John J. Mitchell
Impact in
- Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
- Physiology top 2%
- Lysosomal Storage Disorders Research
Papers in
-
- Metabolism and Genetic Disorders 37
- Physiology 45
- Lysosomal Storage Disorders Research 42
- Co-authors
- Charles R. Scriver (5 shared papers)Yannis J Trakadis (4 shared papers)Janet Woodcock‐Mitchell (12 shared papers)Xiao‐Jian Sun (2 shared papers)Robert B. Low (8 shared papers)Barbara K. Burton (20 shared papers)Nancy Braverman (2 shared papers)Barry H. Thompson (1 shared paper)
- Journals
- Molecular Genetics and Metabolism (26 papers)Orphanet Journal of Rare Diseases (11 papers)Journal of Inherited Metabolic Disease (6 papers)Human Mutation (4 papers)American Journal of Respiratory Cell and Molecular Biology (3 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
John J. Mitchell
114 papers receiving 4.9k citations
John J. Mitchell's Hit Papers
Peers
Comparison fields: 5 of 135
- Clinical Biochemistry 1.7k
- Physiology 828
- Genetics 688
- Rheumatology 210
- Molecular Biology 814
Countries citing papers authored by John J. Mitchell
This map shows the geographic impact of John J. Mitchell'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 John J. Mitchell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John J. Mitchell more than expected).
Fields of papers citing papers by John J. Mitchell
This network shows the impact of papers produced by John J. Mitchell. 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 John J. Mitchell. The network helps show where John J. Mitchell may publish in the future.
Co-authors
The 25 scholars most cited alongside John J. Mitchell, 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 124 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Phenylalanine hydroxylase deficiency: diagnosis and management guideline Hit paper breakdown → | 2014 | 551 |
| 2 | Phenylalanine hydroxylase deficiency Hit paper breakdown → | 2011 | 412 |
| 3 | 2010 | 295 | |
| 4 | 2014 | 204 | |
| 5 | 1999 | 190 | |
| 6 | 2008 | 187 | |
| 7 | 2002 | 180 | |
| 8 | 1988 | 177 | |
| 9 | Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schools. | 1996 | 132 |
| 10 | 2003 | 131 | |
| 11 | 2013 | 119 | |
| 12 | 2012 | 115 | |
| 13 | 1990 | 102 | |
| 14 | 2010 | 102 | |
| 15 | Alpha-smooth muscle actin in parenchymal cells of bleomycin-injured rat lung. | 1989 | 95 |
| 16 | 1990 | 90 | |
| 17 | 2019 | 88 | |
| 18 | 2004 | 87 | |
| 19 | 2016 | 72 | |
| 20 | 2016 | 59 |
About John J. Mitchell
John J. Mitchell is a scholar working on Clinical Biochemistry, Physiology, Rheumatology, Cell Biology and Genetics, having authored 124 papers that have together received 5.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (42 papers), Metabolism and Genetic Disorders (37 papers), Glycogen Storage Diseases and Myoclonus (8 papers), Skin and Cellular Biology Research (6 papers), Cellular Mechanics and Interactions (4 papers), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (4 papers), Neonatal Respiratory Health Research (4 papers) and Pancreatic function and diabetes (3 papers). The work is most often cited by research in Clinical Biochemistry (1.7k citations), Physiology (828 citations), Genetics (688 citations), Rheumatology (210 citations) and Molecular Biology (814 citations). John J. Mitchell has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Charles R. Scriver, Yannis J Trakadis, Janet Woodcock‐Mitchell, Xiao‐Jian Sun, Robert B. Low, Barbara K. Burton, Nancy Braverman, Barry H. Thompson, Susan A. Berry and Hans C. Andersson. Their work appears in journals such as Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, Journal of Inherited Metabolic Disease, Human Mutation and American Journal of Respiratory Cell and Molecular Biology.
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.