Luan T. Tran

867 total citations
25 papers, 205 citations indexed

About

Luan T. Tran is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Rheumatology. According to data from OpenAlex, Luan T. Tran has authored 25 papers receiving a total of 205 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 4 papers in Rheumatology. Recurrent topics in Luan T. Tran's work include RNA regulation and disease (13 papers), RNA modifications and cancer (7 papers) and RNA and protein synthesis mechanisms (5 papers). Luan T. Tran is often cited by papers focused on RNA regulation and disease (13 papers), RNA modifications and cancer (7 papers) and RNA and protein synthesis mechanisms (5 papers). Luan T. Tran collaborates with scholars based in Canada, United States and Netherlands. Luan T. Tran's co-authors include Geneviève Bernard, Kether Guerrero, Isabelle Thiffault, Nicole I. Wolf, Heather D. Durham, Marjo S. van der Knaap, Kathleen E. Sullivan, Benoît J. Gentil, Sylvain Chouinard and Marino Labinaz and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the American College of Cardiology and Annals of Neurology.

In The Last Decade

Luan T. Tran

23 papers receiving 200 citations

Peers

Countries citing papers authored by Luan T. Tran

Since Specialization

Citations

This map shows the geographic impact of Luan T. Tran'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 Luan T. Tran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Luan T. Tran more than expected).

Fields of papers citing papers by Luan T. Tran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luan T. Tran. 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 Luan T. Tran. The network helps show where Luan T. Tran may publish in the future.

