V. Parlier

561 total citations
19 papers, 446 citations indexed

About

V. Parlier is a scholar working on Hematology, Genetics and Genetics. According to data from OpenAlex, V. Parlier has authored 19 papers receiving a total of 446 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Hematology, 8 papers in Genetics and 5 papers in Genetics. Recurrent topics in V. Parlier's work include Acute Myeloid Leukemia Research (13 papers), Chronic Myeloid Leukemia Treatments (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). V. Parlier is often cited by papers focused on Acute Myeloid Leukemia Research (13 papers), Chronic Myeloid Leukemia Treatments (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). V. Parlier collaborates with scholars based in Switzerland, Finland and Netherlands. V. Parlier's co-authors include P Beris, Martine Jotterand, Dominique Mühlematter, Jean‐Jacques Grob, Guy van Melle, M Jotterand-Bellomo, Edouard Haller, A Tobler, J Gmür and U Hess and has published in prestigious journals such as British Journal of Haematology, Leukemia and Genes Chromosomes and Cancer.

In The Last Decade

V. Parlier

19 papers receiving 438 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
V. Parlier Switzerland 13 383 144 121 100 76 19 446
Paola Maria Cavigliano Italy 12 324 0.8× 136 0.9× 94 0.8× 69 0.7× 63 0.8× 27 384
G.W. Dewald United States 9 329 0.9× 103 0.7× 147 1.2× 95 0.9× 61 0.8× 11 416
Laurence Baranger France 12 244 0.6× 104 0.7× 110 0.9× 114 1.1× 49 0.6× 19 362
M. T. Daniel France 7 385 1.0× 240 1.7× 129 1.1× 66 0.7× 48 0.6× 10 494
Dominique Mühlematter Switzerland 14 365 1.0× 160 1.1× 212 1.8× 130 1.3× 78 1.0× 25 528
A. Cantù Rajnoldi Italy 8 379 1.0× 131 0.9× 195 1.6× 115 1.1× 31 0.4× 12 465
Marilena Caresana Italy 10 276 0.7× 131 0.9× 89 0.7× 53 0.5× 48 0.6× 20 314
J. Ritterbach Germany 11 350 0.9× 127 0.9× 161 1.3× 211 2.1× 59 0.8× 19 486
Barbara Rocca Italy 9 274 0.7× 127 0.9× 86 0.7× 52 0.5× 48 0.6× 21 310
Mirjam Klaus Greece 6 343 0.9× 128 0.9× 165 1.4× 111 1.1× 22 0.3× 10 413

Countries citing papers authored by V. Parlier

Since Specialization
Citations

This map shows the geographic impact of V. Parlier'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 V. Parlier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. Parlier more than expected).

Fields of papers citing papers by V. Parlier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. Parlier. 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 V. Parlier. The network helps show where V. Parlier may publish in the future.

Co-authorship network of co-authors of V. Parlier

This figure shows the co-authorship network connecting the top 25 collaborators of V. Parlier. A scholar is included among the top collaborators of V. Parlier 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 V. Parlier. V. Parlier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Benz, Rudolf, Jeroen S. Goede, V. Parlier, et al.. (2008). G-CSF-induced remission in two cases of acute myeloid leukemia. Leukemia Research. 32(7). 1148–1152. 2 indexed citations
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Meyer‐Monard, Sandrine, V. Parlier, Jakob Passweg, et al.. (2006). Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia. Leukemia. 20(2). 247–253. 12 indexed citations
4.
Mühlematter, Dominique, V. Parlier, C Cabrol, et al.. (2005). 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. Cancer Genetics and Cytogenetics. 160(2). 97–119. 13 indexed citations
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Baur, Audrey Sylvia, et al.. (2000). CD34/QBEND10 immunostaining in bone marrow biopsies: an additional parameterfor the diagnosis and classification of myelodysplastic syndromes. European Journal Of Haematology. 64(2). 71–79. 28 indexed citations
8.
Leibundgut, Elisabeth Oppliger, Martine Jotterand, V. Parlier, et al.. (1999). A novel BCR‐ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph‐chromosome and monosomy 7. British Journal of Haematology. 106(4). 1041–1044. 19 indexed citations
9.
Martinet, Danielle, Dominique Mühlematter, Matthew F. Leeman, et al.. (1997). Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML). Leukemia. 11(7). 964–970. 26 indexed citations
10.
Jotterand, Martine & V. Parlier. (1996). Diagnostic and Prognostic Significance of Cytogenetics in Adult Primary Myelodysplastic Syndromes. Leukemia & lymphoma. 23(3-4). 253–266. 29 indexed citations
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Parlier, V., et al.. (1994). Hematologic, clinical, and cytogenetic analysis in 109 patients with primary myelodysplastic syndrome. Cancer Genetics and Cytogenetics. 78(2). 219–231. 55 indexed citations
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Tiainen, Marianne, Sakari Knuutila, Susanne Popp, et al.. (1992). Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies. Genes Chromosomes and Cancer. 4(2). 135–140. 21 indexed citations
17.
Beris, P, et al.. (1991). [Unusual initial manifestation in a case of refractory anemia with excess of blasts].. PubMed. 121(41). 1499–502. 2 indexed citations
18.
Jotterand-Bellomo, M, et al.. (1990). A new case of myelodysplastic syndrome with 6p rearrangement. Cancer Genetics and Cytogenetics. 44(2). 271–274. 6 indexed citations
19.
Jotterand-Bellomo, M, et al.. (1990). Cytogenetic analysis of 54 cases of myelodysplastic syndrome. Cancer Genetics and Cytogenetics. 46(2). 157–172. 51 indexed citations

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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