Austin A Larson
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Metabolism and Genetic Disorders 11
- Genetics 23
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 8
- Co-authors
- Natalie Nokoff (3 shared papers)Penelope E. Bonnen (2 shared papers)Shireen Banerji (1 shared paper)Johan L.K. Van Hove (8 shared papers)Jon Kaufman (1 shared paper)Jasleen Kaur Daljit Singh (1 shared paper)David E. Mandelbaum (1 shared paper)Ellen Roy Elias (1 shared paper)
- Journals
- Molecular Genetics and Metabolism (10 papers)Genetics in Medicine (6 papers)Journal of Inherited Metabolic Disease (5 papers)Mitochondrion (5 papers)The American Journal of Human Genetics (4 papers)
- Partner nations
- United StatesFranceAustralia
In The Last Decade
Austin A Larson
66 papers receiving 1.9k citations
Austin A Larson's Hit Papers
Peers
Comparison fields: 5 of 102
- Clinical Biochemistry 184
- Genetics 506
- Molecular Biology 1.1k
- Genetics 118
- Cell Biology 163
Countries citing papers authored by Austin A Larson
This map shows the geographic impact of Austin A 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 A 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 A Larson more than expected).
Fields of papers citing papers by Austin A Larson
This network shows the impact of papers produced by Austin A 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 A Larson. The network helps show where Austin A Larson may publish in the future.
Co-authors
The 25 scholars most cited alongside Austin A 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 75 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease Hit paper breakdown → | 2019 | 637 |
| 2 | 2014 | 115 | |
| 3 | 2018 | 78 | |
| 4 | 2019 | 76 | |
| 5 | 2020 | 57 | |
| 6 | 2019 | 51 | |
| 7 | 2018 | 49 | |
| 8 | 2020 | 47 | |
| 9 | 2021 | 43 | |
| 10 | 2017 | 37 | |
| 11 | 2018 | 36 | |
| 12 | 2018 | 36 | |
| 13 | 2019 | 35 | |
| 14 | 2020 | 35 | |
| 15 | 2019 | 34 | |
| 16 | 2021 | 34 | |
| 17 | 2021 | 33 | |
| 18 | 2020 | 32 | |
| 19 | 2020 | 29 | |
| 20 | 2013 | 27 |
About Austin A Larson
Austin A Larson is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Cell Biology and Rheumatology, having authored 75 papers that have together received 2.0k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (15 papers), Metabolism and Genetic Disorders (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (8 papers), Cholesterol and Lipid Metabolism (6 papers), Glycosylation and Glycoproteins Research (6 papers) and RNA modifications and cancer (5 papers). The work is most often cited by research in Clinical Biochemistry (184 citations), Genetics (506 citations), Molecular Biology (1.1k citations), Genetics (118 citations) and Cell Biology (163 citations). Austin A Larson has collaborated with scholars based in United States, France and Australia. Frequent co-authors include Natalie Nokoff, Penelope E. Bonnen, Shireen Banerji, Johan L.K. Van Hove, Jon Kaufman, Jasleen Kaur Daljit Singh, David E. Mandelbaum, Ellen Roy Elias, Peter Russell Baker and Naomi J. L. Meeks. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, Journal of Inherited Metabolic Disease, Mitochondrion and The American Journal of Human Genetics.
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.