Marija Volk

575 total citations
36 papers, 378 citations indexed

About

Marija Volk is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marija Volk has authored 36 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marija Volk's work include Prenatal Screening and Diagnostics (9 papers), Retinal Development and Disorders (9 papers) and Retinal Diseases and Treatments (7 papers). Marija Volk is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Retinal Development and Disorders (9 papers) and Retinal Diseases and Treatments (7 papers). Marija Volk collaborates with scholars based in Slovenia, Croatia and Serbia. Marija Volk's co-authors include Borut Peterlin, Saša Ostojić, Miljenko Kapović, Nina Pereza, Luca Lovrečić, Aleš Maver, Branko Zorn, Marko Hawlina, Alenka Hodžić and Ana Fakin and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Marija Volk

35 papers receiving 374 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marija Volk Slovenia 14 155 115 86 76 69 36 378
Suzanne S. Fei United States 13 172 1.1× 55 0.5× 39 0.5× 70 0.9× 69 1.0× 31 412
Emmanouil Manolakos Greece 15 181 1.2× 342 3.0× 23 0.3× 312 4.1× 31 0.4× 70 642
Nathalie Baran France 7 239 1.5× 110 1.0× 109 1.3× 21 0.3× 67 1.0× 7 513
Alison Lashwood United Kingdom 10 141 0.9× 168 1.5× 18 0.2× 268 3.5× 52 0.8× 20 439
Juliette Gimenez Spain 12 286 1.8× 108 0.9× 49 0.6× 72 0.9× 15 0.2× 25 603
Mark A. Garthwaite United States 13 176 1.1× 111 1.0× 89 1.0× 28 0.4× 32 0.5× 15 395
Fabien Guimiot France 13 113 0.7× 125 1.1× 13 0.2× 189 2.5× 53 0.8× 37 475
Geeta Godbole India 10 137 0.9× 66 0.6× 372 4.3× 67 0.9× 100 1.4× 12 590
Alida C. Knegt Netherlands 14 271 1.7× 257 2.2× 64 0.7× 232 3.1× 120 1.7× 35 652
John S. Dallas United States 16 228 1.5× 136 1.2× 135 1.6× 48 0.6× 19 0.3× 28 757

Countries citing papers authored by Marija Volk

Since Specialization
Citations

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

Fields of papers citing papers by Marija Volk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marija Volk

This figure shows the co-authorship network connecting the top 25 collaborators of Marija Volk. A scholar is included among the top collaborators of Marija Volk 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 Marija Volk. Marija Volk 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.
Meglič, Andrej, Marija Volk, Aleš Maver, et al.. (2023). Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the WDR19 Gene. Genes. 14(2). 291–291.
2.
Volk, Marija, et al.. (2023). Oxidative Stress in Antibiotic Toxic Optic Neuropathy Mimicking Acute LHON in a Patient with Exacerbation of Cystic Fibrosis. SHILAP Revista de lepidopterología. 3(1). 387–396. 2 indexed citations
3.
Brecelj, Jelka, Ana Fakin, Marija Volk, et al.. (2023). Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel Variant. Journal of Neuro-Ophthalmology. 43(3). 341–347. 1 indexed citations
4.
Jarc-Vidmar, Martina, Ana Fakin, Jelka Brecelj, et al.. (2022). Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G>A pathogenic variant-case series. Frontiers in Neurology. 13. 1003046–1003046. 4 indexed citations
5.
Pompe, Manca Tekavčič, Marija Volk, Andrej Meglič, et al.. (2021). Disease Progression in CNGA3 and CNGB3 Retinopathy; Characteristics of Slovenian Cohort and Proposed OCT Staging Based on Pooled Data from 126 Patients from 7 Studies. Current Issues in Molecular Biology. 43(2). 941–957. 5 indexed citations
6.
Volk, Marija, Aleš Maver, Alenka Hodžić, Luca Lovrečić, & Borut Peterlin. (2017). Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21. OMICS A Journal of Integrative Biology. 21(10). 565–570. 8 indexed citations
7.
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
8.
Maver, Aleš, et al.. (2016). Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation. Genetics in Medicine. 18(11). 1102–1110. 33 indexed citations
9.
Pereza, Nina, Borut Peterlin, Marija Volk, Miljenko Kapović, & Saša Ostojić. (2015). A critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: genetic association study, systematic review and meta-analyses. Molecular Human Reproduction. 21(5). 466–478. 14 indexed citations
10.
11.
Pereza, Nina, et al.. (2013). Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion. Fertility and Sterility. 99(7). 1923–1929. 7 indexed citations
12.
Volk, Marija, Aleš Maver, Luca Lovrečić, Peter Juvan, & Borut Peterlin. (2013). Expression Signature as a Biomarker for Prenatal Diagnosis of Trisomy 21. PLoS ONE. 8(9). e74184–e74184. 15 indexed citations
13.
Pereza, Nina, Alena Buretić‐Tomljanović, Marija Volk, et al.. (2013). Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review. Fertility and Sterility. 99(6). 1663–1667. 9 indexed citations
14.
Pereza, Nina, Saša Ostojić, Marija Volk, Miljenko Kapović, & Borut Peterlin. (2012). Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion. Reproductive BioMedicine Online. 24(5). 567–575. 36 indexed citations
15.
Pereza, Nina, Saša Ostojić, Marija Volk, et al.. (2012). Third case of 8q23.3‐q24.13 deletion in a patient with Langer–Giedion syndrome phenotype without TRPS1 gene deletion. American Journal of Medical Genetics Part A. 158A(3). 659–663. 15 indexed citations
16.
Madjunkova, Svetlana, Marija Volk, Borut Peterlin, & Dijana Plaseska‐Karanfilska. (2011). Detection of Thrombophilic Mutations Related to Spontaneous Abortions by a Multiplex SNaPshot Method. Genetic Testing and Molecular Biomarkers. 16(4). 259–264. 13 indexed citations
17.
Volk, Marija, et al.. (2011). Association between male infertility and genetic variability at the PON1/2 and GSTM1/T1 gene loci. Reproductive BioMedicine Online. 23(1). 105–110. 25 indexed citations
18.
Ostojić, Saša, Nina Pereza, Marija Volk, Miljenko Kapović, & Borut Peterlin. (2008). ORIGINAL ARTICLE: Genetic Predisposition to Idiopathic Recurrent Spontaneous Abortion: Contribution of Genetic Variations in IGF‐2 and H19 Imprinted Genes. American Journal of Reproductive Immunology. 60(2). 111–117. 21 indexed citations
19.
Medica, Igor, et al.. (2006). Patients with primary cataract as a genetic pool of DMPK protomutation. Journal of Human Genetics. 52(2). 123–128. 10 indexed citations
20.
Šinkovec, Matjaž, Dejan Petrović, Marija Volk, & Borut Peterlin. (2005). Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart‐hand syndrome?. Clinical Genetics. 68(2). 155–160. 13 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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