-G., Khurana, C., Hering, K., Kolb, R., Leipold, A., Abbink, F., Gil-Da-Costa, M. J., Benesch, M., Kerl, K., Lowis, S., Marques, C. H., Graf, N., Nysom, K., Vokuhl, C., Melchior, P., Kröncke, T., Schneppenheim, R., Kordes, U., Gerss, J., Siebert, R., Furtwängler, R. & Frühwald, M. C., 01.2021, In: EUR J CANCER. 142, p. 112-122 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  29. 2020

  30. Age and DNA-methylation subgroup as potential independent risk factors for treatment stratification in children with Atypical Teratoid/Rhabdoid Tumors (ATRT)

    Frühwald, M. C., Hasselblatt, M., Nemes, K., Bens, S., Steinbügl, M., Johann, P. D., Kerl, K., Hauser, P., Quiroga, E., Solano-Paez, P., Biassoni, V., Gil-da-Costa, M. J., Perek-Polnik, M., van de Wetering, M., Sumerauer, D., Pears, J., Stabell, N., Holm, S., Hengartner, H., Gerber, N. U., Grotzer, M., Boos, J., Ebinger, M., Tippelt, S., Paulus, W., Furtwängler, R., Hernáiz-Driever, P., Reinhard, H., Rutkowski, S., Schlegel, P-G., Schmid, I., Kortmann, R-D., Timmermann, B., Warmuth-Metz, M., Kordes, U., Gerss, J., Nysom, K., Schneppenheim, R., Siebert, R., Kool, M. & Graf, N., 07.07.2020, In: NEURO-ONCOLOGY. 22, 7, p. 1006–1017 12 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  31. Infant high grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes

    Clarke, M., Mackay, A., Ismer, B., Pickles, J. C., Tatevossian, R. G., Newman, S., Bale, T. A., Stoler, I., Izquierdo, E., Temelso, S., Carvalho, D. M., Molinari, V., Burford, A., Howell, L., Virasami, A., Fairchild, A. R., Avery, A., Chalker, J., Kristiansen, M., Haupfear, K., Dalton, J. D., Orisme, W., Wen, J., Hubank, M., Kurian, K. M., Rowe, C., Maybury, M., Crosier, S., Knipstein, J., Schuller, U., Kordes, U., Kram, D. E., Snuderl, M., Bridges, L., Martin, A. J., Doey, L. J., Al-Sarraj, S., Chandler, C., Zebian, B., Cairns, C., Natrajan, R., Boult, J. K., Robinson, S. P., Sill, M., Dunkel, I. J., Gilheeney, S. W., Rosenblum, M. K., Hughes, D., Proszek, P. Z., MacDonald, T. J., Preusser, M., Haberler, C., Slavc, I., Packer, R., Ng, H-K., Caspi, S., Popovic, M., Faganel Kotnik, B., Wood, M. D., Baird, L., Davare, M. A., Solomon, D. A., Olsen, T. K., Brandal, P., Farrell, M., Cryan, J. B., Capra, M., Karremann, M., Schittenhelm, J., Schuhmann, M. U., Ebinger, M., Dinjens, W. N. M., Kerl, K., Hettmer, S., Pietsch, T., Andreiuolo, F., Driever, P. H., Korshunov, A., Hiddingh, L., Worst, B. C., Sturm, D., Zuckermann, M., Witt, O., Bloom, T., Mitchell, C., Miele, E., Colafati, G. S., Diomedi-Camassei, F., Bailey, S., Moore, A. S., Hassall, T. E., Lowis, S. P., Tsoli, M., Cowley, M. J., Ziegler, D. S., Karajannis, M. A., Aquilina, K., Hargrave, D. R., Carceller, F., Marshall, L. V., von Deimling, A., Kramm, C. M., Pfister, S. M., Sahm, F., Baker, S. J., Mastronuzzi, A., Carai, A., Vinci, M., Capper, D., Popov, S., Ellison, D. W., Jacques, T. S., Jones, D. T. W. & Jones, C., 07.2020, In: CANCER DISCOV. 10, 7, p. 942-963 22 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  32. Epigenetics impacts upon prognosis and clinical management of choroid plexus tumors