Co-authorship network of co-authors of Luan T. Tran

This figure shows the co-authorship network connecting the top 25 collaborators of Luan T. Tran. A scholar is included among the top collaborators of Luan T. Tran 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 Luan T. Tran. Luan T. Tran 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	Novel Pathogenic Variants in POLR3K Cause POLR3‐Related Leukodystrophy 2024 ·Human Mutation ·(unknown), (unknown), (unknown), (unknown), Kether Guerrero, Luan T. Tran, Christoph W. Müller, Tomi Pastinen, Gustavo Maegawa, Isabelle Thiffault, Geneviève Bernard	0
2	Longitudinal Characterization of the Clinical Course of Intermediate-Severe Salla Disease 2023 ·Pediatric Neurology ·(unknown), (unknown), Luan T. Tran, Chantal Poulin, Geneviève Bernard	2
3	Biallelic pathogenic variants in POLR3D alter tRNA transcription and cause a hypomyelinating leukodystrophy: A case report 2023 ·Frontiers in Neurology ·(unknown), (unknown), Maxime Pinard, Luan T. Tran, Kether Guerrero, Chitra Prasad, Asuri N. Prasad, Tomi Pastinen, Isabelle Thiffault, Benoit Coulombe, Geneviève Bernard	4
4	Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing 2023 ·Frontiers in Neurology ·(unknown), Kether Guerrero, Luan T. Tran, Mackenzie A. Michell‐Robinson, Geneviève Legault, Bernard Brais, Michel Sylvain, (unknown), Michelle Demos, Wolfgang Köhler, Tomi Pastinen, Isabelle Thiffault, Geneviève Bernard	3
5	Hypomyelination caused by a novel homozygous pathogenic variant in FOLR1: complete clinical and radiological recovery with oral folinic acid therapy and review of the literature 2023 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), (unknown), (unknown), Jelena Ostojić, Luan T. Tran, Isabelle Thiffault, Tomi Pastinen, Raphael Schiffmann, Geneviève Bernard	3
6	A Cockayne-like phenotype resulting from a de novo variant in MORC2: expanding the phenotype of MORC2-related disorders 2022 ·Neurogenetics ·(unknown), (unknown), Luan T. Tran, Isabelle De Bie, Amélie Nadeau, (unknown), Anja Raams, Wim Vermeulen, Arjan F. Theil, Geneviève Bernard	2
7	The LORIS MyeliNeuroGene rare disease database for natural history studies and clinical trial readiness 2021 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), (unknown), Luan T. Tran, (unknown), (unknown), (unknown), Cécile Madjar, (unknown), (unknown), Samir Das, Alan C. Evans, Geneviève Bernard	7
8	A Novel De Novo Variant in DYNC1H1 Causes Spinal Muscular Atrophy Lower Extremity Predominant in Identical Twins: A Case Report 2021 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Luan T. Tran, Lei Cao-Lei, Maryam Oskoui, Myriam Srour, Chantal Poulin, Geneviève Bernard	2
9	Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease 2021 ·SHILAP Revista de lepidopterología ·(unknown), Hung‐Yu Shih, Diane Forget, (unknown), Luan T. Tran, Christian Poitras, Kether Guerrero, Sundaresan Tharun, Fowzan S. Alkuraya, Wesam Kurdi, (unknown), Anne‐Marie Laberge, Yue Si, Marie‐Soleil Gauthier, Joshua L. Bonkowsky, Benoit Coulombe, Geneviève Bernard	8
10	Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease 2018 ·Journal of Child Neurology ·Andrea Accogli, Kether Guerrero, Daniela D’Agostino, Luan T. Tran, Cécile Cieuta‐Walti, Isabelle Thiffault, Sébastien Chénier, Jeremy Schwartzentruber, Jacek Majewski, Geneviève Bernard	8
11	Dystonia in RNA Polymerase III‐Related Leukodystrophy 2018 ·Movement Disorders Clinical Practice ·(unknown), Luan T. Tran, Kether Guerrero, Adeline Vanderver, Raphael Schiffmann, Nicole I. Wolf, Sylvain Chouinard, Geneviève Bernard	18
12	Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy 2017 ·Annals of Neurology ·(unknown), (unknown), Martine Tétreault, Luan T. Tran, (unknown), Myriam Srour, (unknown), Catherine Brunel‐Guitton, Jacek Majewski, Long Long, (unknown), Michael J. Gambello, Cas Simons, Adeline Vanderver, Geneviève Bernard	0
13	Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy 2017 ·Clinical Genetics ·(unknown), (unknown), Martine Tétreault, Luan T. Tran, (unknown), Myriam Srour, John J. Mitchell, Catherine Brunel‐Guitton, Jacek Majewski, (unknown), Stephanie Keller, Michael J. Gambello, Cas Simons, Adeline Vanderver, Geneviève Bernard	12
14	Large exonic deletions in POLRB gene cause POLR3-related leukodystrophy 2015 ·Orphanet Journal of Rare Diseases ·Mariana Gutiérrez, Isabelle Thiffault, Kether Guerrero, Gabriel Ángel Martos‐Moreno, Luan T. Tran, William Benko, Marjo S. van der Knaap, Rosalina M.L. van Spaendonk, Nicole I. Wolf, Geneviève Bernard	17
15	Recessive Mutations in POLR3B Encoding RNA Polymerase III Subunit Causing Diffuse Hypomyelination in Patients with 4H Leukodystrophy with Polymicrogyria and Cataracts 2015 ·Clinical Neuroradiology ·Elżbieta Jurkiewicz, Dorota Dunin-Wąsowicz, Dorota Gieruszczak‐Białek, (unknown), Kether Guerrero, Mariana Gutiérrez, Luan T. Tran, Geneviève Bernard	12
16	A pharmacodynamic comparison of a personalized strategy for anti-platelet therapy versus ticagrelor in achieving a therapeutic window 2015 ·International Journal of Cardiology ·(unknown), Joseph Abunassar, George A. Wells, Ruth McPherson, (unknown), Benjamin Hibbert, Marino Labinaz, Michel Le May, Alexander Dick, Chris Glover, Michael Froeschl, Jean-François Marquis, Luan T. Tran, Jordan Bernick, Aun‐Yeong Chong, Derek So	13
17	POLR3A and POLR3B Mutations in Unclassified Hypomyelination 2015 ·Neuropediatrics ·Rosalina van Spaendonk, Miriam Nickel, Annette Bley, Kether Guerrero, Luan T. Tran, Marjo S. van der Knaap, Geneviève Bernard, Ferdy Kurniawan Cayami, Roberta La Piana, Nicole I. Wolf	6
18	A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathy 2014 ·Neurogenetics ·Alireza Kashani, Isabelle Thiffault, Marie-Emmanuelle Dilenge, Christine Saint‐Martin, Kether Guerrero, Luan T. Tran, Eric A. Shoubridge, Marjo S. van der Knaap, Nancy Braverman, Geneviève Bernard	13
19	A PHARMACOGENOMIC APPROACH TO ANTIPLATELET THERAPY IN STEMI PATIENTS: REASSESSMENT OF ANTI-PLATELET THERAPY USING AN INDIVIDUALIZED STRATEGY IN PATIENTS WITH ST-ELEVATION MYOCARDIAL INFARCTION (THE RAPID STEMI STUDY) 2013 ·Journal of the American College of Cardiology ·(unknown), George A. Wells, Ruth McPherson, Marino Labinaz, Chris Glover, Michel Le May, Alexander Dick, Michael Froeschl, Jean-François Marquis, (unknown), Jordan Bernick, Luan T. Tran, Benjamin Hibbert, Jason D. Roberts	1
20	Glucose Is Arrhythmogenic in the Anoxic-Reoxygenated Embryonic Chick Heart 1996 ·Pediatric Research ·Luan T. Tran, Pavel Kučera, Y. de Ribaupierre, (unknown), Eric Raddatz	11

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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