Karin Writzl
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Fetal and Pediatric Neurological Disorders
- Prenatal Screening and Diagnostics
Papers in
- Genetics 19
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genetics and Neurodevelopmental Disorders 4
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- Prenatal Screening and Diagnostics 5
- Co-authors
- Borut Peterlin (17 shared papers)Aleš Maver (11 shared papers)Raoul C. M. Hennekam (5 shared papers)Alida C. Knegt (1 shared paper)Christine M. Pierce (1 shared paper)Barbara Gnidovec Stražišar (2 shared papers)Catherine M. Cale (1 shared paper)Louise C. Wilson (1 shared paper)
- Journals
- PLoS ONE (3 papers)The American Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)Frontiers in Genetics (1 paper)Cell (1 paper)
- Partner nations
- SloveniaNetherlandsUnited Kingdom
In The Last Decade
Karin Writzl
43 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 75
- Genetics 435
- Pediatrics, Perinatology and Child Health 219
- Genetics 78
- Clinical Biochemistry 49
- Psychiatry and Mental health 101
Countries citing papers authored by Karin Writzl
This map shows the geographic impact of Karin Writzl'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 Karin Writzl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Writzl more than expected).
Fields of papers citing papers by Karin Writzl
This network shows the impact of papers produced by Karin Writzl. 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 Karin Writzl. The network helps show where Karin Writzl may publish in the future.
Co-authors
The 25 scholars most cited alongside Karin Writzl, 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 184 | |
| 2 | 2013 | 173 | |
| 3 | 2017 | 71 | |
| 4 | 2009 | 63 | |
| 5 | 2021 | 60 | |
| 6 | 2017 | 55 | |
| 7 | 2007 | 51 | |
| 8 | 2021 | 46 | |
| 9 | 2017 | 43 | |
| 10 | 2013 | 39 | |
| 11 | 2018 | 37 | |
| 12 | 2005 | 34 | |
| 13 | 2012 | 33 | |
| 14 | 2023 | 31 | |
| 15 | 2005 | 26 | |
| 16 | 2014 | 24 | |
| 17 | 2020 | 20 | |
| 18 | 2017 | 19 | |
| 19 | 2016 | 17 | |
| 20 | 2020 | 13 |
About Karin Writzl
Karin Writzl is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics, having authored 45 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (4 papers), Cardiomyopathy and Myosin Studies (4 papers) and Cancer Genomics and Diagnostics (3 papers). The work is most often cited by research in Genetics (435 citations), Pediatrics, Perinatology and Child Health (219 citations), Genetics (78 citations), Clinical Biochemistry (49 citations) and Psychiatry and Mental health (101 citations). Karin Writzl has collaborated with scholars based in Slovenia, Netherlands and United Kingdom. Frequent co-authors include Borut Peterlin, Aleš Maver, Raoul C. M. Hennekam, Alida C. Knegt, Christine M. Pierce, Barbara Gnidovec Stražišar, Catherine M. Cale, Louise C. Wilson, Branko Zorn and Vibhore Kumar. Their work appears in journals such as PLoS ONE, The American Journal of Human Genetics, Clinical Genetics, Frontiers in Genetics and Cell.
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.