M. Jotterand

发表

A novel BCR‐ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph‐chromosome and monosomy 7

A. Tobler, D. Mühlematter, E. O. Leibundgut, 1999, British journal of haematology.

Diagnostic and prognostic significance of cytogenetics in adult primary myelodysplastic syndromes.

M. Jotterand, V. Parlier, 1996, Leukemia & lymphoma.

Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophilia

F. Grand, N. Cross, J. Score, 2006, Leukemia.

The most frequent t(14;19)(q32;q13)-positive B-cell malignancy corresponds to an aggressive subgroup of atypical chronic lymphocytic leukemia

F. Berger, R. Berger, O. Bernard, 2008, Leukemia.

The leukemic fusion gene AML1-MDS1-EVI1 suppresses CEBPA in acute myeloid leukemia by activation of Calreticulin.

J. Rowley, A. Hagemeijer, M. Fey, 2004, Proceedings of the National Academy of Sciences of the United States of America.

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene.

M. Rocchi, B. Johansson, A. Hagemeijer, 2006, Human molecular genetics.

In situ RHAMM protein expression in acute myeloid leukemia blasts suggests poor overall survival

A. Tichelli, A. Tzankov, S. Dirnhofer, 2011, Annals of Hematology.

Determination of cutoff values to detect small aneuploid clones by interphase fluorescence in situ hybridization: the Poisson model is a more appropriate approach. Should single-cell trisomy 8 be considered a clonal defect?

G. van Melle, C. Castagné, D. Mühlematter, 2003, Cancer genetics and cytogenetics.

Expression of pSTAT5 predicts FLT3 internal tandem duplications in acute myeloid leukemia

A. Tichelli, E. Obermann, A. Tzankov, 2010, Annals of Hematology.

Dependency of Survival on Additional Karyotype Anomalies and Bone Marrow Blast Count in Patients Suffering from Myelodysplastic Syndromes with 5q Deletion.

U. Germing, A. Giagounidis, N. Gattermann, 2007 .

Leukemic Cluster Growth in Culture Is an Independent Risk Factor for Acute Myeloid Leukemia and Short Survival in Patients with Myelodysplastic Syndrome

A. Gratwohl, A. Tichelli, M. Stern, 2008, Acta Haematologica.

Comment to “Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO ‘MDS-U’ designation” Haematologica. 2012;97(12):1845-9.

A. Buser, J. Passweg, A. Tichelli, 2013, Haematologica.

CBFB-SMMHC is correlated with increased calreticulin expression and suppresses the granulocytic differentiation factor CEBPA in AML with inv(16).

M. Fey, T. Pabst, D. Betts, 2005, Blood.

Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3

K. Sotlar, P. Went, A. Tzankov, 2008, Journal of Clinical Pathology.

A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL).

Rolf Jaggi, Jörg Hager, Andreas Tobler, 2002, Blood.

Acute myeloid leukemia with myeloid sarcoma and eosinophilia: prolonged remission and molecular response to imatinib.

T. Rausch, D. Muehlematter, O. Spertini, 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Two clonal occurrences of tetrasomy 21 in an atypical chronic myeloid leukemia with wild-type RUNX1 alleles. Additional support for a gene dosage effect of chromosome 21 or RUNX1 in leukemia.

A. Tobler, H. Scott, D. Mühlematter, 2004, Haematologica.

CD34/QBEND10 immunostaining in bone marrow biopsies: an additional parameterfor the diagnosis and classification of myelodysplastic syndromes

M. Jotterand, V. Parlier, P. Schmidt, 2000, European journal of haematology.

Impact of unbalanced minor route versus major route karyotypes at diagnosis on prognosis of CML

Martin C. Müller, J. Hasford, T. Brümmendorf, 2015, Annals of Hematology.

CML Study IV of CML: long-term observation of 1151 patients from the randomized Impact of additional cytogenetic aberrations at diagnosis on prognosis

Martin C. Müller, J. Hasford, K. Spiekermann, 2012 .

