Gisela Haege

1.5k total citations
18 papers, 652 citations indexed

About

Gisela Haege is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gisela Haege has authored 18 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Clinical Biochemistry, 10 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gisela Haege's work include Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (8 papers) and Neonatal Health and Biochemistry (5 papers). Gisela Haege is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (8 papers) and Neonatal Health and Biochemistry (5 papers). Gisela Haege collaborates with scholars based in Germany, Austria and Canada. Gisela Haege's co-authors include Peter Burgard, Georg F. Hoffmann, Martin Lindner, Stefan Kölker, Gwendolyn Gramer, Chris Mühlhausen, Junmin Fang‐Hoffmann, Jana Herınger, Regina Ensenauer and Esther M. Maier and has published in prestigious journals such as Annals of Neurology, Gene and Orphanet Journal of Rare Diseases.

In The Last Decade

Gisela Haege

18 papers receiving 637 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gisela Haege Germany 13 565 348 200 145 139 18 652
Nikolas Boy Germany 13 624 1.1× 483 1.4× 130 0.7× 173 1.2× 103 0.7× 25 710
Ulrike Mütze Germany 18 491 0.9× 321 0.9× 175 0.9× 172 1.2× 155 1.1× 47 750
Gaetano Sabetta Italy 10 402 0.7× 340 1.0× 174 0.9× 62 0.4× 78 0.6× 11 631
Roland Posset Germany 10 386 0.7× 238 0.7× 117 0.6× 103 0.7× 89 0.6× 18 468
Ahmad Monavari Ireland 10 331 0.6× 220 0.6× 129 0.6× 62 0.4× 88 0.6× 26 460
Patrik Feyh Germany 11 349 0.6× 277 0.8× 86 0.4× 49 0.3× 133 1.0× 18 477
L. Kierat Switzerland 13 266 0.5× 271 0.8× 90 0.5× 55 0.4× 139 1.0× 26 496
Amarilis Sanchez‐Valle United States 12 378 0.7× 289 0.8× 82 0.4× 165 1.1× 76 0.5× 26 642
F. J. van Spronsen Netherlands 13 410 0.7× 215 0.6× 80 0.4× 58 0.4× 77 0.6× 27 504
Maria Cristina Schiaffino Italy 13 214 0.4× 190 0.5× 67 0.3× 68 0.5× 117 0.8× 26 453

Countries citing papers authored by Gisela Haege

Since Specialization
Citations

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

Fields of papers citing papers by Gisela Haege

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gisela Haege

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

All Works

18 of 18 papers shown
1.
Gramer, Gwendolyn, et al.. (2016). Long-chain polyunsaturated fatty acid status in children, adolescents and adults with phenylketonuria. Prostaglandins Leukotrienes and Essential Fatty Acids. 109. 52–57. 10 indexed citations
2.
Okun, Jürgen G., Hongying Gan‐Schreier, K Schmidt, et al.. (2016). Newborn Screening for Vitamin B6 Non-responsive Classical Homocystinuria: Systematical Evaluation of a Two-Tier Strategy. JIMD Reports. 32. 87–94. 14 indexed citations
3.
Boy, Nikolas, Jana Herınger, Gisela Haege, et al.. (2015). A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type I. Orphanet Journal of Rare Diseases. 10(1). 163–163. 11 indexed citations
4.
Kölker, Stefan, Ivo Barić, J Zeman, et al.. (2015). Behavioural and emotional problems, intellectual impairment and health‐related quality of life in patients with organic acidurias and urea cycle disorders. Journal of Inherited Metabolic Disease. 39(2). 231–241. 27 indexed citations
5.
Gramer, Gwendolyn, Gisela Haege, Junmin Fang‐Hoffmann, et al.. (2015). Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening. JIMD Reports. 23. 101–112. 21 indexed citations
6.
Burgard, Peter, Stefan Kölker, Gisela Haege, Martin Lindner, & Georg F. Hoffmann. (2015). Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders—review and meta‐analysis of observational studies published over more than 35 years. Journal of Inherited Metabolic Disease. 39(2). 219–229. 50 indexed citations
7.
Haas, Dorothea, Hongying Gan‐Schreier, Claus‐Dieter Langhans, et al.. (2014). Diagnosis and therapeutic monitoring of inborn errors of creatine metabolism and transport using liquid chromatography–tandem mass spectrometry in urine, plasma and CSF. Gene. 538(1). 188–194. 13 indexed citations
8.
Haas, Dorothea, Gisela Haege, Georg F. Hoffmann, & Peter Burgard. (2013). Prenatal Presentation and Diagnostic Evaluation of Suspected Smith–Lemli–Opitz (RSH) Syndrome. American Journal of Medical Genetics Part A. 161(5). 1008–1011. 11 indexed citations
9.
Gramer, Gwendolyn, et al.. (2013). Living with an inborn error of metabolism detected by newborn screening—Parents’ perspectives on child development and impact on family life. Journal of Inherited Metabolic Disease. 37(2). 189–195. 41 indexed citations
10.
Haege, Gisela, et al.. (2013). Usefulness of biochemical parameters in decision‐making on the start of emergency treatment in patients with propionic acidemia. Journal of Inherited Metabolic Disease. 37(1). 31–37. 21 indexed citations
11.
Kölker, Stefan, Jana Herınger, Edith Müller, et al.. (2012). Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience. Molecular Genetics and Metabolism. 107(1-2). 72–80. 38 indexed citations
12.
Gramer, Gwendolyn, C. Springer, Gisela Haege, et al.. (2012). Visual functions in phenylketonuria—evaluating the dopamine and long-chain polyunsaturated fatty acids depletion hypotheses. Molecular Genetics and Metabolism. 108(1). 1–7. 12 indexed citations
13.
Burgard, Peter, Kathrin Rupp, Martin Lindner, et al.. (2012). Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2 – From screening laboratory results to treatment, follow‐up and quality assurance. Journal of Inherited Metabolic Disease. 35(4). 613–625. 77 indexed citations
14.
Haege, Gisela, et al.. (2012). Metabolic decompensation in methylmalonic aciduria: which biochemical parameters are discriminative?. Journal of Inherited Metabolic Disease. 35(5). 797–806. 29 indexed citations
15.
Boy, Nikolas, Gisela Haege, Jana Herınger, et al.. (2012). Low lysine diet in glutaric aciduria type I – effect on anthropometric and biochemical follow‐up parameters. Journal of Inherited Metabolic Disease. 36(3). 525–533. 17 indexed citations
16.
Lindner, Martin, Gwendolyn Gramer, Gisela Haege, et al.. (2011). Efficacy and outcome of expanded newborn screening for metabolic diseases - Report of 10 years from South-West Germany *. Orphanet Journal of Rare Diseases. 6(1). 44–44. 135 indexed citations
17.
Herınger, Jana, Regina Ensenauer, Birgit Assmann, et al.. (2010). Use of guidelines improves the neurological outcome in glutaric aciduria type I. Neuropediatrics. 41(2). 9 indexed citations
18.
Herınger, Jana, Regina Ensenauer, Birgit Assmann, et al.. (2010). Use of guidelines improves the neurological outcome in glutaric aciduria type I. Annals of Neurology. 68(5). 743–752. 116 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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