Martine Jotterand

Publications | Mémoires et thèses

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139 publications

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Bases physiopathologiques en hématologie générale : un aide-mémoire d'hématologie
Schmidt P.M., Cornu P., Angelillo-Scherrer A., Abbal C., Jotterand M., Quarroz S., Canham van Dijken P., 2015., Version 17.0, Centre Hospitalier Universitaire Vaudois, Service d'hématologie.
Basic Physiopathology of General Hematology : a synopsis of hematology.
Schmidt P.M., Cornu P., Angelillo-Scherrer A., Abbal C., Jotterand M., Quarroz S., Canham van Dijken P., 2015., Version 17.0, Centre Hospitalier Universitaire Vaudois, Service d'hématologie.
 
Impact of unbalanced minor route versus major route karyotypes at diagnosis on prognosis of CML.
Fabarius A., Kalmanti L., Dietz C.T., Lauseker M., Rinaldetti S., Haferlach C., Göhring G., Schlegelberger B., Jotterand M., Hanfstein B. et al., 2015. Annals of Hematology, 94 (12) pp. 2015-2024. Peer-reviewed.
Bases physiopathologiques en hématologie générale : un aide-mémoire d'hématologie
Schmidt P.M., Cornu P., Angelillo-Scherrer A., Abbal C., Cairoli A., Jotterand M., Quarroz S., Canham van Dijken P., 2014., Version 16.0, Centre Hospitalier Universitaire Vaudois, Service d'hématologie.
Basic Physiopathology of General Hematology : a synopsis of hematology
Schmidt P.M., Cornu P., Angelillo-Scherrer A., Abbal C., Cairoli A., Jotterand M., Quarroz S., Canham van Dijken P., 2014., Version 16.0, Centre Hospitalier Universitaire Vaudois, Service d'hématologie.
 
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
Holbro A., Jotterand M., Passweg J.R., Buser A., Tichelli A., Rovó A., 2013. Haematologica, 98 (4) pp. e46-e47.
 
Impact of Balanced or Unbalanced Karyotype At Diagnosis On Prognosis of CML: Long-Term Observation From 1346 Patients of the Randomized CML Study IV
Fabarius A., Haferlach C., Hochhaus A., Muller M.C., Hanfstein B., Gohring G., Schlegelberger B., Jotterrand M., Proetel U., Hofmann W.K. et al., 2013. pp. Abstract 913 dans ASH 2012, 54th Annual Meeting of the American Society of Hematology, Blood.
 
High hyperdiploid acute lymphoblastic leukemia in adults shows clonal heterogeneity and chromosomal instability at diagnosis and during the course of the disease.
Talamo A., Marazzi A., Rovo A., Schanz U., Tichelli A., Chalandon Y., Jotterand M., 2012. Annals of Hematology, 91 (5) pp. 793-796. Peer-reviewed.
 
Impact of additional cytogenetic aberrations at diagnosis on prognosis of CML: long-term observation of 1151 patients from the randomized CML Study IV.
Fabarius A., Leitner A., Hochhaus A., Müller M.C., Hanfstein B., Haferlach C., Göhring G., Schlegelberger B., Jotterand M., Reiter A. et al., 2011. Blood, 118 (26) pp. 6760-6768. Peer-reviewed.
 
In situ RHAMM protein expression in acute myeloid leukemia blasts suggests poor overall survival.
Tzankov A., Strasser U., Dirnhofer S., Menter T., Arber C., Jotterand M., Rovo A., Tichelli A., Stauder R., Günthert U., 2011. Annals of Hematology, 90 (8) pp. 901-909.
 
A study on the clinical significance of the who aml subtype inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q chromosomal abnormalities in 6,819 aml cases
Lugthart S., Groeschel S., Beverloo H., Valk P., Schanz U., Bhola S., Vellenga E., Kayser S., Ossenkoppele G., Verhoef G. et al., 2010. p. 482 dans 15th Annual Meeting of the European Hematology Association, Haematologica. Peer-reviewed.
 
Acute myeloid leukemia with myeloid sarcoma and eosinophilia: prolonged remission and molecular response to imatinib.
Vedy Dana, Muehlematter Dominique, Rausch Thierry, Stalder Michele, Jotterand Martine, Spertini Olivier, 2010. Journal of Clinical Oncology, 28 (3) pp. e33-55.
 
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.
Lugthart S., Gröschel S., Beverloo H.B., Kayser S., Valk P.J., van Zelderen-Bhola S.L., Jan Ossenkoppele G., Vellenga E., van den Berg-de Ruiter E., Schanz U. et al., 2010. Journal of Clinical Oncology, 28 (24) pp. 3890-3898.
 
Clonal heterogeneity and chromosomal instability at disease presentation in high hyperdiploid acute lymphoblastic leukemia.
Talamo Anna, Chalandon Yves, Marazzi Alfio, Jotterand Martine, 2010. Cancer Genetics and Cytogenetics, 203 (2) pp. 209-214. Peer-reviewed.
 
