Anzahl der Publikationen: 43
Monographie
Bauer, J.; Bohl, E.; Schneider, S.; Lehmann, R.; Foeckler, F.; Deichner, O.; Krois, A.; Kifinger, B.; Küfmann, Carola; Hubmann, M.; Künz, E.; Moritz, Ch.; Ritzenfeld, T.; Deppisch, C. und Robrecht, D.
(2003):
Integrierte ökologische Bewertung von bayerischen Fließgewässern südlich der Donau.
Bayer. Landesamt für Wasserwirtschaft: Materialien, Bd. 109. München: Bayer. Landesamt für Wasserwirtschaft.
Zeitschriftenartikel
Dressen, M.; Luzius, T.; Lahm, H.; Neb, I.; Doppler, S. A.; Schneider, S.; Dzilic, E.; Lange, R. und Krane, M.
(2022):
Establishment of an induced pluripotent stem cell line DHMi005-A from a healthy male proband.
In: Stem Cell Research, Bd. 59, 102662
Dressen, M.; Lahm, H.; Neb, I.; Luzius, T.; Doppler, S. A.; Schneider, S.; Dzilic, E.; Lange, R. und Krane, M.
(2022):
Establishment of a patient-specific induced pluripotent stem cell line DHMi004-A from a male Holt-Oram syndrome patient with verified TBX5 mutation.
In: Stem Cell Research, Bd. 58, 102617
Haubner, S.; Perna, F.; Koehnke, T.; Schmidt, C.; Berman, S.; Augsberger, C.; Schnorfeil, F. M.; Krupka, C.; Lichtenegger, F. S.; Liu, X.; Kerbs, P.; Schneider, S.; Metzeler, K. H.; Spiekermann, K.; Hiddemann, W.; Greif, P. A.; Herold, T.; Sadelain, M. und Subklewe, M.
(2019):
Coexpression profile of leukemic stem cell markers for combinatorial targeted therapy in AML.
In: Leukemia, Bd. 33, Nr. 1: S. 64-74
Bamopoulos, S. A.; Batcha, A. M. N.; Jurinovic, V.; Metzeler, K. H.; Thurley, M. Rothenberg; Ksienzyk, B.; Hartmann, L.; Greif, P. A.; Phillippou-Massier, J.; Krebs, S.; Blum, H.; Amler, S.; Schneider, S.; Konstandin, N.; Sauerland, M. C.; Berdel, W. E.; Woermann, B. J.; Bohlander, S. K.; Braess, J.; Hiddemann, W.; Mansmann, Ulrich; Spiekermann, K. und Herold, T.
(2017):
Characterization of Spliceosome Mutations in Patients with Acute Myeloid Leukemia.
In: Annals of Hematology, Bd. 96:
S60-S60
Herold, Tobias; Jurinovic, V.; Metzeler, K. H.; Batcha, A. M. N.; Bamopoulos, S. A.; Rothenberg-Thurley, M.; Ksienzyk, B.; Hartmann, L.; Greif, P. A.; Phillippou-Massier, J.; Krebs, S.; Blum, H.; Amler, S.; Schneider, S.; Konstandin, N.; Sauerland, M. C.; Berdel, W. E.; Wörmann, B. J.; Subklewe, M.; Fiegl, M.; Bohlander, S. K.; Braess, J.; Hiddemann, W.; Mansmann, Ulrich und Spiekermann, K.
(2017):
Prediction of Primary Refractory Acute Myeloid Leukemia.
In: Annals of Hematology, Bd. 96:
S25-S25
Vosberg, S.; Hartmann, L.; Metzeler, K. H.; Schumacher, D.; Pastore, F.; Bräundl, K.; Zellmeier, E.; Ksienzyk, B.; Konstandin, N. P.; Schneider, S.; Graf, A.; Krebs, S.; Blum, H.; Neumann, M.; Baldus, C. D.; Bohlander, S. K.; Wolf, S.; Hiddemann, W.; Spiekermann, K. und Greif, P. A.
(2017):
Evolutionary Patterns of Cytogenetically Normal Acute Myeloid Leukemia Correlate with Time to Relapse.
