Sarah C. Grünert

4.5k total citations
86 papers, 1.6k citations indexed

About

Sarah C. Grünert is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Sarah C. Grünert has authored 86 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Clinical Biochemistry, 42 papers in Molecular Biology and 36 papers in Rheumatology. Recurrent topics in Sarah C. Grünert's work include Metabolism and Genetic Disorders (51 papers), Mitochondrial Function and Pathology (22 papers) and Glycogen Storage Diseases and Myoclonus (20 papers). Sarah C. Grünert is often cited by papers focused on Metabolism and Genetic Disorders (51 papers), Mitochondrial Function and Pathology (22 papers) and Glycogen Storage Diseases and Myoclonus (20 papers). Sarah C. Grünert collaborates with scholars based in Germany, Netherlands and United States. Sarah C. Grünert's co-authors include Ute Spiekerkoetter, Luciana Hannibal, Henk J. Blom, Jörn Oliver Sass, Donald W. Jacobsen, Sidney Behringer, Anne‐Lise Bjørke‐Monsen, Vegard Lysne, Karl Otfried Schwab and Anke Schumann and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PEDIATRICS.

In The Last Decade

Sarah C. Grünert

84 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah C. Grünert Germany 22 726 716 564 333 277 86 1.6k
Bernd Schwahn Germany 26 667 0.9× 691 1.0× 1.0k 1.8× 281 0.8× 247 0.9× 61 2.0k
Terry G. J. Derks Netherlands 26 729 1.0× 677 0.9× 834 1.5× 598 1.8× 433 1.6× 106 2.0k
John H. Walter United Kingdom 20 1.2k 1.7× 874 1.2× 589 1.0× 474 1.4× 210 0.8× 39 1.9k
Martina Huemer Austria 26 1.3k 1.7× 855 1.2× 861 1.5× 527 1.6× 227 0.8× 74 2.4k
Elisabetta Pasquini Italy 23 698 1.0× 589 0.8× 366 0.6× 232 0.7× 158 0.6× 59 1.4k
Esther M. Maier Germany 23 857 1.2× 974 1.4× 189 0.3× 251 0.8× 353 1.3× 64 1.7k
Isabel Rivera Portugal 19 421 0.6× 768 1.1× 622 1.1× 168 0.5× 165 0.6× 56 1.5k
Klary E. Niezen‐Koning Netherlands 22 522 0.7× 709 1.0× 395 0.7× 930 2.8× 163 0.6× 59 1.8k
Julian Raiman Canada 24 334 0.5× 559 0.8× 439 0.8× 738 2.2× 228 0.8× 58 1.5k
Ute Spiekerkoetter Germany 30 1.7k 2.3× 1.5k 2.1× 483 0.9× 787 2.4× 278 1.0× 111 2.6k

Countries citing papers authored by Sarah C. Grünert

Since Specialization
Citations

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

Fields of papers citing papers by Sarah C. Grünert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah C. Grünert. 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 Sarah C. Grünert. The network helps show where Sarah C. Grünert may publish in the future.

Co-authorship network of co-authors of Sarah C. Grünert

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah C. Grünert. A scholar is included among the top collaborators of Sarah C. Grünert 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 Sarah C. Grünert. Sarah C. Grünert 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.
Schumann, Anke, Sven F. Garbade, Skadi Beblo, et al.. (2025). Kidney involvement in glycogen storage disease type I: Current knowledge and key challenges. Molecular Genetics and Metabolism. 144(3). 109054–109054.
2.
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
3.
Grünert, Sarah C., Terry G. J. Derks, Helen Mundy, et al.. (2024). Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop. Molecular Genetics and Metabolism. 141(3). 108144–108144. 8 indexed citations
4.
Veiga‐da‐Cunha, Maria, Saskia B. Wortmann, Sarah C. Grünert, & Emile Van Schaftingen. (2023). Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 Inhibitors. Diagnostics. 13(10). 1803–1803. 19 indexed citations
5.
Garbade, Sven F., et al.. (2023). Psychosocial issues and coping strategies in families affected by long‐chain fatty acid oxidation disorders. JIMD Reports. 65(1). 25–38. 2 indexed citations
6.
Derks, Terry G. J., et al.. (2023). Glycogen storage diseases. Nature Reviews Disease Primers. 9(1). 46–46. 33 indexed citations
7.
Grünert, Sarah C., et al.. (2023). Patient‐reported outcomes on empagliflozin treatment in glycogen storage disease type Ib: An international questionnaire study. JIMD Reports. 64(3). 252–258. 16 indexed citations
8.
Grünert, Sarah C., et al.. (2023). Metabolic phenotyping in phenylketonuria reveals disease clustering independently of metabolic control. Molecular Genetics and Metabolism. 138(3). 107509–107509. 10 indexed citations
9.
Yoshimi, Ayami, Kaori Ishikawa, Charlotte M. Niemeyer, & Sarah C. Grünert. (2022). