Janine Reunert

2.1k total citations
45 papers, 880 citations indexed

About

Janine Reunert is a scholar working on Molecular Biology, Physiology and Organic Chemistry. According to data from OpenAlex, Janine Reunert has authored 45 papers receiving a total of 880 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 15 papers in Physiology and 10 papers in Organic Chemistry. Recurrent topics in Janine Reunert's work include Glycosylation and Glycoproteins Research (16 papers), Lysosomal Storage Disorders Research (11 papers) and Carbohydrate Chemistry and Synthesis (10 papers). Janine Reunert is often cited by papers focused on Glycosylation and Glycoproteins Research (16 papers), Lysosomal Storage Disorders Research (11 papers) and Carbohydrate Chemistry and Synthesis (10 papers). Janine Reunert collaborates with scholars based in Germany, Japan and Switzerland. Janine Reunert's co-authors include Thorsten Marquardt, Stephan Rust, Marianne Grüneberg, Julien H. Park, Manfred Fobker, Saskia Biskup, Frank Kannenberg, Charles Marques Lourenço, Eugen Mengel and Richard W.D. Welford and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Janine Reunert

42 papers receiving 876 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janine Reunert Germany 20 507 342 165 115 105 45 880
Sandrine Vuillaumier‐Barrot France 21 858 1.7× 353 1.0× 236 1.4× 195 1.7× 236 2.2× 54 1.3k
Marianne Grüneberg Germany 14 335 0.7× 124 0.4× 54 0.3× 91 0.8× 65 0.6× 30 553
M. Girós Spain 16 556 1.1× 267 0.8× 46 0.3× 48 0.4× 62 0.6× 40 749
Johannis B.C. de Klerk Netherlands 12 441 0.9× 469 1.4× 140 0.8× 80 0.7× 50 0.5× 12 909
Dimitar Gavrilov United States 15 403 0.8× 345 1.0× 83 0.5× 121 1.1× 24 0.2× 35 901
Gerard De Jong Australia 11 235 0.5× 256 0.7× 57 0.3× 33 0.3× 25 0.2× 19 592
Wenjuan Qiu China 22 730 1.4× 378 1.1× 133 0.8× 314 2.7× 29 0.3× 146 1.5k
Clare Beesley United Kingdom 17 288 0.6× 607 1.8× 240 1.5× 108 0.9× 34 0.3× 29 980
Jozef Hertecant United Arab Emirates 19 498 1.0× 157 0.5× 23 0.1× 210 1.8× 61 0.6× 50 995
N. U. Bosshard Switzerland 18 338 0.7× 446 1.3× 223 1.4× 163 1.4× 36 0.3× 27 972

Countries citing papers authored by Janine Reunert

Since Specialization
Citations

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

Fields of papers citing papers by Janine Reunert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janine Reunert

This figure shows the co-authorship network connecting the top 25 collaborators of Janine Reunert. A scholar is included among the top collaborators of Janine Reunert 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 Janine Reunert. Janine Reunert 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.
Iuso, Arcangela, Janine Reunert, Marianne Grüneberg, et al.. (2024). Expanding the genetic and clinical spectrum of SLC25A42‐associated disorders and testing of pantothenic acid to improve CoA level in vitro. JIMD Reports. 65(6). 417–425.
2.
Scarcia, Pasquale, et al.. (2021). Uridine Treatment of the First Known Case of SLC25A36 Deficiency. International Journal of Molecular Sciences. 22(18). 9929–9929. 7 indexed citations
3.
Grüneberg, Marianne, et al.. (2021). A comparison of immediate release and delayed release cysteamine in 17 patients with nephropathic cystinosis. Orphanet Journal of Rare Diseases. 16(1). 387–387. 13 indexed citations
4.
Sidhu, Rohini, Pamela Kell, Dennis J. Dietzen, et al.. (2020). Application of a glycinated bile acid biomarker for diagnosis and assessment of response to treatment in Niemann-pick disease type C1. Molecular Genetics and Metabolism. 131(4). 405–417. 11 indexed citations
5.
Grüneberg, Marianne, et al.. (2020). Dietary mannose supplementation in phosphomannomutase 2 deficiency (PMM2-CDG). Orphanet Journal of Rare Diseases. 15(1). 258–258. 11 indexed citations
6.
Reunert, Janine, et al.. (2020). Cerebro‐oculo‐facio‐skeletal syndrome caused by the homozygous pathogenic variant Gly47Arg in ERCC2. American Journal of Medical Genetics Part A. 185(3). 930–936. 3 indexed citations
7.
Marquardt, Thorsten, Vladimı́r Bzdúch, Stephan Rust, et al.. (2020). SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation. Molecular Genetics and Metabolism Reports. 25. 100636–100636. 5 indexed citations
8.
Sidhu, Rohini, Pamela Kell, Dennis J. Dietzen, et al.. (2020). Application of N-palmitoyl-O-phosphocholineserine for diagnosis and assessment of response to treatment in Niemann-Pick type C disease. Molecular Genetics and Metabolism. 129(4). 292–302. 22 indexed citations
9.
Park, Julien H., Janine Reunert, Michael L. McCormick, et al.. (2019). SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosis. Brain. 142(8). 2230–2237. 62 indexed citations
10.
Park, Julien H., Marianne Grüneberg, Stephan Rust, et al.. (2017). Limitations of galactose therapy in phosphoglucomutase 1 deficiency. Molecular Genetics and Metabolism Reports. 13. 33–40. 27 indexed citations
11.
Murakami, Yoshiko, Martin K. Wild, Martina Ahlmann, et al.. (2016). A novel mutation in PIGW causes glycosylphosphatidylinositol deficiency without hyperphosphatasia. American Journal of Medical Genetics Part A. 170(12). 3319–3322. 19 indexed citations
12.
Kannenberg, Frank, Jerzy–Roch Nofer, Erhard Schulte, et al.. (2016). Determination of serum cholestane-3β,5α,6β-triol by gas chromatography–mass spectrometry for identification of Niemann-Pick type C (NPC) disease. The Journal of Steroid Biochemistry and Molecular Biology. 169. 54–60. 23 indexed citations
13.
Reunert, Janine, Frank Kannenberg, Manfred Fobker, & Thorsten Marquardt. (2015). Improved diagnostics of Niemann–Pick disease type C by the analysis of plasma oxysterols. Molecular Genetics and Metabolism. 114(2). S98–S98. 1 indexed citations
14.
Debus, Volker, Janine Reunert, Sebastian T. Balbach, et al.. (2015). News on Clinical Details and Treatment in PGM1-CDG. JIMD Reports. 26. 77–84. 19 indexed citations
15.
Park, Julien H., Oliver J. Wagner, Yoshinao Wada, et al.. (2015). Congenital nephrotic syndrome with dysmorphic features and death in early infancy: Questions. Pediatric Nephrology. 31(8). 1281–1281.
16.
17.
Park, Julien H., Yoshinao Wada, Claudia Roll, et al.. (2014). The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation. Clinica Chimica Acta. 436. 135–139. 10 indexed citations
18.
Rust, Stephan, Janine Reunert, Friedhelm Meinhardt, et al.. (2013). ALG1-CDG: A new case with early fatal outcome. Gene. 534(2). 345–351. 21 indexed citations
19.
Guan, Ziqiang, Stephan Rust, Janine Reunert, et al.. (2011). Life with too much polyprenol: polyprenol reductase deficiency. Molecular Genetics and Metabolism. 105(4). 642–651. 39 indexed citations
20.
Omran, Heymut, et al.. (2009). Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih. Molecular Genetics and Metabolism. 98(3). 305–309. 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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