Karin Writzl
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and rare skin diseases.
- Sensory Systems top 10%
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
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- Congenital heart defects research 4
- Connexins and lens biology 2
- Co-authors
- Borut Peterlin (16 shared papers)Aleš Maver (9 shared papers)Raoul C. M. Hennekam (5 shared papers)Alida C. Knegt (1 shared paper)Branko Zorn (2 shared papers)Barbara Gnidovec Stražišar (2 shared papers)Christine M. Pierce (1 shared paper)Louise C. Wilson (1 shared paper)
- Journals
- PLoS ONE (3 papers)Clinical Genetics (2 papers)British Journal of Haematology (1 paper)European Journal of Medical Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- SloveniaNetherlandsUnited Kingdom
In The Last Decade
Karin Writzl
29 papers receiving 450 citations
Peers
Comparison fields: 5 of 65
- Genetics 238
- Sensory Systems 27
- Genetics 55
- Clinical Biochemistry 22
- Otorhinolaryngology 14
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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 53 | |
| 2 | 2017 | 51 | |
| 3 | 2021 | 42 | |
| 4 | 2007 | 42 | |
| 5 | 2017 | 34 | |
| 6 | 2013 | 33 | |
| 7 | 2018 | 32 | |
| 8 | 2005 | 29 | |
| 9 | 2012 | 28 | |
| 10 | 2005 | 26 | |
| 11 | 2014 | 21 | |
| 12 | 2016 | 15 | |
| 13 | 2021 | 8 | |
| 14 | 2016 | 8 | |
| 15 | 2009 | 7 | |
| 16 | 2016 | 7 | |
| 17 | Copy number of DAZ genes in Slovenian and Bosnian general population. | 2004 | 5 |
| 18 | 2023 | 4 | |
| 19 | 2023 | 4 | |
| 20 | 2008 | 3 |
About Karin Writzl
Karin Writzl is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cardiology and Cardiovascular Medicine and Surgery, having authored 33 papers that have together received 466 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Cardiomyopathy and Myosin Studies (3 papers) and Connexins and lens biology (2 papers). The work is most often cited by research in Genetics (238 citations), Sensory Systems (27 citations), Genetics (55 citations), Clinical Biochemistry (22 citations) and Otorhinolaryngology (14 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, Branko Zorn, Barbara Gnidovec Stražišar, Christine M. Pierce, Louise C. Wilson, Catherine M. Cale and B. Castle. Their work appears in journals such as PLoS ONE, Clinical Genetics, British Journal of Haematology, European Journal of Medical Genetics and Journal of Medical 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.