Expression of pSTAT5 predicts FLT3 internal tandem duplications in acute myeloid leukemia.
Obermann Ellen Christina, Arber Caroline, Jotterand Martine, Tichelli Andre, Hirschmann Petra, Tzankov Alexandar, 2010. Annals of Hematology, 89 (7) pp. 663-669.
 
Recommendations for the diagnosis and treatment of myelodysplastic syndromes in adult patients in Switzerland
Passweg J.R., Duchosal M.A., Hess U., Blum S., Freiburghaus A.U., Bargetzi M., Binder D., Dirnhofer St., Friess D., Goede J.S. et al., 2010. Swiss Medical Forum = Forum Médical Suisse, 10 (15) pp. 259-265.
Treatment of 5q-syndrome with lenalidomide in an HIV-positive patient under cART.
Blum Sabine, Cavassini Matthias, Lambert Jean-Francois, Fayet Aurelie, Schapira Marc, Jotterand Martine, 2010. Annals of Hematology, 89 (4) pp. 425-426.
A new, automated, four-colour interphase FISH approach for the simultaneous detection of specific aneuploidies of diagnosis and prognosis significance in high hyperdiploid ALL
Talamo Blandin A., Muehlematter D., Bougeon S., Gogniat C., Porter S., Beyer V., Parlier V., Beckmann J., Van Melle G., Jotterand M., 2008. pp. ODE-26, 180 dans Regenerative medicine, CHUV Research Day, January 17, 2008, Université de Lausanne, Faculté de biologie et de médecine.
 
A new, automated, four-colour interphase FISH approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid ALL
Talamo Blandin Anna, Muehlematter Dominique, Bougeon Sandrine, Gogniat Céline, Porter Sarah, Beyer Valérie, Parlier Valérie, Beckmann Jacques S., Van Melle Guy, Jotterand Martine, 2008. pp. 62S dans 76e Assemblée annuelle de la Société suisse de médecine interne (SGIM/SSMI), Swiss Medical Forum = Forum Médical Suisse.
 
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.
Blandin A.T., Mühlematter D., Bougeon S., Gogniat C., Porter S., Beyer V., Parlier V., Beckmann J.S., van Melle G., Jotterand M., 2008. Cancer Genetics and Cytogenetics, 186 (2) pp. 69-77. Peer-reviewed.
 
G-CSF-induced remission in two cases of acute myeloid leukemia.
Benz R., Goede J.S., Parlier V., Mühlematter D., Jotterand M., Fehr J., 2008. Leukemia Research, 32 (7) pp. 1148-1152. Peer-reviewed.
 
Leukemic cluster growth in culture is an independent risk factor for acute myeloid leukemia and short survival in patients with myelodysplastic syndrome.
Bernimoulin M., Stern M., Tichelli A., Jotterand M., Gratwohl A., Nissen C., 2008. Acta Haematologica, 119 (4) pp. 226-235.
 
Monosomal karyotype in acute myeloid leukemia: a better indicator of poor prognosis than a complex karyotype.
Breems D.A., Van Putten W.L., De Greef G.E., Van Zelderen-Bhola S.L., Gerssen-Schoorl K.B., Mellink C.H., Nieuwint A., Jotterand M., Hagemeijer A., Beverloo H.B. et al., 2008. Journal of Clinical Oncology, 26 (29) pp. 4791-4797.
 
Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3.
Tzankov A., Sotlar K., Muhlematter D., Theocharides A., Went P., Jotterand M., Horny H.P., Dirnhofer S., 2008. Journal of Clinical Pathology, 61 (8) pp. 958-961.
 
The most frequent t(14;19)(q32;q13)-positive B-cell malignancy corresponds to an aggressive subgroup of atypical chronic lymphocytic leukemia.
Chapiro E., Radford-Weiss I., Bastard C., Luquet I., Lefebvre C., Callet-Bauchu E., Leroux D., Talmant P., Mozziconacci M.J., Mugneret F. et al., 2008. Leukemia, 22 (11) pp. 2123-2127. Peer-reviewed.
 
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia.
Storlazzi C.T., Albano F., Guastadisegni M.C., Impera L., Mühlematter D., Meyer-Monard S., Wuillemin W., Rocchi M., Jotterand M., 2008. Blood Cells, Molecules and Diseases, 40 (3) pp. 452-455.
 
Case study of intracerebral plasmacytoma as an initial presentation of multiple myeloma.
Wavre A., Baur A.S., Betz M., Mühlematter D., Jotterand M., Zaman K., Ketterer N., 2007. Neuro-oncology, 9 (3) pp. 370-2. Peer-reviewed.
 
Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophilia
Score J., Curtis C., Waghorn K., Stalder M., Jotterand M., Grand F. H., Cross N. C., 2006/05. Leukemia, 20 (5) pp. 827-32.
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
Storlazzi C. T., Fioretos T., Surace C., Lonoce A., Mastrorilli A., Strombeck B., D'Addabbo P., Iacovelli F., Minervini C., Aventin A. et al., 2006/03. Human Molecular Genetics, 15 (6) pp. 933-42.
 
Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia
Meyer-Monard S., Parlier V., Passweg J., Muhlematter D., Hess U., Bargetzi M., Kuhne T., Cabrol C., Gratwohl A., Jotterand M. et al., 2006/02. Leukemia, 20 (2) pp. 247-53.
 
