Borut Peterlin
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Reproductive Medicine top 2%
Papers in
-
- Mitochondrial Function and Pathology 15
- Genetics 87
- Genomics and Rare Diseases 28
- Genomic variations and chromosomal abnormalities 16
- Genetics and Neurodevelopmental Disorders 16
- BRCA gene mutations in cancer 14
- Co-authors
- Aleš Maver (82 shared papers)Dimitar Hristovski (12 shared papers)Daniel Petrovič (32 shared papers)Miljenko Kapović (36 shared papers)Igor Medica (24 shared papers)Luca Lovrečić (43 shared papers)Saša Ostojić (28 shared papers)Mojca Globočnik Petrovič (12 shared papers)
In The Last Decade
Borut Peterlin
281 papers receiving 4.7k citations
Peers
Comparison fields: 5 of 152
- Genetics 1000
- Reproductive Medicine 220
- Biological Psychiatry 57
- Molecular Biology 1.7k
- Obstetrics and Gynecology 167
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-authors
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
Showing the 20 most-cited of 304 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 215 | |
| 2 | 2004 | 175 | |
| 3 | Exploiting semantic relations for literature-based discovery. | 2006 | 116 |
| 4 | 2016 | 113 | |
| 5 | 2008 | 95 | |
| 6 | 2014 | 89 | |
| 7 | Supporting discovery in medicine by association rule mining in Medline and UMLS. | 2001 | 89 |
| 8 | 2005 | 82 | |
| 9 | 2002 | 81 | |
| 10 | 2013 | 71 | |
| 11 | 2018 | 70 | |
| 12 | 2019 | 69 | |
| 13 | 2006 | 62 | |
| 14 | Local and genetic determinants of vascular endothelial growth factor expression in advanced proliferative diabetic retinopathy. | 2008 | 61 |
| 15 | 2004 | 57 | |
| 16 | 2015 | 56 | |
| 17 | 2017 | 54 | |
| 18 | 2007 | 51 | |
| 19 | 2017 | 51 | |
| 20 | 2017 | 49 |
About Borut Peterlin
Borut Peterlin is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience, having authored 304 papers that have together received 4.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (28 papers), Genetic Neurodegenerative Diseases (18 papers), Genomic variations and chromosomal abnormalities (16 papers), Multiple Sclerosis Research Studies (16 papers), Genetics and Neurodevelopmental Disorders (16 papers), Mitochondrial Function and Pathology (15 papers), Prenatal Screening and Diagnostics (15 papers) and BRCA gene mutations in cancer (14 papers). The work is most often cited by research in Genetics (1000 citations), Reproductive Medicine (220 citations), Biological Psychiatry (57 citations), Molecular Biology (1.7k citations) and Obstetrics and Gynecology (167 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, Saša Ostojić, Mojca Globočnik Petrovič, Nina Pereza and Marija Volk. Their work appears in journals such as PLoS ONE, Fertility and Sterility, Clinical Genetics, Genes and Pflügers Archiv - European Journal of Physiology.
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.