Dariusz Rokicki

1.7k total citations
66 papers, 868 citations indexed

About

Dariusz Rokicki is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Dariusz Rokicki has authored 66 papers receiving a total of 868 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 24 papers in Clinical Biochemistry and 16 papers in Rheumatology. Recurrent topics in Dariusz Rokicki's work include Metabolism and Genetic Disorders (24 papers), Mitochondrial Function and Pathology (13 papers) and Glycogen Storage Diseases and Myoclonus (10 papers). Dariusz Rokicki is often cited by papers focused on Metabolism and Genetic Disorders (24 papers), Mitochondrial Function and Pathology (13 papers) and Glycogen Storage Diseases and Myoclonus (10 papers). Dariusz Rokicki collaborates with scholars based in Poland, Netherlands and United States. Dariusz Rokicki's co-authors include Ewa Pronicka, Elżbieta Ciara, Rafał Płoski, Dorota Piekutowska‐Abramczuk, Maciej Pronicki, Paulina Halat, Elżbieta Jurkiewicz, Anna Tylki‐Szymańska, Magdalena Pajdowska and Agnieszka Pollak and has published in prestigious journals such as SHILAP Revista de lepidopterología, Nutrients and Pharmacology Biochemistry and Behavior.

In The Last Decade

Dariusz Rokicki

60 papers receiving 856 citations

Peers

Countries citing papers authored by Dariusz Rokicki

Since Specialization

Citations

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

Fields of papers citing papers by Dariusz Rokicki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dariusz Rokicki

