Ivan Ivanovski

1.7k total citations
47 papers, 368 citations indexed

About

Ivan Ivanovski is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Ivan Ivanovski has authored 47 papers receiving a total of 368 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Surgery, 13 papers in Genetics and 12 papers in Molecular Biology. Recurrent topics in Ivan Ivanovski's work include Genomics and Rare Diseases (5 papers), Connective tissue disorders research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Ivan Ivanovski is often cited by papers focused on Genomics and Rare Diseases (5 papers), Connective tissue disorders research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Ivan Ivanovski collaborates with scholars based in Italy, Serbia and Switzerland. Ivan Ivanovski's co-authors include Eleni Melliou, Miodrag Čolić, Saša Vasilijić, Dragana Vučević, İoanna Chinou, Livia Garavelli, Marzia Pollazzon, Stefano Giuseppe Caraffi, Simonetta Rosato and Marina Atanasković‐Marković and has published in prestigious journals such as SHILAP Revista de lepidopterología, World Journal of Gastroenterology and Allergy.

In The Last Decade

Ivan Ivanovski

41 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ivan Ivanovski Italy	11	93	87	77	75	36	47	368
Qianyu Chen China	11	41 0.4×	98 1.1×	60 0.8×	49 0.7×	40 1.1×	38	392
Deepti Saini India	14	62 0.7×	179 2.1×	48 0.6×	66 0.9×	48 1.3×	26	494
Sanjay Singh India	14	45 0.5×	124 1.4×	18 0.2×	80 1.1×	62 1.7×	28	598
Ayşın Köktürk Türkiye	11	49 0.5×	64 0.7×	13 0.2×	67 0.9×	19 0.5×	25	588
Khimara Naidoo United Kingdom	12	68 0.7×	162 1.9×	14 0.2×	70 0.9×	23 0.6×	21	467
Tatiana Bandaletova United Kingdom	13	34 0.4×	79 0.9×	17 0.2×	66 0.9×	80 2.2×	16	373
Yujun Chen China	11	74 0.8×	96 1.1×	19 0.2×	81 1.1×	10 0.3×	23	374
Munif Allanson Australia	16	25 0.3×	156 1.8×	19 0.2×	31 0.4×	16 0.4×	19	485
Federica Li Pomi Italy	13	19 0.2×	67 0.8×	15 0.2×	46 0.6×	35 1.0×	48	417
Yoonmi Lee South Korea	13	24 0.3×	259 3.0×	46 0.6×	101 1.3×	41 1.1×	19	563

Countries citing papers authored by Ivan Ivanovski

Since Specialization

Citations

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

Fields of papers citing papers by Ivan Ivanovski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivan Ivanovski

This figure shows the co-authorship network connecting the top 25 collaborators of Ivan Ivanovski. A scholar is included among the top collaborators of Ivan Ivanovski 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 Ivan Ivanovski. Ivan Ivanovski 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

Caraffi, Stefano Giuseppe, Simonetta Rosato, Carlotta Spagnoli, et al.. (2025). Axonal motor polyneuropathy in a 13 years old Girl with a de Novo variant in ADNP. Neurogenetics. 26(1). 32–32.

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Carlotta Spagnoli, et al.. (2023). Novel Insights from Clinical Practice: Xia-Gibbs Syndrome with Pes Cavus, Conjunctival Melanosis, and Eye Asymmetry due to a de novo AHDC1 Gene Variant – A Case Report and a Brief Review of the Literature. Molecular Syndromology. 15(1). 63–70. 2 indexed citations

Zanoni, Paolo, Katharina Steindl, Heinrich Sticht, et al.. (2023). The genetic landscape and clinical implication of pediatric Moyamoya angiopathy in an international cohort. European Journal of Human Genetics. 31(7). 784–792. 6 indexed citations

Ćirović, Aleksandar, et al.. (2023). Neonatal hepatitis B vaccination: Reevaluating timing and adjuvants for enhanced safety and effectiveness. SHILAP Revista de lepidopterología. 1(3). e47–e47. 1 indexed citations

Ivanovski, Ivan, Anaïs Begemann, Katharina Steindl, et al.. (2023). The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathies. Molecular Genetics & Genomic Medicine. 11(5). e2148–e2148. 10 indexed citations

Ivanovski, Ivan, Angela Bahr, Markus Zweier, et al.. (2023). A very mild phenotype in six individuals of a three‐generation family with the novel HRAS variant c.176C > G p.(Ala59Gly): Emergence of a new HRAS‐related RASopathy distinct from Costello syndrome. American Journal of Medical Genetics Part A. 191(8). 2074–2082.

Rosato, Simonetta, Sheila Unger, Belinda Campos‐Xavier, et al.. (2022). Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features. Genes. 13(2). 261–261. 9 indexed citations

Ćirović, Aleksandar, et al.. (2021). The adjuvant aluminum fate – Metabolic tale based on the basics of chemistry and biochemistry. Journal of Trace Elements in Medicine and Biology. 68. 126822–126822. 23 indexed citations

Caraffi, Stefano Giuseppe, Ivan Ivanovski, Marzia Pollazzon, et al.. (2019). Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6. Genes. 10(10). 799–799. 15 indexed citations

10.

Bonetti, Silvia, Ivan Ivanovski, Stefano Giuseppe Caraffi, et al.. (2019). Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study. Sleep Medicine. 61. 44–51. 5 indexed citations

11.

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Elisa Magnani, et al.. (2019). Alazami syndrome: the first case of papillary thyroid carcinoma. Journal of Human Genetics. 65(2). 133–141. 15 indexed citations

12.

Elwahab, Sami Abd, et al.. (2019). Over-admission and over-treatment of patients with cellulitis: a 5-year audit against international guidelines. Irish Journal of Medical Science (1971 -). 189(1). 245–249. 6 indexed citations

13.

Ivanovski, Ivan, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.. (2018). Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes. American Journal of Medical Genetics Part A. 176(5). 1166–1174. 13 indexed citations

14.

Ivanovski, Ivan, Stefano Giuseppe Caraffi, Maria Elisabeth Street, et al.. (2018). Prominent and elongated coccyx, a new manifestation of KBG syndrome associated with novel mutation in ANKRD11. American Journal of Medical Genetics Part A. 176(9). 1991–1995. 4 indexed citations

15.

Ivanovski, Ivan, Olivera Djurić, Stefano Giuseppe Caraffi, et al.. (2018). Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 34–34. 4 indexed citations

16.

Ivanovski, Ivan, et al.. (2017). Metabolically based liver damage pathophysiology in patients with urea cycle disorders - A new hypothesis. World Journal of Gastroenterology. 23(44). 7930–7938. 10 indexed citations

17.

Čuturilo, Goran, et al.. (2014). Wiskott-Aldrich syndrome with macrothrombocytopenia. Indian Pediatrics. 51(12). 1015–1016. 8 indexed citations

18.

Ivanovski, Ivan, et al.. (2012). Childhood leukemia genetic bottleneck phenomenon related to TEL-AML1: the postulation by a mathematical model.. PubMed. 125(6). 1182–5. 1 indexed citations

19.

Ivanovski, Ivan. (2010). Erythrocytic transglutaminase inhibition hemolysis at presentation of celiac disease. World Journal of Gastroenterology. 16(44). 5647–5647. 5 indexed citations

20.

Ivanovski, Ognen & Ivan Ivanovski. (2006). Childhood acute lymphoblastic leukemia is triggered by the introduction of immunization against diphtheria. Medical Hypotheses. 68(2). 324–327. 1 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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