Algirdas Utkus
Impact in
- Genetics top 5%
- Genetics and Physical Performance
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cleft Lip and Palate Research
-
- Sports Performance and Training
Papers in
- Genetics 51
- Genomic variations and chromosomal abnormalities 21
- Genomics and Rare Diseases 14
- Genetics and Neurodevelopmental Disorders 14
- Craniofacial Disorders and Treatments 7
- Cleft Lip and Palate Research 7
- Genetics and Physical Performance 6
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- Congenital heart defects research 9
- Mitochondrial Function and Pathology 6
- Co-authors
- Vaidutis Kučinskas (31 shared papers)Eglė Preikšaitienė (28 shared papers)Valentina Ginevičienė (6 shared papers)Birutė Burnytė (19 shared papers)Audronė Jakaitienė (8 shared papers)Laima Ambrozaitytė (20 shared papers)John M. Opitz (4 shared papers)Jurgita Songailienė (11 shared papers)
- Journals
- Genes (8 papers)Cytogenetic and Genome Research (4 papers)Orphanet Journal of Rare Diseases (3 papers)European Journal of Medical Genetics (3 papers)Nutrients (2 papers)
- Partner nations
- LithuaniaUnited StatesUnited Kingdom
In The Last Decade
Algirdas Utkus
115 papers receiving 1.5k citations
Algirdas Utkus's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 580
- Orthopedics and Sports Medicine 88
- Developmental Biology 23
- Clinical Biochemistry 45
- Genetics 69
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 124 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Hit paper breakdown → | 2023 | 124 |
| 2 | 2006 | 72 | |
| 3 | 2016 | 61 | |
| 4 | 2020 | 56 | |
| 5 | 2022 | 51 | |
| 6 | 2014 | 47 | |
| 7 | 2021 | 45 | |
| 8 | 2011 | 42 | |
| 9 | 2021 | 42 | |
| 10 | 2021 | 41 | |
| 11 | 2022 | 40 | |
| 12 | 2017 | 39 | |
| 13 | 2014 | 36 | |
| 14 | 2019 | 35 | |
| 15 | 2020 | 33 | |
| 16 | 2023 | 32 | |
| 17 | 2024 | 30 | |
| 18 | 2015 | 28 | |
| 19 | 2001 | 28 | |
| 20 | 2013 | 25 |
About Algirdas Utkus
Algirdas Utkus is a scholar working on Genetics, Molecular Biology, Genetics, Developmental Biology and Endocrinology, Diabetes and Metabolism, having authored 124 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genomics and Rare Diseases (14 papers), Genetics and Neurodevelopmental Disorders (14 papers), Congenital heart defects research (9 papers), Craniofacial Disorders and Treatments (7 papers), Cleft Lip and Palate Research (7 papers), Mitochondrial Function and Pathology (6 papers) and Genetics and Physical Performance (6 papers). The work is most often cited by research in Genetics (580 citations), Orthopedics and Sports Medicine (88 citations), Developmental Biology (23 citations), Clinical Biochemistry (45 citations) and Genetics (69 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 Biruté Tumiene. Their work appears in journals such as Genes, Cytogenetic and Genome Research, Orphanet Journal of Rare Diseases, European Journal of Medical Genetics and Nutrients.
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.