Bruno Maranda
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
Papers in
-
- Metabolism and Genetic Disorders 18
- Physiology 18
- Lysosomal Storage Disorders Research 16
- Co-authors
- Christiane Auray‐Blais (16 shared papers)Paméla Lavoie (7 shared papers)Ross B. Hodgetts (1 shared paper)Rachel Laframboise (8 shared papers)Sylvain G. Bourgoin (2 shared papers)Vladimir N. Marshansky (2 shared papers)Patrick Vinay (2 shared papers)Grant A. Mitchell (6 shared papers)
- Journals
- The American Journal of Human Genetics (5 papers)Molecular Genetics and Metabolism (5 papers)Journal of Medical Genetics (5 papers)Journal of Inherited Metabolic Disease (4 papers)Orphanet Journal of Rare Diseases (4 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Bruno Maranda
79 papers receiving 3.2k citations
Peers
Comparison fields: 5 of 112
- Clinical Biochemistry 655
- Genetics 769
- Developmental Biology 56
- Cell Biology 363
- Molecular Biology 1.5k
Countries citing papers authored by Bruno Maranda
This map shows the geographic impact of Bruno Maranda'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 Bruno Maranda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bruno Maranda more than expected).
Fields of papers citing papers by Bruno Maranda
This network shows the impact of papers produced by Bruno Maranda. 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 Bruno Maranda. The network helps show where Bruno Maranda may publish in the future.
Co-authors
The 25 scholars most cited alongside Bruno Maranda, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 290 | |
| 2 | 2008 | 252 | |
| 3 | 2016 | 217 | |
| 4 | 2001 | 121 | |
| 5 | 2015 | 115 | |
| 6 | 2012 | 114 | |
| 7 | 2013 | 113 | |
| 8 | 2013 | 108 | |
| 9 | 2012 | 107 | |
| 10 | 2010 | 103 | |
| 11 | 2016 | 91 | |
| 12 | 2011 | 85 | |
| 13 | 2008 | 83 | |
| 14 | 2011 | 81 | |
| 15 | 2012 | 67 | |
| 16 | 2012 | 60 | |
| 17 | 2015 | 59 | |
| 18 | 2016 | 59 | |
| 19 | 2008 | 56 | |
| 20 | 2009 | 56 |
About Bruno Maranda
Bruno Maranda is a scholar working on Clinical Biochemistry, Physiology, Genetics, Molecular Biology and Cell Biology, having authored 80 papers that have together received 3.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (18 papers), Lysosomal Storage Disorders Research (16 papers), Biochemical and Molecular Research (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Biomedical Research and Pathophysiology (5 papers), Neonatal Health and Biochemistry (5 papers), Mitochondrial Function and Pathology (4 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). The work is most often cited by research in Clinical Biochemistry (655 citations), Genetics (769 citations), Developmental Biology (56 citations), Cell Biology (363 citations) and Molecular Biology (1.5k citations). Bruno Maranda has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Christiane Auray‐Blais, Paméla Lavoie, Ross B. Hodgetts, Rachel Laframboise, Sylvain G. Bourgoin, Vladimir N. Marshansky, Patrick Vinay, Grant A. Mitchell, Emmanuelle Lemyre and Marie A. Lambert. Their work appears in journals such as The American Journal of Human Genetics, Molecular Genetics and Metabolism, Journal of Medical Genetics, Journal of Inherited Metabolic Disease and Orphanet Journal of Rare Diseases.
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.