F. Güttler
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Rheumatology top 5%
- Folate and B Vitamins Research
Papers in
-
- Metabolism and Genetic Disorders 44
-
- Metabolomics and Mass Spectrometry Studies 10
- Mitochondrial Function and Pathology 7
- Biochemical and Molecular Research 5
- Co-authors
- Per Guldberg (22 shared papers)K. Henriksen (7 shared papers)Richard Koch (6 shared papers)Reuben Matalon (5 shared papers)Harvey L. Levy (5 shared papers)H. Lou (6 shared papers)P N Jørgensen (4 shared papers)Bobbye Rouse (3 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (17 papers)Acta Paediatrica (10 papers)European Journal of Pediatrics (3 papers)Scandinavian Journal of Immunology (3 papers)Clinical Genetics (3 papers)
- Partner nations
- DenmarkUnited StatesGermany
In The Last Decade
F. Güttler
66 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 99
- Clinical Biochemistry 953
- Rheumatology 263
- Biochemistry 137
- Physiology 305
- Molecular Biology 637
Countries citing papers authored by F. Güttler
This map shows the geographic impact of F. Güttler'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 F. Güttler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Güttler more than expected).
Fields of papers citing papers by F. Güttler
This network shows the impact of papers produced by F. Güttler. 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 F. Güttler. The network helps show where F. Güttler may publish in the future.
Co-authors
The 25 scholars most cited alongside F. Güttler, 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 68 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood. | 1980 | 178 |
| 2 | 2007 | 81 | |
| 3 | Multiple origins for phenylketonuria in Europe. | 1992 | 73 |
| 4 | Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study. | 1996 | 72 |
| 5 | 2000 | 50 | |
| 6 | 1994 | 50 | |
| 7 | 1995 | 48 | |
| 8 | 1996 | 47 | |
| 9 | 1991 | 46 | |
| 10 | 2000 | 43 | |
| 11 | 1979 | 35 | |
| 12 | 1991 | 31 | |
| 13 | 1994 | 28 | |
| 14 | 1990 | 27 | |
| 15 | 1997 | 27 | |
| 16 | 2006 | 27 | |
| 17 | 1967 | 23 | |
| 18 | 1972 | 23 | |
| 19 | 1995 | 22 | |
| 20 | 1987 | 22 |
About F. Güttler
F. Güttler is a scholar working on Clinical Biochemistry, Molecular Biology, Rheumatology, Physiology and Biochemistry, having authored 68 papers that have together received 1.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (44 papers), Folate and B Vitamins Research (20 papers), Metabolomics and Mass Spectrometry Studies (10 papers), Mitochondrial Function and Pathology (7 papers), Amino Acid Enzymes and Metabolism (6 papers), Diet and metabolism studies (6 papers), Biochemical and Molecular Research (5 papers) and Neonatal Health and Biochemistry (4 papers). The work is most often cited by research in Clinical Biochemistry (953 citations), Rheumatology (263 citations), Biochemistry (137 citations), Physiology (305 citations) and Molecular Biology (637 citations). F. Güttler has collaborated with scholars based in Denmark, United States and Germany. Frequent co-authors include Per Guldberg, K. Henriksen, Richard Koch, Reuben Matalon, Harvey L. Levy, H. Lou, P N Jørgensen, Bobbye Rouse, Felix de la Cruz and Savio L.C. Woo. Their work appears in journals such as Journal of Inherited Metabolic Disease, Acta Paediatrica, European Journal of Pediatrics, Scandinavian Journal of Immunology and Clinical 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.