V. Parlier
Impact in
- Hematology top 2%
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
- Genetics top 10%
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Chronic Lymphocytic Leukemia Research
- Genomic variations and chromosomal abnormalities
Papers in
- Hematology 15
- Acute Myeloid Leukemia Research 13
- Chronic Myeloid Leukemia Treatments 6
- Genetics 8
- Myeloproliferative Neoplasms: Diagnosis and Treatment 5
- Genomic variations and chromosomal abnormalities 5
- Chronic Lymphocytic Leukemia Research 3
- Co-authors
- P Beris (8 shared papers)Martine Jotterand (10 shared papers)Dominique Mühlematter (9 shared papers)Jean‐Jacques Grob (1 shared paper)Guy van Melle (7 shared papers)M Jotterand-Bellomo (3 shared papers)A Tobler (3 shared papers)Edouard Haller (3 shared papers)
- Journals
- Leukemia (2 papers)Leukemia Research (2 papers)British Journal of Haematology (2 papers)Genes Chromosomes and Cancer (1 paper)Cancer Genetics and Cytogenetics (9 papers)
- Partner nations
- SwitzerlandFinlandNetherlands
In The Last Decade
V. Parlier
19 papers receiving 439 citations
Peers
Comparison fields: 5 of 29
- Hematology 368
- Genetics 137
- Public Health, Environmental and Occupational Health 93
- Emergency Medicine 28
- Pathology and Forensic Medicine 49
Countries citing papers authored by V. Parlier
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
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-authors
The 25 scholars most cited alongside V. Parlier, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 86 | |
| 2 | 1994 | 55 | |
| 3 | 1990 | 51 | |
| 4 | 2004 | 31 | |
| 5 | 1996 | 29 | |
| 6 | 2000 | 28 | |
| 7 | 1997 | 26 | |
| 8 | 1995 | 24 | |
| 9 | 1992 | 21 | |
| 10 | 1999 | 19 | |
| 11 | 1992 | 19 | |
| 12 | 2005 | 13 | |
| 13 | 2006 | 12 | |
| 14 | 2008 | 11 | |
| 15 | 2003 | 10 | |
| 16 | 1990 | 6 | |
| 17 | 2008 | 2 | |
| 18 | [Unusual initial manifestation in a case of refractory anemia with excess of blasts]. | 1991 | 2 |
| 19 | 1994 | 1 |
About V. Parlier
V. Parlier is a scholar working on Hematology, Genetics, Genetics, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 19 papers that have together received 446 indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (13 papers), Chronic Myeloid Leukemia Treatments (6 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Acute Lymphoblastic Leukemia research (4 papers), Chronic Lymphocytic Leukemia Research (3 papers), Prenatal Screening and Diagnostics (3 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Hematology (368 citations), Genetics (137 citations), Public Health, Environmental and Occupational Health (93 citations), Emergency Medicine (28 citations) and Pathology and Forensic Medicine (49 citations). V. Parlier has collaborated with scholars based in Switzerland, Finland and Netherlands. Frequent co-authors include P Beris, Martine Jotterand, Dominique Mühlematter, Jean‐Jacques Grob, Guy van Melle, M Jotterand-Bellomo, A Tobler, Edouard Haller, Marianne Tiainen and J Gmür. Their work appears in journals such as Leukemia, Leukemia Research, British Journal of Haematology, Genes Chromosomes and Cancer and Cancer Genetics and Cytogenetics.
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.