Karin Writzl

1.5k total citations
33 papers, 466 citations indexed

About

Karin Writzl is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karin Writzl has authored 33 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karin Writzl's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Karin Writzl is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Karin Writzl collaborates with scholars based in Slovenia, Netherlands and United Kingdom. Karin Writzl's co-authors include Borut Peterlin, Aleš Maver, Raoul C. M. Hennekam, Alida C. Knegt, Branko Zorn, Catherine M. Cale, Barbara Gnidovec Stražišar, Christine M. Pierce, Louise C. Wilson and A. J. van Essen and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Karin Writzl

29 papers receiving 450 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Karin Writzl Slovenia 12 238 219 57 55 44 33 466
Morad Khayat Israel 16 162 0.7× 422 1.9× 38 0.7× 36 0.7× 29 0.7× 50 664
Flavio Faletra Italy 15 267 1.1× 251 1.1× 26 0.5× 32 0.6× 40 0.9× 84 649
Eveliina Jakkula Finland 10 283 1.2× 230 1.1× 64 1.1× 21 0.4× 26 0.6× 20 610
Vassos Neocleous Cyprus 15 261 1.1× 444 2.0× 15 0.3× 60 1.1× 38 0.9× 61 728
Pagon Ra United States 6 260 1.1× 450 2.1× 96 1.7× 70 1.3× 38 0.9× 291 791
Olaf Rittinger Austria 17 384 1.6× 433 2.0× 16 0.3× 74 1.3× 47 1.1× 40 785
Elisa Tassano Italy 15 272 1.1× 310 1.4× 14 0.2× 47 0.9× 47 1.1× 54 596
Ayse Bilge Ozel United States 14 131 0.6× 245 1.1× 53 0.9× 111 2.0× 17 0.4× 26 635
Deborah Morrogh United Kingdom 9 299 1.3× 247 1.1× 16 0.3× 26 0.5× 45 1.0× 13 542
Oscar F. Chacón‐Camacho Mexico 12 211 0.9× 348 1.6× 20 0.4× 46 0.8× 18 0.4× 62 533

Countries citing papers authored by Karin Writzl

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Karin Writzl

This figure shows the co-authorship network connecting the top 25 collaborators of Karin Writzl. A scholar is included among the top collaborators of Karin Writzl based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karin Writzl. Karin Writzl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Maver, Aleš, et al.. (2024). Clinical Outcome of Hypertrophic Cardiomyopathy in Probands with the Founder Variant c.913_914del in MYBPC3: A Slovenian Cohort Study. Journal of Cardiovascular Translational Research. 18(1). 110–120.
2.
Bertok, Sara, Karin Writzl, Luca Lovrečić, et al.. (2024). The Genetic Architecture of Congenital Heart Disease in Neonatal Intensive Care Unit Patients—The Experience of University Medical Centre, Ljubljana. Life. 14(9). 1118–1118. 1 indexed citations
3.
Writzl, Karin, et al.. (2024). Genetic background of high myopia in children. PLoS ONE. 19(11). e0313121–e0313121.
4.
5.
6.
Oblak, Janja Pretnar, et al.. (2021). Preceding Head Trauma in Four Cases of Sporadic Cerebral Amyloid Angiopathy – Case Report Series. Journal of Stroke and Cerebrovascular Diseases. 31(2). 106260–106260. 8 indexed citations
7.
Writzl, Karin, et al.. (2021). Improving diagnostics of rare genetic diseases with NGS approaches. Journal of Community Genetics. 12(2). 247–256. 42 indexed citations
8.
Maver, Aleš, et al.. (2018). Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss. PLoS ONE. 13(1). e0188578–e0188578. 32 indexed citations
9.
Writzl, Karin, Aleš Maver, Lidija Kovačič, et al.. (2017). De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise. The American Journal of Human Genetics. 101(5). 844–855. 51 indexed citations
10.
Stražišar, Barbara Gnidovec, et al.. (2014). Early-onset epileptic encephalopathy with hearing loss in two siblings with TBC1D24 recessive mutations. European Journal of Paediatric Neurology. 19(2). 251–256. 21 indexed citations
11.
Writzl, Karin & Alida C. Knegt. (2013). 6p21.3 microdeletion involving the SYNGAP1 gene in a patient with intellectual disability, seizures, and severe speech impairment. American Journal of Medical Genetics Part A. 161(7). 1682–1685. 33 indexed citations
12.
Writzl, Karin, Barbara Gnidovec Stražišar, Damjan Osredkar, et al.. (2012). Early onset West syndrome with severe hypomyelination and coloboma‐like optic discs in a girl with SPTAN1 mutation. Epilepsia. 53(6). e106–10. 28 indexed citations
13.
Geršak, Ksenija, et al.. (2010). Premature ovarian failure with FMR1 premutation, X chromosome mosaicism and blood lymphocyte microchimerism. Climacteric. 14(2). 289–293. 2 indexed citations
14.
Maas, Saskia M., Maria Lombardi, A. J. van Essen, et al.. (2009). Phenotype and genotype in 17 patients with Goltz–Gorlin syndrome. Journal of Medical Genetics. 46(10). 716–720. 53 indexed citations
15.
Writzl, Karin, Jera Jeruc, Michael Oldridge, Borut Peterlin, & Raoul C. M. Hennekam. (2008). Genital anomalies in a patient with Treacher Collins syndrome. American Journal of Medical Genetics Part A. 146A(16). 2169–2171. 3 indexed citations
16.
Writzl, Karin, Catherine M. Cale, Christine M. Pierce, Louise C. Wilson, & Raoul C. M. Hennekam. (2007). Immunological abnormalities in CHARGE syndrome. European Journal of Medical Genetics. 50(5). 338–345. 42 indexed citations
17.
Writzl, Karin, Branko Zorn, & Borut Peterlin. (2005). Preliminary analysis of AZFb region duplication by quantitative real-time PCR. Human Reproduction. 21(3). 753–754. 1 indexed citations
18.
Fermo, Elisa, Paola Bianchi, Laurent R. Chiarelli, et al.. (2005). Red cell pyruvate kinase deficiency: 17 new mutations of the PK‐LR gene. British Journal of Haematology. 129(6). 839–846. 29 indexed citations
19.
Writzl, Karin, Branko Zorn, & Borut Peterlin. (2005). Copy number of DAZ genes in infertile men. Fertility and Sterility. 84(5). 1522–1525. 26 indexed citations
20.
Writzl, Karin, et al.. (2004). Copy number of DAZ genes in Slovenian and Bosnian general population.. PubMed. 28 Suppl 2. 283–9. 5 indexed citations

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.

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