CBFB-SMMHC is correlated with increased calreticulin expression and suppresses the granulocytic differentiation factor CEBPA in AML with inv(16)
Helbling D., Mueller B. U., Timchenko N. A., Schardt J., Eyer M., Betts D. R., Jotterand M., Meyer-Monard S., Fey M. F., Pabst T., 2005/08. Blood, 106 (4) pp. 1369-75.
 
Broad molecular screening of an unclassifiable myeloproliferative disorder reveals an unexpected ETV6/ABL1 fusion transcript
Meyer-Monard S., Muhlematter D., Streit A., Chase A. J., Gratwohl A., Cross N. C., Jotterand M., Tichelli A., 2005/06. Leukemia, 19 (6) pp. 1096-9.
 
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.
Beyer V., Mühlematter D., Parlier V., Cabrol C., Bougeon-Mamin S., Solenthaler M., Tobler A., Pugin P., Gregor M., Hitz F. et al., 2005. Cancer genetics and cytogenetics, 160 (2) pp. 97-119. Peer-reviewed.
 
The leukemic fusion gene AML1-MDS1-EVI1 suppresses CEBPA in acute myeloid leukemia by activation of Calreticulin
Helbling D., Mueller B. U., Timchenko N. A., Hagemeijer A., Jotterand M., Meyer-Monard S., Lister A., Rowley J. D., Huegli B., Fey M. F. et al., 2004/09. Proceedings of the National Academy of Sciences of the United States of America, 101 (36) pp. 13312-7.
 
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
Escher R., Muhlematter D., Scott H. S., Jotterand M., Tobler A., 2004/08. Haematologica, 89 (8) pp. ECR26.
 
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
Beyer V., Castagne C., Muhlematter D., Parlier V., Gmur J., Hess U., Kovacsovics T., Meyer-Monard S., Tichelli A., Tobler A. et al., 2004/07. Cancer Genetics and Cytogenetics, 152 (1) pp. 29-41.
 
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?
Castagne C., Muhlematter D., Beyer V., Parlier V., van Melle G., Jotterand M., 2003/12. Cancer Genetics and Cytogenetics, 147 (2) pp. 99-109.
 
Cytogénétique des hémopathies malignes
Jotterand M., 2003. Labmed Suisse, 30 pp. 321-326.
 
La perception du génie génétique sous l'angle des rapports sociaux de sexes Science and technology : gender matters.
Sommer N., Jotterand M, 2003. Commission nationale Suisse pour l'UNESCO pp. 209-224.
 
A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL)
Novak U., Oppliger Leibundgut E., Hager J., Muhlematter D., Jotterand M., Besse C., Leupin N., Ratschiller D., Papp J., Kearsey G. et al., 2002/09. Blood, 100 (5) pp. 1787-94.
 
Cytogénétique des hémopathies malignes
Jotterand M., 2002. Médecine et Hygiène, 60 (2389) pp. 838-842.
 
Hybridation in situ fluorescente (FISH), un complement a l'analyse cytogenetique des hemopathies malignes. [Fluorescent in situ hybridization (FISH), cytogenetic analytical complement for the diagnosis of malignant blood diseases]
Muhlematter D., Castagne C., Beyer V., Martinet D., Parlier V., Jotterand M., 2000/05. Revue Médicale de la Suisse Romande, 120 (5) pp. 393-400.
 
CD34/QBEND10 immunostaining in bone marrow biopsies: an additional parameter for the diagnosis and classification of myelodysplastic syndromes.
Baur A.S., Meugé-Moraw C., Schmidt P.M., Parlier V., Jotterand M., Delacrétaz F., 2000/02. European Journal of Haematology, 64 (2) pp. 71-79. Peer-reviewed.
 
Der, die, das ... Gentechnik?
Rey Lucienne, Jotterand Martine, 2000. 24.
 
Génie génétique: masculin, féminin?
Rey Lucienne, Jotterand Martine, 2000. 45.
 
A novel BCR-ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph-chromosome and monosomy 7
Leibundgut E. O., Jotterand M., Rigamonti V., Parlier V., Muhlematter D., Tobler A., Solenthaler M., 1999/09. British Journal of Haematology, 106 (4) pp. 1041-4.
 
Dicentric translocation (9;12) presenting as refractory Philadelphia chromosome-positive acute B-cell lymphoblastic leukemia
Bargetzi M. J., Muhlematter D., Tichelli A., Jotterand M., Wernli M., 1999/08. Cancer Genetics and Cytogenetics, 113 (1) pp. 90-2.
 
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
Castagne C., Muhlematter D., Martinet D., Jotterand M., 1999/03. Cancer Genetics and Cytogenetics, 109 (2) pp. 166-71.
 
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered.
van der Reijden B.A., Dauwerse H.G., Giles R.H., Jagmohan-Changur S., Wijmenga C., Liu P.P., Smit B., Wessels H.W., Beverstock G.C., Jotterand-Bellomo M. et al., 1999/01/14. Oncogene, 18 (2) pp. 543-550. Peer-reviewed.
 
