M. Baiget
Impact in
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- Neurogenetic and Muscular Disorders Research
- BRCA gene mutations in cancer
- Hemoglobinopathies and Related Disorders
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- Genetic Neurodegenerative Diseases
Papers in
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- RNA modifications and cancer 4
- DNA Repair Mechanisms 3
- Cancer therapeutics and mechanisms 2
- Genetics 10
- Hemoglobinopathies and Related Disorders 6
- Neurogenetic and Muscular Disorders Research 4
- BRCA gene mutations in cancer 3
- Co-authors
- Enric Álvarez (1 shared paper)Víctor Pérez (1 shared paper)Vı́ctor Volpini (1 shared paper)José Ignacio Emparanza (2 shared papers)Loreto Martorell (2 shared papers)Eduardo F. Tizzano (5 shared papers)J.F. Martí-Massó (2 shared papers)José M. Millán (2 shared papers)
- Journals
- Human Mutation (2 papers)Acta Haematologica (2 papers)Journal of Clinical Oncology (2 papers)Neuromuscular Disorders (2 papers)European Journal of Human Genetics (1 paper)
- Partner nations
- SpainItalyUnited States
In The Last Decade
M. Baiget
29 papers receiving 281 citations
Peers
Comparison fields: 5 of 45
- Genetics 73
- Cellular and Molecular Neuroscience 66
- Hematology 34
- Ophthalmology 23
- Biological Psychiatry 6
Countries citing papers authored by M. Baiget
This map shows the geographic impact of M. Baiget'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 M. Baiget with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Baiget more than expected).
Fields of papers citing papers by M. Baiget
This network shows the impact of papers produced by M. Baiget. 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 M. Baiget. The network helps show where M. Baiget may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Baiget, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 44 | |
| 2 | 2006 | 42 | |
| 3 | 1993 | 38 | |
| 4 | 2013 | 30 | |
| 5 | 1999 | 29 | |
| 6 | 1986 | 18 | |
| 7 | 2006 | 18 | |
| 8 | 1994 | 13 | |
| 9 | 1983 | 10 | |
| 10 | 1994 | 9 | |
| 11 | 1996 | 6 | |
| 12 | 1996 | 6 | |
| 13 | 2011 | 4 | |
| 14 | 1994 | 3 | |
| 15 | 1982 | 3 | |
| 16 | 2001 | 2 | |
| 17 | 1979 | 2 | |
| 18 | 2008 | 2 | |
| 19 | Serum ferritin concentration and bone marrow iron stores. | 1980 | 2 |
| 20 | [Mutations in the BRCA1 gene in young Spanish women with breast cancer]. | 1999 | 2 |
About M. Baiget
M. Baiget is a scholar working on Molecular Biology, Genetics, Hematology, Oncology and Cellular and Molecular Neuroscience, having authored 30 papers that have together received 292 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (6 papers), Neurogenetic and Muscular Disorders Research (4 papers), RNA modifications and cancer (4 papers), Iron Metabolism and Disorders (3 papers), BRCA gene mutations in cancer (3 papers), DNA Repair Mechanisms (3 papers), Genetic factors in colorectal cancer (2 papers) and Cancer therapeutics and mechanisms (2 papers). The work is most often cited by research in Genetics (73 citations), Cellular and Molecular Neuroscience (66 citations), Hematology (34 citations), Ophthalmology (23 citations) and Biological Psychiatry (6 citations). M. Baiget has collaborated with scholars based in Spain, Italy and United States. Frequent co-authors include Enric Álvarez, Víctor Pérez, Vı́ctor Volpini, José Ignacio Emparanza, Loreto Martorell, Eduardo F. Tizzano, J.F. Martí-Massó, José M. Millán, J J Poza and Orland Dı́ez. Their work appears in journals such as Human Mutation, Acta Haematologica, Journal of Clinical Oncology, Neuromuscular Disorders and European Journal of Human Genetics.
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.