Rami Massie

2.4k total citations
27 papers, 454 citations indexed

About

Rami Massie is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Rami Massie has authored 27 papers receiving a total of 454 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Neurology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Rami Massie's work include Hereditary Neurological Disorders (6 papers), Mitochondrial Function and Pathology (4 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (4 papers). Rami Massie is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Mitochondrial Function and Pathology (4 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (4 papers). Rami Massie collaborates with scholars based in Canada, United States and Japan. Rami Massie's co-authors include Margherita Milone, C G Savory, Champ L. Baker, Peter James Dyck, Nathan P. Staff, Kimberly K. Amrami, Michelle L. Mauermann, Christopher J. Klein, Pierre R. Bourque and Jodi Warman‐Chardon and has published in prestigious journals such as Blood, Brain and Neurology.

In The Last Decade

Rami Massie

23 papers receiving 436 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rami Massie Canada 11 165 124 118 104 75 27 454
Andrew J. Waclawik United States 11 116 0.7× 100 0.8× 232 2.0× 136 1.3× 49 0.7× 36 534
Maria del Mar Amador France 11 231 1.4× 74 0.6× 133 1.1× 47 0.5× 33 0.4× 25 482
Bum Chun Suh South Korea 12 194 1.2× 32 0.3× 101 0.9× 191 1.8× 39 0.5× 44 451
Masamichi Fukushima Japan 10 157 1.0× 47 0.4× 118 1.0× 38 0.4× 31 0.4× 11 339
T. Morioka Japan 15 117 0.7× 119 1.0× 148 1.3× 53 0.5× 34 0.5× 32 567
Xiaodi Han China 10 137 0.8× 57 0.5× 92 0.8× 49 0.5× 27 0.4× 27 381
Robert‐Yves Carlier France 12 68 0.4× 57 0.5× 253 2.1× 103 1.0× 135 1.8× 37 546
Rati Choksi United States 16 321 1.9× 43 0.3× 209 1.8× 223 2.1× 220 2.9× 30 747
Gianna Berti Italy 13 77 0.5× 31 0.3× 222 1.9× 103 1.0× 35 0.5× 31 404
Naoki Nitta Japan 13 71 0.4× 147 1.2× 142 1.2× 262 2.5× 51 0.7× 42 625

Countries citing papers authored by Rami Massie

Since Specialization
Citations

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

Fields of papers citing papers by Rami Massie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rami Massie

This figure shows the co-authorship network connecting the top 25 collaborators of Rami Massie. A scholar is included among the top collaborators of Rami Massie 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 Rami Massie. Rami Massie 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.
Chen, Lijun, et al.. (2025). Beyond the Heart: Exploring Extracardiac Manifestations in Cardiac Amyloidosis for Early Diagnosis. Current Cardiology Reports. 27(1). 105–105.
2.
Massie, Rami, et al.. (2023). An adult patient with Tatton–Brown–Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy. American Journal of Medical Genetics Part A. 194(4). e63484–e63484. 1 indexed citations
3.
Hasıloğlu, Zehra Işık, et al.. (2023). Prevalence of Peripheral Nervous System Involvement in Adult Leukodystrophies (P2-5.031). Neurology. 100(17_supplement_2).
4.
Martin, Florence, Eric Bareke, Annie Laplante, et al.. (2022). Novel homozygous nonsense mutation of MLIP and compensatory alternative splicing. npj Genomic Medicine. 7(1). 36–36. 2 indexed citations
5.
Karamchandani, Jason, Bruno‐Pierre Dubé, Océane Landon‐Cardinal, et al.. (2022). Myositis with prominent B-cell aggregates causing shrinking lung syndrome in systemic lupus erythematosus: a case report. BMC Rheumatology. 6(1). 11–11. 1 indexed citations
6.
Pellerin, David, Rami Massie, Michael Ashley Stein, et al.. (2021). Breakthrough of Granulomatosis with Polyangiitis-Associated CNS Vasculitis Amidst Adequate B-cell Depletion. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 50(1). 152–154.
7.
Alcántara, Mónica, Michelle M. Mezei, Steven K. Baker, et al.. (2021). Canadian Guidelines for Hereditary Transthyretin Amyloidosis Polyneuropathy Management. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49(1). 7–18. 13 indexed citations
8.
Massie, Rami, et al.. (2021). MTP deficiency caused by HADHB mutations: Pathophysiology and clinical manifestations. Molecular Genetics and Metabolism. 133(1). 1–7. 20 indexed citations
9.
Chalk, Colin, et al.. (2020). Poor Yield of Routine Transthyretin Screening in Patients with Idiopathic Neuropathy. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 47(6). 816–819. 3 indexed citations
10.
Hodgkinson, Victoria, Ario Mirian, Angela Genge, et al.. (2018). Provincial Differences in the Diagnosis and Care of Amyotrophic Lateral Sclerosis. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45(6). 652–659. 13 indexed citations
11.
Gentil, Benoît J., Erin O’Ferrall, Colin Chalk, et al.. (2017). A New Mutation in FIG4 Causes a Severe Form of CMT4J Involving TRPV4 in the Pathogenic Cascade. Journal of Neuropathology & Experimental Neurology. 76(9). 789–799. 12 indexed citations
12.
Gagnon, Cynthia, et al.. (2017). Traduction française de l’échelle Charcot-Marie-Tooth Disease Pediatric Scale. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 44(6). 740–743. 8 indexed citations
13.
Parente, Fabienne, et al.. (2016). An unusual cause of Achilles tendon xanthoma. Journal of clinical lipidology. 10(4). 1040–1044. 7 indexed citations
14.
Bourque, Pierre R., Jodi Warman‐Chardon, & Rami Massie. (2015). Autoimmune peripheral neuropathies. Clinica Chimica Acta. 449. 37–42. 28 indexed citations
15.
Gupta, Gaurav, Rami Massie, Timothy J. Doherty, et al.. (2015). Diabetic Cranio‐Cervico‐Radiculoplexus Neuropathy. PM&R. 7(11). 1189–1193. 3 indexed citations
16.
Massie, Rami, Jing Wang, Victor Wei Zhang, et al.. (2012). Mitochondrial myopathy due to novel missense mutation in the cytochrome c oxidase 1 gene. Journal of the Neurological Sciences. 319(1-2). 158–163. 6 indexed citations
17.
Massie, Rami, Lee‐Jun C. Wong, & Margherita Milone. (2010). Exercise intolerance due to cytochrome b mutation. Muscle & Nerve. 42(1). 136–140. 15 indexed citations
18.
Milone, Margherita & Rami Massie. (2010). Polymerase Gamma 1 Mutations. The Neurologist. 16(2). 84–91. 68 indexed citations
19.
Baker, Champ L., et al.. (2007). Arthroscopic Bursectomy for Recalcitrant Trochanteric Bursitis. Arthroscopy The Journal of Arthroscopic and Related Surgery. 23(8). 827–832. 85 indexed citations
20.
Massie, Rami, Denis Sirhan, & Frédérick Andermann. (2006). Chronic Cluster-Like Headache Secondary to an Epidermoid Clival Lesion. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 33(4). 421–422. 5 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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