Flemming Güttler

3.3k total citations
58 papers, 2.3k citations indexed

About

Flemming Güttler is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Flemming Güttler has authored 58 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Clinical Biochemistry, 35 papers in Molecular Biology and 18 papers in Rheumatology. Recurrent topics in Flemming Güttler's work include Metabolism and Genetic Disorders (49 papers), Folate and B Vitamins Research (18 papers) and Mitochondrial Function and Pathology (17 papers). Flemming Güttler is often cited by papers focused on Metabolism and Genetic Disorders (49 papers), Folate and B Vitamins Research (18 papers) and Mitochondrial Function and Pathology (17 papers). Flemming Güttler collaborates with scholars based in Denmark, United States and Germany. Flemming Güttler's co-authors include Per Guldberg, Savio L.C. Woo, Alan S. Lidsky, Richard Koch, T.S. Chandra, Kathryn Robson, Anthony G. DiLella, Joshua Marvit, Karen Friis Henriksen and Anne Romstad and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Flemming Güttler

57 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Flemming Güttler Denmark 24 1.7k 1.4k 608 568 296 58 2.3k
Edwin W. Naylor United States 27 1.6k 1.0× 1.5k 1.1× 408 0.7× 479 0.8× 725 2.4× 66 2.8k
Esther M. Maier Germany 23 857 0.5× 974 0.7× 189 0.3× 251 0.4× 221 0.7× 64 1.7k
Haruo Shintaku Japan 25 693 0.4× 777 0.6× 236 0.4× 698 1.2× 374 1.3× 116 2.1k
Maria Giżewska Poland 15 1.3k 0.8× 830 0.6× 327 0.5× 776 1.4× 275 0.9× 51 1.6k
Yoshiyuki Okano Japan 24 1.3k 0.8× 905 0.6× 322 0.5× 391 0.7× 381 1.3× 62 1.7k
Deborah Marsden United States 24 1.2k 0.7× 854 0.6× 283 0.5× 532 0.9× 391 1.3× 65 1.8k
Chris Mühlhausen Germany 23 1.2k 0.7× 1.1k 0.8× 228 0.4× 286 0.5× 227 0.8× 43 1.8k
Can Fıçıcıoğlu United States 23 890 0.5× 790 0.6× 289 0.5× 551 1.0× 295 1.0× 102 1.7k
Douglas S. Kerr United States 22 1.1k 0.7× 969 0.7× 102 0.2× 492 0.9× 191 0.6× 48 1.9k
E. Christensen Denmark 26 1.6k 1.0× 1.6k 1.1× 229 0.4× 224 0.4× 257 0.9× 70 2.2k

Countries citing papers authored by Flemming Güttler

Since Specialization
Citations

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

Fields of papers citing papers by Flemming Güttler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Flemming 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 Flemming Güttler. The network helps show where Flemming Güttler may publish in the future.

