Sara Bertok

582 total citations
35 papers, 354 citations indexed

About

Sara Bertok is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Sara Bertok has authored 35 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Surgery. Recurrent topics in Sara Bertok's work include Metabolism and Genetic Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Congenital Ear and Nasal Anomalies (3 papers). Sara Bertok is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Congenital Ear and Nasal Anomalies (3 papers). Sara Bertok collaborates with scholars based in Slovenia, Italy and Slovakia. Sara Bertok's co-authors include Tadej Battelino, Katarina Trebušak Podkrajšek, Antonio Amoroso, Mojca Žerjav Tanšek, Jernej Kovač, Urh Grošelj, Primož Kotnik, Luca Lovrečić, Magdalena Avbelj Stefanija and Barbka Repič Lampret and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Nephrology Dialysis Transplantation.

In The Last Decade

Sara Bertok

35 papers receiving 345 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sara Bertok Slovenia	10	166	122	85	54	42	35	354
Dina Marek‐Yagel Israel	12	358 2.2×	78 0.6×	39 0.5×	122 2.3×	63 1.5×	26	507
Erwin Lankes Germany	11	158 1.0×	74 0.6×	29 0.3×	31 0.6×	72 1.7×	20	342
Jennifer Lee United States	8	95 0.6×	94 0.8×	27 0.3×	14 0.3×	23 0.5×	11	319
Ilham Ratbi Morocco	15	332 2.0×	162 1.3×	26 0.3×	27 0.5×	65 1.5×	45	617
Chiyoko N. Inoue Japan	12	292 1.8×	45 0.4×	73 0.9×	35 0.6×	55 1.3×	24	426
Kei Fukuda Japan	14	388 2.3×	104 0.9×	22 0.3×	30 0.6×	14 0.3×	27	552
Shixin Tao United States	14	256 1.5×	139 1.1×	63 0.7×	38 0.7×	8 0.2×	20	450
Shoichiro Kanda Japan	13	267 1.6×	56 0.5×	165 1.9×	41 0.8×	5 0.1×	36	442
Artemis Doulgeraki Greece	12	145 0.9×	89 0.7×	14 0.2×	8 0.1×	44 1.0×	33	358
Gianna Costa Italy	13	168 1.0×	129 1.1×	16 0.2×	159 2.9×	17 0.4×	24	505

Countries citing papers authored by Sara Bertok

Since Specialization

Citations

This map shows the geographic impact of Sara Bertok'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 Sara Bertok with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sara Bertok more than expected).

Fields of papers citing papers by Sara Bertok

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sara Bertok. 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 Sara Bertok. The network helps show where Sara Bertok may publish in the future.

Co-authorship network of co-authors of Sara Bertok

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Bertok. A scholar is included among the top collaborators of Sara Bertok 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 Sara Bertok. Sara Bertok is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

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

Stražišar, Barbara Gnidovec, Matjaž Homan, Sara Bertok, et al.. (2024). VIPAS39 related arthrogryposis-renal dysfunction-cholestasis syndrome—case report and systematic review. Orphanet Journal of Rare Diseases. 19(1). 496–496. 1 indexed citations

Dolžan, Vita, Mojca Žerjav Tanšek, Andrea Pastorakova, et al.. (2023). Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Frontiers in Endocrinology. 14. 1134133–1134133. 5 indexed citations

Bertok, Sara, et al.. (2023). Challenges in establishing optimal pediatric palliative care at the university hospital in Slovenia. European Journal of Pediatrics. 182(3). 1393–1401. 3 indexed citations

Urlep, Darja, Mojca Žerjav Tanšek, Sara Bertok, et al.. (2023). Non-alcoholic fatty liver disease in a pediatric patient with heterozygous familial hypobetalipoproteinemia due to a novel APOB variant: a case report and systematic literature review. Frontiers in Medicine. 10. 1106441–1106441. 3 indexed citations

Šikonja, Jaka, Matej Mlinarič, Sara Bertok, et al.. (2023). Clinical and genetic characteristics of a patient with phosphoribosyl pyrophosphate synthetase 1 deficiency and a systematic literature review. Molecular Genetics and Metabolism Reports. 36. 100986–100986. 1 indexed citations

Homan, Matjaž, Maruša Debeljak, Mojca Žerjav Tanšek, et al.. (2022). Compound Heterozygote Mutation in the SMPD1 Gene Leading to Nieman-Pick Disease Type A. American Journal of Case Reports. 23. e937220–e937220. 3 indexed citations

Bertok, Sara, et al.. (2021). A novel mutation of congenital nephrotic syndrome in a Slovenian child eventually receiving a renal transplant. Croatian Medical Journal. 62(2). 187–191. 1 indexed citations

Šikonja, Jaka, Jernej Brecelj, Mojca Žerjav Tanšek, et al.. (2021). Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia – A novel fumarylacetoacetate hydrolase (FAH) intronic disease-causing variant. Molecular Genetics and Metabolism Reports. 30. 100836–100836. 2 indexed citations

10.

Stefanija, Magdalena Avbelj, Sara Bertok, Katarina Trebušak Podkrajšek, et al.. (2021). Novel Insights Into Monogenic Obesity Syndrome Due to INPP5E Gene Variant: A Case Report of a Female Patient. Frontiers in Endocrinology. 12. 581134–581134. 7 indexed citations

11.

Lovrečić, Luca, Marija Volk, Sara Bertok, et al.. (2018). Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotyping. Journal of Applied Genetics. 59(2). 179–185. 13 indexed citations

12.

Bertok, Sara, Vita Dolžan, Katja Goričar, et al.. (2017). The association of SCN1A p.Thr1067Ala polymorphism with epilepsy risk and the response to antiepileptic drugs in Slovenian children and adolescents with epilepsy. Seizure. 51. 9–13. 12 indexed citations

13.

Lampret, Barbka Repič, Urh Grošelj, Mojca Žerjav Tanšek, et al.. (2017). Next generation sequencing as a follow-up test in an expanded newborn screening programme. Clinical Biochemistry. 52. 48–55. 48 indexed citations

14.

Bertok, Sara, Jernej Kovač, Marija Volk, et al.. (2017). Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic features. Molecular Cytogenetics. 10(1). 10–10. 4 indexed citations

15.

Cini, Giulia, Massimo Mezzavilla, Lara Della Puppa, et al.. (2016). Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy. BMC Medical Genetics. 17(1). 11–11. 11 indexed citations

16.

Lovrečić, Luca, Sara Bertok, & Mojca Žerjav Tanšek. (2016). A New Case of an Extremely Rare 3p21.31 Interstitial Deletion. Molecular Syndromology. 7(2). 93–98. 5 indexed citations

17.

Podkrajšek, Katarina Trebušak, et al.. (2014). Painful micturition in a small child: an unusual clinical picture of paroxysmal extreme pain disorder. Pediatric Nephrology. 29(9). 1643–1646. 11 indexed citations

18.

Bisceglia, Luigi, Giuseppina Cerullo, Paola Forabosco, et al.. (2006). Genetic Heterogeneity in Italian Families with IgA Nephropathy: Suggestive Linkage for Two Novel IgA Nephropathy Loci. The American Journal of Human Genetics. 79(6). 1130–1134. 81 indexed citations

19.

Biolo, Gianni, Antonio Amoroso, Silvana Savoldi, et al.. (2006). Association of interferon-γ +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients. Nephrology Dialysis Transplantation. 21(5). 1317–1322. 28 indexed citations

20.

Miertuš, Ján, Wiktor Borozdin, Vladimı́r Frecer, et al.. (2006). A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndrome. Human Genetics. 119(1-2). 154–161. 28 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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