Dominique Mühlematter

826 citations

25 papers · 528 indexed · h-index 14

Co-authors: V. Parlier Martine Jotterand P Beris Jean‐Jacques Grob André Tichelli A Hagemeijer J Schwaller MF Fey
Topics: Acute Myeloid Leukemia Research (13 papers)Acute Lymphoblastic Leukemia research (9 papers)Chronic Lymphocytic Leukemia Research (9 papers)
Cited by: Hematology Genetics Pathology and Forensic Medicine
Journals: Blood Oncogene Molecular Cancer
Partner nations: Switzerland Netherlands United Kingdom

In The Last Decade

Dominique Mühlematter

25 papers receiving 518 citations

Peers

Countries citing papers authored by Dominique Mühlematter

Since Specialization

Citations

This map shows the geographic impact of Dominique Mühlematter's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dominique Mühlematter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dominique Mühlematter more than expected).

Fields of papers citing papers by Dominique Mühlematter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dominique Mühlematter. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dominique Mühlematter. The network helps show where Dominique Mühlematter may publish in the future.

Co-authorship network of co-authors of Dominique Mühlematter

This figure shows the co-authorship network connecting the top 25 collaborators of Dominique Mühlematter. A scholar is included among the top collaborators of Dominique Mühlematter based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Dominique Mühlematter. Dominique Mühlematter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders 2015 ·Molecular Cancer ·Alberto L’Abbate,Doron Tolomeo,(unknown),Angelo Lonoce,Crocifissa Lo Cunsolo,Dominique Mühlematter,Jacqueline Schoumans,Peter Vandenberghe,A Van Hoof,Orazio Palumbo,Massimo Carella,Tommaso Mazza,Clelia Tiziana Storlazzi	14
2	G-CSF-induced remission in two cases of acute myeloid leukemia 2008 ·Leukemia Research ·Rudolf Benz,Jeroen S. Goede,V. Parlier,Dominique Mühlematter,Martine Jotterand,Jörg Fehr	2
3	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 2008 ·Cancer Genetics and Cytogenetics ·(unknown),Dominique Mühlematter,(unknown),(unknown),Sarah Porter,(unknown),V. Parlier,J. Beckmann,Guy van Melle,Martine Jotterand	11
4	Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3 2008 ·Journal of Clinical Pathology ·Alexandar Tzankov,(unknown),Dominique Mühlematter,Alexandre Theocharides,Philip Went,Martine Jotterand,H.‐P. Horny,S Dirnhofer	21
5	Case study of intracerebral plasmacytoma as an initial presentation of multiple myeloma 2007 ·Neuro-Oncology ·(unknown),Audrey Sylvia Baur,Michael Betz,Dominique Mühlematter,Martine Jotterand,Khalil Zaman,Nicolas Ketterer	21
6	Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia 2006 ·Leukemia ·Sandrine Meyer‐Monard,V. Parlier,Jakob Passweg,Dominique Mühlematter,U Hess,Mario Bargetzi,Thomas Kühne,C Cabrol,Aloïs Gratwohl,Martine Jotterand,André Tichelli	12
7	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 2005 ·Cancer Genetics and Cytogenetics ·(unknown),Dominique Mühlematter,V. Parlier,C Cabrol,(unknown),Max Solenthaler,Andreas Tobler,P Pugin,Michael Gregor,Felicitas Hitz,U Hess,B Chapuis,(unknown),Urs Schanz,(unknown),Guy van Melle,Martine Jotterand	13
8	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 2004 ·Cancer Genetics and Cytogenetics ·(unknown),(unknown),Dominique Mühlematter,V. Parlier,J Gmür,U Hess,Tibor Kovacsovics,Sandrine Meyer‐Monard,André Tichelli,Andreas Tobler,E Jacky,Urs Schanz,Mario Bargetzi,Anne Hagemeijer,Théo de Witte,Guy van Melle,Martine Jotterand	31
9	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? 2003 ·Cancer Genetics and Cytogenetics ·(unknown),Dominique Mühlematter,(unknown),V. Parlier,Guy van Melle,Martine Jotterand	10
