Michal Malina

1.2k total citations
22 papers, 282 citations indexed

About

Michal Malina is a scholar working on Nephrology, Immunology and Molecular Biology. According to data from OpenAlex, Michal Malina has authored 22 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Nephrology, 8 papers in Immunology and 6 papers in Molecular Biology. Recurrent topics in Michal Malina's work include Complement system in diseases (8 papers), Renal Diseases and Glomerulopathies (7 papers) and Adenosine and Purinergic Signaling (3 papers). Michal Malina is often cited by papers focused on Complement system in diseases (8 papers), Renal Diseases and Glomerulopathies (7 papers) and Adenosine and Purinergic Signaling (3 papers). Michal Malina collaborates with scholars based in Czechia, United Kingdom and Germany. Michal Malina's co-authors include Tomáš Seeman, Franz Schaefer, Ondřej Cinek, Eva Šimková, Ashima Gulati, Arvind Bagga, J Janda, Jakub Zieg, Neil Sheerin and Štěpánka Průhová and has published in prestigious journals such as Blood, PLoS ONE and PEDIATRICS.

In The Last Decade

Michal Malina

22 papers receiving 280 citations

Peers

Michal Malina

NEPHR

IMMUN

HEMAT

GENET

Nobuaki Takagi Japan

Caroline Rousset‐Rouvière France

Ortraud Beringer Germany

Reem Raafat United States

Jan Schmidtko Germany

Gesa Schalk Germany

L Moulonguet France

Idris Boudhabhay France

Emma Diletta Stea Italy

Beatriz Arrizabalaga Spain

Nobuaki Takagi Japan

Michal Malina

191 ×1.2

NEPHR

223 ×1.6

IMMUN

26 ×0.4

125 ×2.6

HEMAT

30 ×0.9

GENET

Citations per year, relative to Michal Malina Michal Malina (= 1×) peers Nobuaki Takagi

Countries citing papers authored by Michal Malina

Since Specialization

Citations

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

Fields of papers citing papers by Michal Malina

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michal Malina

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

Tse, Yincent, et al.. (2023). 1 Low yield from imaging after non E. coli urine tract infections in children treated in primary care and emergency department. A70–A71. 1 indexed citations

Brocklebank, Vicky, Patrick R. Walsh, Thomas M Hallam, et al.. (2023). Atypical hemolytic uremic syndrome in the era of terminal complement inhibition: an observational cohort study. Blood. 142(16). 1371–1386. 22 indexed citations

Tse, Yincent, et al.. (2023). Low yield from imaging after non-E. coliurine tract infections in children treated in primary care and emergency department. Archives of Disease in Childhood. 108(6). 474–480. 1 indexed citations

Bryant, Andrew, Sonya Carnell, Thomas Chadwick, et al.. (2022). Safety and impact of eculizumab withdrawal in patients with atypical haemolytic uraemic syndrome: protocol for a multicentre, open-label, prospective, single-arm study. BMJ Open. 12(9). e054536–e054536. 5 indexed citations

Plumb, Lucy, Winnie Magadi, Anna Casula, et al.. (2022). Advanced chronic kidney disease among UK children. Archives of Disease in Childhood. 107(11). 1043–1045. 5 indexed citations

Ryan, Kate, et al.. (2022). Perioperative fluid management and associated complications in children receiving kidney transplants in the UK. Pediatric Nephrology. 38(4). 1299–1307. 5 indexed citations

Brocklebank, Vicky, Valerie Wilson, Patrick R. Walsh, et al.. (2022). Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic Syndrome. Transplantation. 107(4). 994–1003. 18 indexed citations

Seeman, Tomáš, et al.. (2018). Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93. Pediatric Nephrology. 33(8). 1347–1363. 35 indexed citations

Bartosova, Maria, Betti Schaefer, Niels Grabe, et al.. (2016). Reduced Microvascular Density in Omental Biopsies of Children with Chronic Kidney Disease. PLoS ONE. 11(11). e0166050–e0166050. 13 indexed citations

10.

Ažukaitis, Karolis, et al.. (2013). Macrovascular involvement in a child with atypical hemolytic uremic syndrome. Pediatric Nephrology. 29(7). 1273–1277. 15 indexed citations

11.

Malina, Michal, et al.. (2012). Late recovery of renal function by rituximab in a patient with Wegener’s granulomatosis. Pediatric Nephrology. 28(3). 511–514. 3 indexed citations

12.

Malina, Michal, et al.. (2012). Peripheral gangrenes in children with atypical hemolytic uremic syndrome. Immunobiology. 217(11). 1192–1193. 2 indexed citations

13.

Malina, Michal, Lubka T. Roumenina, Tomáš Seeman, et al.. (2012). Genetics of hemolytic uremic syndromes. La Presse Médicale. 41(3). e105–e114. 22 indexed citations

14.

Malina, Michal, et al.. (2011). Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP. Pediatric Nephrology. 27(1). 73–81. 16 indexed citations

15.

Boppel, Tobias, Franz Schaefer, Chiara Gaudino, et al.. (2011). Extensive hemispheric diffusion restriction in haemolytic uremic syndrome. Clinical Radiology. 67(3). 292–294. 1 indexed citations

16.

Uhlı́k, Jir̆ı́, et al.. (2011). Remodeling of fetoplacental arteries in rats due to chronic hypoxia. Experimental and Toxicologic Pathology. 65(1-2). 97–103. 10 indexed citations

17.

Malina, Michal, et al.. (2011). Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome. European Journal of Pediatrics. 171(1). 121–124. 11 indexed citations

18.

Malina, Michal, Ondřej Cinek, J Janda, & Tomáš Seeman. (2009). Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation. Pediatric Nephrology. 24(10). 2051–2053. 25 indexed citations

19.

Hernychová, Lenka, Jiří Stulík, Petr Halada, et al.. (2001). Construction of aFrancisella tularensis two-dimensional electrophoresis protein database. PROTEOMICS. 1(4). 508–515. 25 indexed citations

20.

Hernychová, Lenka, Jiří Stulík, Petr Halada, et al.. (2001). Construction of a Francisella tularensis two-dimensional electrophoresis protein database. PROTEOMICS. 1(4). 508–515. 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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