Elisabet Lloveras
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- Prenatal Screening and Diagnostics 10
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- Genomic variations and chromosomal abnormalities 12
- Chronic Lymphocytic Leukemia Research 7
- Genomics and Rare Diseases 2
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- Genomic variations and chromosomal abnormalities 12
- Chronic Lymphocytic Leukemia Research 7
- Genomics and Rare Diseases 2
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- Multiple Myeloma Research and Treatments 2
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- Lymphoma Diagnosis and Treatment 3
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- Immunodeficiency and Autoimmune Disorders 2
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- Chromosomal and Genetic Variations 2
- Co-authors
- M. Paz CañadasCarme FusterGianfranco VoglinoVincenzo CiriglianoElena OrdóñezMatteo AdinolfíAlberto PlajaFrançesc Solé
- Journals
- Cytogenetic and Genome Research (5 papers)Fertility and Sterility (1 paper)Annals of the New York Academy of Sciences (1 paper)
- Partner nations
- SpainUnited StatesUnited Kingdom
In The Last Decade
Elisabet Lloveras
19 papers receiving 220 citations
Peers
Comparison fields: 5 of 31
- Pediatrics, Perinatology and Child Health 132
- Genetics 153
- Genetics 57
- Hematology 29
- Pathology and Forensic Medicine 42
Countries citing papers authored by Elisabet Lloveras
This map shows the geographic impact of Elisabet Lloveras'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 Elisabet Lloveras with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elisabet Lloveras more than expected).
Fields of papers citing papers by Elisabet Lloveras
This network shows the impact of papers produced by Elisabet Lloveras. 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 Elisabet Lloveras. The network helps show where Elisabet Lloveras may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Elisabet Lloveras, 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 | 2021 | 0 | |
| 2 | 2019 | 6 | |
| 3 | 2015 | 1 | |
| 4 | 2015 | 6 | |
| 5 | 2014 | 5 | |
| 6 | 2013 | 2 | |
| 7 | 2013 | 20 | |
| 8 | 2011 | 1 | |
| 9 | 2009 | 85 | |
| 10 | 2006 | 36 | |
| 11 | 2006 | 1 | |
| 12 | 2003 | 17 | |
| 13 | 2003 | 14 | |
| 14 | 2002 | 7 | |
| 15 | Collection of Philadelphia-negative stem cells using recombinant human granulocyte colony-stimulating factor in chronic myeloid leukemia patients treated with alpha-interferon. | 2002 | 7 |
| 16 | 2000 | 1 | |
| 17 | 2000 | 4 | |
| 18 | 1999 | 7 | |
| 19 | 1999 | 22 | |
| 20 | 1998 | 8 |
About Elisabet Lloveras
Elisabet Lloveras is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 20 papers that have together received 250 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (10 papers), Chronic Lymphocytic Leukemia Research (7 papers), Lymphoma Diagnosis and Treatment (3 papers), Genomics and Rare Diseases (2 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Multiple Myeloma Research and Treatments (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (132 citations), Genetics (153 citations) and Genetics (57 citations). Elisabet Lloveras has collaborated with scholars based in Spain, United States and United Kingdom. Frequent co-authors include M. Paz Cañadas, Carme Fuster, Gianfranco Voglino, Vincenzo Cirigliano, Elena Ordóñez, Matteo Adinolfí, Alberto Plaja, Françesc Solé, Blanca Espinet and Lourdes Florensa. Their work appears in journals such as Cytogenetic and Genome Research, Fertility and Sterility, Annals of the New York Academy of Sciences, Prenatal Diagnosis 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.