Alexandre Janer

1.6k citations

20 papers · 1.1k · h-index 16

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Molecular Biology top 10%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- Ubiquitin and proteasome pathways
- RNA modifications and cancer

Papers in

Molecular Biology 17
- Mitochondrial Function and Pathology 14
- ATP Synthase and ATPases Research 5
- RNA modifications and cancer 3
Clinical Biochemistry 8
- Metabolism and Genetic Disorders 8

Co-authors: Eric A. Shoubridge (14 shared papers)Hana Antonická (7 shared papers)Anne‐Claude Gingras (5 shared papers)Zhen‐Yuan Lin (4 shared papers)Woranontee Weraarpachai (3 shared papers)Alexis Brice (4 shared papers)Annie Sittler (4 shared papers)Brian H. Robinson (1 shared paper)
Journals: Human Molecular Genetics (3 papers)Life Science Alliance (2 papers)The American Journal of Human Genetics (2 papers)Cell Metabolism (1 paper)Molecular Genetics and Metabolism (1 paper)
Partner nations: Canada United States France

In The Last Decade

Alexandre Janer

19 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Alexandre Janer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Alexandre Janer Line = papers co-authored together Alexandre Janer links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	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 ·Jessie M. Cameron, Alexandre Janer, Valeriy Levandovskiy, Nevena MacKay, Tracey A. Rouault, Wing-Hang Tong, Isla Ogilvie, Eric A. Shoubridge, Brian H. Robinson	2011	222
2	SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome EMBO Molecular Medicine ·Alexandre Janer, Julien Prudent, Vincent Paupe, Somayyeh Fahiminiya, Jacek Majewski, Nicolas Sgarioto, Christine Des Rosiers, Anik Forest, Zhen‐Yuan Lin, Anne‐Claude Gingras, Grant A. Mitchell, Heidi M. McBride, Eric A. Shoubridge	2016	156
3	A High-Density Human Mitochondrial Proximity Interaction Network Cell Metabolism ·Hana Antonická, Zhen‐Yuan Lin, Alexandre Janer, Mari J. Aaltonen, Woranontee Weraarpachai, Anne‐Claude Gingras, Eric A. Shoubridge	2020	122
4	SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7 Human Molecular Genetics ·Alexandre Janer, Andreas Werner, Junko Takahashi‐Fujigasaki, Aurélie Daret, Hiroto Fujigasaki, Koji Takada, Charles Duyckaerts, Alexis Brice, Anne Dejean, Annie Sittler	2009	84
5	PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins The Journal of Cell Biology ·Alexandre Janer, Elodie Martin, Marie‐Paule Muriel, Morwena Latouche, Hiroto Fujigasaki, Merle Ruberg, Alexis Brice, Yvon Trottier, Annie Sittler	2006	76
6	Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice Brain ·Alice Chort, Sandro Alves, Martina Marinello, Béatrice Dufresnois, Jean-Gabriel Dornbierer, Christelle Tesson, Morwena Latouche, Darren P. Baker, Martine Barkats, Khalid Hamid El Hachimi, Merle Ruberg, Alexandre Janer, Giovanni Stévanin, Alexis Brice, Annie Sittler	2013	64
7	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 ·Michito Namekawa, M.-P. Muriel, Alexandre Janer, Morwena Latouche, Aurélien Dauphin, Thomas Debeir, Elodie Martin, Charles Duyckaerts, A.F. Prigent, Christel Depienne, Annie Sittler, Alexis Brice, Merle Ruberg	2007	59
8	Loss of CHCHD10–CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS Human Molecular Genetics ·Isabella R. Straub, Alexandre Janer, Woranontee Weraarpachai, Lorne Zinman, Janice Robertson, Ekaterina Rogaeva, Eric A. Shoubridge	2017	59
9	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 ·Florin Sasarman, Isabelle Thiffault, Woranontee Weraarpachai, Steven Salomon, Catalina Maftei, Julie D. Gauthier, Benjamin Ellazam, Neil Webb, Hana Antonická, Alexandre Janer, Catherine Brunel‐Guitton, Orly Elpeleg, Grant A. Mitchell, Eric A. Shoubridge	2015	58
10	An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect 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	2012	58
11	Subcellular location of MMACHC and MMADHC, two human proteins central to intracellular vitamin B12 metabolism Molecular Genetics and Metabolism ·Wayne Mah, Justin C. Deme, David Watkins, Stephen Fung, Alexandre Janer, Eric A. Shoubridge, David S. Rosenblatt, James W. Coulton	2012	26
