Ivo Barić

5.3k total citations
81 papers, 1.8k citations indexed

About

Ivo Barić is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Ivo Barić has authored 81 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 39 papers in Clinical Biochemistry and 29 papers in Rheumatology. Recurrent topics in Ivo Barić's work include Metabolism and Genetic Disorders (39 papers), Folate and B Vitamins Research (27 papers) and Biochemical and Molecular Research (19 papers). Ivo Barić is often cited by papers focused on Metabolism and Genetic Disorders (39 papers), Folate and B Vitamins Research (27 papers) and Biochemical and Molecular Research (19 papers). Ivo Barić collaborates with scholars based in Croatia, Germany and United States. Ivo Barić's co-authors include Ksenija Fumić, Georg F. Hoffmann, Danijela Petković Ramadža, Oliver Vugrek, Johannes Zschocke, Vladimir Sarnavka, S. Harvey Mudd, Sally P. Stabler, Robert H. Allen and Conrad Wagner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Brain.

In The Last Decade

Ivo Barić

78 papers receiving 1.8k citations

Peers

Countries citing papers authored by Ivo Barić

Since Specialization

Citations

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

Fields of papers citing papers by Ivo Barić

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivo Barić

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

#	Work	Indexed citations
1	Comparison of Model‐Predicted and Observed Evinacumab Pharmacokinetics and Efficacy in Children Aged < 5 Years With Homozygous Familial Hypercholesterolemia 2025 ·CPT Pharmacometrics & Systems Pharmacology ·(unknown), Robert Dingman, Jeanne Mendell, Katy C. Norman, Richard T. De George, Xue‐Qiao Zhao, Robert Pordy, (unknown), Wendy S. Putnam, Geetha Raghuveer, Brian W. McCrindle, Elena Fornari, Ivo Barić, Shubha Srinivasan, (unknown), Eliot A. Brinton, John D. Davis, (unknown), Lutz Harnisch	1
2	Succinic semialdehyde dehydrogenase deficiency in mice and in humans: An untargeted metabolomics perspective 2023 ·Journal of Inherited Metabolic Disease ·(unknown), Udo F. H. Engelke, (unknown), (unknown), Jean‐Baptiste Roullet, Sanne Broekman, Erik de Vrieze, Erwin van Wijk, Mirjam M. C. Wamelink, Rafael Artuch, Ivo Barić, Jona Merx, Thomas J. Boltje, (unknown), Michèl A.A.P. Willemsen, Marcel M. Verbeek, Ron A. Wevers, K. Michael Gibson, Karlien L. M. Coene	3
3	A biallelic loss-of-function variant in MYZAP is associated with a recessive form of severe dilated cardiomyopathy 2022 ·Molecular Case Studies ·Aleš Maver, (unknown), Ashraf Yusuf Rangrez, Marijana Ćorić, Jan Homolak, (unknown), (unknown), Mario Udovičić, (unknown), Umber Saleem, Sandra D. Laufer, Arne Hansen, Norbert Frey, Ivo Barić, Borut Peterlin	4
4	Case Report: Advanced Skeletal Muscle Imaging in S-Adenosylhomocysteine Hydrolase Deficiency and Further Insight Into Muscle Pathology 2022 ·Frontiers in Pediatrics ·Danijela Petković Ramadža, (unknown), Kamelija Žarković, Hanns Lochmüller, (unknown), (unknown), Ivo Barić, (unknown)	1
5	Diagnosis and the importance of early treatment of tyrosinemia type 1: A case report 2019 ·PubMed ·(unknown), (unknown), Ksenija Fumić, Dunja Rogić, (unknown), Danijela Petković Ramadža, (unknown), Ivo Barić	1
6	Hypogammaglobulinemia and imaging features in a patient with infantile free sialic acid storage disease (ISSD) and a novel mutation in the SLC17A5 gene 2018 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown), Danijela Petković Ramadža, (unknown), (unknown), (unknown), (unknown), Kristina Potočki, (unknown), (unknown), Kamelija Žarković, Jennifer Kerkhof, Marija Ljubojević, (unknown), (unknown), Ksenija Fumić, Bekim Sadiković, Ivo Barić	1