    Thomas, C., Metrock, K., Kordes, U., Hasselblatt, M. & Dhall, G., 05.2020, In: J NEURO-ONCOL. 148, 1, p. 39-45 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Review article › Research

  33. Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults

    Thomas, C., Wefers, A., Bens, S., Nemes, K., Agaimy, A., Oyen, F., Vogelgesang, S., Rodriguez, F. J., Brett, F. M., McLendon, R., Bodi, I., Burel-Vandenbos, F., Keyvani, K., Tippelt, S., Poulsen, F. R., Lipp, E. S., Giannini, C., Reifenberger, G., Kuchelmeister, K., Pietsch, T., Kordes, U., Siebert, R., Frühwald, M. C., Johann, P. D., Sill, M., Kool, M., von Deimling, A., Paulus, W. & Hasselblatt, M., 02.2020, In: ACTA NEUROPATHOL. 139, 2, p. 277-286 10 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  34. 2019

  35. Phase I/II intra-patient dose escalation study of vorinostat in children with relapsed solid tumor, lymphoma, or leukemia

    van Tilburg, C. M., Milde, T., Witt, R., Ecker, J., Hielscher, T., Seitz, A., Schenk, J-P., Buhl, J. L., Riehl, D., Frühwald, M. C., Pekrun, A., Rossig, C., Wieland, R., Flotho, C., Kordes, U., Gruhn, B., Simon, T., Linderkamp, C., Sahm, F., Taylor, L., Freitag, A., Burhenne, J., Foerster, K. I., Meid, A. D., Pfister, S. M., Karapanagiotou-Schenkel, I. & Witt, O., 10.12.2019, In: CLIN EPIGENETICS. 11, 1, p. 188

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  36. Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1

    Thomas, C., Knerlich-Lukoschus, F., Reinhard, H., Johann, P. D., Sturm, D., Sahm, F., Bens, S., Vogt, J., Nemes, K., Oyen, F., Kordes, U., Siebert, R., Schneppenheim, R., Messing-Jünger, M., Pietsch, T., von Deimling, A., Paulus, W., Pfister, S. M., Kool, M., Frühwald, M. C. & Hasselblatt, M., 05.2019, In: ACTA NEUROPATHOL. 137, 5, p. 847-850 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  37. Manifestations and Treatment of Adult-onset Symptomatic Optic Pathway Glioma in Neurofibromatosis Type 1

    Mehlan, J., Schüttauf, F., Salamon, J. M., Kordes, U., Friedrich, R. E. & Mautner, V-F., 02.2019, In: ANTICANCER RES. 39, 2, p. 827-831 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  38. 2018

  39. Biological material collection to advance translational research and treatment of children with CNS tumours: position paper from the SIOPE Brain Tumour Group

    Rutkowski, S., Modena, P., Williamson, D., Kerl, K., Nysom, K., Pizer, B., Bartels, U., Puget, S., Doz, F., Michalski, A., von Hoff, K., Chevignard, M., Avula, S., Murray, M. J., Schönberger, S., Czech, T., Schouten-van Meeteren, A. Y. N., Kordes, U., Kramm, C. M., van Vuurden, D. G., Hulleman, E., Janssens, G. O., Solanki, G. A., van Veelen, M-L. C., Thomale, U., Schuhmann, M. U., Jones, C., Giangaspero, F., Figarella-Branger, D., Pietsch, T., Clifford, S. C., Pfister, S. M. & Van Gool, S. W., 08.2018, In: LANCET ONCOL. 19, 8, p. e419-e428

    Research output: SCORING: Contribution to journal › SCORING: Review article › Research

  40. Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis

    Holsten, T., Bens, S., Oyen, F., Nemes, K., Hasselblatt, M., Kordes, U., Siebert, R., Frühwald, M. C., Schneppenheim, R. & Schüller, U., 08.2018, In: EUR J HUM GENET. 26, 8, p. 1083-1093 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Review article › Research

  41. Differences in maxillomandibular morphology among patients with mucopolysaccharidoses I, II, III, IV and VI: a retrospective MRI study

    Koehne, T., Köhn, A., Friedrich, R. E., Kordes, U., Schinke, T., Muschol, N. & Kahl-Nieke, B., 04.2018, In: CLIN ORAL INVEST. 22, 3, p. 1541-1549 9 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  42. Group 3 medulloblastoma in a patient with a GYS2 germline mutation and glycogen storage disease 0a