Co-authorship network of co-authors of Flemming Güttler

This figure shows the co-authorship network connecting the top 25 collaborators of Flemming Güttler. A scholar is included among the top collaborators of Flemming 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 Flemming Güttler. Flemming 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.
Rohr, Frances, Ann Wessel, Steven F. Dobrowolski, et al.. (2019). Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study. Molecular Genetics and Metabolism. 128(4). 415–421. 10 indexed citations
2.
Wang, Lin, Sankar Surendran, Kimberlee Michals‐Matalon, et al.. (2007). Mutations in the Regulatory Domain of Phenylalanine Hydroxylase and Response to Tetrahydrobiopterin. Genetic Testing. 11(2). 174–178. 8 indexed citations
3.
Michals‐Matalon, Kimberlee, Gita Bhatia, Flemming Güttler, Stephen K. Tyring, & Reuben Matalon. (2007). Response of Phenylketonuria to Tetrahydrobiopterin. Journal of Nutrition. 137(6). 1564S–1567S. 15 indexed citations
4.
Møller, Lisbeth Birk, Anders O.H. Nygren, Patrick Scott, et al.. (2007). Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany. Human Mutation. 28(2). 207–207. 23 indexed citations
5.
Møller, Lisbeth Birk, Anne Romstad, Aída Ormazábal, et al.. (2005). Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency. Prenatal Diagnosis. 25(8). 671–675. 13 indexed citations
6.
Møller, Lisbeth Birk, et al.. (2005). Inter-individual variation in brain phenylalanine concentration in patients with PKU is not caused by genetic variation in the 4F2hc/LAT1 complex. Molecular Genetics and Metabolism. 86. 119–123. 14 indexed citations
7.
Kalkanoğlu, H. Serap, Kirsten Ahring, Lisbeth Birk Møller, et al.. (2005). Behavioural effects of phenylalanine‐free amino acid tablet supplementation in intellectually disabled adults with untreated phenylketonuria. Acta Paediatrica. 94(9). 1218–1222. 20 indexed citations
8.
Matalon, Reuben, Richard Koch, Kimberlee Michals‐Matalon, et al.. (2004). Biopterin responsive phenylalanine hydroxylase deficiency. Genetics in Medicine. 6(1). 27–32. 50 indexed citations
9.
Koch, Richard, Flemming Güttler, & Nenad Blau. (2002). Mental Illness in Mild PKU Responds to Biopterin. Molecular Genetics and Metabolism. 75(3). 284–286. 21 indexed citations
10.
Kalkanoğlu, H. Serap, Anne Romstad, Turgay Coşkun, & Flemming Güttler. (2001). Evaluation of a fetus at risk for dihydropteridine reductase deficiency by direct mutation analysis using denaturing gradient gel electrophoresis. Prenatal Diagnosis. 21(10). 868–870. 4 indexed citations
11.
Koch, Richard & Flemming Güttler. (2000). Benefits of Mutation Analysis and Examination of Brain Phenylalanine Levels in the Management of Phenylketonuria. PEDIATRICS. 106(5). 1136–1136. 2 indexed citations
12.
Koch, Richard, et al.. (1999). Long-Term Beneficial Effects of the Phenylalanine-Restricted Diet in Late-Diagnosed Individuals with Phenylketonuria. Molecular Genetics and Metabolism. 67(2). 148–155. 38 indexed citations
13.
Guldberg, Per, Françoise Rey, Johannes Zschocke, et al.. (1998). A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype. The American Journal of Human Genetics. 63(1). 71–79. 278 indexed citations
14.
Levy, Harvey L., Debra K. Sullivan, Kimberlee Michals‐Matalon, et al.. (1994). Maternal mild hyperphenylalaninemia: Results of treated and untreated pregnancies in two sisters. The Journal of Pediatrics. 125(3). 467–469. 4 indexed citations
15.
Guldberg, Per & Flemming Güttler. (1993). A simple method for identification of point mutations using denaturing gradient gel electrophoresis. Nucleic Acids Research. 21(9). 2261–2262. 50 indexed citations
16.
Guldberg, Per, Valentino Romano, N. Ceratto, et al.. (1993). Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenyl-alaninemia in Southern Europe. Human Molecular Genetics. 2(10). 1703–1707. 104 indexed citations
17.
Guldberg, Per & Flemming Güttler. (1992). PCR in the Diagnosis of Phenylketonuria. Annals of Medicine. 24(3). 187–190. 3 indexed citations
18.
Okano, Yoshiyuki, Randy C. Eisensmith, Flemming Güttler, et al.. (1991). Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria. New England Journal of Medicine. 324(18). 1232–1238. 206 indexed citations
19.
Güttler, Flemming. (1989). Impact of medical genetics concerning phenylketonuria: accomplishments, status and practical future possibilities. Clinical Genetics. 36(5). 333–334. 1 indexed citations
20.
Güttler, Flemming, et al.. (1969). Diurnal Variations of Serum Phenylalanine in Phenylketonuric Children on Low Phenylalanine Diet. American Journal of Clinical Nutrition. 22(12). 1568–1570. 19 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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