In: Annals of Hematology, Bd. 96:
S55-S55
Prassek, V. V.; Rothenberg-Thurley, M.; Sauerland, M. C.; Amler, S.; Görlich, D.; Herold, T.; Janke, H.; Schneider, S.; Subklewe, M.; Krug, U.; Faldum, A.; Berdel, W.; Wörmann, B.; Bräss, J.; Spiekermann, K.; Hiddemann, W. und Metzeler, K.
(2017):
AML patients aged >= 75 years enrolled into AMLCG trials: do genetic alterations impact clinical outcome in very old, intensively treated patients?
In: Oncology Research and Treatment, Bd. 40: S. 29
Herold, Tobias; Metzeler, Klaus H.; Vosberg, Sebastian; Hartmann, Luise; Jurinovic, Vindi; Opatz, Sabrina; Konstandin, Nikola P.; Schneider, S.; Zellmeier, Evelyn; Ksienzyk, Bianka; Graf, A.; Krebs, S.; Blum, H.; Sauerland, Maria Cristina; Büchner, T.; Berdel, W. E.; Wörmann, Bernhard; Mansmann, Ulrich; Hiddemann, Wolfgang; Bohlander, Stefan K.; Spiekermann, Karsten und Greif, Philipp A.
(2017):
Acute Myeloid Leukemia with Del(9q) is Characterized by Frequent Mutations of NPM1, DNMT3A, WT1 and Low Expression of TLE4.
In: Genes, Chromosomes and Cancer, Bd. 56, Nr. 1: S. 75-86
Bremova, T.; Sztatecsny, C.; Rominger, A.; Havla, J.; Bamberger, A.; Hartmann, K.; Clevert, D. A.; Strupp, M. und Schneider, S.
(2017):
Niemann Pick Type C heterozygosity may predispose to late-onset neurodegeneration.
In: European Journal of Neurology, Bd. 24: S. 448
Prassek, V.; Rothenberg-Thurley, M.; Sauerland, M. C.; Amler, S.; Görlich, D.; Herold, T.; Janke, H.; Schneider, S.; Subklewe, M.; Krug, U.; Faldum, A.; Berdel, W. E.; Wörmann, B.; Braess, J.; Hiddemann, W.; Spiekermann, K. und Metzeler, K. H.
(2017):
AML patients aged >= 75 years enrolled into AMLCG trials: do genetic alterations impact clinical outcome in very old, intensively treated patients?
In: Haematologica, Bd. 102: S. 209-210
Konstandin, N. P.; Pastore, F.; Dufour, A.; Metzeler, K. H.; Rothenberg-Thurley, M.; Herold, T.; Schneider, S.; Ksienzyk, B.; Tschuri, S.; Berdel, W. E.; Wörmann, B. J.; Sauerland, C.; Bräss, J.; Stefan, B. K.; Hiddemann, W. und Spiekermann, K.
(2017):
Genetic Characterization of a Large Group of CEBPA Mutated AML Patients and the Effect of TET2 and GATA2 Mutations on Outcome.
In: Haematologica, Bd. 102: S. 363-364
Herold, Tobias; Schneider, S.; Metzeler, Klaus H.; Neumann, Martin; Hartmann, Luise; Roberts, Kathryn G.; Konstandin, Nikola P.; Greif, Philipp A.; Bräundl, Kathrin; Ksienzyk, Bianka; Huk, Natalia; Schneider, Irene; Zellmeier, Evelyn; Jurinovic, Vindi; Mansmann, Ulrich; Hiddemann, Wolfgang; Mullighan, Charles G.; Bohlander, Stefan K.; Spiekermann, Karsten; Hölzel, Dieter; Brüggemann, Monika; Baldus, Claudia D.; Dreyling, Martin und Gökbuget, Nicola
(2017):
Adults with Philadelphia chromosome–like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis.
In: Haematologica, Bd. 102, Nr. 1: S. 130-138
[PDF, 1MB]
Prassek, V. V.; Rothenberg-Thurley, M.; Herold, T.; Amler, S.; Sauerland, M. C.; Goerlich, D.; Janke, H.; Schneider, S.; Subklewe, Marion; Krug, U.; Faldum, A.; Berdel, W. E.; Woermann, B.; Buechner, T.; Braess, J.; Hiddemann, W.; Spiekermann, K. und Metzeler, K. H.
(2017):
AML Patients Aged >= 75 Years Enrolled into AMLCG Trials: Do Gene Mutations Impact Clinical Outcome in Very Old, Intensively Treated Patients?
