Borut Peterlin
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 96
- Genomics and Rare Diseases 32
- Genomic variations and chromosomal abnormalities 16
- BRCA gene mutations in cancer 16
- Genetics and Neurodevelopmental Disorders 16
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- Mitochondrial Function and Pathology 16
- Co-authors
- Aleš Maver (84 shared papers)Dimitar Hristovski (15 shared papers)Daniel Petrovič (33 shared papers)Miljenko Kapović (39 shared papers)Igor Medica (25 shared papers)Luca Lovrečić (44 shared papers)Mojca Globočnik Petrovič (13 shared papers)Saša Ostojić (27 shared papers)
In The Last Decade
Borut Peterlin
315 papers receiving 6.5k citations
Borut Peterlin's Hit Papers
Peers
Comparison fields: 5 of 167
- Genetics 1.5k
- Pediatrics, Perinatology and Child Health 685
- Reproductive Medicine 277
- Molecular Biology 2.4k
- Biological Psychiatry 69
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 331 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 406 |
| 2 | Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening Hit paper breakdown → | 2015 | 277 |
| 3 | 2016 | 248 | |
| 4 | 2004 | 209 | |
| 5 | Exploiting semantic relations for literature-based discovery. | 2006 | 135 |
| 6 | 2016 | 123 | |
| 7 | 2008 | 115 | |
| 8 | 2017 | 109 | |
| 9 | 2014 | 107 | |
| 10 | 2018 | 106 | |
| 11 | Supporting discovery in medicine by association rule mining in Medline and UMLS. | 2001 | 99 |
| 12 | 2013 | 93 | |
| 13 | 2005 | 92 | |
| 14 | 2002 | 84 | |
| 15 | 2018 | 81 | |
| 16 | 2019 | 74 | |
| 17 | 2015 | 73 | |
| 18 | 2019 | 65 | |
| 19 | Local and genetic determinants of vascular endothelial growth factor expression in advanced proliferative diabetic retinopathy. | 2008 | 65 |
| 20 | 2006 | 63 |
About Borut Peterlin
Borut Peterlin is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Hematology, having authored 331 papers that have together received 6.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (32 papers), Genetic Neurodegenerative Diseases (20 papers), Prenatal Screening and Diagnostics (18 papers), Multiple Sclerosis Research Studies (17 papers), Mitochondrial Function and Pathology (16 papers), Genomic variations and chromosomal abnormalities (16 papers), BRCA gene mutations in cancer (16 papers) and Genetics and Neurodevelopmental Disorders (16 papers). The work is most often cited by research in Genetics (1.5k citations), Pediatrics, Perinatology and Child Health (685 citations), Reproductive Medicine (277 citations), Molecular Biology (2.4k citations) and Biological Psychiatry (69 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, Marija Volk and Nina Pereza. Their work appears in journals such as PLoS ONE, Clinical Genetics, European Journal of Human 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.