Sampling bias and logistical problems of molecular analyses in a clinical leukaemia trial. Swiss Group for Clinical Cancer Research (SAKK)
Fey M. F., Blaser M., Wernli M., Jotterand M., Maibach R., Gratwohl A., Tobler A., 1998/11. British Journal of Haematology, 103 (2) pp. 585-7.
 
Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML)
Martinet D., Muhlematter D., Leeman M., Parlier V., Hess U., Gmur J., Jotterand M., 1997/07. Leukemia, 11 (7) pp. 964-70.
 
Effect of conditioned media, nutritive elements, and mitotic synchronization on the accuracy of the cytogenetic analysis in acute nonlymphocytic leukemia patients presenting with inv(16)/t(16;16) or t(15;17).
Castagné C., Mühlematter D., van Melle G., Gachoud V., Jotterand Bellomo M., 1997/04. Cancer genetics and cytogenetics, 94 (2) pp. 106-112. Peer-reviewed.
 
Cytogénétique des hémopathies malignes III. Hybridation in situ fluorescente (FISH)
Mühlematter D, Martinet D, Castagné C, Jotterand Bellomo M, 1997. Génétique médicale 38 pp. 16-21.
 
Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16).
Giles R.H., Dauwerse J.G., Higgins C., Petrij F., Wessels J.W., Beverstock G.C., Döhner H., Jotterand-Bellomo M., Falkenburg J.H., Slater R.M. et al., 1997. Leukemia, 11 (12) pp. 2087-2096.
 
Effect of conditioned media, nutritive elements, and mitotic synchronization on the accuracy of the cytogenetic analysis in acute nonlymphocytic leukemia patients presenting with inv(16)/t(16;16) or t(15;17).
Castagné C., Mühlematter D., van Melle G., Gachoud V., Jotterand Bellomo M., 1997. Cancer Genetics and Cytogenetics, 94 (2) pp. 106-112.
 
Le génie génétique au-delà des slogans : 20 entretiens
Jotterand M, 1997. 45.
 
Zwischentöne : 20 Interviews zur Gentechnologie
Jotterand M, 1997..
 
Diagnostic and prognostic significance of cytogenetics in adult primary myelodysplastic syndromes
Jotterand M., Parlier V., 1996/10. Leukemia and Lymphoma, 23 (3-4) pp. 253-66.
 
Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia.
van der Reijden B.A., Martinet D., Dauwerse J.G., Giles R.H., Wessels J.W., Beverstock G.C., Smit B., Mühlematter D., Jotterand Bellomo M., Gabert J. et al., 1996/09. Leukemia, 10 (9) pp. 1459-1462. Peer-reviewed.
 
Application de la technique d'hybridation in situ fluorescente (FISH) au diagnostic de la translocation de Philadelphie dans la leucémie myéloïde chronique [Fluorescent in-situ hybridization technique (FISH) in the diagnosis of Philadelphia translocation in chronic myeloid leukemia]
Martinet D., Mühlematter D., Jotterand Bellomo M., 1996. Schweizerische Medizinische Wochenschrift = Journal Suisse de Médecine, 126 (20) pp. 855-863.
 
Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias.
Pabst T., Schwaller J., Bellomo M.J., Oestreicher M., Mühlematter D., Tichelli A., Tobler A., Fey M.F., 1996. Blood, 88 (3) pp. 1026-1034.
 
Krebscytogenetik
Jotterand Bellomo M, 1996. Therapiewoche Schweiz 12 pp. 29-34.
 
Signification diagnostique et pronostique de l'analyse cytogénétique dans les leucémies aiguës et les syndromes myélodysplasiques. [Significance, diagnosis and prognosis in the cytogenetic analysis in acute leukemias and myelodysplastic syndromes].
Jotterand Bellomo M., 1996. Therapeutische Umschau. Revue Thérapeutique, 53 (2) pp. 103-110.
 
Tetrasomy 8 in a patient with acute nonlymphocytic leukemia: a metaphase and interphase study with fluorescence in situ hybridization.
Mühlematter D., Castagné C., Bruzzese O., Clément F., Schmidt P.M., Bellomo M.J., 1996. Cancer Genetics and Cytogenetics, 89 (1) pp. 44-48. Peer-reviewed.
 
A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11).
Slater R., Smit E., Kroes W., Bellomo M.J., Mühlematter D., Harbott J., Behrendt H., Hählen K., Veerman A.J., Hagemeijer A., 1995. Leukemia, 9 (10) pp. 1613-1619.
 
Prediction of 18-month survival in patients with primary myelodysplastic syndrome. A regression model and scoring system based on the combination of chromosome findings and the Bournemouth score.
Parlier V., Van Melle G., Beris P., Schmidt P.M., Tobler A., Haller E., Bellomo M.J., 1995. Cancer genetics and cytogenetics, 81 (2) pp. 158-165. Peer-reviewed.
 