In: Annals of Hematology, Bd. 96:
S63-S63
Reiter, K.; Hubmann, M.; Harin, E.; Vosberg, S.; Braeundl, K.; Ksienzyk, B.; Schneider, S.; Dufour, A.; Zellmeier, E.; Bohlander, S. K.; Sauerland, C.; Berdel, W. E.; Woermann, B.; Buechner, T.; Braess, J.; Hiddemann, W.; Spiekermann, K. und Greif, A.
(2017):
Comparison of FLT3-ITD Detection of High-Throughput Amplicon Sequencing to Routine Diagnostics - A Retrospective Analysis of AMLCG Study Patients.
In: Annals of Hematology, Bd. 96:
S62-S62
Rothenberg-Thurley, M.; Amler, S.; Goerlich, D.; Sauerland, M. C.; Schneider, S.; Konstandin, N. P.; Batcha, A. M.; Ksienzyk, B.; Zellmeier, E.; Mansmann, Ulrich; Subklewe, Marion; Bohlander, S. K.; Faldum, A.; Hiddemann, W.; Spiekermann, K.; Braess, J. und Metzeler, Klaus H.
(2017):
Persistence of Driver Mutations during Complete Remission Associates with Shorter Survival and Contributes to the Inferior Outcomes of Elderly Patients with Acute Myeloid Leukemia.
In: Annals of Hematology, Bd. 96:
S31-S32
Rothenberg-Thurley, M.; Amler, S.; Goerlich, D.; Sauerland, M. C.; Schneider, S.; Konstandin, N. P.; Schaaf, S.; Batcha, A. M. Nazeer; Bräundl, K.; Ksienzyk, B.; Zellmeier, E.; Mansmann, Ulrich; Fiegl, M.; Subklewe, M.; Bohlander, S. K.; Faldum, A.; Hiddemann, W.; Spiekermann, K.; Braess, J. und Metzeler, K. H.
(2016):
Persistence of driver mutations during complete remission associates with shorter survival and contributes to the inferior outcomes of elderly patients with acute myeloid leukemia.
In: Haematologica, Bd. 101: S. 23
Rothenberg-Thurley, M.; Amler, S.; Görlich, D.; Sauerland, M. C.; Schneider, S.; Konstandin, N. P.; Schaaf, S.; Nazeer Batcha, A. M.; Bräundl, K.; Ksienzyk, B.; Zellmaier, E.; Mansmann, Ulrich; Fiegl, M.; Subklewe, M.; Bohlander, S. K.; Faldum, A.; Hiddemann, W.; Spiekermann, K.; Braess, J. und Metzeler, K. H.
(2016):
Persistence of driver mutations during complete remission associates with shorter survival and contributes to the inferior outcomes of elderly patients with acute myeloid leukemia.
In: Oncology Research and Treatment, Bd. 39: S. 110-111
Hartmann, L.; Dutta, S.; Opatz, S.; Vosberg, S.; Reiter, K.; Leubolt, G.; Metzeler, K. H.; Herold, T.; Bamopoulos, S. A.; Bräundl, K.; Zellmeier, E.; Ksienzyk, B.; Konstandin, N. P.; Schneider, S.; Hopfner, K. P.; Graf, A.; Krebs, S.; Blum, H.; Middeke, J. M.; Stölzel, F.; Thiede, C.; Wolf, S.; Bohlander, S. K.; Preiss, C.; Chen-Wichmann, L.; Wichmann, C.; Sauerland, M. C.; Büchner, T.; Berdel, W. E.; Wörmann, B. J.; Braess, J.; Hiddemann, W.; Spiekermann, K. und Greif, P. A.
(2016):
Frequent recurring mutations disrupt the anti-proliferative function of ZBTB7A in acute myeloid leukemia with t(8;21) translocation.
In: Haematologica, Bd. 101: S. 11
Krupka, C.; Kufer, P.; Kischel, R.; Zugmaier, G.; Lichtenegger, F. S.; Köhnke, T.; Vick, B.; Jeremias, I.; Metzeler, K. H.; Altmann, T.; Schneider, S.; Fiegl, M.; Spiekermann, K.; Bauerle, P. A.; Hiddemann, W.; Riethmüller, G. und Subklewe, M.