    Holsten, T., Tsiakas, K., Kordes, U., Bison, B., Pietsch, T., Rutkowski, S., Santer, R. & Schüller, U., 03.2018, In: CHILD NERV SYST. 34, 3, p. 581-584 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  43. 2017

  44. Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology

    Ripperger, T., Bielack, S. S., Borkhardt, A., Brecht, I. B., Burkhardt, B., Calaminus, G., Debatin, K-M., Deubzer, H., Dirksen, U., Eckert, C., Eggert, A., Erlacher, M., Fleischhack, G., Frühwald, M. C., Gnekow, A., Goehring, G., Graf, N., Hanenberg, H., Hauer, J., Hero, B., Hettmer, S., von Hoff, K., Horstmann, M., Hoyer, J., Illig, T., Kaatsch, P., Kappler, R., Kerl, K., Klingebiel, T., Kontny, U., Kordes, U., Körholz, D., Koscielniak, E., Kramm, C. M., Kuhlen, M., Kulozik, A. E., Lamottke, B., Leuschner, I., Lohmann, D. R., Meinhardt, A., Metzler, M., Meyer, L. H., Moser, O., Nathrath, M., Niemeyer, C. M., Nustede, R., Pajtler, K. W., Paret, C., Rasche, M., Reinhardt, D., Rieß, O., Russo, A., Rutkowski, S., Schlegelberger, B., Schneider, D., Schneppenheim, R., Schrappe, M., Schroeder, C., von Schweinitz, D., Simon, T., Sparber-Sauer, M., Spix, C., Stanulla, M., Steinemann, D., Strahm, B., Temming, P., Thomay, K., von Bueren, A. O., Vorwerk, P., Witt, O., Wlodarski, M., Wössmann, W., Zenker, M., Zimmermann, S., Pfister, S. M. & Kratz, C. P., 04.2017, In: AM J MED GENET A. 173, 4, p. 1017-1037 21 p.

    Research output: SCORING: Contribution to journal › SCORING: Review article › Research

  45. 2016

  46. Methylation profiling of choroid plexus tumors reveals 3 clinically distinct subgroups

    Thomas, C., Sill, M., Ruland, V., Witten, A., Hartung, S., Kordes, U., Jeibmann, A., Beschorner, R., Keyvani, K., Bergmann, M., Mittelbronn, M., Pietsch, T., Felsberg, J., Monoranu, C. M., Varlet, P., Hauser, P., Olar, A., Grundy, R. G., Wolff, J. E., Korshunov, A., Jones, D. T., Bewerunge-Hudler, M., Hovestadt, V., von Deimling, A., Pfister, S. M., Paulus, W., Capper, D. & Hasselblatt, M., 06.2016, In: NEURO-ONCOLOGY. 18, 6, p. 790-6 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  47. 2015

  48. Strategies to improve the quality of survival for childhood brain tumour survivors

    Tallen, G., Resch, A., Calaminus, G., Wiener, A., Leiss, U., Pletschko, T., Friedrich, C., Langer, T., Grabow, D., Driever, P. H., Kortmann, R-D., Timmermann, B., Pietsch, T., Warmuth-Metz, M., Bison, B., Thomale, U-W., Krauss, J., Mynarek, M., von Hoff, K., Ottensmeier, H., Frühwald, M., Kramm, C. M., Temming, P., Müller, H. L., Witt, O., Kordes, U., Fleischhack, G., Gnekow, A., Rutkowski, S. & German Paediatric Brain Tumour Consortium (HIT-Network), 11.2015, In: EUR J PAEDIATR NEURO. 19, 6, p. 619-39 21 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  49. Pediatric atypical choroid plexus papilloma reconsidered: increased mitotic activity is prognostic only in older children

    Thomas, C., Ruland, V., Kordes, U., Hartung, S., Capper, D., Pietsch, T., Gerß, J., Wolff, J. E. A., Paulus, W. & Hasselblatt, M., 06.2015, In: ACTA NEUROPATHOL. 129, 6, p. 925-7 3 p.

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  50. Radiation therapy for choroid plexus carcinoma patients with Li-Fraumeni Syndrome: advantageous or detrimental?