7	Program proširenog novorođenačkog probira u Republici Hrvatskoj – zahtjevi i izazovi pravilnog uzimanja suhe kapi krvi 2018 ·(unknown), Ivo Barić, (unknown), (unknown), (unknown), Danijela Petković Ramadža, (unknown), (unknown)	1
8	The ethical framework for performing research with rare inherited neurometabolic disease patients 2017 ·European Journal of Pediatrics ·Viviana Giannuzzi, Hugo Devlieger, Lucia Margari, Viveca Odlind, (unknown), Cinzia Maria Bellettato, Francesca D’Avanzo, Christina Lampe, (unknown), Elisenda Cortès‐Saladelafont, Àngels García Cazorla, Ivo Barić, Ljerka Cvitanović-Šojat, Ksenija Fumić, Christine í Dali, (unknown), Fedele Bonifazi, Maurizio Scarpa, Adriana Ceci	10
9	Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature 2016 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown), Vladimir Sarnavka, (unknown), Mario Ćuk, Danijela Petković Ramadža, Ksenija Fumić, Vesna Kuŝec, René Santer, Ivo Barić	9
10	Behavioural and emotional problems, intellectual impairment and health‐related quality of life in patients with organic acidurias and urea cycle disorders 2015 ·Journal of Inherited Metabolic Disease ·(unknown), Stefan Kölker, (unknown), Ivo Barić, J Zeman, Matthias R. Baumgartner, Chris Mühlhausen, Àngels García‐Cazorla, Florian Gleich, Gisela Haege, Peter Burgard	27
11	Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome 2013 ·European Journal of Human Genetics ·Denise Horn, Dagmar Wieczorek, Kay Metcalfe, Ivo Barić, (unknown), Mario Ćuk, Danijela Petković Ramadža, Ulrike Krüger, Stephanie Demuth, Wolfram Heinritz, Tobias Linden, Jens Koenig, Peter N. Robinson, Peter Krawitz	31
12	Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNATrp gene 2012 ·European Journal of Human Genetics ·Ivo Barić, Ksenija Fumić, Danijela Petković Ramadža, Wolfgang Sperl, Franz Zimmermann, (unknown), Zoran D‎. Mitrović, Leo Pažanin, (unknown), (unknown), Željko Reiner, Johannes A. Mayr	11
13	Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Toshiyuki Fukao, Jörn Oliver Sass, Petri Kursula, Eva Thimm, U. Wendel, Can Fıçıcıoğlu, Kamel Monastiri, Nathalie Guffon, Ivo Barić, M. T. Zabot, Naomi Kondo	26
14	Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene. 2009 ·PubMed ·Danijela Petković Ramadža, Feodora Stipoljev, Vladimir Sarnavka, (unknown), Kristina Potočki, Ksenija Fumić, Étienne Mornet, Ivo Barić	4
15	Mitochondriopathy presenting with immune disorder 2008 ·European Journal of Human Genetics ·(unknown), Alenka Gagro, Rita Horváth, Mario Ćuk, Vladimir Sarnavka, Goran Tešović, Hanns Lochmüller, Nina Barišić, (unknown), (unknown), (unknown), Marija Jelušić, (unknown), (unknown), Lana Tambić-Bukovac, (unknown), Ivo Barić	1
16	Differential metabolic consequences of fumarate hydratase and respiratory chain defects 2008 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Nuno Raimundo, (unknown), Ksenija Fumić, Ivo Barić, Anne M. Remes, Risto Renkonen, Risto Lapatto, Anu Suomalainen	22
17	Studies of S-adenosylhomocysteine-hydrolase polymorphism in a Croatian population 2005 ·Journal of Human Genetics ·Doris Kloor, Ksenija Fumić, Sebastian Attig, (unknown), Hartmut Oßwald, Ivo Barić, Jürgen Tomiuk, J. Kömpf	3
18	Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC). Report of a New Case 2005 ·Neuropediatrics ·Saadet Mercimek‐Mahmutoglu, Marjo S. van der Knaap, Ivo Barić, Daniela Prayer, Sylvia Stoeckler-Ipsiroglu	19
19	Inborn errors of metabolism at the turn of the millennium. 2001 ·PubMed ·Ivo Barić, Ksenija Fumić, Georg F. Hoffmann	9
20	Expand Long PCR for fragile X mutation detection 1997 ·Clinical Genetics ·Silva Hečimović, Ingeborg Barišić, Andreas Müller, Iskra Petković, Ivo Barić, (unknown), Krešimir Pavelić	39

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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