RT-PCR diagnosis of patients with acute nonlymphocytic leukemia and inv(16)(p13q22) and identification of new alternative splicing in CBFB-MYH11 transcripts.
van der Reijden B.A., Lombardo M., Dauwerse H.G., Giles R.H., Mühlematter D., Bellomo M.J., Wessels H.W., Beverstock G.C., van Ommen G.J., Hagemeijer A. et al., 1995. Blood, 86 (1) pp. 277-282.
 
Cytogénétique des hémopathies malignes I. Introduction
Jotterand Bellomo M, Parlier V, Mühlematter D, 1994. Génétique médicale 32 pp. 19-21.
 
Cytogénétique des hémopathies malignes II. Syndromes myéloprolifératifs
Jotterand Bellomo M, Mühlematter D, 1994. Génétique médicale 33 pp. 12-4.
 
Hematologic, clinical, and cytogenetic analysis in 109 patients with primary myelodysplastic syndrome. Prognostic significance of morphology and chromosome findings.
Parlier V., van Melle G., Beris P., Schmidt P.M., Tobler A., Haller E., Jotterand Bellomo M., 1994. Cancer genetics and cytogenetics, 78 (2) pp. 219-31.
 
Importance clinique du caryotype en hématologie. [Clinical importance of karyotype in hematology.]
Jotterand Bellomo M., 1994. Schweizerische medizinische Wochenschrift, 124 (1-2) pp. 26-36.
 
Autoimmune myelodysplasia
Miescher P, Jotterand Bellomo M, 1993. pp. 93-100 dans Raghavachar A, Schrezenmeier H, Frickhofen N (eds.) Aplastic anemia: current perspectives on the pathogenesis and treatment, Wien : Blackwell-MZV. 166 p.
 
Cytogénétique des hémopathies malignes [Cytogenetics of malignant hemopathies]
Jotterand Bellomo M., Mühlematter D., Parlier V., 1993. Revue médicale de la Suisse romande, 113 (4) pp. 291-303.
 
Etoposide and secondary haematological malignancies: coincidence or causality?
Zulian G.B., Jotterand Bellomo M., Cabrol C., Beris P., Mermillod B., Alberto P., 1993. Annals of oncology, 4 (7) pp. 559-66.
 
Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies.
Tiainen M., Popp S., Parlier V., Emmerich P., Bellomo M.J., Ruutu T., Cremer T., Knuutila S., 1992. Genes, chromosomes & cancer, 4 (2) pp. 135-40.
 
t(8;9)(p11;q32) in atypical chronic myeloid leukaemia: a new cytogenetic-clinicopathologic association?
Jotterand Bellomo M., Mühlematter D., Wicht M., Delacrétaz F., Schmidt P.M., 1992. British journal of haematology, 81 (2) pp. 307-8.
 
Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome.
Jotterand Bellomo M., Parlier V., Mühlematter D., Grob J.P., Beris P., 1992. Cancer genetics and cytogenetics, 59 (2) pp. 138-60.
 
Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria.
Parlier V., Tiainen M., Beris P., Miescher P.A., Knuutila S., Jotterand Bellomo M., 1992. British journal of haematology, 81 (2) pp. 296-304.
 
Présentation initiale inhabituelle d'un cas d'anémie réfractaire avec excès de blastes"[Unusual initial manifestation in a case of refractory anemia with excess of blasts]
Beris P., Soulier-Lauper M., Parlier V., Jotterand-Bellomo M., 1991. Schweizerische medizinische Wochenschrift, 121 (41) pp. 1499-502.
 
A new case of myelodysplastic syndrome with 6p rearrangement.
Jotterand-Bellomo M., Parlier V., Petite J., Beris J., 1990. Cancer genetics and cytogenetics, 44 (2) pp. 271-4.
 
Cytogenetic analysis of 54 cases of myelodysplastic syndrome.
Jotterand-Bellomo M., Parlier V., Schmidt P.M., Beris P., 1990. Cancer genetics and cytogenetics, 46 (2) pp. 157-72.
 
Inducible and constitutive MHC class II gene expression. Distinct tissue-specific genetic controls.
Sartoris S., Scupoli M.T., Scarpellino L., Paiola F., Jotterand-Bellomo M., Tridente G., Accolla R.S., 1990. Journal of immunology, 145 (6) pp. 1960-7.
 
Karyotypic analysis of the AKR/J mouse thymoma cell line BW5147.G.1.4.OUAR.1.
Fernandez-Ruiz E., Silva A., Jotterand-Bellomo M., 1990. Hybridoma, 9 (3) pp. 285-8.
 
Short-term culture of spleen lymphocytes for chromosome analysis of small rodents.
Jotterand Bellomo M., Mühlematter D., Nabholz M., 1990. Genetica, 83 (1) pp. 51-60.
 
Constitutional karyotype in retinoblastoma. Case report and review of literature
Munier F., Pescia G., Jotterand-Bellomo M., Balmer A., Gailloud C., Thonney F., 1989/06. Ophthalmic Paediatrics and Genetics, 10 (2) pp. 129-50.
 
Chromosomes et cancer
Jotterand Bellomo M, 1989. Uni Lausanne : bulletin d'information de l'Université de Lausanne, 60 (3) pp. 46-9.
 
