Identification of PML as novel PAX5 fusion partner in childhood acute lymphoblastic leukaemiaNEBRAL, Karin; KÖNIG, Margit; HARDER, Lana et al.British journal of haematology. 2007, Vol 139, Num 2, pp 269-274, issn 0007-1048, 6 p.Article

Fatigue, emotional functioning, and executive dysfunction in pediatric multiple sclerosisHOLLAND, Alice Ann; GRAVES, Donna; GREENBERG, Benjamin M et al.Neuropsychology, development, and cognition. Section C, Child neuropsychology. 2014, Vol 20, Num 1-2, pp 71-85, issn 0929-7049, 15 p.Article

Cognitive functioning in pediatric transverse myelitisHARDER, Lana L; HOLLAND, Alice Ann; FROHMAN, Elliot et al.Multiple sclerosis. 2013, Vol 19, Num 7, pp 947-952, issn 1352-4585, 6 p.Article

Interphase cytogenetics of hematological neoplasms under the perspective of the novel WHO classificationMARTIN-SUBERO, José Ignacio; GESK, Stefan; HARDER, Lana et al.Anticancer research. 2003, Vol 23, Num 2A, pp 1139-1148, issn 0250-7005, 10 p.Conference Paper

GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphomaVATER, Inga; WAGNER, Florian; GESK, Stefan et al.British journal of haematology. 2009, Vol 144, Num 3, pp 317-331, issn 0007-1048, 15 p.Article

Interphase FISH assays for the detection of translocations with breakpoints in immunoglobulin light chain lociMARTIN-SUBERO, José I; HARDER, Lana; GESK, Stefan et al.International journal of cancer. 2002, Vol 98, Num 3, pp 470-474, issn 0020-7136Article

Translocations activating IRF4 identify a subtype of germinal center-derived B-cell lymphoma affecting predominantly children and young adultsSALAVERRIA, Itziar; PHILIPP, Claudia; BERGER, Hilmar et al.Blood. 2011, Vol 118, Num 1, pp 139-147, issn 0006-4971, 9 p.Article

Common clonal T-cell origin in a patient with T-prolymphocytic leukaemia and associated cutaneous T-cell lymphomasASSAF, Chalid; HUMMEL, Michael; GOERDT, Sergij et al.British journal of haematology. 2003, Vol 120, Num 3, pp 488-491, issn 0007-1048, 4 p.Article

Recurrent involvement of the REL and BCL11A loci in classical Hodgkin lymphomaMARTIN-SUBERO, José I; GESK, Stefan; DYER, Martin J. S et al.Blood. 2002, Vol 99, Num 4, pp 1474-1477, issn 0006-4971Article

Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluorescence in situ hybridizationKAHL, Christina; GESK, Stefan; HARDER, Lana et al.Cancer genetics and cytogenetics. 2001, Vol 129, Num 1, pp 80-84, issn 0165-4608Article

Pediatric Multiple Sclerosis: What we know and where are we headed?MACALLISTER, William S; CHRISTODOULOU, Christopher; MILAZZO, Maria et al.Neuropsychology, development, and cognition. Section C, Child neuropsychology. 2013, Vol 19, Num 1, pp 1-22, issn 0929-7049, 22 p.Article

Recurrent loss of the Y chromosome and homozygous deletions within the pseudoautosomal region 1: association with male predominance in mantle cell lymphomaNIELÄNDER, Inga; MARTIN-SUBERO, José I; MARTINEZ-CLIMENT, José A et al.Haematologica (Roma). 2008, Vol 93, Num 6, pp 949-950, issn 0390-6078, 2 p.Article

Trisomy 19 is associated with trisomy 12 and mutated IGHV genes in B-chronic lymphocytic leukaemiaSELLMANN, Ludger; GESK, Stefan; DÜHRSEN, Ulrich et al.British journal of haematology. 2007, Vol 138, Num 2, pp 217-220, issn 0007-1048, 4 p.Article

Chromosomal breakpoints affecting immunoglobulin loci are recurrent in hodgkin and reed-sternberg cells of classical hodgkin lymphomaMARTIN-SUBERO, José I; KLAPPER, Wolfram; BARTH, Thomas F. E et al.Cancer research (Baltimore). 2006, Vol 66, Num 21, pp 10332-10338, issn 0008-5472, 7 p.Article

Identification of the gene encoding cyclin E1 (CCNE1) as a novel IGH translocation partner in t(14;19)(q32;q12) in diffuse large B-cell lymphomaNAGEL, Inga; AKASAKA, Takashi; KLAPPER, Wolfram et al.Haematologica (Roma). 2009, Vol 94, Num 7, pp 1020-1023, issn 0390-6078, 4 p.Article

Quantitative assessment of molecular remission after high-dose therapy with autologous stem cell transplantation predicts long-term remission in mantle cell lymphomaPOTT, Christiane; SCHRADER, Carsten; DREYLING, Martin et al.Blood. 2006, Vol 107, Num 6, pp 2271-2278, issn 0006-4971, 8 p.Article

Multicolor-FICTION: Expanding the possibilities of combined morphologic, immunophenotypic, and genetic single cell analysesMARTIN-SUBERO, Josh Ignacio; CHUDOBA, Use; HARDER, Lana et al.The American journal of pathology. 2002, Vol 161, Num 2, pp 413-420, issn 0002-9440Article

The BCL11 gene family : involvement of BCL11A in lymphoid malignanciesSATTERWHITE, Ed; SONOKI, Takashi; SCHLEGELBERGER, Brigitte et al.Blood. 2001, Vol 98, Num 12, pp 3413-3420, issn 0006-4971Article

Deregulation of the telomerase reverse transcriptase (TERT) gene by chromosomal translocations in B-cell malignanciesNAGEL, Inga; SZCZEPANOWSKI, Monika; KLAPPER, Wolfram et al.Blood. 2010, Vol 116, Num 8, pp 1317-1320, issn 0006-4971, 4 p.Article

Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemiaRUSSELL, Lisa J; CAPASSO, Melania; GUTTERY, David S et al.Blood. 2009, Vol 114, Num 13, pp 2688-2698, issn 0006-4971, 11 p.Article

t(6;14)(p22;q32) : a new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)RUSSELL, Lisa J; AKASAKA, Takashi; ROSS, Fiona et al.Blood. 2008, Vol 111, Num 1, pp 387-391, issn 0006-4971, 5 p.Article

Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in b-cell precursor acute lymphoblastic leukemia (BCP-ALL)AKASAKA, Takashi; BALASAS, Theodore; GESK, Stefan et al.Blood. 2007, Vol 109, Num 8, pp 3451-3461, issn 0006-4971, 11 p.Article

Follicular lymphoma lacking the t(14;18)(q32;q21): identification of two disease subtypesHORSMAN, Douglas E; OKAMOTO, Ichiro; GASCOYNE, Randy D et al.British journal of haematology. 2003, Vol 120, Num 3, pp 424-433, issn 0007-1048, 10 p.Article

Cytogenetic and molecular characterization of a patient with simultaneous B-cell chronic lymphocytic leukemia and peripheral T-cell lymphomaMARTIN-SUBERO, J. Ignacio; SIEBERT, Reiner; GROTE, Werner et al.American journal of hematology. 2001, Vol 68, Num 4, pp 276-279, issn 0361-8609Article

Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical managementHEIDEMANN, Simone; FISCHER, Christine; JONAT, Waiter et al.Breast cancer research and treatment. 2012, Vol 134, Num 3, pp 1229-1239, issn 0167-6806, 11 p.Article