F. Ajmar
Impact in
- Hematology top 5%
- Chronic Myeloid Leukemia Treatments
- Acute Myeloid Leukemia Research
- Genetics top 5%
- Chronic Lymphocytic Leukemia Research
- Myeloproliferative Neoplasms: Diagnosis and Treatment
Papers in
- Hematology 18
- Chronic Myeloid Leukemia Treatments 13
- Acute Myeloid Leukemia Research 11
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- Genetic Neurodegenerative Diseases 8
- Hereditary Neurological Disorders 8
- Co-authors
- Paola Mandich (20 shared papers)Emilia Bellone (18 shared papers)Mario Sessarego (17 shared papers)E Salvidio (8 shared papers)Emilio Di Maria (11 shared papers)Roberto Ravazzolo (11 shared papers)Cecilia Garrè (8 shared papers)Raffaella Defferrari (7 shared papers)
- Journals
- Human Genetics (2 papers)Biochemical Genetics (2 papers)Acta Haematologica (2 papers)Journal of the Peripheral Nervous System (2 papers)Human Mutation (2 papers)
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
F. Ajmar
52 papers receiving 732 citations
Peers
Comparison fields: 5 of 68
- Hematology 203
- Genetics 187
- Cellular and Molecular Neuroscience 253
- Neurology 153
- Neurology 82
Countries citing papers authored by F. Ajmar
This map shows the geographic impact of F. Ajmar'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 F. Ajmar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Ajmar more than expected).
Fields of papers citing papers by F. Ajmar
This network shows the impact of papers produced by F. Ajmar. 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 F. Ajmar. The network helps show where F. Ajmar may publish in the future.
Co-authors
The 25 scholars most cited alongside F. Ajmar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 63 | |
| 2 | Terminal erythroid differentiation in the K-562 cell line by 1-beta-D-arabinofuranosylcytosine: accompaniment by c-myc messenger RNA decrease. | 1986 | 58 |
| 3 | 1989 | 57 | |
| 4 | 1994 | 48 | |
| 5 | 1999 | 42 | |
| 6 | 1997 | 40 | |
| 7 | 1991 | 34 | |
| 8 | 1967 | 32 | |
| 9 | 1987 | 27 | |
| 10 | 1983 | 25 | |
| 11 | 2001 | 25 | |
| 12 | 1999 | 24 | |
| 13 | Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families. | 1992 | 23 |
| 14 | 1998 | 22 | |
| 15 | 1995 | 22 | |
| 16 | 1985 | 22 | |
| 17 | Effects of fibroblasts on the growth of erythroid progenitor cells in vitro. | 1977 | 19 |
| 18 | 1995 | 14 | |
| 19 | 1968 | 13 | |
| 20 | 1981 | 13 |
About F. Ajmar
F. Ajmar is a scholar working on Hematology, Cellular and Molecular Neuroscience, Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 57 papers that have together received 779 indexed citations. Recurring topics across this work include Chronic Myeloid Leukemia Treatments (13 papers), Acute Myeloid Leukemia Research (11 papers), Neonatal Health and Biochemistry (8 papers), Genetic Neurodegenerative Diseases (8 papers), Hereditary Neurological Disorders (8 papers), Chronic Lymphocytic Leukemia Research (7 papers), Erythrocyte Function and Pathophysiology (5 papers) and Cholinesterase and Neurodegenerative Diseases (4 papers). The work is most often cited by research in Hematology (203 citations), Genetics (187 citations), Cellular and Molecular Neuroscience (253 citations), Neurology (153 citations) and Neurology (82 citations). F. Ajmar has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Paola Mandich, Emilia Bellone, Mario Sessarego, E Salvidio, Emilio Di Maria, Roberto Ravazzolo, Cecilia Garrè, Raffaella Defferrari, Domenico Coviello and Gianluigi Mancardi. Their work appears in journals such as Human Genetics, Biochemical Genetics, Acta Haematologica, Journal of the Peripheral Nervous System and Human Mutation.
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.