Alexandre Janer

1.5k total citations
20 papers, 1.1k citations indexed

About

Alexandre Janer is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alexandre Janer has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alexandre Janer's work include Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (8 papers) and ATP Synthase and ATPases Research (5 papers). Alexandre Janer is often cited by papers focused on Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (8 papers) and ATP Synthase and ATPases Research (5 papers). Alexandre Janer collaborates with scholars based in Canada, United States and France. Alexandre Janer's co-authors include Eric A. Shoubridge, Hana Antonická, Anne‐Claude Gingras, Zhen‐Yuan Lin, Woranontee Weraarpachai, Alexis Brice, Annie Sittler, Wing-Hang Tong, Isla Ogilvie and Valeriy Levandovskiy and has published in prestigious journals such as Nucleic Acids Research, The Journal of Cell Biology and Nature Cell Biology.

In The Last Decade

Alexandre Janer

19 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexandre Janer Canada 15 842 242 190 138 127 20 1.1k
Teresa Rizza Italy 23 783 0.9× 338 1.4× 84 0.4× 84 0.6× 76 0.6× 43 1.1k
Stéphane Schmucker France 12 724 0.9× 50 0.2× 351 1.8× 212 1.5× 186 1.5× 14 876
Metodi D. Metodiev France 15 1.4k 1.7× 291 1.2× 93 0.5× 92 0.7× 18 0.1× 21 1.6k
Florin Sasarman Canada 26 2.3k 2.7× 831 3.4× 106 0.6× 100 0.7× 45 0.4× 33 2.5k
Woranontee Weraarpachai Canada 13 972 1.2× 333 1.4× 67 0.4× 64 0.5× 16 0.1× 16 1.1k
Elisa Fassone Italy 13 705 0.8× 365 1.5× 51 0.3× 34 0.2× 28 0.2× 19 880
Elena J. Tucker Australia 19 1.3k 1.5× 580 2.4× 58 0.3× 46 0.3× 104 0.8× 41 1.7k
Shotaro Saita Japan 13 936 1.1× 260 1.1× 85 0.4× 229 1.7× 13 0.1× 14 1.2k
Sze Chern Lim Australia 11 766 0.9× 355 1.5× 39 0.2× 33 0.2× 56 0.4× 13 899
Anne P. Døskeland Norway 17 554 0.7× 255 1.1× 54 0.3× 118 0.9× 11 0.1× 28 899

Countries citing papers authored by Alexandre Janer

Since Specialization
Citations

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

Fields of papers citing papers by Alexandre Janer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandre Janer

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandre Janer. A scholar is included among the top collaborators of Alexandre Janer 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 Alexandre Janer. Alexandre Janer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Collier, Jack J., Geneviève Morin, Vanessa Goyon, et al.. (2025). MAPL regulates gasdermin-mediated release of mtDNA from lysosomes to drive pyroptotic cell death. Nature Cell Biology. 27(10). 1708–1724. 1 indexed citations
2.
Zhong, Hui, Alexandre Janer, Oleh Khalimonchuk, et al.. (2023). BOLA3 and NFU1 link mitoribosome iron–sulfur cluster assembly to multiple mitochondrial dysfunctions syndrome. Nucleic Acids Research. 51(21). 11797–11812. 17 indexed citations
3.
Janer, Alexandre, et al.. (2023). The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusion. Life Science Alliance. 6(6). e202301914–e202301914. 18 indexed citations
4.
5.
Janer, Alexandre, Jordan L. Morris, Michiel Krols, et al.. (2023). ESYT1 tethers the ER to mitochondria and is required for mitochondrial lipid and calcium homeostasis. Life Science Alliance. 7(1). e202302335–e202302335. 13 indexed citations
6.
Antonická, Hana, Zhen‐Yuan Lin, Alexandre Janer, et al.. (2020). A High-Density Human Mitochondrial Proximity Interaction Network. Cell Metabolism. 32(3). 479–497.e9. 116 indexed citations
7.
Janer, Alexandre, et al.. (2018). Modular Orekit-based Flight Dynamics Software. 2018 SpaceOps Conference. 1 indexed citations
8.
Straub, Isabella R., Alexandre Janer, Woranontee Weraarpachai, et al.. (2017). Loss of CHCHD10–CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS. Human Molecular Genetics. 27(1). 178–189. 58 indexed citations
9.
Janer, Alexandre, Julien Prudent, Vincent Paupe, et al.. (2016). SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome. 5. 14 indexed citations
10.
Janer, Alexandre, Julien Prudent, Vincent Paupe, et al.. (2016). SLC 25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome. EMBO Molecular Medicine. 8(9). 1019–1038. 153 indexed citations
11.
Pupavac, Mihaela, David Watkins, Somayyeh Fahiminiya, et al.. (2016). Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations inZNF143, Which Codes for a Transcriptional Activator. Human Mutation. 37(9). 976–982. 24 indexed citations
12.
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
13.
Sasarman, Florin, Isabelle Thiffault, Woranontee Weraarpachai, et al.. (2015). The 3′ addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1. Human Molecular Genetics. 24(10). 2841–2847. 56 indexed citations
14.
Alves, Sandro, Martina Marinello, Christelle Tesson, et al.. (2013). Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice. Brain. 136(6). 1732–1745. 59 indexed citations
15.
Deme, Justin C., David Watkins, Stephen Fung, et al.. (2012). Subcellular location of MMACHC and MMADHC, two human proteins central to intracellular vitamin B12 metabolism. Molecular Genetics and Metabolism. 108(2). 112–118. 26 indexed citations
16.
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
17.
Cameron, Jessie M., Alexandre Janer, Valeriy Levandovskiy, et al.. (2011). Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes. The American Journal of Human Genetics. 89(4). 486–495. 209 indexed citations
18.
Janer, Alexandre, Andreas Werner, Junko Takahashi‐Fujigasaki, et al.. (2009). SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7. Human Molecular Genetics. 19(1). 181–195. 80 indexed citations
19.
Namekawa, Michito, Alexandre Janer, Morwena Latouche, et al.. (2007). Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis. Molecular and Cellular Neuroscience. 35(1). 1–13. 58 indexed citations
20.
Janer, Alexandre, Elodie Martin, Marie‐Paule Muriel, et al.. (2006). PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins. The Journal of Cell Biology. 174(1). 65–76. 72 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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