Algirdas Utkus
Impact in
- Genetics top 5%
- Genetics and Physical Performance
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Sports Performance and Training
Papers in
-
- Congenital heart defects research 9
- Mitochondrial Function and Pathology 6
- Genetics 43
- Genomic variations and chromosomal abnormalities 18
- Genetics and Neurodevelopmental Disorders 8
- Cleft Lip and Palate Research 7
- Genomics and Rare Diseases 7
- Craniofacial Disorders and Treatments 7
- Congenital Ear and Nasal Anomalies 6
- Co-authors
- Vaidutis Kučinskas (30 shared papers)Eglė Preikšaitienė (27 shared papers)Valentina Ginevičienė (6 shared papers)Birutė Burnytė (19 shared papers)Audronė Jakaitienė (7 shared papers)Laima Ambrozaitytė (20 shared papers)John M. Opitz (4 shared papers)Jurgita Songailienė (12 shared papers)
- Journals
- Genes (8 papers)Cytogenetic and Genome Research (4 papers)Orphanet Journal of Rare Diseases (3 papers)European Journal of Medical Genetics (2 papers)Journal of Cellular Biochemistry (2 papers)
- Partner nations
- LithuaniaUnited StatesUnited Kingdom
In The Last Decade
Algirdas Utkus
105 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 113
- Genetics 421
- Orthopedics and Sports Medicine 83
- Developmental Biology 22
- Drug Discovery 1
- Genetics 52
Countries citing papers authored by Algirdas Utkus
This map shows the geographic impact of Algirdas Utkus'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 Algirdas Utkus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Algirdas Utkus more than expected).
Fields of papers citing papers by Algirdas Utkus
This network shows the impact of papers produced by Algirdas Utkus. 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 Algirdas Utkus. The network helps show where Algirdas Utkus may publish in the future.
Co-authors
The 25 scholars most cited alongside Algirdas Utkus, 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 113 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 63 | |
| 2 | 2016 | 55 | |
| 3 | 2022 | 48 | |
| 4 | 2021 | 42 | |
| 5 | 2014 | 40 | |
| 6 | 2011 | 40 | |
| 7 | 2017 | 38 | |
| 8 | 2021 | 36 | |
| 9 | 2022 | 33 | |
| 10 | 2014 | 33 | |
| 11 | 2015 | 25 | |
| 12 | 2001 | 25 | |
| 13 | 2013 | 23 | |
| 14 | 2014 | 20 | |
| 15 | 2016 | 19 | |
| 16 | 2017 | 19 | |
| 17 | 2005 | 18 | |
| 18 | 2021 | 15 | |
| 19 | 2020 | 15 | |
| 20 | 2014 | 15 |
About Algirdas Utkus
Algirdas Utkus is a scholar working on Molecular Biology, Genetics, Genetics, Endocrinology, Diabetes and Metabolism and Pediatrics, Perinatology and Child Health, having authored 113 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Congenital heart defects research (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Cleft Lip and Palate Research (7 papers), Genomics and Rare Diseases (7 papers), Craniofacial Disorders and Treatments (7 papers), Congenital Ear and Nasal Anomalies (6 papers) and Mitochondrial Function and Pathology (6 papers). The work is most often cited by research in Genetics (421 citations), Orthopedics and Sports Medicine (83 citations), Developmental Biology (22 citations), Drug Discovery (1 citation) and Genetics (52 citations). Algirdas Utkus has collaborated with scholars based in Lithuania, United States and United Kingdom. Frequent co-authors include Vaidutis Kučinskas, Eglė Preikšaitienė, Valentina Ginevičienė, Birutė Burnytė, Audronė Jakaitienė, Laima Ambrozaitytė, John M. Opitz, Jurgita Songailienė, Erinija Pranckevičienė and Dalius Jatužis. Their work appears in journals such as Genes, Cytogenetic and Genome Research, Orphanet Journal of Rare Diseases, European Journal of Medical Genetics and Journal of Cellular Biochemistry.
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.