    Bahar, M., Kordes, U., Tekautz, T. & Wolff, J., 05.2015, In: ANTICANCER RES. 35, 5, p. 3013-3017 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  51. High-resolution genomic analysis does not qualify atypical plexus papilloma as a separate entity among choroid plexus tumors

    Japp, A. S., Gessi, M., Messing-Jünger, M., Denkhaus, D., Zur Mühlen, A., Wolff, J. E., Hartung, S., Kordes, U., Klein-Hitpass, L. & Pietsch, T., 02.2015, In: J NEUROPATH EXP NEUR. 74, 2, p. 110-20 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  52. 2014

  53. Methylation of the hTERT promoter is frequent in choroid plexus tumors but not of independent prognostic value

    Ruland, V., Hartung, S., Kordes, U., Wolff, J. E., Paulus, W. & Hasselblatt, M., 01.08.2014, In: J NEURO-ONCOL. 119, 1, p. 215-6 2 p.

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  54. Choroid plexus carcinomas are characterized by complex chromosomal alterations related to patient age and prognosis

    Ruland, V., Hartung, S., Kordes, U., Wolff, J. E., Paulus, W. & Hasselblatt, M., 01.05.2014, In: GENE CHROMOSOME CANC. 53, 5, p. 373-80 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  55. Favorable outcome of patients affected by rhabdoid tumors due to rhabdoid tumor predisposition syndrome (RTPS)

    Kordes, U., Bartelheim, K., Modena, P., Massimino, M., Biassoni, V., Reinhard, H., Hasselblatt, M., Schneppenheim, R. & Frühwald, M. C., 01.05.2014, In: PEDIATR BLOOD CANCER. 61, 5, p. 919-21 3 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  56. High-dose chemotherapy (HDCT) with auto-SCT in children with atypical teratoid/rhabdoid tumors (AT/RT): a report from the European Rhabdoid Registry (EU-RHAB)

    Benesch, M., Bartelheim, K., Fleischhack, G., Gruhn, B., Schlegel, P. G., Witt, O., Stachel, K. D., Hauch, H., Urban, C., Quehenberger, F., Massimino, M., Pietsch, T., Hasselblatt, M., Giangaspero, F., Kordes, U., Schneppenheim, R., Hauser, P., Klingebiel, T. & Frühwald, M. C., 01.03.2014, In: BONE MARROW TRANSPL. 49, 3, p. 370-5 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  57. Neuroonkologie

    Rutkowski, S. J., Hornung, D., Kordes, U., Kammler, G., Hagel, C., Löbel, U., Ebinger, M., Rössler, J., Resch, A. & Linhart, D., 2014, Neuropädiatrie - Evidenzbasierte Therapie. Korinthenberg, R., Panteliadis, C. P. & Hagel, C. (eds.). 2 ed. München: Elsevier, 27 p. 12

    Research output: SCORING: Contribution to book/anthology › SCORING: Contribution to collected editions/anthologies › Education › peer-review

  58. 2013

  59. Supra- and infratentorial pediatric ependymomas differ significantly in NeuN, p75 and GFAP expression

    Hagel, C., Treszl, A., Fehlert, J., Harder, J., von Haxthausen, F., Kern, M., von Bueren, A. O. & Kordes, U., 01.04.2013, In: J NEURO-ONCOL. 112, 2, p. 191-7 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  60. High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.

    Hasselblatt, M., Isken, S., Linge, A., Eikmeier, K., Jeibmann, A., Oyen, F., Nagel, I., Richter, J., Bartelheim, K., Kordes, U., Schneppenheim, R., Frühwald, M., Siebert, R. & Paulus, W., 2013, In: GENE CHROMOSOME CANC. 52, 2, p. 185-190 6 p., 2.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  61. 2012

  62. Mismatch repair deficiency: a temozolomide resistance factor in medulloblastoma cell lines that is uncommon in primary medulloblastoma tumours.

    von Bueren, A., Bacolod, M. D., Hagel, C., Heinimann, K., Fedier, A., Kordes, U., Pietsch, T., Koster, J., Grotzer, M. A., Friedman, H. S., Marra, G., Kool, M. & Rutkowski, S., 09.10.2012, In: BRIT J CANCER. 107, 8, p. 1399-1408 10 p., 8.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

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