Luan T. Tran

867 citations

25 papers · 205 indexed · h-index 9

Internal Medicine
Cardiology and Cardiovascular Medicine
- Antiplatelet Therapy and Cardiovascular Diseases 3
Clinical Biochemistry
Molecular Biology
- RNA regulation and disease 13
- RNA modifications and cancer 7
- RNA and protein synthesis mechanisms 5
- RNA Research and Splicing 4
- Mitochondrial Function and Pathology 3
Structural Biology
Genetics
- Genetics and Neurodevelopmental Disorders 4
Rheumatology
- Glycogen Storage Diseases and Myoclonus 2

Co-authors: Geneviève Bernard Kether Guerrero Isabelle Thiffault Nicole I. Wolf Heather D. Durham Marjo S. van der Knaap Kathleen E. Sullivan Benoît J. Gentil
Cited by: Internal Medicine Cardiology and Cardiovascular Medicine Clinical Biochemistry
Journals: SHILAP Revista de lepidopterología (2 papers)Journal of the American College of Cardiology (1 paper)Annals of Neurology (1 paper)
Partner nations: Canada United States Netherlands

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

The 25 scholars most cited alongside Luan T. Tran, 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 Luan T. Tran Line = papers co-authored together Luan T. Tran links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Novel Pathogenic Variants in POLR3K Cause POLR3‐Related Leukodystrophy Human Mutation ·Stefanie Perrier,Julia Macintosh,Agata D. Misiaszek,Gabrielle Lambert,Kether Guerrero,Luan T. Tran,Christoph W. Müller,Tomi Pastinen,Gustavo Maegawa,Isabelle Thiffault,Geneviève Bernard	2024	0
2	Longitudinal Characterization of the Clinical Course of Intermediate-Severe Salla Disease Pediatric Neurology ·Alexandra Chapleau,Amytice Mirchi,Luan T. Tran,Chantal Poulin,Geneviève Bernard	2023	2
3	Biallelic pathogenic variants in POLR3D alter tRNA transcription and cause a hypomyelinating leukodystrophy: A case report Frontiers in Neurology ·Julia Macintosh,Stefanie Perrier,Maxime Pinard,Luan T. Tran,Kether Guerrero,Chitra Prasad,Asuri N. Prasad,Tomi Pastinen,Isabelle Thiffault,Benoit Coulombe,Geneviève Bernard	2023	4
4	Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing Frontiers in Neurology ·Stefanie Perrier,Kether Guerrero,Luan T. Tran,Mackenzie A. Michell‐Robinson,Geneviève Legault,Bernard Brais,Michel Sylvain,James Dorman,Michelle Demos,Wolfgang Köhler,Tomi Pastinen,Isabelle Thiffault,Geneviève Bernard	2023	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 Orphanet Journal of Rare Diseases ·Ana Potic,Stefanie Perrier,Tijana Radović,Svetlana Gavrilović,Jelena Ostojić,Luan T. Tran,Isabelle Thiffault,Tomi Pastinen,Raphael Schiffmann,Geneviève Bernard	2023	3
6	A Cockayne-like phenotype resulting from a de novo variant in MORC2: expanding the phenotype of MORC2-related disorders Neurogenetics ·Amytice Mirchi,Alexa Derksen,Luan T. Tran,Isabelle De Bie,Amélie Nadeau,Audrey Lovett,Anja Raams,Wim Vermeulen,Arjan F. Theil,Geneviève Bernard	2022	2
7	The LORIS MyeliNeuroGene rare disease database for natural history studies and clinical trial readiness Orphanet Journal of Rare Diseases ·Aaron Spahr,Zaliqa Rosli,Mélanie Legault,Luan T. Tran,Simon Fournier,Helia Toutounchi,Lama Darbelli,Cécile Madjar,Cassandra Lucia,Marie-Lou St-Jean,Samir Das,Alan C. Evans,Geneviève Bernard	2021	7
8	A Novel De Novo Variant in DYNC1H1 Causes Spinal Muscular Atrophy Lower Extremity Predominant in Identical Twins: A Case Report SHILAP Revista de lepidopterología ·Alexa Derksen,Amytice Mirchi,Luan T. Tran,Lei Cao-Lei,Maryam Oskoui,Myriam Srour,Chantal Poulin,Geneviève Bernard	2021	2
9	Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease SHILAP Revista de lepidopterología ·Alexa Derksen,Hung‐Yu Shih,Diane Forget,Lama Darbelli,Luan T. Tran,Christian Poitras,Kether Guerrero,Sundaresan Tharun,Fowzan S. Alkuraya,Wesam Kurdi,Cam‐Tu Émilie Nguyen,Anne‐Marie Laberge,Yue Si,Marie‐Soleil Gauthier,Joshua L. Bonkowsky,Benoit Coulombe,Geneviève Bernard	2021	8
