Austin Larson
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
-
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA and protein synthesis mechanisms
- Coenzyme Q10 studies and effects
Papers in
-
- Mitochondrial Function and Pathology 9
- ATP Synthase and ATPases Research 4
- Glycosylation and Glycoproteins Research 3
- Genetics 10
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 4
- Co-authors
- Shireen Banerji (1 shared paper)Jon Kaufman (1 shared paper)Natalie Nokoff (3 shared papers)David E. Mandelbaum (1 shared paper)Penelope E. Bonnen (2 shared papers)Johan L.K. Van Hove (8 shared papers)Jasleen Singh (1 shared paper)Johan Van Hove (2 shared papers)
- Journals
- Molecular Genetics and Metabolism (7 papers)Mitochondrion (5 papers)Journal of Inherited Metabolic Disease (2 papers)Genetics in Medicine (2 papers)Frontiers in Pediatrics (1 paper)
- Partner nations
- United StatesAustraliaCanada
In The Last Decade
Austin Larson
32 papers receiving 348 citations
Peers
Comparison fields: 5 of 64
- Clinical Biochemistry 58
- Molecular Biology 179
- Genetics 67
- Aging 4
- Nephrology 14
Countries citing papers authored by Austin Larson
This map shows the geographic impact of Austin Larson'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 Austin Larson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Austin Larson more than expected).
Fields of papers citing papers by Austin Larson
This network shows the impact of papers produced by Austin Larson. 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 Austin Larson. The network helps show where Austin Larson may publish in the future.
Co-authors
The 25 scholars most cited alongside Austin Larson, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 43 | |
| 2 | 2017 | 35 | |
| 3 | 2018 | 30 | |
| 4 | 2013 | 28 | |
| 5 | 2018 | 20 | |
| 6 | 2019 | 18 | |
| 7 | 2020 | 16 | |
| 8 | 2021 | 15 | |
| 9 | 2022 | 13 | |
| 10 | 2023 | 13 | |
| 11 | 2019 | 12 | |
| 12 | 2016 | 12 | |
| 13 | Genetic causes of pituitary hormone deficiencies. | 2015 | 12 |
| 14 | 2012 | 11 | |
| 15 | 2018 | 11 | |
| 16 | Disorders of sex development: clinically relevant genes involved in gonadal differentiation. | 2012 | 10 |
| 17 | 2021 | 8 | |
| 18 | 2021 | 7 | |
| 19 | 2022 | 6 | |
| 20 | 2024 | 5 |
About Austin Larson
Austin Larson is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cell Biology and Physiology, having authored 40 papers that have together received 356 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (8 papers), Genetics and Neurodevelopmental Disorders (4 papers), ATP Synthase and ATPases Research (4 papers), Genomics and Rare Diseases (4 papers), Lysosomal Storage Disorders Research (4 papers), Cellular transport and secretion (3 papers) and Glycosylation and Glycoproteins Research (3 papers). The work is most often cited by research in Clinical Biochemistry (58 citations), Molecular Biology (179 citations), Genetics (67 citations), Aging (4 citations) and Nephrology (14 citations). Austin Larson has collaborated with scholars based in United States, Australia and Canada. Frequent co-authors include Shireen Banerji, Jon Kaufman, Natalie Nokoff, David E. Mandelbaum, Penelope E. Bonnen, Johan L.K. Van Hove, Jasleen Singh, Johan Van Hove, Ellen Roy Elias and Peter R. Baker. Their work appears in journals such as Molecular Genetics and Metabolism, Mitochondrion, Journal of Inherited Metabolic Disease, Genetics in Medicine and Frontiers in Pediatrics.
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.