This figure shows the co-authorship network connecting the top 25 collaborators of Dariusz Rokicki. A scholar is included among the top collaborators of Dariusz Rokicki 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 Dariusz Rokicki. Dariusz Rokicki 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	Family Occurrence of an m.3303C>T Point Mutation in the MT-TL1 Gene, Which Induces Cardiomyopathy Syndrome with/without Skeletal Muscle Myopathy 2024 ·Genes ·(unknown), (unknown), Ewa Starostecka, Dariusz Rokicki, (unknown), (unknown), Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, (unknown)	1
2	Efficacy and Safety of Ketogenic Diet Treatment in Pediatric Patients with Mitochondrial Disease 2024 ·Nutrients ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Dorota Piekutowska‐Abramczuk, (unknown), Elżbieta Ciara, Maciej Jaworski, Aleksandra Jezela‐Stanek, Dariusz Rokicki	2
3	Neutrophil functions in patients with neutropenia due to glycogen storage disease type 1b treated with empagliflozin 2024 ·Blood Advances ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Barbara Piątosa, Emilia Samborowska, Joanna Madzio, Janusz Książyk, (unknown), (unknown), Jan Potempa, Wojciech Młynarski, Dariusz Rokicki, Florian Veillard	4
4	The fibroblast growth factor 21 concentration in children with mitochondrial disease does not depend on the disease stage, but rather on the disease genotype 2022 ·Pediatric Endocrinology Diabetes and Metabolism ·(unknown), Dariusz Rokicki, (unknown), (unknown), (unknown), Dorota Piekutowska‐Abramczuk, (unknown), Elżbieta Ciara, Maciej Jaworski, Aleksandra Jezela‐Stanek	0
5	Clinical characteristics and long-term outcomes of patients with glycogen storage disease type 1b: a retrospective multi-center experience in Poland 2022 ·Pediatric Endocrinology Diabetes and Metabolism ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Elżbieta Ciara, Janusz Książyk, Dariusz Rokicki	6
6	Noncoding sequence variants define a novel regulatory element in the first intron of the N ‐acetylglutamate synthase gene 2021 ·Human Mutation ·Johannes Häberle, (unknown), (unknown), Véronique Rüfenacht, Dariusz Rokicki, M. Estela Rubio‐Gozalbo, Mendel Tuchman, Nicola Longo, Mark Yandell, Ashley Andrews, (unknown), Ljubica Caldovic	5
7	NBAS deficiency due to biallelic c.2809C > G variant presenting with recurrent acute liver failure with severe hyperammonemia, acquired microcephaly and progressive brain atrophy 2021 ·Metabolic Brain Disease ·Patryk Lipiński, (unknown), Dorota Piekutowska‐Abramczuk, Elżbieta Jurkiewicz, (unknown), Piotr Socha, Irena Jankowska, Dariusz Rokicki, Anna Tylki‐Szymańska	4
8	Neonatal cholestasis due to citrin deficiency: diagnostic pitfalls 2020 ·Acta Biochimica Polonica ·Patryk Lipiński, Dorota Jurkiewicz, Elżbieta Ciara, Rafał Płoski, Sabina Więcek, (unknown), (unknown), Piotr Socha, Dariusz Rokicki, Anna Tylki‐Szymańska, Irena Jankowska	4
9	Clinical picture and treatment effects in 5 patients with Methylmalonic aciduria related to MMAA mutations 2020 ·Molecular Genetics and Metabolism Reports ·(unknown), (unknown), Magdalena Pajdowska, (unknown), (unknown), (unknown), Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, Dariusz Rokicki	5
10	Mild phenotype of glutaric aciduria type 1 in polish patients – novel data from a group of 13 cases 2018 ·Metabolic Brain Disease ·(unknown), Aleksandra Jezela‐Stanek, Agnieszka Różdżyńska‐Świątkowska, Elżbieta Jurkiewicz, (unknown), Edyta Szymańska, Dariusz Rokicki, Elżbieta Ciara, Małgorzata Rydzanicz, Piotr Stawiński, Rafał Płoski, Anna Tylki‐Szymańska	7
11	Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH cases 2017 ·Journal of Applied Genetics ·Ewa Pronicka, Elżbieta Ciara, Paulina Halat, (unknown), Marek Wójcik, (unknown), Dariusz Rokicki, Paweł Płudowski, Ewa Wojciechowska, Aldona Wierzbicka, Janusz Książyk, (unknown), Martin Konrad, Karl P. Schlingmann, Mieczysław Litwin	60
12	Difficulties in recognition of pyruvate dehydrogenase complex deficiency on the basis of clinical and biochemical features. The role of next-generation sequencing 2016 ·Molecular Genetics and Metabolism Reports ·Elżbieta Ciara, Dariusz Rokicki, Paulina Halat, Agnieszka Karkucińska‐Więckowska, Dorota Piekutowska‐Abramczuk, Johannes A. Mayr, Joanna Trubicka, (unknown), Maciej Pronicki, Magdalena Pajdowska, (unknown), Maria Giżewska, Małgorzata Krajewska‐Walasek, Janusz Książyk, Wolfgang Sperl, Rafał Płoski, Ewa Pronicka	14
13	New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre 2016 ·Journal of Translational Medicine ·Ewa Pronicka, Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, Joanna Trubicka, Dariusz Rokicki, Agnieszka Karkucińska‐Więckowska, Magdalena Pajdowska, Elżbieta Jurkiewicz, Paulina Halat, Joanna Kosińska, Agnieszka Pollak, Małgorzata Rydzanicz, Piotr Stawiński, Maciej Pronicki, Małgorzata Krajewska‐Walasek, Rafał Płoski	159
14	Bilateral striatal necrosis caused by ADAR mutations in two siblings with dystonia and freckles-like skin changes that should be differentiated from Leigh syndrome 2016 ·Folia Neuropathologica ·Dorota Piekutowska‐Abramczuk, Hanna Mierzewska, Monika Bekiesińska‐Figatowska, Elżbieta Ciara, Joanna Trubicka, Maciej Pronicki, Dariusz Rokicki, Małgorzata Rydzanicz, Rafał Płoski, Ewa Pronicka	7
15	Tyrosinemia type III in an asymptomatic girl 2015 ·SHILAP Revista de lepidopterología ·Edyta Szymańska, (unknown), Elżbieta Ciara, Dorota Piekutowska‐Abramczuk, Rafał Płoski, Dariusz Rokicki, Anna Tylki‐Szymańska	14
16	Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis—A Case Report 2015 ·Journal of Oral and Maxillofacial Surgery ·(unknown), (unknown), Dariusz Rokicki, (unknown)	2
17	Angiomodulatory properties of <i>Rhodiola</i> spp. and other natural antioxidants 2015 ·Central European Journal of Immunology ·Dorota M. Radomska-Leśniewska, Piotr Skopiński, Barbara J. Bałan, (unknown), Jarosław Jóźwiak, Dariusz Rokicki, Ewa Skopińska-Różewska, Anna Borecka, (unknown)	24
18	Schimke immuno-osseous dysplasia: two cases 2002 ·Pediatric Radiology ·Anna Tylki‐Szymańska, (unknown), Małgorzata Krajewska‐Walasek, Jacek Michałkiewicz, (unknown), Dariusz Rokicki	4
19	The anxiolytic-like effect of nicotine undergoes rapid tolerance in a model of contextual fear conditioning in rats 2001 ·Pharmacology Biochemistry and Behavior ·Janusz Szyndler, Halina Sienkiewicz‐Jarosz, Piotr Maciejak, Marek Siemiątkowski, Dariusz Rokicki, Anna Członkowska, Adam Płaźnik	41
20	Ornithine transcarbamylase gene mutations and genotype-phenotype correlation in Polish patients with hyperammonemia type 2 1999 ·Journal of Applied Genetics ·Ewa Popowska, Elżbieta Ciara, Dariusz Rokicki, Ewa Pronicka	1

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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