Hans C. Andersson
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Physiology top 1%
- Lysosomal Storage Disorders Research
- Diet and metabolism studies
Papers in
-
- DNA Repair Mechanisms 11
- Plant tissue culture and regeneration 7
-
- Plant Genetic and Mutation Studies 8
- Co-authors
- Paige Kaplan (7 shared papers)B.A. Kihlman (16 shared papers)Joel Charrow (5 shared papers)Barry E. Rosenbloom (5 shared papers)Neal J. Weinreb (5 shared papers)Pramod K. Mistry (5 shared papers)Gregory M. Pastores (4 shared papers)Rebecca S. Wappner (4 shared papers)
- Journals
- The Journal of Pediatrics (11 papers)Hereditas (8 papers)Genetics in Medicine (7 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (5 papers)Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (4 papers)
- Partner nations
- United StatesSwedenPakistan
In The Last Decade
Hans C. Andersson
99 papers receiving 3.6k citations
Hit Papers
Peers
Comparison fields: 5 of 146
- Clinical Biochemistry 583
- Physiology 1.6k
- Cell Biology 731
- Chemical Health and Safety 17
- Biochemistry 182
Countries citing papers authored by Hans C. Andersson
This map shows the geographic impact of Hans C. Andersson'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 Hans C. Andersson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hans C. Andersson more than expected).
Fields of papers citing papers by Hans C. Andersson
This network shows the impact of papers produced by Hans C. Andersson. 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 Hans C. Andersson. The network helps show where Hans C. Andersson may publish in the future.
Co-authors
The 25 scholars most cited alongside Hans C. Andersson, 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 104 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 | 465 |
| 2 | 2002 | 404 | |
| 3 | 2000 | 398 | |
| 4 | 2001 | 281 | |
| 5 | 2006 | 150 | |
| 6 | 2008 | 120 | |
| 7 | 1994 | 99 | |
| 8 | 2021 | 96 | |
| 9 | 2005 | 89 | |
| 10 | 2012 | 83 | |
| 11 | 2004 | 82 | |
| 12 | 2002 | 81 | |
| 13 | 1980 | 71 | |
| 14 | 2016 | 63 | |
| 15 | 2010 | 58 | |
| 16 | 1990 | 57 | |
| 17 | 1998 | 53 | |
| 18 | 2013 | 53 | |
| 19 | 1999 | 46 | |
| 20 | 1999 | 43 |
About Hans C. Andersson
Hans C. Andersson is a scholar working on Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Physiology, having authored 104 papers that have together received 3.8k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (16 papers), Carcinogens and Genotoxicity Assessment (15 papers), DNA Repair Mechanisms (11 papers), Lysosomal Storage Disorders Research (11 papers), Neonatal Health and Biochemistry (11 papers), Biomedical Research and Pathophysiology (8 papers), Plant Genetic and Mutation Studies (8 papers) and Plant tissue culture and regeneration (7 papers). The work is most often cited by research in Clinical Biochemistry (583 citations), Physiology (1.6k citations), Cell Biology (731 citations), Chemical Health and Safety (17 citations) and Biochemistry (182 citations). Hans C. Andersson has collaborated with scholars based in United States, Sweden and Pakistan. Frequent co-authors include Paige Kaplan, B.A. Kihlman, Joel Charrow, Barry E. Rosenbloom, Neal J. Weinreb, Pramod K. Mistry, Gregory M. Pastores, Rebecca S. Wappner, Edwin H. Kolodny and C. Ronald Scott. Their work appears in journals such as The Journal of Pediatrics, Hereditas, Genetics in Medicine, Mutation research. Fundamental and molecular mechanisms of mutagenesis and Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis.
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.