Goranka Tanačković
Impact in
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- Neurogenetic and Muscular Disorders Research
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- RNA Research and Splicing
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- Retinal Development and Disorders
- RNA regulation and disease
- CRISPR and Genetic Engineering
Papers in
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- RNA modifications and cancer 5
- RNA Research and Splicing 5
- RNA regulation and disease 4
- Retinal Development and Disorders 2
- RNA and protein synthesis mechanisms 2
- Co-authors
- Angela Krämer (3 shared papers)Carlo Rivolta (4 shared papers)Adriana Ransijn (4 shared papers)Eliot L. Berson (3 shared papers)Dobrila Nešić (1 shared paper)Shyana Harper (1 shared paper)Carmen Ayuso (1 shared paper)Sherif Abou Elela (2 shared papers)
- Journals
- Human Molecular Genetics (1 paper)The American Journal of Human Genetics (1 paper)Journal of Thrombosis and Thrombolysis (1 paper)Molecular Biology of the Cell (1 paper)BMJ Open (1 paper)
- Partner nations
- SwitzerlandUnited StatesAustralia
In The Last Decade
Goranka Tanačković
16 papers receiving 523 citations
Peers
Comparison fields: 5 of 62
- Genetics 63
- Molecular Biology 435
- Aging 9
- Internal Medicine 10
- Ophthalmology 25
Countries citing papers authored by Goranka Tanačković
This map shows the geographic impact of Goranka Tanačković'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 Goranka Tanačković with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Goranka Tanačković more than expected).
Fields of papers citing papers by Goranka Tanačković
This network shows the impact of papers produced by Goranka Tanačković. 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 Goranka Tanačković. The network helps show where Goranka Tanačković may publish in the future.
Co-authors
The 25 scholars most cited alongside Goranka Tanačković, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 110 | |
| 2 | 2011 | 103 | |
| 3 | 2011 | 98 | |
| 4 | 2004 | 74 | |
| 5 | 2010 | 48 | |
| 6 | 2017 | 27 | |
| 7 | 2005 | 20 | |
| 8 | 2012 | 17 | |
| 9 | 2009 | 13 | |
| 10 | 2023 | 6 | |
| 11 | 2017 | 5 | |
| 12 | 2019 | 3 | |
| 13 | Two cases of alleles with complex genotypes among cystic fibrosis patients from Croatia | 2002 | 2 |
| 14 | 2007 | 1 | |
| 15 | Generalized Defects In Spliceosome Composition And Pre-mRNA Splicing Are Associated With Retinitis Pigmentosa In Humans | 2011 | 1 |
| 16 | 2016 | 1 |
About Goranka Tanačković
Goranka Tanačković is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine, Public Health, Environmental and Occupational Health and Genetics, having authored 16 papers that have together received 529 indexed citations. Recurring topics across this work include RNA modifications and cancer (5 papers), RNA Research and Splicing (5 papers), RNA regulation and disease (4 papers), Cystic Fibrosis Research Advances (2 papers), Retinal Development and Disorders (2 papers), RNA and protein synthesis mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (1 paper) and Venous Thromboembolism Diagnosis and Management (1 paper). The work is most often cited by research in Genetics (63 citations), Molecular Biology (435 citations), Aging (9 citations), Internal Medicine (10 citations) and Ophthalmology (25 citations). Goranka Tanačković has collaborated with scholars based in Switzerland, United States and Australia. Frequent co-authors include Angela Krämer, Carlo Rivolta, Adriana Ransijn, Eliot L. Berson, Dobrila Nešić, Shyana Harper, Carmen Ayuso, Sherif Abou Elela, Philippe Thibault and Roscoe Klinck. Their work appears in journals such as Human Molecular Genetics, The American Journal of Human Genetics, Journal of Thrombosis and Thrombolysis, Molecular Biology of the Cell and BMJ Open.
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.