Nina Barišić

5.4k total citations
61 papers, 860 citations indexed

About

Nina Barišić is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Nina Barišić has authored 61 papers receiving a total of 860 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 15 papers in Neurology and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in Nina Barišić's work include Hereditary Neurological Disorders (10 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Metabolism and Genetic Disorders (8 papers). Nina Barišić is often cited by papers focused on Hereditary Neurological Disorders (10 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Metabolism and Genetic Disorders (8 papers). Nina Barišić collaborates with scholars based in Croatia, Germany and Italy. Nina Barišić's co-authors include Peter De Jonghe, Kristl G. Claeys, Vincent Timmerman, Eva Nelis, A. Löfgren, Maja Sirotković-Skerlev, Hanns Lochmüller, Goran Šimić, Jadranka Sertić and Atiqul Islam and has published in prestigious journals such as Neurology, Epilepsia and Acta Neuropathologica.

In The Last Decade

Nina Barišić

55 papers receiving 848 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nina Barišić Croatia 17 396 261 184 161 121 61 860
Wladimir Bocca Vieira de Rezende Pinto Brazil 15 267 0.7× 241 0.9× 174 0.9× 293 1.8× 66 0.5× 84 765
Amets Sáenz Spain 18 522 1.3× 334 1.3× 60 0.3× 222 1.4× 177 1.5× 41 949
Paulo Victor Sgobbi de Souza Brazil 14 250 0.6× 240 0.9× 179 1.0× 277 1.7× 55 0.5× 82 707
Francesca Madia Italy 18 351 0.9× 290 1.1× 81 0.4× 438 2.7× 95 0.8× 62 1.0k
Kimiko Tamagawa Japan 17 392 1.0× 163 0.6× 136 0.7× 80 0.5× 28 0.2× 35 764
Claudia Castiglioni Chile 15 320 0.8× 111 0.4× 125 0.7× 61 0.4× 54 0.4× 47 566
Michiya Ohta Japan 19 421 1.1× 305 1.2× 114 0.6× 235 1.5× 89 0.7× 36 990
Tsutomu Takahashi Japan 18 386 1.0× 187 0.7× 54 0.3× 77 0.5× 68 0.6× 51 966
Elisabetta Tasca Italy 15 539 1.4× 195 0.7× 90 0.5× 106 0.7× 162 1.3× 23 761
C. Ortez Spain 15 422 1.1× 146 0.6× 121 0.7× 92 0.6× 78 0.6× 76 691

