Vladimir Sarnavka
- Molecular Biology
- Rheumatology top 5%
- Clinical Biochemistry top 2%
- Physiology
- Pediatrics, Perinatology and Child Health
- Co-authors
- Ksenija FumićIvo BarićS. Harvey MuddOliver VugrekIgor P. PogribnyAndreas SchulzeLeo PažaninConrad Wagner
- Topics
- Metabolism and Genetic Disorders (11 papers)Folate and B Vitamins Research (7 papers)Amino Acid Enzymes and Metabolism (3 papers)
- Journals
- Proceedings of the National Academy of SciencesHuman MutationEuropean Journal of Human Genetics
- Partner nations
- CroatiaUnited StatesGermany
In The Last Decade
Vladimir Sarnavka
24 papers receiving 429 citations
Peers
Comparison fields: 5 of 65
- Molecular Biology 272
- Rheumatology 186
- Clinical Biochemistry 179
- Physiology 52
- Pediatrics, Perinatology and Child Health 48
Countries citing papers authored by Vladimir Sarnavka
This map shows the geographic impact of Vladimir Sarnavka'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 Vladimir Sarnavka with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vladimir Sarnavka more than expected).
Fields of papers citing papers by Vladimir Sarnavka
This network shows the impact of papers produced by Vladimir Sarnavka. 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 Vladimir Sarnavka. The network helps show where Vladimir Sarnavka may publish in the future.
Co-authorship network of co-authors of Vladimir Sarnavka
This figure shows the co-authorship network connecting the top 25 collaborators of Vladimir Sarnavka. A scholar is included among the top collaborators of Vladimir Sarnavka based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Vladimir Sarnavka. Vladimir Sarnavka is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 9 | |
| 2 | New symptomatic patients with glutaric aciduria type 3: further evidence of high prevalence of the c.1006C>T (p.Arg336Trp) mutation | 3 |
| 3 | 0 | |
| 4 | Pallister Killian syndrome: unusual significant postnatal overgrowth in a girl with otherwise typical presentation. | 8 |
| 5 | Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene. | 4 |
| 6 | 58 | |
| 7 | 12 | |
| 8 | Mitochondriopathy presenting with immune disorder | 1 |
| 9 | The fourth S-adenosylhomocysteine hydrolase deficient patient : Further evidence of congenital miopathy | 8 |
| 10 | 15 | |
| 11 | Rezultati metaboličkog probira u Hrvatskoj | 1 |
| 12 | S-Adenosylhomocysteine (AdoHcy) hydrolase deficiency: myopathy seems to be congenital | 1 |
| 13 | 162 | |
| 14 | [Glutaric aciduria type 1: an example of the importance of early detection of so-called cerebral organic aciduria]. | 3 |
| 15 | 17 | |
| 16 | 1 | |
| 17 | 4 | |
| 18 | 11 | |
| 19 | 22 | |
| 20 | 11 |
About Vladimir Sarnavka
Vladimir Sarnavka is a scholar working on Clinical Biochemistry, Rheumatology and Biochemistry, having authored 25 papers that have together received 445 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (11 papers), Folate and B Vitamins Research (7 papers) and Amino Acid Enzymes and Metabolism (3 papers). The work is most often cited by research in Clinical Biochemistry (179 citations), Rheumatology (186 citations) and Biochemistry (41 citations). Vladimir Sarnavka has collaborated with scholars based in Croatia, United States and Germany. Frequent co-authors include Ksenija Fumić, Ivo Barić, S. Harvey Mudd, Oliver Vugrek, Igor P. Pogribny, Andreas Schulze, Leo Pažanin, Conrad Wagner, Sally P. Stabler and Robert H. Allen. Their work appears in journals such as Proceedings of the National Academy of Sciences, Human Mutation 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.