Janet Marcadier
Impact in
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
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- RNA modifications and cancer 2
- RNA and protein synthesis mechanisms 1
- Surgery 3
- Congenital Anomalies and Fetal Surgery 2
- Co-authors
- Jeremy Schwartzentruber (2 shared papers)Kym M. Boycott (2 shared papers)Jacek Majewski (2 shared papers)Mark A. Tarnopolsky (3 shared papers)Hilde Van Esch (1 shared paper)Lysanne Patry (1 shared paper)Mark E. Samuels (1 shared paper)Jean‐Pierre Fryns (1 shared paper)
- Journals
- Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (2 papers)Clinical Genetics (2 papers)Human Mutation (1 paper)BMJ Open (1 paper)Canadian Journal of Cardiology (1 paper)
- Partner nations
- CanadaUnited States
In The Last Decade
Janet Marcadier
8 papers receiving 237 citations
Peers
Comparison fields: 5 of 47
- Genetics 44
- Genetics 110
- Pediatrics, Perinatology and Child Health 47
- Molecular Biology 119
- Psychiatry and Mental health 24
Countries citing papers authored by Janet Marcadier
This map shows the geographic impact of Janet Marcadier'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 Janet Marcadier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Janet Marcadier more than expected).
Fields of papers citing papers by Janet Marcadier
This network shows the impact of papers produced by Janet Marcadier. 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 Janet Marcadier. The network helps show where Janet Marcadier may publish in the future.
Co-authors
The 25 scholars most cited alongside Janet Marcadier, 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 | 2011 | 81 | |
| 2 | 2014 | 64 | |
| 3 | 2011 | 36 | |
| 4 | 2020 | 26 | |
| 5 | 2010 | 20 | |
| 6 | 2021 | 12 | |
| 7 | 2014 | 4 | |
| 8 | 2011 | 1 |
About Janet Marcadier
Janet Marcadier is a scholar working on Molecular Biology, Surgery, Genetics, Public Health, Environmental and Occupational Health and Genetics, having authored 8 papers that have together received 244 indexed citations. Recurring topics across this work include Congenital Anomalies and Fetal Surgery (2 papers), RNA modifications and cancer (2 papers), Genomics and Rare Diseases (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Metabolism and Genetic Disorders (1 paper), Gestational Trophoblastic Disease Studies (1 paper), RNA and protein synthesis mechanisms (1 paper) and Parvovirus B19 Infection Studies (1 paper). The work is most often cited by research in Genetics (44 citations), Genetics (110 citations), Pediatrics, Perinatology and Child Health (47 citations), Molecular Biology (119 citations) and Psychiatry and Mental health (24 citations). Janet Marcadier has collaborated with scholars based in Canada and United States. Frequent co-authors include Jeremy Schwartzentruber, Kym M. Boycott, Jacek Majewski, Mark A. Tarnopolsky, Hilde Van Esch, Lysanne Patry, Mark E. Samuels, Jean‐Pierre Fryns, Jacques L. Michaud and Fergus E. McKiernan. Their work appears in journals such as Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Clinical Genetics, Human Mutation, BMJ Open and Canadian Journal of Cardiology.
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.