F. G�ttler

537 total citations
16 papers, 448 citations indexed

About

F. G�ttler is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, F. G�ttler has authored 16 papers receiving a total of 448 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Clinical Biochemistry, 10 papers in Molecular Biology and 7 papers in Rheumatology. Recurrent topics in F. G�ttler's work include Metabolism and Genetic Disorders (13 papers), Folate and B Vitamins Research (6 papers) and Mitochondrial Function and Pathology (3 papers). F. G�ttler is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Folate and B Vitamins Research (6 papers) and Mitochondrial Function and Pathology (3 papers). F. G�ttler collaborates with scholars based in Denmark, United States and Germany. F. G�ttler's co-authors include C. Lykkelund, H. Lou, Alan S. Lidsky, Savio L.C. Woo, Anthony G. DiLella, A. Niederwieser, Susan Sullivan, Peter Bruhn, Stephen P. Daiger and Anne‐Marie Gerdes and has published in prestigious journals such as The Journal of Pediatrics, Human Genetics and Molecular Genetics and Metabolism.

In The Last Decade

F. G�ttler

16 papers receiving 440 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. G�ttler Denmark	10	341	278	127	120	60	16	448
Baudouin François Belgium	8	462 1.4×	330 1.2×	170 1.3×	145 1.2×	74 1.2×	10	530
Hildgund Schmidt Germany	8	462 1.4×	319 1.1×	215 1.7×	146 1.2×	49 0.8×	12	529
Kikumaro Aoki Japan	13	431 1.3×	361 1.3×	182 1.4×	96 0.8×	97 1.6×	18	618
Martijn J. de Groot Netherlands	11	348 1.0×	252 0.9×	174 1.4×	51 0.4×	95 1.6×	14	450
Norma Spécola Argentina	11	206 0.6×	154 0.6×	181 1.4×	61 0.5×	37 0.6×	19	376
Enrica Riva Italy	12	590 1.7×	416 1.5×	225 1.8×	214 1.8×	69 1.1×	20	707
F. Güttler Denmark	9	389 1.1×	270 1.0×	226 1.8×	76 0.6×	58 1.0×	15	491
Marina A. Schwab Germany	6	323 0.9×	339 1.2×	72 0.6×	61 0.5×	62 1.0×	6	453
Marina Morath Germany	10	283 0.8×	224 0.8×	52 0.4×	105 0.9×	45 0.8×	16	393
J. B. de Klerk Netherlands	5	208 0.6×	213 0.8×	66 0.5×	30 0.3×	35 0.6×	5	303

Countries citing papers authored by F. G�ttler

Since Specialization

Citations

This map shows the geographic impact of F. G�ttler'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. G�ttler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. G�ttler more than expected).

Fields of papers citing papers by F. G�ttler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. G�ttler. 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. G�ttler. The network helps show where F. G�ttler may publish in the future.

Co-authorship network of co-authors of F. G�ttler

This figure shows the co-authorship network connecting the top 25 collaborators of F. G�ttler. A scholar is included among the top collaborators of F. G�ttler 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. G�ttler. F. G�ttler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Gjetting, Torben, Anne Romstad, Jan Haavik, et al.. (2001). A Phenylalanine Hydroxylase Amino Acid Polymorphism with Implications for Molecular Diagnostics. Molecular Genetics and Metabolism. 73(3). 280–284. 11 indexed citations

G�ttler, F., Per Guldberg, Randy C. Eisensmith, & Savio L.C. Woo. (1999). Molecular genetics and outcome in PKU. Mental Retardation and Developmental Disabilities Research Reviews. 5(2). 113–116. 1 indexed citations

Koch, Richard, Eva Friedman, C. Azen, et al.. (1999). The International Collaborative Study of Maternal Phenylketonuria status report 1998. Mental Retardation and Developmental Disabilities Research Reviews. 5(2). 117–121. 9 indexed citations

Guldberg, Per, et al.. (1995). In vivo assessment of mutations in the phenylalanine hydroxylase gene by phenylalanine loading: characterization of seven common mutations. European Journal of Pediatrics. 154(7). 551–556. 1 indexed citations

Apold, Jaran, Hans Geir Eiken, Elisabeth Svensson, et al.. (1993). The phenylketonuria G272X haplotype 7 mutation in European populations. Human Genetics. 92(2). 107–9. 7 indexed citations

Jaruzelska, Jadwiga, et al.. (1991). The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria. Human Genetics. 86(3). 247–50. 14 indexed citations

Konecki, David, Uta Lichter‐Konecki, Randy C. Eisensmith, et al.. (1991). Molecular characterization of PKU allele prevalent in southern Europe and Ireland. Somatic Cell and Molecular Genetics. 17(3). 303–309. 27 indexed citations

Gerdes, Anne‐Marie, et al.. (1988). Variability in clinical expression of Menkes syndrome. European Journal of Pediatrics. 148(2). 132–135. 37 indexed citations

Lykkelund, C., Jytte Bieber Nielsen, H. Lou, et al.. (1988). Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine. European Journal of Pediatrics. 148(3). 238–245. 59 indexed citations

10.

G�ttler, F., Fred D. Ledley, Alan S. Lidsky, et al.. (1987). Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria. The Journal of Pediatrics. 110(1). 68–71. 48 indexed citations

11.

Lidsky, Alan S., Stephen P. Daiger, F. G�ttler, et al.. (1987). Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Human Genetics. 76(1). 40–6. 98 indexed citations

12.

G�ttler, F., Anthony G. DiLella, Fred D. Ledley, et al.. (1987). Molecular biology of phenylketonuria. European Journal of Pediatrics. 146(1). A5–A11. 13 indexed citations

13.

Lou, H., F. G�ttler, C. Lykkelund, Peter Bruhn, & A. Niederwieser. (1985). Decreased vigilance and neurotransmitter synthesis after discontinuation of dietary treatment for phenylketonuria in adolescents. European Journal of Pediatrics. 144(1). 17–20. 93 indexed citations

14.

G�ttler, F., H. C. Lou, C. Lykkelund, & A. Niederwieser. (1984). Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis. European Journal of Pediatrics. 142(2). 126–129. 16 indexed citations

15.

G�ttler, F., et al.. (1983). Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome. Human Genetics. 64(4). 371–375. 5 indexed citations

16.

Lykkelund, C., et al.. (1982). Diagnosis of Hunter's syndrome carriers; Radioactive sulphate incorporation into fibroblasts in the presence of fructose 1-phosphate. Human Genetics. 60(2). 167–171. 9 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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