Jana Herınger

982 total citations
14 papers, 557 citations indexed

About

Jana Herınger is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jana Herınger has authored 14 papers receiving a total of 557 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Clinical Biochemistry, 12 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jana Herınger's work include Metabolism and Genetic Disorders (14 papers), Mitochondrial Function and Pathology (12 papers) and Biochemical and Molecular Research (6 papers). Jana Herınger is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Mitochondrial Function and Pathology (12 papers) and Biochemical and Molecular Research (6 papers). Jana Herınger collaborates with scholars based in Germany, Austria and United States. Jana Herınger's co-authors include Stefan Kölker, Inga Harting, Nikolas Boy, Peter Burgard, Chris Mühlhausen, Georg F. Hoffmann, Angelika Seitz, Esther M. Maier, Birgit Assmann and Johannes Zschocke and has published in prestigious journals such as Annals of Neurology, Orphanet Journal of Rare Diseases and Molecular Genetics and Metabolism.

In The Last Decade

Jana Herınger

14 papers receiving 553 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jana Herınger Germany 12 502 387 131 101 100 14 557
Nikolas Boy Germany 13 624 1.2× 483 1.2× 173 1.3× 125 1.2× 103 1.0× 25 710
Roland Posset Germany 10 386 0.8× 238 0.6× 103 0.8× 94 0.9× 89 0.9× 18 468
Marina Morath Germany 10 283 0.6× 224 0.6× 31 0.2× 45 0.4× 105 1.1× 16 393
F. J. van Spronsen Netherlands 13 410 0.8× 215 0.6× 58 0.4× 91 0.9× 77 0.8× 27 504
Akiko Ichinohe Japan 10 162 0.3× 200 0.5× 49 0.4× 178 1.8× 63 0.6× 17 396
Helen Prunty United Kingdom 8 160 0.3× 162 0.4× 46 0.4× 61 0.6× 121 1.2× 19 356
Norma Spécola Argentina 11 206 0.4× 154 0.4× 49 0.4× 37 0.4× 61 0.6× 19 376
Rianne Jahja Netherlands 12 414 0.8× 288 0.7× 52 0.4× 92 0.9× 52 0.5× 16 499
Geralyn Creadon‐Swindell United States 6 205 0.4× 203 0.5× 35 0.3× 107 1.1× 23 0.2× 7 297
F. G�ttler Denmark 10 341 0.7× 278 0.7× 47 0.4× 60 0.6× 120 1.2× 16 448

Countries citing papers authored by Jana Herınger

Since Specialization
Citations

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

Fields of papers citing papers by Jana Herınger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jana Herınger

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

All Works

14 of 14 papers shown
1.
Boy, Nikolas, Sven F. Garbade, Jana Herınger, et al.. (2019). Patterns, evolution, and severity of striatal injury in insidious‐ vs acute‐onset glutaric aciduria type 1. Journal of Inherited Metabolic Disease. 42(1). 117–127. 23 indexed citations
2.
Garbade, Sven F., Nikolas Boy, Jana Herınger, Stefan Kölker, & Inga Harting. (2018). Age-Related Changes and Reference Values of Bicaudate Ratio and Sagittal Brainstem Diameters on MRI. Neuropediatrics. 49(4). 269–275. 12 indexed citations
3.
Boy, Nikolas, Sven F. Garbade, Jana Herınger, et al.. (2018). Patterns, evolution, and severity of striatal injury in insidious- versus acute-onset glutaric aciduria type 1. Journal of Inherited Metabolic Disease. 42(1). 117–127. 23 indexed citations
4.
Boy, Nikolas, Jana Herınger, Olaf A. Bodamer, et al.. (2017). Extrastriatal changes in patients with late-onset glutaric aciduria type I highlight the risk of long-term neurotoxicity. Orphanet Journal of Rare Diseases. 12(1). 77–77. 40 indexed citations
5.
Boy, Nikolas, Chris Mühlhausen, Esther M. Maier, et al.. (2016). Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision. Journal of Inherited Metabolic Disease. 40(1). 75–101. 147 indexed citations
6.
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
7.
Herınger, Jana, Vassili Valayannopoulos, Allan M. Lund, et al.. (2015). Impact of age at onset and newborn screening on outcome in organic acidurias. Journal of Inherited Metabolic Disease. 39(3). 341–353. 64 indexed citations
8.
Harting, Inga, Nikolas Boy, Jana Herınger, et al.. (2015). 1H‐MRS in glutaric aciduria type 1: impact of biochemical phenotype and age on the cerebral accumulation of neurotoxic metabolites. Journal of Inherited Metabolic Disease. 38(5). 829–838. 45 indexed citations
9.
Herınger, Jana, Nikolas Boy, Peter Burgard, Jürgen G. Okun, & Stefan Kölker. (2015). Newborn Screening for Glutaric Aciduria Type I: Benefits and limitations. International Journal of Neonatal Screening. 1(2). 57–68. 11 indexed citations
10.
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
11.
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
12.
Opp, Silvana, et al.. (2011). Glutaric aciduria type I: A translational approach to an enigmatic disease. DergiPark (Istanbul University). 1 indexed citations
13.
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
14.
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

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026