Loss of interleukin 2 dependence in cloned interleukin 2-dependent rat T lymphocyte x BW5147 hybridomas is not associated with segregation of a specific pair of rat chromosomes.
Somoza C., Fernández-Ruiz E., Jotterand-Bellomo M., Sanz E., Nabholz M., Silva A., 1989. European journal of immunology, 19 (7) pp. 1177-81.
 
Active suppression of major histocompatibility complex class II gene expression during differentiation from B cells to plasma cells.
Latron F., Jotterand-Bellomo M., Maffei A., Scarpellino L., Bernard M., Strominger J.L., Accolla R.S., 1988. Proceedings of the National Academy of Sciences of the United States of America, 85 (7) pp. 2229-33.
 
Chromosome analysis of five specimens of Mus bufo-triton (Muridae) from Burundi (Africa): three cytogenetic entities, a special type of chromosomal sex determination, taxonomy and phylogeny
Jotterand M, 1988. Cytogenetics and cell genetics, 48 (2) pp. 88-91.
 
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and results.
Jotterand-Bellomo M., Pescia G., Nguyen The H., Gaide A. C., Thonney F., Marguerat P., Paccaud F., Munier F., 1988. Annales de Génétique, 31 (1) pp. 14-20.
 
Les chromosomes du rat de Cuming, Phloeomys cumingi Waterhouse, 1839 (Mammalia: Rodentia) [Chromosomes of the Cuming rat, Phloeomys cumingi Waterhouse, 1839 (Mammalia: Rodentia)]
Jotterand-Bellomo M., Schauenberg P., 1988. Genetica, 76 (3) pp. 181-90.
 
Rétinoblastoma Héréditaire, Estérase D, et Trophoblaste: perspective de diagnostic prénatal précoce? [Hereditary Retinoblastoma, Esterase D, and Trophoblast: Perspective for Prenatal Diagnosis?]
Munier F, Pescia G, Roth M, Balmer A, Jotterand-Bellomo M, Gailloud C, Dimo N, 1988. Klinische Monatsblätter für Augenheilkunde, 192 (5) pp. 586-88.
 
Distinct mechanisms regulate MHC class II gene expression in B cells and macrophages.
Maffei A., Scarpellino L., Bernard M., Carra G., Jotterand-Bellomo M., Guardiola J., Accolla R.S., 1987. Journal of immunology, 139 (3) pp. 942-8.
 
Les chromosomes du trophoblaste embryonnaire: preparation et colorations [Chromosomes of the embryonic trophoblast: preparation and staining]
Jotterand-Bellomo M., Gaide A.C., Thonney F., Pescia G., 1987. Archives of gynecology and obstetrics, 241 (Suppl.) pp. S93-100.
 
Les chromosomes humains: un testament phylogénétique [Human chromosomes: a phylogenetic testament]
Jotterand-Bellomo M., 1987. Revue médicale de la Suisse romande, 107 (7) pp. 567-75.
aIr-1, a newly found locus on mouse chromosome 16 encoding a trans-acting activator factor for MHC class II gene expression.
Accolla R.S., Jotterand-Bellomo M., Scarpellino L., Maffei A., Carra G., Guardiola J., 1986. Journal of Experimental Medicine, 164 (1) pp. 369-374.
 
Chromosome analysis of chorionic villi: technique and results.
Jotterand-Bellomo M., Gaide A.C., Thonney F., 1986. Contributions to Gynecology and Obstetrics, 15 pp. 70-79.
 
Le genre Mus africain, un exemple d'homogénéité caryotypique: étude cytogénétique de Mus minutoides/musculoides (Côte d'Ivoire), de Mus setulosus (République Centrafricaine) et de Mus mattheyi (Burkina Faso) [The African Mus genus, an example of karyotypic homogeneity: cytogenetic study of Mus minutoides/musculoides (Ivory Coast), M. setulosus (Central African Republic), and M. mattheyi (Burkina Faso)]
Jotterand Bellomo M, 1986. Cytogenetics and cell genetics, 42 (1-2) pp. 99-104.
 
L'analyse cytogénétique de deux espèces de Muridae africains, Mus oubanguii et Mus minutoides/musculoides: polymorphisme chromosomique et ébauche d'une phylogénie [Cytogenetic analysis of two species of African Murids, Mus oubanguiiand Mus minutoides/musculoides: chromosomal polymorphism and outline of a phylogeny]
Jotterand Bellomo M, 1984. Cytogenetics and cell genetics, 38 (3) pp. 182-8.
 
Les sites fragiles autosomiques. [[Autosomal fragile sites].
Jotterand-Bellomo M., 1984. Journal de Génétique Humaine, 32 (3) pp. 155-166.
 
New developments in vertebrate cytotaxonomy VII Les chromosomes des Rongeurs (ordre Rodentia Bowdich, 1821)
Jotterand-Bellomo M, 1984. Genetica, 64 (1) pp. 3-64.
 
Les effets de la distamycine A sur les cellules du liquide amniotique cultivées in vitro
Jotterand Bellomo M, 1983. Annales de genetique, 26 (1) pp. 27-30.
 
