Alex MacKenzie
Impact in
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research
- Genomics and Rare Diseases
- Molecular Biology top 1%
- Cell death mechanisms and regulation
- Mitochondrial Function and Pathology
- RNA modifications and cancer
- RNA Interference and Gene Delivery
Papers in
- Genetics 39
- Neurogenetic and Muscular Disorders Research 37
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- RNA modifications and cancer 31
- Cell death mechanisms and regulation 19
- Mitochondrial Function and Pathology 15
- RNA Research and Splicing 15
- Co-authors
- Robert G. KornelukStephen BairdEric C. LaCasseKym M. BoycottDennis E. BulmanMegan R. VanstoneKatsuyuki TamaiCharles Lefebvre
- Journals
- Human Molecular Genetics (5 papers)Genomics (5 papers)Orphanet Journal of Rare Diseases (4 papers)The Science of The Total Environment (4 papers)Neurology (4 papers)
- Partner nations
- CanadaUnited StatesSpain
In The Last Decade
Alex MacKenzie
120 papers receiving 6.7k citations
Hit Papers
Peers
Comparison fields: 5 of 160
- Genetics 739
- Molecular Biology 4.6k
- Cellular and Molecular Neuroscience 784
- Cancer Research 588
- Genetics 1.1k
Countries citing papers authored by Alex MacKenzie
This map shows the geographic impact of Alex MacKenzie'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 Alex MacKenzie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alex MacKenzie more than expected).
Fields of papers citing papers by Alex MacKenzie
This network shows the impact of papers produced by Alex MacKenzie. 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 Alex MacKenzie. The network helps show where Alex MacKenzie may publish in the future.
Co-authors
The 25 scholars most cited alongside Alex MacKenzie, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2024 | 0 | |
| 3 | 2024 | 2 | |
| 4 | 2023 | 1 | |
| 5 | 2023 | 5 | |
| 6 | 2022 | 76 | |
| 7 | 2021 | 1 | |
| 8 | 2017 | 11 | |
| 9 | 2017 | 11 | |
| 10 | 2016 | 47 | |
| 11 | 2015 | 11 | |
| 12 | The study of drugs for rare disorders: harnessing research contributions by Canadian academic institutions. | 2014 | 2 |
| 13 | Rare-disease genetics in the era of next-generation sequencing: discovery to translation Hit paper breakdown → | 2013 | 496 |
| 14 | 2002 | 12 | |
| 15 | 2000 | 59 | |
| 16 | 1999 | 43 | |
| 17 | The inhibitors of apoptosis (IAPs) and their emerging role in cancer Hit paper breakdown → | 1998 | 837 |
| 18 | 1997 | 50 | |
| 19 | Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome Hit paper breakdown → | 1996 | 593 |
| 20 | 1991 | 2 |
About Alex MacKenzie
Alex MacKenzie is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Cellular and Molecular Neuroscience and Biochemistry, having authored 125 papers that have together received 6.8k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (37 papers), RNA modifications and cancer (31 papers), Cell death mechanisms and regulation (19 papers), Mitochondrial Function and Pathology (15 papers), RNA Research and Splicing (15 papers), Congenital Anomalies and Fetal Surgery (13 papers), Genetic Neurodegenerative Diseases (11 papers) and SARS-CoV-2 detection and testing (10 papers). The work is most often cited by research in Genetics (739 citations), Molecular Biology (4.6k citations), Cellular and Molecular Neuroscience (784 citations), Cancer Research (588 citations) and Genetics (1.1k citations). Alex MacKenzie has collaborated with scholars based in Canada, United States and Spain. Frequent co-authors include Robert G. Korneluk, Stephen Baird, Eric C. LaCasse, Kym M. Boycott, Dennis E. Bulman, Megan R. Vanstone, Katsuyuki Tamai, Charles Lefebvre, Reza Mastery Farahani and Natalie Roy. Their work appears in journals such as Human Molecular Genetics, Genomics, Orphanet Journal of Rare Diseases, The Science of The Total Environment and Neurology.
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.