(2016):
Blockade of the PD-1/PD-L1 axis augments lysis of AML cells by the CD33/CD3 BiTE antibody construct AMG 330: reversing a T-cell-induced immune escape mechanism.
In: Leukemia, Bd. 30, Nr. 2: S. 484-491
Vosberg, Sebastian; Herold, Tobias; Hartmann, Luise; Neumann, Martin; Opatz, Sabrina; Metzeler, Klaus H.; Schneider, S.; Graf, A.; Krebs, S.; Blum, H.; Baldus, Claudia D.; Hiddemann, Wolfgang; Spiekermann, Karsten; Bohlander, Stefan K.; Mansmann, Ulrich und Greif, Philipp A.
(2016):
Close Correlation of Copy Number Aberrations Detected by Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia.
In: Genes, Chromosomes and Cancer, Bd. 55, Nr. 7: S. 553-567
Dufour, A.; Schneider, F.; Hoster, Eva; Benthaus, T.; Ksienzyk, Bianka; Schneider, S.; Kakadia, P. M.; Sauerland, M. C.; Berdel, W. E.; Büchner, T.; Wörmann, Bernhard; Braess, J.; Subklewe, M.; Hiddemann, Wolfgang; Bohlander, Stefan K. und Spiekermann, Karsten
(2012):
Monoallelic CEBPA mutations in normal karyotype acute myeloid leukemia: independent favorable prognostic factor within NPM1 mutated patients.
In: Annals of Hematology, Bd. 91, Nr. 7: S. 1051-1063
Schneider, F.; Hoster, Eva; Schneider, S.; Dufour, A.; Benthaus, T.; Kakadia, P. M.; Bohlander, Stefan K.; Braess, J.; Heinecke, A.; Sauerland, M. C.; Berdel, W. E.; Büchner, T.; Wörmann, Bernhard; Feuring-Buske, M.; Buske, C.; Creutzig, U.; Thiede, C.; Zwaan, M. C.; Heuvel-Eibrink, M. M. van den; Reinhardt, D.; Hiddemann, Wolfgang und Spiekermann, Karsten
(2012):
Age-dependent frequencies of NPM1 mutations and FLT3-ITD in patients with normal karyotype AML (NK-AML).
In: Annals of Hematology, Bd. 91, Nr. 1: S. 9-18
Schneider, F.; Hoster, Eva; Unterhalt, Michael; Schneider, S.; Dufour, A.; Benthaus, T.; Mellert, G.; Zellmeier, Evelyn; Kakadia, P. M.; Bohlander, Stefan K.; Feuring-Buske, M.; Buske, C.; Braess, J.; Heinecke, A.; Sauerland, M. C.; Berdel, W. E.; Büchner, T.; Wörmann, Bernhard; Hiddemann, Wolfgang und Spiekermann, Karsten
(2012):
The FLT3ITD level has a high prognostic impact in NPM1 mutated, but not NPM1 unmutated AML with a normal karyotype.
In: Blood, Bd. 119, Nr. 19: S. 4383-4386
Greif, Philipp A.; Dufour, A.; Konstandin, Nikola P.; Ksienzyk, Bianka; Zellmeier, Evelyn; Tizazu, B.; Sturm, J.; Benthaus, T.; Herold, Tobias; Yaghmaie, M.; Dorge, P.; Hopfner, K. P.; Hauser, A.; Graf, A.; Krebs, S.; Blum, H.; Kakadia, P. M.; Schneider, S.; Hoster, Eva; Schneider, F.; Stanulla, M.; Braess, J.; Sauerland, M. C.; Berdel, W. E.; Büchner, T.; Wörmann, Bernhard; Hiddemann, Wolfgang; Spiekermann, Karsten und Bohlander, Stefan K.
(2012):
GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia.
In: Blood, Bd. 120, Nr. 2: S. 395-403
Herold, Tobias; Mulaw, M. A.; Jurinovic, Vindi; Seiler, T.; Metzeler, Klaus H.; Dufour, A.; Schneider, S.; Kakadia, P. M.; Spiekermann, Karsten; Mansmann, Ulrich; Hiddemann, Wolfgang; Buske, C.; Dreyling, Martin und Bohlander, Stefan K.
(2012):
High expression of MZB1 predicts adverse prognosis in chronic lymphocytic leukemia, follicular lymphoma and diffuse large B-cell lymphoma and is associated with a unique gene expression signature.
