Florin Sasarman

3.5k citations

33 papers · 2.5k indexed · h-index 26

Co-authors: Eric A. Shoubridge Hana Antonická Tamiko Nishimura Catherine Brunel‐Guitton Woranontee Weraarpachai Scot C. Leary Timothy Wai Vincent Paupe
Topics: Mitochondrial Function and Pathology (26 papers)Metabolism and Genetic Disorders (20 papers)ATP Synthase and ATPases Research (18 papers)
Cited by: Clinical Biochemistry Molecular Biology Aging
Journals: New England Journal of Medicine Cell Journal of Biological Chemistry
Partner nations: Canada United States United Kingdom

In The Last Decade

Florin Sasarman

33 papers receiving 2.5k citations

Peers

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

#	Work	Indexed citations
1	D-2-hydroxyglutaric aciduria in a patient with speech delay due to a novel homozygous deletion in the D2HGDH gene 2019 ·Molecular Genetics and Metabolism Reports ·(unknown),Florin Sasarman,David S. Sinasac,Walla Al‐Hertani	2
2	RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement 2015 ·European Journal of Human Genetics ·Alexandre Janer,Clara DM van Karnebeek,Florin Sasarman,Hana Antonická,(unknown),Casper Shyr,Mary Dunbar,(unknown),Colin J.D. Ross,Hilary Vallance,Janis M. Dionne,Wyeth W. Wasserman,Eric A. Shoubridge	23
3	LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy 2015 ·SHILAP Revista de lepidopterología ·Inge A. Meijer,Florin Sasarman,(unknown),Elsa Rossignol,Michel Vanasse,(unknown),Grant A. Mitchell,Catherine Brunel‐Guitton	19
4	An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase 2015 ·Human Molecular Genetics ·Reetta Hinttala,Florin Sasarman,Takashi Nishimura,Hana Antonická,Catherine Brunel‐Guitton,Jeremy Schwartzentruber,Somayyeh Fahiminiya,Jacek Majewski,Denis Faubert,Elsebet Østergaard,Jan Smeıtınk,Eric A. Shoubridge	21
5	The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression 2013 ·Cell Metabolism ·Hana Antonická,Florin Sasarman,Tamiko Nishimura,Vincent Paupe,Eric A. Shoubridge	178
6	Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans 2012 ·PLoS Biology ·Vafa Bayat,Isabelle Thiffault,Manish Jaiswal,Martine Tétreault,Taraka Donti,Florin Sasarman,Geneviève Bernard,(unknown),Marie‐Josée Dicaire,Jean Mathieu,Michel Vanasse,Jean‐Pierre Bouchard,Marie‐France Rioux,Charles Marques Lourenço,Zhihong Li,Claire Haueter,Eric A. Shoubridge,Brett H. Graham,Bernard Brais,Hugo J. Bellen	121
7	Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis 2012 ·The American Journal of Human Genetics ·Woranontee Weraarpachai,Florin Sasarman,Tamiko Nishimura,Hana Antonická,Karine Auré,Agnès Rötig,Anne Lombès,Eric A. Shoubridge	78
8	The conserved interaction of C7orf30 with MRPL14 promotes biogenesis of the mitochondrial large ribosomal subunit and mitochondrial translation 2012 ·Molecular Biology of the Cell ·Stephen Fung,Tamiko Nishimura,Florin Sasarman,Eric A. Shoubridge	46
9	A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia 2012 ·Human Mutation ·Florin Sasarman,Tamiko Nishimura,Isabelle Thiffault,Eric A. Shoubridge	41
10	An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect 2012 ·The American Journal of Human Genetics ·Alexandre Janer,Hana Antonická,Emilie Lalonde,Tamiko Nishimura,Florin Sasarman,Garry K. Brown,Ruth M. Brown,Jacek Majewski,Eric A. Shoubridge	55
11	MITRAC Links Mitochondrial Protein Translocation to Respiratory-Chain Assembly and Translational Regulation 2012 ·Cell ·David U. Mick,Sven Dennerlein,Heike Wiese,Robert Reinhold,David Pacheu‐Grau,Isotta Lorenzi,Florin Sasarman,Woranontee Weraarpachai,Eric A. Shoubridge,Bettina Warscheid,Peter Rehling	174
12	The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation 2011 ·Human Molecular Genetics ·Florin Sasarman,Hana Antonická,Rita Horváth,Eric A. Shoubridge	46
13	LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria 2010 ·Molecular Biology of the Cell ·Florin Sasarman,Catherine Brunel‐Guitton,Hana Antonická,Timothy Wai,Eric A. Shoubridge	215
14	Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect 2010 ·The American Journal of Human Genetics ·Hana Antonická,Elsebet Østergaard,Florin Sasarman,Woranontee Weraarpachai,Flemming Wibrand,(unknown),Richard J. Rodenburg,Marjo S. van der Knaap,Jan Smeıtınk,Zofia M. Chrzanowska‐Lightowlers,Eric A. Shoubridge	115
15	Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1 2009 ·Human Molecular Genetics ·Scot C. Leary,Florin Sasarman,Tamiko Nishimura,Eric A. Shoubridge	135
16	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 2008 ·Human Molecular Genetics ·Florin Sasarman,Hana Antonická,Eric A. Shoubridge	116
17	Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs 2006 ·The American Journal of Human Genetics ·Jan Smeıtınk,Orly Elpeleg,Hana Antonická,(unknown),Ann Saada,P. Smits,Florin Sasarman,Gert Vriend,Jasmine Jacob‐Hirsch,Avraham Shaag,Gideon Rechavi,(unknown),Jürgen Horst,Richard J. Rodenburg,Bert van den Heuvel,Eric A. Shoubridge	142
18	The P174L Mutation in Human Sco1 Severely Compromises Cox17-dependent Metallation but Does Not Impair Copper Binding 2006 ·Journal of Biological Chemistry ·Paul A. Cobine,Fabien Pierrel,Scot C. Leary,Florin Sasarman,Yih‐Chern Horng,Eric A. Shoubridge,Dennis R. Winge	32
19	Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency 2004 ·New England Journal of Medicine ·Marieke J. H. Coenen,Hana Antonická,Cristina Ugalde,Florin Sasarman,(unknown),J. G. A. M. Heister,Robert F. Newbold,Frans J.M. Trijbels,Lambert P. van den Heuvel,Eric A. Shoubridge,Jan Smeıtınk	152
20	Nuclear genetic control of mitochondrial translation in skeletal muscle revealed in patients with mitochondrial myopathy 2002 ·Human Molecular Genetics ·Florin Sasarman	22

About Florin Sasarman

Florin Sasarman is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry, having authored 33 papers that have together received 2.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (26 papers), Metabolism and Genetic Disorders (20 papers) and ATP Synthase and ATPases Research (18 papers). The work is most often cited by research in Clinical Biochemistry (831 citations), Molecular Biology (2.3k citations) and Aging (19 citations). Florin Sasarman has collaborated with scholars based in Canada, United States and United Kingdom. Frequent 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. Their work appears in journals such as New England Journal of Medicine, Cell and Journal of Biological Chemistry.

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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