Treatment of 5q-syndrome with lenalidomide in an HIV-positive patient under cART

M. Cavassini, A. Fayet, M. Schapira, 2010, Annals of Hematology.

POSSIBLE EVIDENCE OF X-Y INTERCHANGE IN AN XX MALE

G. Pescia, M. Jotterand, 1977, The Lancet.

A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21)

E. Juillard, M. Jotterand, 1976, Human Genetics.

Impact of additional cytogenetic aberrations at diagnosis on prognosis of CML: long-term observation of 1151 patients from the randomized CML Study IV.

Martin C. Müller, H. Einsele, J. Hasford, 2011, Blood.

Clonal heterogeneity and chromosomal instability at disease presentation in high hyperdiploid acute lymphoblastic leukemia.

A. Marazzi, Y. Chalandon, M. Jotterand, 2010, Cancer genetics and cytogenetics.

Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia

A. Gratwohl, A. Tichelli, T. Kühne, 2006, Leukemia.

Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.

A. Hagemeijer, G. van Melle, A. Tobler, 2004, Cancer genetics and cytogenetics.

Monosomal karyotype in acute myeloid leukemia: a better indicator of poor prognosis than a complex karyotype.

A. Hagemeijer, W. van Putten, B. Löwenberg, 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Clinical, molecular, and prognostic significance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia.

K. Döhner, R. Schlenk, H. Döhner, 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases.

G. van Melle, A. Tobler, M. Gregor, 2005, Cancer genetics and cytogenetics.

Various Other 3 q Abnormalities in Acute Myeloid Leukemia

K. Döhner, R. Schlenk, H. Döhner, 2010 .

Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML)

D. Martinet, D. Mühlematter, J. Gmür, 1997, Leukemia.

[New non-Robertsonian polymorphous system in the "Leggadas" (Mus sp.) of the Centrafricain Republic].

M. Jotterand, R. Matthey, 1970, Revue suisse de zoologie; annales de la Societe zoologique suisse et du Museum d'histoire naturelle de Geneve.

Effect of conditioned medium, nutritive elements and mitotic synchronization on the accuracy of the cytogenetic analysis in patients with chronic myeloid leukemia at diagnosis and during alpha-interferon therapy.

D. Martinet, C. Castagné, D. Mühlematter, 1999, Cancer genetics and cytogenetics.

Case study of intracerebral plasmacytoma as an initial presentation of multiple myeloma.

K. Zaman, D. Mühlematter, M. Betz, 2007, Neuro-oncology.

Broad molecular screening of an unclassifiable myeloproliferative disorder reveals an unexpected ETV6/ABL1 fusion transcript

A. Gratwohl, A. Tichelli, A. Chase, 2005, Leukemia.

22q11 Deletion Syndrome and Urogenital Manifestations: A Clinicopathological Case Report

A. Feki, N. Ben Ali, M. Jotterand, 2016, Front. Med..

High hyperdiploid acute lymphoblastic leukemia in adults shows clonal heterogeneity and chromosomal instability at diagnosis and during the course of the disease

A. Marazzi, A. Tichelli, Y. Chalandon, 2012, Annals of Hematology.

Dicentric translocation (9;12) presenting as refractory Philadelphia chromosome-positive acute B-cell lymphoblastic leukemia.

A. Tichelli, M. Bargetzi, D. Mühlematter, 1999, Cancer genetics and cytogenetics.

Impact of additional cytogenetic aberrations at diagnosis on prognosis of CML: long-term observation of 1151 patients from the randomized CML Study IV.

Martin C. Müller, H. Einsele, J. Hasford, 2011, Blood.

Automated four-color interphase fluorescence in situ hybridization approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid acute lymphoblastic leukemia.

J. Beckmann, G. van Melle, Sarah Porter, 2008, Cancer genetics and cytogenetics.