F. Güttler

1.6k total citations
67 papers, 1.2k citations indexed

About

F. Güttler is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, F. Güttler has authored 67 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Clinical Biochemistry, 31 papers in Molecular Biology and 19 papers in Rheumatology. Recurrent topics in F. Güttler's work include Metabolism and Genetic Disorders (43 papers), Folate and B Vitamins Research (19 papers) and Metabolomics and Mass Spectrometry Studies (10 papers). F. Güttler is often cited by papers focused on Metabolism and Genetic Disorders (43 papers), Folate and B Vitamins Research (19 papers) and Metabolomics and Mass Spectrometry Studies (10 papers). F. Güttler collaborates with scholars based in Denmark, United States and Germany. F. Güttler's co-authors include Per Guldberg, K. Henriksen, Richard Koch, Reuben Matalon, H. Lou, Harvey L. Levy, Bobbye Rouse, Felix de la Cruz, Savio L.C. Woo and P N Jørgensen and has published in prestigious journals such as Human Molecular Genetics, Infection and Immunity and Biochimica et Biophysica Acta (BBA) - General Subjects.

In The Last Decade

F. Güttler

65 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
F. Güttler Denmark 21 917 681 346 302 143 67 1.2k
Jean Rey France 20 692 0.8× 585 0.9× 237 0.7× 252 0.8× 114 0.8× 45 1.1k
B. William Uhlendorf United States 20 650 0.7× 714 1.0× 431 1.2× 575 1.9× 148 1.0× 26 1.6k
Philip P. Dembure United States 16 606 0.7× 403 0.6× 200 0.6× 184 0.6× 304 2.1× 26 1.0k
M. van Rijn Netherlands 15 994 1.1× 547 0.8× 628 1.8× 257 0.9× 228 1.6× 28 1.3k
Ellen S. Kang United States 18 393 0.4× 324 0.5× 284 0.8× 94 0.3× 87 0.6× 51 811
Jennifer R. Toone Canada 17 627 0.7× 600 0.9× 314 0.9× 123 0.4× 157 1.1× 39 1.2k
Cristina Amat Di San Filippo United States 13 594 0.6× 554 0.8× 178 0.5× 115 0.4× 134 0.9× 13 858
Ertan Mayatepek Germany 9 381 0.4× 439 0.6× 154 0.4× 85 0.3× 70 0.5× 12 716
Shigeaki Miyabayashi Japan 20 708 0.8× 1.0k 1.5× 131 0.4× 110 0.4× 59 0.4× 62 1.3k
Wenjuan Qiu China 22 606 0.7× 730 1.1× 378 1.1× 373 1.2× 283 2.0× 146 1.5k

Countries citing papers authored by F. Güttler

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of F. Güttler

This figure shows the co-authorship network connecting the top 25 collaborators of F. Güttler. A scholar is included among the top collaborators of F. Güttler based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with F. Güttler. F. Güttler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hertz, Jens Michael, Karen Østergaard, Susanne S. Pedersen, et al.. (2006). Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early‐onset Parkinson's Disease. European Journal of Neurology. 13(4). 385–390. 26 indexed citations
2.
Koch, Richard, Will Hanley, Harvey L. Levy, et al.. (2000). Maternal Phenylketonuria: An International Study. Molecular Genetics and Metabolism. 71(1-2). 233–239. 39 indexed citations
3.
Guldberg, Per, K. Henriksen, H. Lou, & F. Güttler. (1998). Aberrant phenylalanine metabolism in phenylketonuria heterozygotes. Journal of Inherited Metabolic Disease. 21(4). 365–372. 15 indexed citations
4.
Weglage, J., Kurt Ullrich, Michael Pietsch, et al.. (1997). Intellectual, Neurologic, and Neuropsychologic Outcome in Untreated Subjects with Nonphenylketonuria Hyperphenylalaninemia. Pediatric Research. 42(3). 378–384. 24 indexed citations
5.
Güttler, F. & Per Guldberg. (1996). The influence of mutations on enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiency. European Journal of Pediatrics. 155(S1). S6–S10. 46 indexed citations
6.
Guldberg, Per, Harvey L. Levy, Richard Koch, et al.. (1996). Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study.. PubMed. 59(1). 84–94. 66 indexed citations
7.
Andresen, Jente, et al.. (1994). Unchanged MRI of myelin in adolescents with PKU supplied with non‐phe essential amino acids after dietary relaxation. Acta Paediatrica. 83(12). 1312–1314. 12 indexed citations
8.
Güttler, F. & Per Guldberg. (1994). Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemia. Acta Paediatrica. 83(s407). 49–56. 20 indexed citations
9.
Romano, Valentino, Friedemann Call, Per Guldberg, et al.. (1994). Association between haplotypes, Hind III‐VNTR alleles and mutations at the PAH locus in Sicily. Acta Paediatrica. 83(s407). 39–40. 5 indexed citations
10.
Guldberg, Per & F. Güttler. (1994). Mutations in the phenylalanine hydroxylase gene: methods for their characterization. Acta Paediatrica. 83(s407). 27–33. 13 indexed citations
11.
Koch, Richard, Reuben Matalon, Bobbye Rouse, et al.. (1994). The international collaborative study of maternal phenylketonuria: status report 1994. Acta Paediatrica. 83(s407). 111–119. 46 indexed citations
12.
Fisch, Robert O., et al.. (1994). Phenylketonuric patients decades after diet. Journal of Inherited Metabolic Disease. 18(3). 347–353. 28 indexed citations
13.
Güttler, F., et al.. (1994). Genotype‐phenotype correlation in 11 Romanian PKU families. Journal of Inherited Metabolic Disease. 17(3). 374–375. 6 indexed citations
14.
Guldberg, Per, et al.. (1993). A novel missense mutation in the phenylalanine hydroxylase gene of a homozygous Pakistani patient with non-PKU hyperphenylalaninemia. Human Molecular Genetics. 2(7). 1061–1062. 5 indexed citations
15.
Okano, Y, et al.. (1991). A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia. European Journal of Pediatrics. 150(5). 347–352. 31 indexed citations
16.
Gerdes, Anne‐Marie, Jytte Bieber Nielsen, H. Lou, & F. Güttler. (1990). Plasma Amino Acids in Phenylketonuric Children Treated Either with Phenylalanine‐free Amino Acids or a Protein Hydrolysate. Acta Paediatrica. 79(1). 69–72. 6 indexed citations
17.
Gerdes, Anne‐Marie, et al.. (1990). Plasma Amino Acids in Term Neonates and Infants with Phenylketonuria before and after Institution of the Diet. Acta Paediatrica. 79(1). 64–68. 4 indexed citations
18.
Herrmann, F. H., et al.. (1988). Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic Republic. Clinical Genetics. 34(3). 176–180. 13 indexed citations
19.
Güttler, F., et al.. (1967). Cellular Compartmentalization of Lactate Dehydrogenase Isoenzymes. Enzymologia biologica et clinica. 8(6). 456–470. 19 indexed citations
20.
Güttler, F.. (1967). The Metabolic Activity Acquired by the Media of Cultivated Malignant and Non-Malignant Cells Compared to that of Human Effusions. Enzymologia biologica et clinica. 8(3). 228–234. 3 indexed citations

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.

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