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Chromosomal aberrations in congenital bone marrow failure disorders—an early indicator for leukemogenesis?
Published in:
Annals of Hematology, 2007, v. 86, n. 10, p. 733, doi. 10.1007/s00277-007-0337-z
By:
- Göhring, G.;
- Karow, A.;
- Steinemann, D.;
- Wilkens, L.;
- Lichter, P.;
- Zeidler, C.;
- Niemeyer, C.;
- Welte, K.;
- Schlegelberger, B.
Publication type:
Article
Fluorescence in situ hybridization using the subtelomeric 11q probe as a diagnostic tool for congenital thrombocytopenia.
Published in:
2006
By:
- Göhring, G.;
- Hanke, C.;
- Kratz, C.;
- Kontny, U.;
- Steinemann, D.;
- Niemeyer, C.;
- Schlegelberger, B.
Publication type:
Letter
Frequency and prognostic impact of casein kinase 1A1 mutations in MDS patients with deletion of chromosome 5q.
Published in:
Leukemia (08876924), 2015, v. 29, n. 9, p. 1942, doi. 10.1038/leu.2015.49
By:
- Heuser, M;
- Meggendorfer, M;
- Cruz, M M A;
- Fabisch, J;
- Klesse, S;
- Köhler, L;
- Göhring, G;
- Ganster, C;
- Shirneshan, K;
- Gutermuth, A;
- Cerny-Reiterer, S;
- Krönke, J;
- Panagiota, V;
- Haferlach, C;
- Koenecke, C;
- Platzbecker, U;
- Thiede, C;
- Schroeder, T;
- Kobbe, G;
- Ehrlich, S
Publication type:
Article
Low frequency of calreticulin mutations in MDS patients.
Published in:
Leukemia (08876924), 2014, v. 28, n. 9, p. 1933, doi. 10.1038/leu.2014.165
By:
- Heuser, M;
- Panagiota, V;
- Koenecke, C;
- Fehse, B;
- Alchalby, H;
- Badbaran, A;
- Shahswar, R;
- Stadler, M;
- Eder, M;
- Göhring, G;
- Trummer, A;
- Schroeder, T;
- Kobbe, G;
- Thiede, C;
- Platzbecker, U;
- Schlegelberger, B;
- Kroeger, N;
- Ganser, A;
- Thol, F
Publication type:
Article
Prognostic effect of calreticulin mutations in patients with myelofibrosis after allogeneic hematopoietic stem cell transplantation.
Published in:
Leukemia (08876924), 2014, v. 28, n. 7, p. 1552, doi. 10.1038/leu.2014.66
By:
- Panagiota, V;
- Thol, F;
- Markus, B;
- Fehse, B;
- Alchalby, H;
- Badbaran, A;
- Lehmann, U;
- Koenecke, C;
- Shahswar, R;
- Chaturvedi, A;
- Stadler, M;
- Eder, M;
- Göhring, G;
- Koenigsmann, M;
- Kloos, A;
- Trummer, A;
- Schroeder, T;
- Kobbe, G;
- Thiede, C;
- Platzbecker, U
Publication type:
Article
The clinical relevance of minor paroxysmal nocturnal hemoglobinuria clones in refractory cytopenia of childhood: a prospective study by EWOG-MDS.
Published in:
Leukemia (08876924), 2014, v. 28, n. 1, p. 189, doi. 10.1038/leu.2013.195
By:
- Aalbers, A M;
- van der Velden, V H J;
- Yoshimi, A;
- Fischer, A;
- Noellke, P;
- Zwaan, C M;
- Baumann, I;
- Beverloo, H B;
- Dworzak, M;
- Hasle, H;
- Locatelli, F;
- De Moerloose, B;
- Göhring, G;
- Schmugge, M;
- Stary, J;
- Zecca, M;
- Langerak, A W;
- van Dongen, J J M;
- Pieters, R;
- Niemeyer, C M
Publication type:
Article
Analysis of NUP98/NSD1 translocations in adult AML and MDS patients.