Hommage au Professeur Robert Matthey. [Dedication to Professor Robert Matthey.]
Jotterand-Bellomo M., 1982. Cytogenetics and Cell Genetics, 34 (1-2) pp. 5-9.
 
Monosomie/trisomie 4q12 leads to q13 en mosaïque chez une enfant arriérée et dysmorphique. [Monosomy/trisomy 4q12 to q13 mosaicism in a retarded and dysmorphic girl.]
Pescia G., Tonella A., Jotterand-Bellomo M., 1982. Annales de Génétique, 25 (2) pp. 110-112.
 
Achalasie avec dolicho-méga-oesophage associée à une surdité de perception et à une translocation balancée 4:9 familiale. [Achalasia with dolichomegaesophagus associated with perceptual deafness of perception and familial 4:9 balanced translocation.]
Pescia G., Jotterand-Bellomo M., Vecerina S., Lanao C., 1981. Revue Médicale de la Suisse Romande, 101 (4) pp. 263-268.
 
Aspects cliniques et génétiques des translocations balancées: à propos de 7 observations. [Clinical and genetic aspects of balanced translocations: apropos of 7 cases.]
Pescia G., Gaide A.C., Jotterand-Bellomo M., Carrel C.F., 1981. Revue Médicale de la Suisse Romande, 101 (4) pp. 295-301.
 
Etude cytogénétique de deux sangliers (Sus scrofa L.) de couleur claire, capturés aux environs de Genève (Suisse)
Jotterand Bellomo M, Baettig M, 1981. Revue suisse de zoologie, 88 pp. 787-95.
 
Extra microchromosome mosaicism in amniotic cells confirmed in fetal tissues.
Pescia G., Jotterand-Bellomo M., Flury R., 1981. Journal de Génétique Humaine, 28 (5) pp. 175-183.
 
Hommage au professeur Robert Matthey. [Homage to Professor Robert Matthey.]
Jotterand-Bellomo M., 1981. Revue Médicale de la Suisse Romande, 101 (4) pp. 253-262.
 
Is it always the same NOR that is more active in a pair of acrocentrics with distinct AG-stainings?
Jotterand-Bellomo M., van Melle G., 1981. Human Genetics, 59 (2) p. 185.
 
Le caryotype et la spermatogenèse de Mus setulosus
Jotterand Bellomo M, 1981. Genetica, 56 (3) pp. 217-27.
 
Le diagnostic anténatal à Lausanne: à propos de 1500 observations. [Prenatal diagnosis in Lausanne: apropos of 1500 cases.]
Pescia G., Nguyen-The H., Jotterand-Bellomo M., Gaide A.C., 1981. Revue Médicale de la Suisse Romande, 101 (4) pp. 285-288.
 
Un cas de trisomie 22 incomplète due à la malségrégation méiotique d'une translocation familiale 11:12. [Incomplete trisomy 22 due to meiotic malsegregation of a familial 11:12 translocation.]
Pescia G., Jotterand-Bellomo M., Gaide A.C., 1981. Revue Médicale de la Suisse Romande, 101 (4) pp. 325-359.
 
Variability of the nucleolar organizer activity in human lymphocytes via Ag-staining.
Jotterand-Bellomo M., van Melle G., 1981. Human Genetics, 59 (2) pp. 141-147.
 
Attitude pratique face a l'hypertension arterielle de l'enfant. [Practical approach to arterial hypertension in children]
Guignard J. P., Dorner F., Jotterand M., Spahr A., Gautier E., 1980/03. Revue Médicale de la Suisse Romande, 100 (3) pp. 213-9.
 
Fusion telomérique de deux chromosomes X par leurs bras courts chez une patiente présentant un syndrome de Turner atypique. [Telomeric fusion of the short arms of both X chromosomes in a patient presenting an atypical Turner syndrome.]
Pescia G., Jotterand-Bellomo M., Nguyen T.H., Scholberg-Hermann B., 1980. Journal de Génétique Humaine, 28 (4) pp. 131-140.
 
La formule chromosomique de Mus setulosus (Leggada): description du caryotype et de la spermatogenèse (bandes Q, C, G et coloration argentique) et quelques considérations sur la différenciation du genre Mus
Jotterand-Bellomo Martine, 1980. pp. 44-57 dans Müller Hansjakob (eds.) Wirbeltierzytogenetik : Moderne Aspekte; Symposium zu Ehren von Robert Matthey, Pully, Jahrbuch der Schweizerischen Naturforschenden Gesellschaft. Wissenschaftlicher und administrativer Teil = Annuaire de la Société Helvétique des Sciences Naturelles. Partie scientifique et administrative, Basel : Birkhäuser.
 
Fausses-couches precoces iteratives et caryotype. Etude cytogenetique de 80 couples consecutifs. [Early repeated abortions and karyotypes. A cytogenic study of 80 consecutive couples (author's transl)]
Pescia G., Jotterand M., Gaide A. C., 1979/02. Journal de Gynécologie, Obstétrique et Biologie de la Reproduction, 8 (1) pp. 35-8.
 