Countries citing papers authored by Nina Barišić

Since Specialization
Citations

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

Fields of papers citing papers by Nina Barišić

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nina Barišić

This figure shows the co-authorship network connecting the top 25 collaborators of Nina Barišić. A scholar is included among the top collaborators of Nina Barišić 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 Nina Barišić. Nina Barišić 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.
Barišić, Nina, et al.. (2025). Spinal cord stimulation (SCS) induced favorable neuromodulative outcome in the treatment of chronic neuropathic pain syndrome in children. European Journal of Paediatric Neurology. 54. 186–192.
2.
Wendel, Eva‐Maria, Daniel Tibussek, Nina Barišić, et al.. (2024). Children with MOG-IgG positive bilateral optic neuritis misdiagnosed as fulminant idiopathic intracranial hypertension. Multiple Sclerosis and Related Disorders. 93. 106205–106205. 1 indexed citations
3.
Chudy, Darko, et al.. (2023). GPi DBS treatment outcome in children with monogenic dystonia: a case series and review of the literature. Frontiers in Neurology. 14. 1151900–1151900. 3 indexed citations
4.
Leko, Mirjana Babić, et al.. (2023). Molecular Biomarkers for the Diagnosis, Prognosis, and Pharmacodynamics of Spinal Muscular Atrophy. Journal of Clinical Medicine. 12(15). 5060–5060. 13 indexed citations
5.
Mercuri, Eugenio, Nina Barišić, Odile Boespflug‐Tanguy, et al.. (2020). SUNFISH Part 2: Efficacy and Safety of Risdiplam (RG7916) in Patients with Type 2 or Non-Ambulant Type 3 Spinal Muscular Atrophy (SMA) (1260). Neurology. 94(15_supplement). 20 indexed citations
6.
Lepej, Snježana Židovec, Ivana Grgić, Vladimir Trkulja, et al.. (2017). Chemokines CXCL10, CXCL11, and CXCL13 in acute disseminated encephalomyelitis, non-polio enterovirus aseptic meningitis, and neuroborreliosis: CXCL10 as initial discriminator in diagnostic algorithm?. Neurological Sciences. 39(3). 471–479. 15 indexed citations
7.
Juraški, Romana Gjergja, et al.. (2012). SMJERNICE HRVATSKOG DRUŠTVA ZA DJEČJU NEUROLOGIJU ZA DIJAGNOSTIKU I TERAPIJU FEBRILNIH KONVULZIJA. Paediatria Croatica. 56(2). 171–174. 1 indexed citations
8.
Barišić, Nina, Amina Chaouch, Juliane S. Müller, & Hanns Lochmüller. (2011). Genetic heterogeneity and pathophysiological mechanisms in congenital myasthenic syndromes. European Journal of Paediatric Neurology. 15(3). 189–196. 16 indexed citations
9.
Dumić, Miroslav, Nina Barišić, Vesna Kuŝec, et al.. (2010). Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy. European Journal of Pediatrics. 170(3). 393–396. 19 indexed citations
10.
Kutleša, Marko, et al.. (2009). Ischemic stroke associated with adenoviral infection in a 4-year-old boy. Wiener klinische Wochenschrift. 121(23-24). 776–779. 4 indexed citations
11.
Gagro, Alenka, Rita Horváth, Mario Ćuk, et al.. (2008). Mitochondriopathy presenting with immune disorder. European Journal of Human Genetics. 116. 1 indexed citations
12.
Šimić, Goran, Mihovil Mladinov, Nataša Jovanov Milošević, et al.. (2007). Abnormal motoneuron migration, differentiation, and axon outgrowth in spinal muscular atrophy. Acta Neuropathologica. 115(3). 313–326. 41 indexed citations
13.
Barišić, Nina, et al.. (2006). Progressive chronic inflammatory demyelinating polyneuropathy in a child with central nervous system involvement and myopathy.. University of Zagreb University Computing Centre (SRCE). 30(4). 945–9. 3 indexed citations
14.
Barišić, Nina, Jasminka Jakić‐Razumović, Miroslav Harjaček, et al.. (2006). Childhood dermatomyositis associated with intracranial tumor and liver cysts. European Journal of Paediatric Neurology. 11(2). 76–80. 2 indexed citations
15.
Barišić, Nina, et al.. (2005). Rizik javljanja drugog napadaja u neliječene djece s benignom parcijalnom epilepsijom s centrotemporalnim šiljcima — prospektivno istraživanje. 59. 59–62. 2 indexed citations
16.
Barišić, Nina, et al.. (2005). [The risk of second seizure in children with benign childhood epilepsy with centrotemporal spikes without treatment--a prospective study].. PubMed. 59(1). 59–62. 8 indexed citations
17.
Barišić, Nina, Juliane S. Müller, Michaela A. Gazdik, et al.. (2004). Clinical variability of CMS-EA (congenital myasthenic syndrome with episodic apnea) due to identical CHAT mutations in two infants. European Journal of Paediatric Neurology. 9(1). 7–12. 28 indexed citations
18.
Barišić, Nina, et al.. (2002). Spinal dysraphism associated with congenital heart disorder in a girl with MELAS syndrome and point mutation at mitochondrial DNA nucleotide 3271.. PubMed. 43(1). 37–41. 9 indexed citations
19.
Barišić, Nina, Cornelia Schmidt, Ágnes Herczegfalvi, et al.. (2002). Congenital Myasthenic Syndrome (CMS) in Three European Kinships due to a Novel Splice Mutation (IVS7 - 2 A/G) in the Epsilon Acetylcholine Receptor (AChR) Subunit Gene. Neuropediatrics. 33(5). 249–254. 5 indexed citations
20.
Barišić, Nina, Jadranka Sertić, Ivo Barić, et al.. (1998). Molecular Analysis and Electromyoneurographic Abnormalities in Croatian Children with Proximal Spinal Muscular Atrophies. Clinical Chemistry and Laboratory Medicine (CCLM). 36(8). 667–669. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Wladimir Bocca Vieira de Rezende Pinto Breakdown of academic impact, for papers by Amets Sáenz Breakdown of academic impact, for papers by Paulo Victor Sgobbi de Souza Breakdown of academic impact, for papers by Francesca Madia Breakdown of academic impact, for papers by Kimiko Tamagawa Breakdown of academic impact, for papers by Claudia Castiglioni Breakdown of academic impact, for papers by Michiya Ohta Breakdown of academic impact, for papers by Tsutomu Takahashi Breakdown of academic impact, for papers by Elisabetta Tasca Breakdown of academic impact, for papers by C. Ortez
Rankless by CCL
2026