Published in:
Leukemia (08876924), 2013, v. 27, n. 3, p. 750, doi. 10.1038/leu.2012.249
By:
- Thol, F;
- Kölking, B;
- Hollink, I H I;
- Damm, F;
- van den Heuvel-Eibrink, M M;
- Michel Zwaan, C;
- Bug, G;
- Ottmann, O;
- Wagner, K;
- Morgan, M;
- Hofmann, W K;
- Göhring, G;
- Schlegelberger, B;
- Krauter, J;
- Ganser, A;
- Heuser, M
Publication type:
Article
Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML)
Published in:
2012
By:
- Hanfstein B;
- Müller MC;
- Hehlmann R;
- Erben P;
- Lauseker M;
- Fabarius A;
- Schnittger S;
- Haferlach C;
- Göhring G;
- Proetel U;
- Kolb HJ;
- Krause SW;
- Hofmann WK;
- Schubert J;
- Einsele H;
- Dengler J;
- Hänel M;
- Falge C;
- Kanz L;
- Neubauer A
Publication type:
Journal Article
Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML).
Published in:
Leukemia (08876924), 2012, v. 26, n. 9, p. 2096, doi. 10.1038/leu.2012.85
By:
- Hanfstein, B;
- Müller, M C;
- Hehlmann, R;
- Erben, P;
- Lauseker, M;
- Fabarius, A;
- Schnittger, S;
- Haferlach, C;
- Göhring, G;
- Proetel, U;
- Kolb, H-J;
- Krause, S W;
- Hofmann, W-K;
- Schubert, J;
- Einsele, H;
- Dengler, J;
- Hänel, M;
- Falge, C;
- Kanz, L;
- Neubauer, A
Publication type:
Article
SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications.
Published in:
Leukemia (08876924), 2012, v. 26, n. 5, p. 1137, doi. 10.1038/leu.2011.321
By:
- Damm, F;
- Thol, F;
- Kosmider, O;
- Kade, S;
- Löffeld, P;
- Dreyfus, F;
- Stamatoullas-Bastard, A;
- Tanguy-Schmidt, A;
- Beyne-Rauzy, O;
- de Botton, S;
- Guerci-Bresler, A;
- Göhring, G;
- Schlegelberger, B;
- Ganser, A;
- Bernard, O A;
- Fontenay, M;
- Heuser, M
Publication type:
Article
Long-term transfusion independence in del(5q) MDS patients who discontinue lenalidomide.
Published in:
Leukemia (08876924), 2012, v. 26, n. 4, p. 855, doi. 10.1038/leu.2011.268
By:
- Giagounidis, A A N;
- Kulasekararaj, A;
- Germing, U;
- Radkowski, R;
- Haase, S;
- Petersen, P;
- Göhring, G;
- Büsche, G;
- Aul, C;
- Mufti, G J;
- Platzbecker, U
Publication type:
Article
Prognostic implications and molecular associations of NADH dehydrogenase subunit 4 (ND4) mutations in acute myeloid leukemia.
Published in:
Leukemia (08876924), 2012, v. 26, n. 2, p. 289, doi. 10.1038/leu.2011.200
By:
- Damm, F;
- Bunke, T;
- Thol, F;
- Markus, B;
- Wagner, K;
- Göhring, G;
- Schlegelberger, B;
- Heil, G;
- Reuter, C W M;
- Püllmann, K;
- Schlenk, R F;
- Döhner, K;
- Heuser, M;
- Krauter, J;
- Döhner, H;
- Ganser, A;
- Morgan, M A
Publication type:
Article
Telomere shortening, clonal evolution and disease progression in myelodysplastic syndrome patients with 5q deletion treated with lenalidomide.
Published in:
2012
By:
- Göhring, G;
- Lange, K;
- Hofmann, W;
- Nielsen, K V;
- Hellström-Lindberg, E;
- Roy, L;
- Morgan, M;
- Kreipe, H;
- Büsche, G;
- Giagounidis, A;
- Schlegelberger, B
Publication type:
Letter
Stable and reproducible engraftment of primary adult and pediatric acute myeloid leukemia in NSG mice.