In: Leukemia & Lymphoma, Bd. 54, Nr. 8: S. 1652-1657
Herold, Tobias; Jurinovic, Vindi; Metzeler, Klaus H.; Boulesteix, Anne-Laure; Bergmann, M.; Seiler, T.; Mulaw, M.; Thoene, S.; Dufour, A.; Pasalic, Z.; Schmidberger, Markus; Schmidt, M.; Schneider, S.; Kakadia, P. M.; Feuring-Buske, M.; Braess, J.; Spiekermann, Karsten; Mansmann, Ulrich; Hiddemann, Wolfgang; Buske, C. und Bohlander, Stefan K.
(2011):
An eight-gene expression signature for the prediction of survival and time to treatment in chronic lymphocytic leukemia.
In: Leukemia, Bd. 25, Nr. 10: S. 1639-1645
Herold, Tobias; Jurinovic, Vindi; Mulaw, M.; Seiler, T.; Dufour, A.; Schneider, S.; Kakadia, P. M.; Feuring-Buske, M.; Braess, J.; Spiekermann, Karsten; Mansmann, Ulrich; Hiddemann, Wolfgang; Buske, C. und Bohlander, Stefan K.
(2011):
Expression analysis of genes located in the minimally deleted regions of 13q14 and 11q22-23 in chronic lymphocytic leukemia-unexpected expression pattern of the RHO GTPase activator ARHGAP20.
In: Genes, Chromosomes and Cancer, Bd. 50, Nr. 7: S. 546-558
Dufour, A.; Schneider, F.; Metzeler, Klaus H.; Hoster, Eva; Schneider, S.; Zellmeier, Evelyn; Benthaus, T.; Sauerland, M. C.; Berdel, W. E.; Büchner, T.; Wörmann, Bernhard; Braess, J.; Hiddemann, Wolfgang; Bohlander, Stefan K. und Spiekermann, Karsten
(2010):
Acute myeloid leukemia with biallelic CEBPA gene mutations and normal karyotype represents a distinct genetic entity associated with a favorable clinical outcome.
In: Journal of Clinical Oncology, Bd. 28, Nr. 4: S. 570-577
Schneider, F.; Hoster, Eva; Unterhalt, Michael; Schneider, S.; Dufour, A.; Benthaus, T.; Mellert, G.; Zellmeier, Evelyn; Bohlander, Stefan K.; Feuring-Buske, M.; Buske, C.; Braess, J.; Fritsch, S.; Heinecke, A.; Sauerland, M. C.; Berdel, W. E.; Büchner, T.; Wörmann, Bernhard; Hiddemann, Wolfgang und Spiekermann, Karsten
(2009):
NPM1, but not FLT3-ITD mutations predict early blast cell clearance and CR rate in patients with normal karyotype AML (NK-AML) or high risk myelodysplastic syndrome (MDS).
In: Blood, Bd. 113, Nr. 21: S. 5250-5253
Schneider, S.; Seither, Berenike; Tönges, S. und Schmitt, H.
(2006):
Sports injuries: population based representative data on incidence, diagnosis, sequelae, and high risk groups.
In: British Journal of Sports Medicine, Bd. 40, Nr. 4: S. 334-339
[PDF, 182kB]
Buchbeitrag
Schmidt, G.; Siebzehnrübl, S.; Fischer, R. und Scheer, Hugo
(1988):
Photochromic properties of C-phycocyanin.
In: Scheer, Hugo und Schneider, S. (Hrsg.):
Photosynthetic light-harvesting systems : organization and function. Berlin: De Gruyter. S. 77-88
[PDF, 1MB]
Konferenzbeitrag
Geiselhart, P.; Schneider, S.; Fischer, R.; Siebzehnrübl, S. und Scheer, Hugo
(1989):
Energy transfer in C-phycocyanin in different states of aggregation studied by picosecond time-resolved fluorescence.
International Symposium on Photobiology and Biotechnology, Poznan, Polen, 27. - 30. Juni 1989.
In: Photobiology and biotechnology: proceedings of international symposium ; June 27 - 30, 1989 ; Poznań, Poland. Poznań Technical University, Polish Biophysical Society,
Poznań: S. 47-51
[PDF, 777kB]
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