A. Micheil Innes
- Genetics top 2%
- Genomics and Rare Diseases 21
- Genetics and Neurodevelopmental Disorders 17
- Genomic variations and chromosomal abnormalities 16
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 10
- Molecular Biology top 5%
- Congenital heart defects research 12
- RNA modifications and cancer 11
- Mitochondrial Function and Pathology 11
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- Prenatal Screening and Diagnostics 12
- Sensory Systems top 5%
- Co-authors
- Jillian S. ParboosinghKym M. BoycottDavid A. DymentFrançois P. BernierJacek MajewskiLina Basel‐VanagaiteJeremy SchwartzentruberRyan E. Lamont
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
A. Micheil Innes
110 papers receiving 3.4k citations
Peers
Comparison fields: 5 of 130
- Genetics 1.1k
- Clinical Biochemistry 206
- Molecular Biology 2.0k
- Pediatrics, Perinatology and Child Health 531
- Sensory Systems 106
Countries citing papers authored by A. Micheil Innes
This map shows the geographic impact of A. Micheil Innes'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 A. Micheil Innes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Micheil Innes more than expected).
Fields of papers citing papers by A. Micheil Innes
This network shows the impact of papers produced by A. Micheil Innes. 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 A. Micheil Innes. The network helps show where A. Micheil Innes may publish in the future.
Co-authorship network
The 25 scholars most cited alongside A. Micheil Innes, 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 | 1 | |
| 2 | 2024 | 4 | |
| 3 | 2024 | 5 | |
| 4 | 2024 | 1 | |
| 5 | 2024 | 0 | |
| 6 | 2024 | 0 | |
| 7 | 2023 | 6 | |
| 8 | 2022 | 5 | |
| 9 | 2019 | 16 | |
| 10 | 2019 | 45 | |
| 11 | 2018 | 13 | |
| 12 | 2016 | 13 | |
| 13 | 2014 | 21 | |
| 14 | 2013 | 28 | |
| 15 | 2012 | 8 | |
| 16 | 2012 | 2 | |
| 17 | 2006 | 17 | |
| 18 | 2005 | 4 | |
| 19 | 2004 | 405 | |
| 20 | 2003 | 6 |
About A. Micheil Innes
A. Micheil Innes is a scholar working on Genetics, Clinical Biochemistry and Developmental Biology, having authored 113 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (21 papers), Genetics and Neurodevelopmental Disorders (17 papers), Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (12 papers), Congenital heart defects research (12 papers), RNA modifications and cancer (11 papers), Mitochondrial Function and Pathology (11 papers) and Metabolism and Genetic Disorders (10 papers). The work is most often cited by research in Genetics (1.1k citations), Clinical Biochemistry (206 citations) and Molecular Biology (2.0k citations). A. Micheil Innes has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Jillian S. Parboosingh, Kym M. Boycott, David A. Dyment, François P. Bernier, Jacek Majewski, Lina Basel‐Vanagaite, Jeremy Schwartzentruber, Ryan E. Lamont, A. James Barkovich and Rachel Straussberg.
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.