Diagnostic prénatal des maladies gététiques. A propos de 500 observations. [Prenatal diagnosis of genetic illnesses. 500 cases.]
Pescia G., Nguyen The H., Vajda D., Tolck P., Cruz J., Jotterand-Bellomo M., 1979. Revue Médicale de la Suisse Romande, 99 (9) pp. 637-642.
 
Phénotype de la trisomie 9q distale chez un enfant présentant un chromosome surnuméraire remanié [t(X;9)]. [Distal 9q trisomy phenotype in a patient with a supernumerary rearranged chromosome [t(X:9)] (author's transl).]
Pescia G., Jotterand-Bellomo M., de Crousaz H., Payot M., Martin D., 1979. Annales de Génétique, 22 (3) pp. 158-62.
 
Les chromosomes humains: matériel et méthodes. [Human chromosomes: material and methods.]
Jotterand-Bellomo M., 1978. Revue Médicale de la Suisse Romande, 98 (1) pp. 3-16.
 
Les nouvelles méthodes d'analyses chromosomiques en cytogénétique humaine. [New methods for human chromosome analysis (author's transl).]
Jotterand-Bellomo M., 1978. Schweizerische Rundschau für Medizin Praxis = Revue suisse de médecine Praxis, 67 (30) pp. 1093-1102.
 
One case of a Ph1 chromosome resulting from translocation of the distal end 22q onto the short arm of chromosome 15.
Jotterand-Bellomo M., 1978. Cytogenetics and Cell Genetics, 21 (3) pp. 168-169.
 
Possible evidence of X-Y interchange in an XX male
Pescia G., Jotterand M., 1977/03. Lancet, 1 (8010) p. 550.
 
Etude familiale d'une translocation t(2;14)
Jotterand Bellomo M, Voumard C F, 1977. Archiv fur Genetik, 49/50 p. 186.
 
Association d'atteintes oculaires et otologiques dans une institution pour handicapes visuels et mentaux [Association of ocular and otological damage in an institution for the visually and mentally handicapped]
Cuendet J. F., Juillard E., Catti A., Verellen C., Dutoit M. L., Jotterand M., 1976/11. Journal de Genetique Humaine, 24 Suppl pp. 215-20.
 
A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21)
Jotterand M., Juillard E., 1976/08. Human Genetics, 33 (3) pp. 213-22.
 
Trisomie 22. [Trisomy 22.]
Jotterand-Bellomo M., 1976. Archiv für Genetik, 49-50 (2-3) pp. 134-166.
 
A propos de quelques anomalies chromosomiques mineures [Several minor chromosome anomalies]
Grosset L., Jotterand M., Catti A., 1975/10. Journal de Genetique Humaine, 23 SUPPL pp. 115-7.
 
Le manul Otocolobus manul (Pallas 1776): son caryotype et sa position dans la classification des Felides [The manul Octocolobus manul (Pallas 1776): its karyotype and position in the classification of the Felidae]
Schauenberg P., Jotterand M., 1975/07. Revue Suisse de Zoologie, 82 (2) pp. 425-9.
 
The African Mus (Pigmy-mice): the role of chromosome polymorphism in speciation
Jotterand M., 1975. Caryologia, 28 pp. 335-44.
 
A chromosome mutation affecting the number of nucleoli in Xenopus borealis Parker
Jotterand M., Fischberg M., 1974/09. Experientia, 30 (9) pp. 1003-5.
 
Chromosomes of Felidae
Jotterand M, 1972. Carnivore Genetics Newsletter 2 pp. 83-4.
 
Deux espèces cryptiques sont confondues sous le nom de Taterillus gracilis Th. (Gerbillinae)
Matthey R, Jotterand M, 1972. Revue Suisse de Zoologie, 79 (3) pp. 1104-1105.
 
L'analyse du caryotype permet de reconnaître deux espèces cryptiques confondues sous le nom de Taterillus gracilis Th (Rongeurs-Gerbillidae)
Matthey R, Jotterand M, 1972. Mammalia, 36 (2) pp. 193-209.
 
Le polymorphisme chromosomique des Mus (Leggadas) africains. Cytogenetique, zoogeographie, evolution. [Chromosome polymorphism of Mus (Leggadas) africains. Cytogenetics, zoogeography and evolution]
Jotterand M., 1972. Revue Suisse de Zoologie, 79 (1) pp. 287-359.
 
La formule chromosomique de quatre especes de Felidae. [Chromosome arrangement of 4 species of Felidae]
Jotterand M., 1971/12. Revue Suisse de Zoologie, 78 (4) pp. 1248-51.
 
Un nouveau système polymorphe robertsonien chez une nouvelle espece de "Leggada" (Mus goundae Petter) [A new robertsonian polymorphic system in a new species of "Leggada" (Mus goundae Petter)]
Jotterand M., 1970/12. Experientia, 26 (12) pp. 1360-1.
 
Nouveau systeme polymorphe non-robertsonien chez des "Leggadas" (Mus sp.) de republique Centrafricaine. [New non-Robertsonian polymorphous system in the "Leggadas" (Mus sp.) of the Centrafricain Republic]
Matthey R., Jotterand M., 1970/09. Revue Suisse de Zoologie, 77 (3) pp. 630-5.
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