Borut Peterlin
- Genetics top 1%
- Genomics and Rare Diseases 33
- Genomic variations and chromosomal abnormalities 19
- BRCA gene mutations in cancer 17
- Genetics and Neurodevelopmental Disorders 16
- Reproductive Medicine top 2%
- Obstetrics and Gynecology top 2%
- Molecular Biology top 5%
- Biological Psychiatry top 5%
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- Prenatal Screening and Diagnostics 20
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- Multiple Sclerosis Research Studies 18
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- Genetic Neurodegenerative Diseases 18
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- Reproductive System and Pregnancy 16
Borut Peterlin
281 papers receiving 4.6k citations
Peers
Comparison fields: 5 of 155
- Genetics 1.2k
- Reproductive Medicine 311
- Obstetrics and Gynecology 243
- Molecular Biology 2.1k
- Biological Psychiatry 64
Countries citing papers authored by Borut Peterlin
This map shows the geographic impact of Borut Peterlin'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 Borut Peterlin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Borut Peterlin more than expected).
Fields of papers citing papers by Borut Peterlin
This network shows the impact of papers produced by Borut Peterlin. 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 Borut Peterlin. The network helps show where Borut Peterlin may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Borut Peterlin, 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 | 2025 | 0 | |
| 2 | 2024 | 0 | |
| 3 | 2024 | 0 | |
| 4 | 2024 | 2 | |
| 5 | 2023 | 9 | |
| 6 | 2022 | 12 | |
| 7 | 2021 | 5 | |
| 8 | 2021 | 10 | |
| 9 | 2021 | 2 | |
| 10 | 2020 | 28 | |
| 11 | 2019 | 17 | |
| 12 | 2018 | 68 | |
| 13 | 2018 | 23 | |
| 14 | 2013 | 7 | |
| 15 | Implementation of molecular karyotyping in clinical genetics | 2013 | 1 |
| 16 | The role of chitotriosidase duplication gene polymorphism in the susceptibility to sarcoidosis | 2010 | 4 |
| 17 | Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina. | 2006 | 5 |
| 18 | 2004 | 9 | |
| 19 | Copy number of DAZ genes in Slovenian and Bosnian general population. | 2004 | 5 |
| 20 | 2001 | 28 |
About Borut Peterlin
Borut Peterlin is a scholar working on Genetics, Reproductive Medicine and Hematology, having authored 302 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (33 papers), Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (19 papers), Multiple Sclerosis Research Studies (18 papers), Genetic Neurodegenerative Diseases (18 papers), BRCA gene mutations in cancer (17 papers), Reproductive System and Pregnancy (16 papers) and Genetics and Neurodevelopmental Disorders (16 papers). The work is most often cited by research in Genetics (1.2k citations), Reproductive Medicine (311 citations) and Obstetrics and Gynecology (243 citations). Borut Peterlin has collaborated with scholars based in Slovenia, Croatia and Serbia. Frequent co-authors include Aleš Maver, Dimitar Hristovski, Daniel Petrovič, Miljenko Kapović, Igor Medica, Luca Lovrečić, Mojca Globočnik Petrovič, Saša Ostojić, Nina Pereza and Marija Volk. Their work appears in journals such as PLoS ONE, Fertility and Sterility, Pflügers Archiv - European Journal of Physiology, Clinical Genetics 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.