Published in:
2011
By:
- Malaisé, M;
- Neumeier, M;
- Botteron, C;
- Döhner, K;
- Reinhardt, D;
- Schlegelberger, B;
- Göhring, G;
- Gruhn, B;
- Debatin, K-M;
- Corbacioglu, S
Publication type:
Letter
Systemic mastocytosis (SM) with associated BCR-ABL-positive myelogenous leukaemia (SM-AHNMD): evidence that mast cells do not belong to the leukaemic clone.
Published in:
Leukemia (08876924), 2011, v. 25, n. 6, p. 1050, doi. 10.1038/leu.2011.41
By:
- Hussein, K.;
- Horny, H.-P.;
- Büsche, G.;
- Görner, M.;
- Göhring, G.;
- Kreipe, H.;
- Bock, O.
Publication type:
Article
ICSBP promoter methylation in myelodysplastic syndromes and acute myeloid leukaemia.
Published in:
2011
By:
- Otto, N.;
- Göhring, G.;
- Hofmann, W.;
- Scherer, R.;
- Luna, J. Chacon;
- Lehmann, U.;
- Ganser, A.;
- Welte, K.;
- Schlegelberger, B.;
- Steinemann, D.
Publication type:
Letter
A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation?
Published in:
2009
By:
- Ripperger, T.;
- Steinemann, D.;
- Göhring, G.;
- Finke, J.;
- Niemeyer, C. M.;
- Strahm, B.;
- Schlegelberger, B.
Publication type:
Letter
Global increase in DNA methylation in patients with myelodysplastic syndrome.
Published in:
Leukemia (08876924), 2008, v. 22, n. 10, p. 1954, doi. 10.1038/leu.2008.76
By:
- Römermann, D.;
- Hasemeier, B.;
- Metzig, K.;
- Göhring, G.;
- Schlegelberger, B.;
- Länger, F.;
- Kreipe, H.;
- Lehmann, U.
Publication type:
Article
Marrow fibrosis predicts early fatal marrow failure in patients with myelodysplastic syndromes.
Published in:
Leukemia (08876924), 2008, v. 22, n. 2, p. 313, doi. 10.1038/sj.leu.2405030
By:
- Buesche, G.;
- Teoman, H.;
- Wilczak, W.;
- Ganser, A.;
- Hecker, H.;
- Wilkens, L.;
- Göhring, G.;
- Schlegelberger, B.;
- Bock, O.;
- Georgii, A.;
- Kreipe, H.
Publication type:
Article
Familial polycythemia vera with non-germ line JAK2<sup>V617F</sup> mutation sparing the abnormal and clonal granulopoiesis.
Published in:
2007
By:
- Hussein, K.;
- Bock, O.;
- Ballmaier, M.;
- Göhring, G.;
- Steinemann, D.;
- Lehmann, U.;
- Kemper, J.;
- Buhr, T.;
- Kreipe, H.
Publication type:
Letter
Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome.
Published in:
2007
By:
- Karow, A.;
- Steinemann, D.;
- Göhring, G.;
- Hasle, H.;
- Greiner, J.;
- Harila-Saari, A.;
- Flotho, C.;
- Zenker, M.;
- Schlegelberger, B.;
- Niemeyer, C. M.;
- Kratz, C. P.
Publication type:
Letter
Prenatal diagnosis of an epignathus associated with a 49,XXXXY karyotype--a case report.
Published in:
2008
By:
- Staboulidou I;
- Miller K;
- Göhring G;
- Hillemanns P;
- Wüstemann M;
- Staboulidou, Ismini;
- Miller, Konstantin;
- Göhring, Gudrun;
- Hillemanns, Peter;
- Wüstemann, Max
Publication type:
journal article
Chromosomal Instability and Telomere Shortening in Long-Term Culture of Hematopoietic Stem Cells: Insights from a Cell Culture Model of RPS14 Haploinsufficiency.
Published in:
Cytogenetic & Genome Research, 2013, v. 142, n. 1, p. 14, doi. 10.1159/000356096
By:
- Thomay, K.;
- Schienke, a.;
- Vajen, B.;
- Modlich, U.;
- Schambach, a.;
- Hofmann, W.;
- Schlegelberger, B.;
- Göhring, G.
Publication type:
Article

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