Florian Gleich

1.7k total citations
26 papers, 437 citations indexed

About

Florian Gleich is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Florian Gleich has authored 26 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Clinical Biochemistry, 9 papers in Molecular Biology and 9 papers in Rheumatology. Recurrent topics in Florian Gleich's work include Metabolism and Genetic Disorders (23 papers), Folate and B Vitamins Research (9 papers) and Neonatal Health and Biochemistry (8 papers). Florian Gleich is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Folate and B Vitamins Research (9 papers) and Neonatal Health and Biochemistry (8 papers). Florian Gleich collaborates with scholars based in Germany, Switzerland and United States. Florian Gleich's co-authors include Stefan Kölker, Sven F. Garbade, Ulrike Mütze, Georg F. Hoffmann, Thomas Opladen, Matthias R. Baumgartner, Roland Posset, Peter Burgard, Martina Pötschke-Langer and Ute Mons and has published in prestigious journals such as PEDIATRICS, Nutrients and Frontiers in Endocrinology.

In The Last Decade

Florian Gleich

26 papers receiving 431 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florian Gleich Germany 15 293 179 120 98 94 26 437
Junmin Fang‐Hoffmann Germany 13 439 1.5× 204 1.1× 103 0.9× 210 2.1× 247 2.6× 15 528
Susan Marczewski United States 7 47 0.2× 136 0.8× 22 0.2× 124 1.3× 144 1.5× 7 459
Jarmo K. Visakorpi Finland 9 125 0.4× 63 0.4× 98 0.8× 25 0.3× 44 0.5× 16 535
Huma Arshad Cheema Pakistan 9 53 0.2× 52 0.3× 74 0.6× 37 0.4× 23 0.2× 48 267
Ghassan Abdoh Qatar 10 182 0.6× 74 0.4× 48 0.4× 138 1.4× 154 1.6× 16 308
Marilyn Hill United Kingdom 10 44 0.2× 90 0.5× 27 0.2× 36 0.4× 180 1.9× 19 315
Malak Alghamdi Saudi Arabia 9 50 0.2× 84 0.5× 42 0.3× 24 0.2× 21 0.2× 31 224
K Gellissen Germany 10 68 0.2× 128 0.7× 47 0.4× 112 1.1× 73 0.8× 18 443
Reza Alibakhshi Iran 10 77 0.3× 98 0.5× 46 0.4× 39 0.4× 25 0.3× 47 326
Naziha Kaabachi Tunisia 8 32 0.1× 84 0.5× 111 0.9× 20 0.2× 55 0.6× 19 329

Countries citing papers authored by Florian Gleich

Since Specialization
Citations

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

Fields of papers citing papers by Florian Gleich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florian Gleich

This figure shows the co-authorship network connecting the top 25 collaborators of Florian Gleich. A scholar is included among the top collaborators of Florian Gleich 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 Florian Gleich. Florian Gleich 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.
Mütze, Ulrike, Florian Gleich, Sarah C. Grünert, et al.. (2025). Long-Term Outcomes of Adolescents and Young Adults Identified by Metabolic Newborn Screening. PEDIATRICS. 155(4). 2 indexed citations
2.
Morris, Andrew A. M., Jitka Sokolová, Markéta Pavlı́ková, et al.. (2025). Cystathionine β‐Synthase Deficiency in the E‐HOD Registry—Part II: Dietary and Pharmacological Treatment. Journal of Inherited Metabolic Disease. 48(1). e12844–e12844. 1 indexed citations
3.
Mütze, Ulrike, Florian Gleich, Dorothea Haas, et al.. (2024). Vitamin B12 Deficiency Newborn Screening. PEDIATRICS. 154(2). 2 indexed citations
4.
Zielonka, Matthias, Stefan Kölker, Sven F. Garbade, et al.. (2024). Severity-adjusted evaluation of initial dialysis on short-term health outcomes in urea cycle disorders. Molecular Genetics and Metabolism. 143(1-2). 108566–108566. 1 indexed citations
5.
Schnabel‐Besson, Elena, Sven F. Garbade, Florian Gleich, et al.. (2024). Parental and child's psychosocial and financial burden living with an inherited metabolic disease identified by newborn screening. Journal of Inherited Metabolic Disease. 48(1). e12784–e12784. 4 indexed citations
6.
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
7.
Posset, Roland, Matthias Zielonka, Florian Gleich, et al.. (2023). The challenge of understanding and predicting phenotypic diversity in urea cycle disorders. Journal of Inherited Metabolic Disease. 46(6). 1007–1016. 3 indexed citations
8.
Schnabel‐Besson, Elena, Stefan Kölker, Florian Gleich, et al.. (2023). Combined Newborn Screening Allows Comprehensive Identification also of Attenuated Phenotypes for Methylmalonic Acidurias and Homocystinuria. Nutrients. 15(15). 3355–3355. 15 indexed citations
9.
Posset, Roland, Sven F. Garbade, Florian Gleich, et al.. (2022). Predicting the disease severity in male individuals with ornithine transcarbamylase deficiency. Annals of Clinical and Translational Neurology. 9(11). 1715–1726. 7 indexed citations
10.
Opladen, Thomas, Florian Gleich, Viktor Kožich, et al.. (2021). U-IMD: the first Unified European registry for inherited metabolic diseases. Orphanet Journal of Rare Diseases. 16(1). 95–95. 16 indexed citations
11.
Brennenstuhl, Heiko, Julian Schröter, Federico Baronio, et al.. (2021). Phenotypic diversity, disease progression, and pathogenicity of MVK missense variants in mevalonic aciduria. Journal of Inherited Metabolic Disease. 44(5). 1272–1287. 22 indexed citations
12.
Landolt, Markus A., Matthias R. Baumgartner, Stefan Kölker, et al.. (2020). Health‐related quality of life in paediatric patients with intoxication‐type inborn errors of metabolism: Analysis of an international data set. Journal of Inherited Metabolic Disease. 44(1). 215–225. 22 indexed citations
13.
Posset, Roland, Stefan Kölker, Florian Gleich, et al.. (2020). Severity-adjusted evaluation of newborn screening on the metabolic disease course in individuals with cytosolic urea cycle disorders. Molecular Genetics and Metabolism. 131(4). 390–397. 15 indexed citations
14.
Kožich, Viktor, Jitka Sokolová, Andrew A. M. Morris, et al.. (2020). Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis. Journal of Inherited Metabolic Disease. 44(3). 677–692. 27 indexed citations
15.
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
16.
Zielonka, Matthias, Stefan Kölker, Florian Gleich, et al.. (2019). Early prediction of phenotypic severity in Citrullinemia Type 1. Annals of Clinical and Translational Neurology. 6(9). 1858–1871. 25 indexed citations
17.
Molema, Femke, Florian Gleich, Peter Burgard, et al.. (2019). Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea‐cycle disorders: On the basis of information from a European multicenter registry. Journal of Inherited Metabolic Disease. 42(6). 1162–1175. 26 indexed citations
18.
Kölker, Stefan, Daniela Karall, Johannes Häberle, et al.. (2017). Incidence, disease onset and short-term outcome in urea cycle disorders –cross-border surveillance in Germany, Austria and Switzerland. Orphanet Journal of Rare Diseases. 12(1). 111–111. 41 indexed citations
19.
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
20.
Gleich, Florian, Ute Mons, & Martina Pötschke-Langer. (2011). Air Contamination Due to Smoking in German Restaurants, Bars, and Other Venues--Before and After the Implementation of a Partial Smoking Ban. Nicotine & Tobacco Research. 13(11). 1155–1160. 25 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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