10	Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease 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	2018	8
11	Dystonia in RNA Polymerase III‐Related Leukodystrophy Movement Disorders Clinical Practice ·Ghalia Al Yazidi,Luan T. Tran,Kether Guerrero,Adeline Vanderver,Raphael Schiffmann,Nicole I. Wolf,Sylvain Chouinard,Geneviève Bernard	2018	18
12	Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy Annals of Neurology ·Stefanie Perrier,Laurence Gauquelin,Martine Tétreault,Luan T. Tran,Neil Webb,Myriam Srour,Joshua R. Mitchell,Catherine Brunel‐Guitton,Jacek Majewski,Long Long,S Keller,Michael J. Gambello,Cas Simons,Adeline Vanderver,Geneviève Bernard	2017	0
13	Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy Clinical Genetics ·Stefanie Perrier,Laurence Gauquelin,Martine Tétreault,Luan T. Tran,Neil Webb,Myriam Srour,John J. Mitchell,Catherine Brunel‐Guitton,Jacek Majewski,V. Long,Stephanie Keller,Michael J. Gambello,Cas Simons,Adeline Vanderver,Geneviève Bernard	2017	12
14	Large exonic deletions in POLRB gene cause POLR3-related leukodystrophy 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	2015	17
15	Recessive Mutations in POLR3B Encoding RNA Polymerase III Subunit Causing Diffuse Hypomyelination in Patients with 4H Leukodystrophy with Polymicrogyria and Cataracts Clinical Neuroradiology ·Elżbieta Jurkiewicz,Dorota Dunin-Wąsowicz,Dorota Gieruszczak‐Białek,Katarzyna Malczyk,Kether Guerrero,Mariana Gutiérrez,Luan T. Tran,Geneviève Bernard	2015	12
16	A pharmacodynamic comparison of a personalized strategy for anti-platelet therapy versus ticagrelor in achieving a therapeutic window International Journal of Cardiology ·Nikita Malhotra,Joseph Abunassar,George A. Wells,Ruth McPherson,Angel Fu,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	2015	13
17	POLR3A and POLR3B Mutations in Unclassified Hypomyelination 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	2015	6
18	A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathy 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	2014	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) Journal of the American College of Cardiology ·Derek Yiu Fai So,George A. Wells,Ruth McPherson,Marino Labinaz,Chris Glover,Michel Le May,Alexander Dick,Michael Froeschl,Jean-François Marquis,Nitan Garg,Jordan Bernick,Luan T. Tran,Benjamin Hibbert,Jason D. Roberts	2013	1
20	Glucose Is Arrhythmogenic in the Anoxic-Reoxygenated Embryonic Chick Heart Pediatric Research ·Luan T. Tran,Pavel Kučera,Y. de Ribaupierre,Anne-Catherine Rochat,Eric Raddatz	1996	11

About Luan T. Tran

Luan T. Tran is a scholar working on Rheumatology, Molecular Biology and Cardiology and Cardiovascular Medicine, having authored 25 papers that have together received 205 indexed citations. Recurring topics across this work include RNA regulation and disease (13 papers), RNA modifications and cancer (7 papers), RNA and protein synthesis mechanisms (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), RNA Research and Splicing (4 papers), Mitochondrial Function and Pathology (3 papers), Antiplatelet Therapy and Cardiovascular Diseases (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). The work is most often cited by research in Internal Medicine (12 citations), Cardiology and Cardiovascular Medicine (52 citations) and Clinical Biochemistry (15 citations). Luan T. Tran has collaborated with scholars based in Canada, United States and Netherlands. Frequent 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. Their work appears in journals such as SHILAP Revista de lepidopterología, Journal of the American College of Cardiology and Annals of Neurology.

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