Goran Čuturilo

1.1k total citations
32 papers, 323 citations indexed

About

Goran Čuturilo is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Goran Čuturilo has authored 32 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Genetics and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Goran Čuturilo's work include Congenital heart defects research (11 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital Heart Disease Studies (6 papers). Goran Čuturilo is often cited by papers focused on Congenital heart defects research (11 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital Heart Disease Studies (6 papers). Goran Čuturilo collaborates with scholars based in Serbia, Slovenia and United States. Goran Čuturilo's co-authors include Borut Peterlin, Aleš Maver, Alenka Hodžić, Danijela Drakulić, Milena Stevanović, Luca Lovrečić, Karin Writzl, Sanaa Muheisen, Brian A. Link and Anja Kovanda and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Goran Čuturilo

32 papers receiving 319 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Goran Čuturilo Serbia 11 167 149 47 43 32 32 323
Marije Meuwissen Belgium 11 153 0.9× 186 1.2× 25 0.5× 25 0.6× 40 1.3× 23 368
Pietro Sirleto Italy 12 221 1.3× 137 0.9× 48 1.0× 31 0.7× 34 1.1× 25 399
Magdalena Badura‐Stronka Poland 12 183 1.1× 141 0.9× 40 0.9× 22 0.5× 18 0.6× 32 357
Alper Gezdirici Türkiye 9 209 1.3× 129 0.9× 17 0.4× 20 0.5× 34 1.1× 55 337
Teresa Giugliano Italy 12 189 1.1× 94 0.6× 37 0.8× 24 0.6× 31 1.0× 21 339
Francesco Benedicenti Italy 10 165 1.0× 123 0.8× 23 0.5× 37 0.9× 28 0.9× 21 417
Pamela Trapane United States 7 82 0.5× 131 0.9× 26 0.6× 53 1.2× 14 0.4× 16 247
Julie M. Joyce Canada 10 176 1.1× 174 1.2× 88 1.9× 20 0.5× 17 0.5× 26 470
Tiffany Busa France 11 174 1.0× 163 1.1× 16 0.3× 26 0.6× 27 0.8× 27 312
Laurence Lœuillet France 11 145 0.9× 106 0.7× 44 0.9× 50 1.2× 50 1.6× 20 361

Countries citing papers authored by Goran Čuturilo

Since Specialization
Citations

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

Fields of papers citing papers by Goran Čuturilo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Goran Čuturilo

This figure shows the co-authorship network connecting the top 25 collaborators of Goran Čuturilo. A scholar is included among the top collaborators of Goran Čuturilo 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 Goran Čuturilo. Goran Čuturilo 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.
Čuturilo, Goran, et al.. (2024). Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion. Children. 11(4). 489–489. 2 indexed citations
2.
3.
Tylki‐Szymańska, Anna, Zsuzsanna Almássy, Ingeborg Barišić, et al.. (2022). The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers. Orphanet Journal of Rare Diseases. 17(1). 136–136. 4 indexed citations
4.
Drakulić, Danijela, et al.. (2021). Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit. European Journal of Pediatrics. 180(10). 3219–3227. 1 indexed citations
5.
Gallagher, Louise, Severin Rakić, Paula Jorge, et al.. (2020). Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature. International Journal of Environmental Research and Public Health. 17(24). 9253–9253. 4 indexed citations
6.
Maver, Aleš, et al.. (2018). Rare missense TUBGCP5 gene variant in a patient with primary microcephaly. European Journal of Medical Genetics. 62(12). 103598–103598. 20 indexed citations
7.
Čuturilo, Goran, Danijela Drakulić, Slobodan Ilić, et al.. (2017). The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome. Pediatric Cardiology. 38(8). 1680–1685. 10 indexed citations
8.
Maver, Aleš, et al.. (2017). Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases. Genetics in Medicine. 20(3). 303–312. 51 indexed citations
9.
Harms, Frederike L., Malik Alawi, David J. Amor, et al.. (2017). The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumor. American Journal of Medical Genetics Part A. 176(2). 470–476. 13 indexed citations
10.
11.
Čuturilo, Goran, et al.. (2016). Improving the diagnosis of children with 22q11.2 deletion syndrome: A single-center experience from Serbia. Indian Pediatrics. 53(9). 786–789. 4 indexed citations
12.
Čuturilo, Goran, et al.. (2014). Wiskott-Aldrich syndrome with macrothrombocytopenia. Indian Pediatrics. 51(12). 1015–1016. 8 indexed citations
13.
Čuturilo, Goran, et al.. (2014). Ectodermal Defects and Anal Atresia in a Child with a TP63 Mutation‐Expanding the Phenotypic Spectrum. Pediatric Dermatology. 32(3). 421–422. 3 indexed citations
14.
15.
Medjo, Biljana, et al.. (2012). Inhaled nitric oxide therapy for acute respiratory distress syndrome in children. Indian Pediatrics. 49(7). 573–576. 3 indexed citations
16.
Čuturilo, Goran, et al.. (2011). 4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome. European Journal of Pediatrics. 170(11). 1465–1470. 16 indexed citations
17.
Medjo, Biljana, et al.. (2008). INDICATIONS AND COMPLICATIONS OF MECHANICAL VENTILATION IN PEDIATRIC INTENSIVE CARE UNIT PATIENTS. Archives of Disease in Childhood. 93. 2 indexed citations
18.
Atanasković‐Marković, Marina, Marija Gavrović‐Jankulović, Tanja Ćirković Veličković, et al.. (2008). Intraoperative anaphylactic shock in a child with no history of type I hypersensitivity.. PubMed. 7(2). 97–9. 3 indexed citations
19.
Čuturilo, Goran, et al.. (2008). Prenatal growth retardation, microcephaly, and eye coloboma in infant with multiple congenital anomalies: Further delineation of presumed new dysmorphic syndrome. Birth Defects Research Part A Clinical and Molecular Teratology. 82(3). 166–168. 4 indexed citations
20.
Čuturilo, Goran, et al.. (2007). A rare association of interrupted aortic arch type C and microdeletion 22q11.2. European Journal of Pediatrics. 167(10). 1195–1198. 4 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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