10	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 α-Interferon Therapy 1999 ·Cancer Genetics and Cytogenetics ·(unknown),Dominique Mühlematter,Danielle Martinet,Martine Jotterand	7
11	Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered 1999 ·Oncogene ·Bert A. van der Reijden,Hans G. Dauwerse,Rachel H. Giles,Shantie Jagmohan–Changur,Cisca Wijmenga,(unknown),Bep Smit,(unknown),(unknown),M Jotterand-Bellomo,Danielle Martinet,Dominique Mühlematter,Mårina Lafage‐Pochitaloff,Jean Gabert,Josy Reiffers,Chrystèle Bilhou‐Nabera,Gert‐Jan B. van Ommen,Anne Hagemeijer,Martijn H. Breuning	25
12	Dicentric Translocation (9;12) Presenting as Refractory Philadelphia Chromosome-Positive Acute B-Cell Lymphoblastic Leukemia 1999 ·Cancer Genetics and Cytogenetics ·Mario Bargetzi,Dominique Mühlematter,André Tichelli,Martine Jotterand,Martin Wernli	6
13	A novel BCR‐ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph‐chromosome and monosomy 7 1999 ·British Journal of Haematology ·Elisabeth Oppliger Leibundgut,Martine Jotterand,(unknown),V. Parlier,Dominique Mühlematter,Andreas Tobler,Max Solenthaler	19
14	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) 1997 ·Cancer Genetics and Cytogenetics ·(unknown),Dominique Mühlematter,Guy van Melle,(unknown),(unknown)	8
15	Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML) 1997 ·Leukemia ·Danielle Martinet,Dominique Mühlematter,Matthew F. Leeman,V. Parlier,U Hess,J Gmür,Martine Jotterand	26
16	Tetrasomy 8 in a patient with acute nonlymphocytic leukemia: A metaphase and interphase study with fluorescence in situ hybridization 1996 ·Cancer Genetics and Cytogenetics ·Dominique Mühlematter,(unknown),(unknown),(unknown),(unknown),(unknown)	16
17	A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11). 1995 ·PubMed ·Rosalyn Slater,E.M.E. Smit,Wilma G. M. Kroes,(unknown),Dominique Mühlematter,Jochen Harbott,H. Behrendt,K. Hählen,A. Veerman,A Hagemeijer	21
18	RT-PCR diagnosis of patients with acute nonlymphocytic leukemia and inv(16)(p13q22) and identification of new alternative splicing in CBFB- MYH11 transcripts 1995 ·Blood ·(unknown),(unknown),(unknown),Rachel H. Giles,Dominique Mühlematter,(unknown),(unknown),G.C. Beverstock,GJ van Ommen,A Hagemeijer	50
19	t(8;9)(p11;q32) IN ATYPICAL CHRONIC MYELOID LEUKAEMIA: A NEW CYTOGENETTC‐CLINICOPATHOLOGIC ASSOCIATION? 1992 ·British Journal of Haematology ·(unknown),Dominique Mühlematter,(unknown),(unknown),(unknown)	23
20	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 1992 ·Cancer Genetics and Cytogenetics ·(unknown),V. Parlier,Dominique Mühlematter,Jean‐Jacques Grob,P Beris	86

About Dominique Mühlematter

Dominique Mühlematter is a scholar working on Hematology, Genetics and Public Health, Environmental and Occupational Health, having authored 25 papers that have together received 528 indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (13 papers), Acute Lymphoblastic Leukemia research (9 papers) and Chronic Lymphocytic Leukemia Research (9 papers). The work is most often cited by research in Hematology (365 citations), Genetics (160 citations) and Pathology and Forensic Medicine (102 citations). Dominique Mühlematter has collaborated with scholars based in Switzerland, Netherlands and United Kingdom. Frequent co-authors include V. Parlier, Martine Jotterand, P Beris, Jean‐Jacques Grob, André Tichelli, A Hagemeijer, J Schwaller, MF Fey, M Oestreicher and A Tobler. Their work appears in journals such as Blood, Oncogene and Molecular Cancer.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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