12	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 ·Mihaela Pupavac, David Watkins, Francis Petrella, Somayyeh Fahiminiya, Alexandre Janer, Warren Cheung, Anne‐Claude Gingras, Tomi Pastinen, Joseph Muenzer, Jacek Majewski, Eric A. Shoubridge, David S. Rosenblatt	2016	26
13	RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement European Journal of Human Genetics ·Alexandre Janer, Clara DM van Karnebeek, Florin Sasarman, Hana Antonická, Malak Al Ghamdi, Casper Shyr, Mary Dunbar, Sylvia Stockler-Ispiroglu, Colin J.D. Ross, Hilary Vallance, Janis M. Dionne, Wyeth W. Wasserman, Eric A. Shoubridge	2015	24
14	BOLA3 and NFU1 link mitoribosome iron–sulfur cluster assembly to multiple mitochondrial dysfunctions syndrome Nucleic Acids Research ·Hui Zhong, Alexandre Janer, Oleh Khalimonchuk, Hana Antonická, Eric A. Shoubridge, Antoni Barrientos	2023	20
15	The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusion Life Science Alliance ·Jana Schuettpelz, Alexandre Janer, Hana Antonická, Eric A. Shoubridge	2023	18
16	ESYT1 tethers the ER to mitochondria and is required for mitochondrial lipid and calcium homeostasis Life Science Alliance ·Alexandre Janer, Jordan L. Morris, Michiel Krols, Hana Antonická, Mari J. Aaltonen, Zhen‐Yuan Lin, Hanish Anand, Anne‐Claude Gingras, Julien Prudent, Eric A. Shoubridge	2023	15
17	SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome Alexandre Janer, Julien Prudent, Vincent Paupe, Somayyeh Fahiminiya, Jacek Majewski, Nicolas Sgarioto, Christine Des Rosiers, Anick Forest, Zhen‐Yuan Lin, Anne‐Claude Gingras, Grant A. Mitchell, Heidi M. McBride, Eric A. Shoubridge	2016	14
18	Loss of mitochondrial Chchd10 or Chchd2 in zebrafish leads to an ALS‐like phenotype and Complex I deficiency independent of the mitochondrial integrated stress response Developmental Neurobiology ·Virginie Petel Légaré, Christian J. Rampal, Tyler J.N. Gurberg, Mari J. Aaltonen, Alexandre Janer, Lorne Zinman, Eric A. Shoubridge, Gary A.B. Armstrong	2023	9
19	MAPL regulates gasdermin-mediated release of mtDNA from lysosomes to drive pyroptotic cell death Nature Cell Biology ·Benjamin Nguyen, Jack J. Collier, Olesia Ignatenko, Geneviève Morin, Vanessa Goyon, Alexandre Janer, Camila Tiefensee Ribeiro, Austen J. Milnerwood, Sidong Huang, Michel Desjardins, Heidi M. McBride	2025	3
20	Modular Orekit-based Flight Dynamics Software 2018 SpaceOps Conference ·Maxime Journot, Nicolas Frouvelle, Cosmin I. Udroiu, Lucian-Florentin Bărbulescu, Oana M. Hogoiu, Maria Teodorescu, Alexandre Janer, Pol Sola Romeu	2018	1

About Alexandre Janer

Alexandre Janer is a scholar working on Molecular Biology, Clinical Biochemistry, Cellular and Molecular Neuroscience, Neurology and Rheumatology, having authored 20 papers that have together received 1.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (8 papers), ATP Synthase and ATPases Research (5 papers), Genetic Neurodegenerative Diseases (4 papers), Amyotrophic Lateral Sclerosis Research (3 papers), RNA modifications and cancer (3 papers), Metalloenzymes and iron-sulfur proteins (2 papers) and Folate and B Vitamins Research (2 papers). The work is most often cited by research in Clinical Biochemistry (235 citations), Molecular Biology (834 citations), Cellular and Molecular Neuroscience (195 citations), Cell Biology (137 citations) and Renewable Energy, Sustainability and the Environment (126 citations). Alexandre Janer has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Eric A. Shoubridge, Hana Antonická, Anne‐Claude Gingras, Zhen‐Yuan Lin, Woranontee Weraarpachai, Alexis Brice, Annie Sittler, Brian H. Robinson, Jessie M. Cameron and Valeriy Levandovskiy. Their work appears in journals such as Human Molecular Genetics, Life Science Alliance, The American Journal of Human Genetics, Cell Metabolism and Molecular Genetics and Metabolism.

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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