Sergio Arias
Impact in
- Developmental Biology top 10%
- Congenital limb and hand anomalies
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
-
- Mitochondrial Function and Pathology 3
- RNA regulation and disease 2
- Genetics 7
- Congenital Ear and Nasal Anomalies 2
- Dermatoglyphics and Human Traits 2
- Co-authors
- Alba Hernández (3 shared papers)J Pinto-Cisternas (2 shared papers)John M. Opitz (1 shared paper)Víctor B. Penchaszadeh (1 shared paper)Álvaro Rodríguez (2 shared papers)Manuel Pedro Rodríguez Bolívar (1 shared paper)Linda Teresa Orcasita (1 shared paper)Peter Günczler (1 shared paper)
In The Last Decade
Sergio Arias
29 papers receiving 403 citations
Peers
Comparison fields: 5 of 61
- Developmental Biology 23
- Sensory Systems 36
- Cellular and Molecular Neuroscience 95
- Cell Biology 73
- Genetics 105
Countries citing papers authored by Sergio Arias
This map shows the geographic impact of Sergio Arias'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 Sergio Arias with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sergio Arias more than expected).
Fields of papers citing papers by Sergio Arias
This network shows the impact of papers produced by Sergio Arias. 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 Sergio Arias. The network helps show where Sergio Arias may publish in the future.
Co-authors
The 13 scholars most cited alongside Sergio Arias, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic heterogeneity in the Waardenburg syndrome. | 1971 | 98 |
| 2 | 1980 | 49 | |
| 3 | Apparent non-penetrance for dystopia in Waardenburg syndrome type I, with some hints on the diagnosis of dystopia canthorum. | 1978 | 49 |
| 4 | 2007 | 46 | |
| 5 | 2007 | 35 | |
| 6 | 2015 | 34 | |
| 7 | 2012 | 20 | |
| 8 | 2014 | 15 | |
| 9 | 1980 | 15 | |
| 10 | 2010 | 11 | |
| 11 | 1975 | 11 | |
| 12 | 2017 | 10 | |
| 13 | PI locus (alpha-1-antitrypsin) allelic frequencies in an Andean Venezuelan population. | 1996 | 6 |
| 14 | 1980 | 6 | |
| 15 | 1985 | 6 | |
| 16 | Hemoglobin S/hemoglobin City of Hope compound heterozygote with a SubSaharan genetic background and severe bone marrow hypoplasia. | 2010 | 4 |
| 17 | 1987 | 3 | |
| 18 | 1972 | 3 | |
| 19 | Inherited congenital profound deafness in a genetic isolate. | 1974 | 3 |
| 20 | 1971 | 2 |
About Sergio Arias
Sergio Arias is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Cellular and Molecular Neuroscience, having authored 33 papers that have together received 435 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (4 papers), Mitochondrial Function and Pathology (3 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Reproductive Physiology in Livestock (2 papers), RNA regulation and disease (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Dermatoglyphics and Human Traits (2 papers) and Reproductive Biology and Fertility (2 papers). The work is most often cited by research in Developmental Biology (23 citations), Sensory Systems (36 citations), Cellular and Molecular Neuroscience (95 citations), Cell Biology (73 citations) and Genetics (105 citations). Sergio Arias has collaborated with scholars based in Venezuela, Colombia and Brazil. Frequent co-authors include Alba Hernández, J Pinto-Cisternas, John M. Opitz, Víctor B. Penchaszadeh, Álvaro Rodríguez, Manuel Pedro Rodríguez Bolívar, Linda Teresa Orcasita, Peter Günczler, Z. Layrisse and Charles C. White. Their work appears in journals such as Annals of Human Genetics, Journal of Inherited Metabolic Disease, Immunogenetics, Human Genetics and Computers in Biology and Medicine.
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.