Luis E. Figuera
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Dermatological and Skeletal Disorders
- Cell Biology top 5%
- Plant Pathogens and Fungal Diseases
- Skin and Cellular Biology Research
Papers in
-
- Glutathione Transferases and Polymorphisms 11
- Genetics 42
- Genomic variations and chromosomal abnormalities 15
- Connective tissue disorders research 6
- Co-authors
- Martha Patricia Gallegos‐Arreola (51 shared papers)Guillermo Moisés Zúñiga‐González (38 shared papers)Ana María Puebla‐Pérez (32 shared papers)M.L. Abarca (2 shared papers)J. M. Cantú (9 shared papers)J. Cano (2 shared papers)Francesc Accensi (2 shared papers)Pragna I. Patel (4 shared papers)
- Journals
- Clinical Genetics (7 papers)Blood Cells Molecules and Diseases (3 papers)Archives of Medical Research (3 papers)BioMed Research International (2 papers)Disease Markers (2 papers)
- Partner nations
- MexicoUnited StatesSpain
In The Last Decade
Luis E. Figuera
125 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 106
- Genetics 602
- Cell Biology 283
- Rheumatology 159
- Urology 65
- Developmental Biology 25
Countries citing papers authored by Luis E. Figuera
This map shows the geographic impact of Luis E. Figuera'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 Luis E. Figuera with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Luis E. Figuera more than expected).
Fields of papers citing papers by Luis E. Figuera
This network shows the impact of papers produced by Luis E. Figuera. 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 Luis E. Figuera. The network helps show where Luis E. Figuera may publish in the future.
Co-authors
The 25 scholars most cited alongside Luis E. Figuera, 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 135 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients. | 1996 | 111 |
| 2 | 2000 | 104 | |
| 3 | 1999 | 100 | |
| 4 | 2010 | 96 | |
| 5 | 2006 | 58 | |
| 6 | 2001 | 57 | |
| 7 | 1995 | 51 | |
| 8 | 2011 | 51 | |
| 9 | 2010 | 48 | |
| 10 | 2006 | 44 | |
| 11 | 2000 | 44 | |
| 12 | 2009 | 43 | |
| 13 | 2010 | 37 | |
| 14 | 2013 | 33 | |
| 15 | Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRs. | 2000 | 32 |
| 16 | 2005 | 31 | |
| 17 | 2010 | 29 | |
| 18 | 2002 | 27 | |
| 19 | 2014 | 27 | |
| 20 | 2013 | 24 |
About Luis E. Figuera
Luis E. Figuera is a scholar working on Molecular Biology, Genetics, Physiology, Cancer Research and Rheumatology, having authored 135 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Lysosomal Storage Disorders Research (13 papers), Glutathione Transferases and Polymorphisms (11 papers), Folate and B Vitamins Research (6 papers), Chromosomal and Genetic Variations (6 papers), Prenatal Screening and Diagnostics (6 papers), Alzheimer's disease research and treatments (6 papers) and Connective tissue disorders research (6 papers). The work is most often cited by research in Genetics (602 citations), Cell Biology (283 citations), Rheumatology (159 citations), Urology (65 citations) and Developmental Biology (25 citations). Luis E. Figuera has collaborated with scholars based in Mexico, United States and Spain. Frequent co-authors include Martha Patricia Gallegos‐Arreola, Guillermo Moisés Zúñiga‐González, Ana María Puebla‐Pérez, M.L. Abarca, J. M. Cantú, J. Cano, Francesc Accensi, Pragna I. Patel, Lucila Sandoval-Ramı́rez and Diana García‐Cruz. Their work appears in journals such as Clinical Genetics, Blood Cells Molecules and Diseases, Archives of Medical Research, BioMed Research International and Disease Markers.
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.