Goražd Rudolf

1.1k total citations · 1 hit paper
23 papers, 598 citations indexed

About

Goražd Rudolf is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Goražd Rudolf has authored 23 papers receiving a total of 598 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Goražd Rudolf's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Multiple Sclerosis Research Studies (3 papers). Goražd Rudolf is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Multiple Sclerosis Research Studies (3 papers). Goražd Rudolf collaborates with scholars based in Slovenia, Croatia and Serbia. Goražd Rudolf's co-authors include Debra Kennedy, Ingunn Björnsdóttir, Katri Hämeen‐Anttila, Hedvig Nordeng, Mariola Drozd, Angela Lupattelli, Myla E. Moretti, Ksenia Zagorodnikova, Alice Panchaud and Anneke Passier and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Goražd Rudolf

19 papers receiving 581 citations

Hit Papers

Medication use in pregnancy: a cross-sectional, multinati... 2014 2026 2018 2022 2014 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Goražd Rudolf Slovenia 10 351 184 138 78 60 23 598
Andrea Gallinelli Italy 17 239 0.7× 269 1.5× 101 0.7× 87 1.1× 122 2.0× 29 728
Henry Bohler United States 13 190 0.5× 108 0.6× 111 0.8× 75 1.0× 71 1.2× 22 608
Agnieszka Podfigurna-Stopa Poland 17 363 1.0× 79 0.4× 45 0.3× 123 1.6× 46 0.8× 34 891
Rosita Gallo Italy 10 107 0.3× 76 0.4× 116 0.8× 146 1.9× 55 0.9× 12 590
R. J. Woods United Kingdom 12 72 0.2× 162 0.9× 151 1.1× 81 1.0× 92 1.5× 17 645
Eng‐Cheng Chan Australia 14 129 0.4× 146 0.8× 76 0.6× 163 2.1× 90 1.5× 24 565
Krzysztof Katulski Poland 11 266 0.8× 50 0.3× 33 0.2× 108 1.4× 30 0.5× 32 656
Laura Toso United States 15 111 0.3× 283 1.5× 115 0.8× 64 0.8× 13 0.2× 28 479
Helmut Pschera Sweden 12 72 0.2× 151 0.8× 123 0.9× 55 0.7× 15 0.3× 38 515
M. Fadalti Italy 7 172 0.5× 97 0.5× 132 1.0× 40 0.5× 23 0.4× 8 419

Countries citing papers authored by Goražd Rudolf

Since Specialization
Citations

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

Fields of papers citing papers by Goražd Rudolf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Goražd Rudolf

This figure shows the co-authorship network connecting the top 25 collaborators of Goražd Rudolf. A scholar is included among the top collaborators of Goražd Rudolf 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 Goražd Rudolf. Goražd Rudolf 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.
Kovanda, Anja, Luca Lovrečić, Goražd Rudolf, et al.. (2023). Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular Dystrophy. Genes. 14(12). 2166–2166. 2 indexed citations
2.
Wirth, Thomas, Louise‐Laure Mariani, Michel Baulac, et al.. (2020). Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism. Movement Disorders. 35(5). 880–885. 21 indexed citations
3.
Rudolf, Goražd, et al.. (2019). The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy. Molecular Genetics & Genomic Medicine. 7(6). e658–e658. 3 indexed citations
4.
Rudolf, Goražd, Aleš Maver, Alenka Hodžić, et al.. (2018). Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis. PLoS ONE. 13(1). e0190601–e0190601. 39 indexed citations
5.
Maver, Aleš, Smiljana Ristič, Saša Simčič, et al.. (2017). Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis. Scientific Reports. 7(1). 3715–3715. 49 indexed citations
6.
Rudolf, Goražd, Nataša Tul, Ivan Verdenik, et al.. (2017). Impact of prenatal screening on the prevalence of Down syndrome in Slovenia. PLoS ONE. 12(6). e0180348–e0180348. 9 indexed citations
7.
Lovrečić, Luca, et al.. (2016). Clinical utility of array comparative genomic hybridisation in prenatal setting. BMC Medical Genetics. 17(1). 81–81. 15 indexed citations
8.
Blinc, Aleš, Aleš Maver, Goražd Rudolf, et al.. (2015). Clinical Exome Sequencing as a Novel Tool for Diagnosing Loeys-Dietz Syndrome Type 3. European Journal of Vascular and Endovascular Surgery. 50(6). 816–821. 11 indexed citations
9.
Rudolf, Goražd, et al.. (2015). Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss. Molecular Cytogenetics. 8(1). 83–83. 5 indexed citations
10.
Živković, Maja, Nada Starčević Čizmarević, Luca Lovrečić, et al.. (2014). The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis. Disease Markers. 2014. 1–8. 14 indexed citations
11.
Lupattelli, Angela, Olav Spigset, Michael Twigg, et al.. (2014). Medication use in pregnancy: a cross-sectional, multinational web-based study. BMJ Open. 4(2). e004365–e004365. 338 indexed citations breakdown →
12.
Čizmarević, Nada Starčević, Borut Peterlin, Juraj Sepčić, et al.. (2011). CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients. International Journal of Immunogenetics. 38(5). 419–426. 9 indexed citations
13.
Lovrečić, Luca, et al.. (2011). A new case of rare proximal 3q13 interstitial deletion. SHILAP Revista de lepidopterología. 6(5). 625–630. 2 indexed citations
14.
Rudolf, Goražd & Borut Peterlin. (2009). DNA testiranje u medicini. University of Zagreb University Computing Centre (SRCE). 45(1). 38–43.
15.
Rudolf, Goražd, et al.. (2008). A Down syndrome female infant with partial trisomy of chromosome 21--abnormal nuchal translucency screening test.. PubMed. 19(4). 429–32.
16.
Medica, Igor, et al.. (2005). C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairment. PubMed. 5(1). 11–11. 10 indexed citations
17.
Medica, Igor, Goražd Rudolf, Igor Prpić, Milan Stanojević, & Borut Peterlin. (2005). Incidence of the del35G/GJB2 mutation in Croatian newborns with hearing impairment.. PubMed. 11(11). CR533–5. 8 indexed citations
18.
Rudolf, Goražd. (1968). Duration of Sleep. BMJ. 2(5606). 701.3–701. 1 indexed citations
19.
Rudolf, Goražd. (1966). Institute of Neurology. BMJ. 2(5504). 53–53. 17 indexed citations
20.
Rudolf, Goražd. (1955). DRUGS IN THE TREATMENT OF DEPRESSION. The Lancet. 265(6875). 1178–1178.

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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