Florin Sasarman

3.5k total citations
33 papers, 2.5k citations indexed

About

Florin Sasarman is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, Florin Sasarman has authored 33 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 2 papers in Cell Biology. Recurrent topics in Florin Sasarman's work include Mitochondrial Function and Pathology (26 papers), Metabolism and Genetic Disorders (20 papers) and ATP Synthase and ATPases Research (18 papers). Florin Sasarman is often cited by papers focused on Mitochondrial Function and Pathology (26 papers), Metabolism and Genetic Disorders (20 papers) and ATP Synthase and ATPases Research (18 papers). Florin Sasarman collaborates with scholars based in Canada, United States and United Kingdom. Florin Sasarman's co-authors include Eric A. Shoubridge, Hana Antonická, Tamiko Nishimura, Catherine Brunel‐Guitton, Woranontee Weraarpachai, Scot C. Leary, Timothy Wai, Vincent Paupe, Jan Smeıtınk and Rita Horváth and has published in prestigious journals such as New England Journal of Medicine, Cell and Journal of Biological Chemistry.

In The Last Decade

Florin Sasarman

33 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Florin Sasarman Canada	26	2.3k	831	124	120	109	33	2.5k
Hana Antonická Canada	25	2.8k 1.2×	1.0k 1.2×	142 1.1×	150 1.3×	150 1.4×	42	3.0k
Emmanuelle Sarzi France	17	1.6k 0.7×	865 1.0×	103 0.8×	104 0.9×	109 1.0×	25	1.7k
Teresa Rizza Italy	23	783 0.3×	338 0.4×	98 0.8×	68 0.6×	93 0.9×	43	1.1k
Eva Richard Spain	23	820 0.4×	609 0.7×	87 0.7×	85 0.7×	104 1.0×	61	1.2k
Metodi D. Metodiev France	15	1.4k 0.6×	291 0.4×	92 0.7×	200 1.7×	77 0.7×	21	1.6k
Cassandra Obie United States	16	1.4k 0.6×	345 0.4×	185 1.5×	163 1.4×	171 1.6×	22	1.7k
Elena J. Tucker Australia	19	1.3k 0.6×	580 0.7×	56 0.5×	146 1.2×	348 3.2×	41	1.7k
Stephanie Grünewald United Kingdom	28	1.4k 0.6×	558 0.7×	516 4.2×	52 0.4×	354 3.2×	85	2.1k
Anne-Marie J. Shearwood Australia	21	1.7k 0.8×	225 0.3×	144 1.2×	382 3.2×	85 0.8×	22	1.9k
Alexandre Janer Canada	15	842 0.4×	242 0.3×	86 0.7×	33 0.3×	67 0.6×	20	1.1k

Countries citing papers authored by Florin Sasarman

Since Specialization

Citations

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

Fields of papers citing papers by Florin Sasarman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florin Sasarman

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

Sasarman, Florin, et al.. (2019). D-2-hydroxyglutaric aciduria in a patient with speech delay due to a novel homozygous deletion in the D2HGDH gene. Molecular Genetics and Metabolism Reports. 20. 100482–100482. 2 indexed citations

Janer, Alexandre, Clara DM van Karnebeek, Florin Sasarman, et al.. (2015). RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement. European Journal of Human Genetics. 23(10). 1301–1307. 23 indexed citations

Meijer, Inge A., Florin Sasarman, Elsa Rossignol, et al.. (2015). LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy. SHILAP Revista de lepidopterología. 5. 85–88. 19 indexed citations

Hinttala, Reetta, Florin Sasarman, Takashi Nishimura, et al.. (2015). An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase. Human Molecular Genetics. 24(14). 4103–4113. 21 indexed citations

Antonická, Hana, Florin Sasarman, Tamiko Nishimura, Vincent Paupe, & Eric A. Shoubridge. (2013). The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression. Cell Metabolism. 17(3). 386–398. 178 indexed citations

Leary, Scot C., Hana Antonická, Florin Sasarman, et al.. (2013). Novel Mutations inSCO1as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis. Human Mutation. 34(10). 1366–1370. 40 indexed citations

Bayat, Vafa, Isabelle Thiffault, Manish Jaiswal, et al.. (2012). Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans. PLoS Biology. 10(3). e1001288–e1001288. 121 indexed citations

Fung, Stephen, Tamiko Nishimura, Florin Sasarman, & Eric A. Shoubridge. (2012). The conserved interaction of C7orf30 with MRPL14 promotes biogenesis of the mitochondrial large ribosomal subunit and mitochondrial translation. Molecular Biology of the Cell. 24(3). 184–193. 46 indexed citations

Sasarman, Florin, Tamiko Nishimura, Isabelle Thiffault, & Eric A. Shoubridge. (2012). A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia. Human Mutation. 33(8). 1201–1206. 41 indexed citations

10.

Weraarpachai, Woranontee, Florin Sasarman, Tamiko Nishimura, et al.. (2012). Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis. The American Journal of Human Genetics. 90(1). 142–151. 78 indexed citations

11.

Janer, Alexandre, Hana Antonická, Emilie Lalonde, et al.. (2012). An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect. The American Journal of Human Genetics. 91(4). 737–743. 55 indexed citations

12.

Sasarman, Florin, Hana Antonická, Rita Horváth, & Eric A. Shoubridge. (2011). The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation. Human Molecular Genetics. 20(23). 4634–4643. 46 indexed citations

13.

Sasarman, Florin, Catherine Brunel‐Guitton, Hana Antonická, Timothy Wai, & Eric A. Shoubridge. (2010). LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria. Molecular Biology of the Cell. 21(8). 1315–1323. 215 indexed citations

14.

Antonická, Hana, Elsebet Østergaard, Florin Sasarman, et al.. (2010). Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect. The American Journal of Human Genetics. 87(1). 115–122. 115 indexed citations

15.

Leary, Scot C., Florin Sasarman, Tamiko Nishimura, & Eric A. Shoubridge. (2009). Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1. Human Molecular Genetics. 18(12). 2230–2240. 135 indexed citations

16.

Sasarman, Florin, Hana Antonická, & Eric A. Shoubridge. (2008). The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2. Human Molecular Genetics. 17(23). 3697–3707. 116 indexed citations

17.

Smeıtınk, Jan, Orly Elpeleg, Hana Antonická, et al.. (2006). Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs. The American Journal of Human Genetics. 79(5). 869–877. 142 indexed citations

18.

Antonická, Hana, Florin Sasarman, Nancy G. Kennaway, & Eric A. Shoubridge. (2006). The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1. Human Molecular Genetics. 15(11). 1835–1846. 111 indexed citations

19.

Coenen, Marieke J. H., Hana Antonická, Cristina Ugalde, et al.. (2004). Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency. New England Journal of Medicine. 351(20). 2080–2086. 152 indexed citations

20.

Sasarman, Florin. (2002). Nuclear genetic control of mitochondrial translation in skeletal muscle revealed in patients with mitochondrial myopathy. Human Molecular Genetics. 11(14). 1669–1681. 22 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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