Nikolas Boy

1.6k total citations
25 papers, 710 citations indexed

About

Nikolas Boy is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics. According to data from OpenAlex, Nikolas Boy has authored 25 papers receiving a total of 710 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Clinical Biochemistry, 15 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Nikolas Boy's work include Metabolism and Genetic Disorders (24 papers), Mitochondrial Function and Pathology (13 papers) and Genomics and Rare Diseases (8 papers). Nikolas Boy is often cited by papers focused on Metabolism and Genetic Disorders (24 papers), Mitochondrial Function and Pathology (13 papers) and Genomics and Rare Diseases (8 papers). Nikolas Boy collaborates with scholars based in Germany, United States and United Kingdom. Nikolas Boy's co-authors include Stefan Kölker, Inga Harting, Sven F. Garbade, Georg F. Hoffmann, Jana Herınger, Angelika Seitz, Esther M. Maier, Chris Mühlhausen, Johannes Zschocke and Peter Burgard and has published in prestigious journals such as Brain, PEDIATRICS and Gene.

In The Last Decade

Nikolas Boy

24 papers receiving 704 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nikolas Boy Germany 13 624 483 173 130 125 25 710
Jana Herınger Germany 12 502 0.8× 387 0.8× 131 0.8× 88 0.7× 101 0.8× 14 557
Gisela Haege Germany 13 565 0.9× 348 0.7× 145 0.8× 200 1.5× 89 0.7× 18 652
Roland Posset Germany 10 386 0.6× 238 0.5× 103 0.6× 117 0.9× 94 0.8× 18 468
Ahmad Monavari Ireland 10 331 0.5× 220 0.5× 62 0.4× 129 1.0× 84 0.7× 26 460
F. J. van Spronsen Netherlands 13 410 0.7× 215 0.4× 58 0.3× 80 0.6× 91 0.7× 27 504
Marina Morath Germany 10 283 0.5× 224 0.5× 31 0.2× 78 0.6× 45 0.4× 16 393
Jaime Campistol Spain 7 342 0.5× 220 0.5× 67 0.4× 86 0.7× 49 0.4× 8 469
Akiko Ichinohe Japan 10 162 0.3× 200 0.4× 49 0.3× 37 0.3× 178 1.4× 17 396
F. X. Coudé France 16 484 0.8× 292 0.6× 39 0.2× 177 1.4× 97 0.8× 33 709
Helen Prunty United Kingdom 8 160 0.3× 162 0.3× 46 0.3× 63 0.5× 61 0.5× 19 356

Countries citing papers authored by Nikolas Boy

Since Specialization
Citations

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

Fields of papers citing papers by Nikolas Boy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nikolas Boy

This figure shows the co-authorship network connecting the top 25 collaborators of Nikolas Boy. A scholar is included among the top collaborators of Nikolas Boy 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 Nikolas Boy. Nikolas Boy 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.
Boy, Nikolas, Sven F. Garbade, Saskia Haupt, et al.. (2024). Digital-Tier Strategy Improves Newborn Screening for Glutaric Aciduria Type 1. International Journal of Neonatal Screening. 10(4). 83–83.
2.
Forny, Patrick, Friederike Hörster, Matthias R. Baumgartner, Stefan Kölker, & Nikolas Boy. (2023). How guideline development has informed clinical research for organic acidurias (et vice versa). Journal of Inherited Metabolic Disease. 46(3). 520–535. 3 indexed citations
3.
Boy, Nikolas, et al.. (2023). Phenotypic prediction in glutaric aciduria type 1 combining in silico and in vitro modeling with real‐world data. Journal of Inherited Metabolic Disease. 46(3). 391–405. 4 indexed citations
4.
Mütze, Ulrike, Sven F. Garbade, Gwendolyn Gramer, et al.. (2020). Long-term Outcomes of Individuals With Metabolic Diseases Identified Through Newborn Screening. PEDIATRICS. 146(5). 43 indexed citations
5.
Brügger, Melanie, et al.. (2020). Locus heterogeneity in two siblings presenting with developmental delay, intellectual disability and autism spectrum disorder. Gene. 768. 145260–145260. 1 indexed citations
6.
Boy, Nikolas, et al.. (2020). Impact of newborn screening and quality of therapy on the neurological outcome in glutaric aciduria type 1: a meta-analysis. Genetics in Medicine. 23(1). 13–21. 36 indexed citations
7.
Mhanni, Aziz, et al.. (2020). Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba: 1980–2020. Molecular Genetics and Metabolism Reports. 25. 100666–100666. 1 indexed citations
8.
Posset, Roland, Sven F. Garbade, Nikolas Boy, et al.. (2019). Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—A successful strategy for clinical research of rare diseases. Journal of Inherited Metabolic Disease. 42(1). 93–106. 25 indexed citations
9.
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
10.
Posset, Roland, Sven F. Garbade, Nikolas Boy, et al.. (2018). Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—a successful strategy for clinical research of rare diseases. Journal of Inherited Metabolic Disease. 3 indexed citations
11.
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
12.
Boy, Nikolas, et al.. (2018). Organic acidurias in adults: late complications and management. Journal of Inherited Metabolic Disease. 41(5). 765–776. 27 indexed citations
13.
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
14.
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
15.
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
16.
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
17.
Zielonka, Matthias, et al.. (2014). Severe Acute Subdural Hemorrhage in a Patient With Glutaric Aciduria Type I After Minor Head Trauma. Journal of Child Neurology. 30(8). 1065–1069. 9 indexed citations
18.
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
19.
Harting, Inga, Eva Neumaier‐Probst, Angelika Seitz, et al.. (2009). Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I. Brain. 132(7). 1764–1782. 121 indexed citations
20.
Kölker, Stefan, Sven F. Garbade, Nikolas Boy, et al.. (2007). Decline of Acute Encephalopathic Crises in Children with Glutaryl-CoA Dehydrogenase Deficiency Identified by Newborn Screening in Germany. Pediatric Research. 62(3). 357–363. 88 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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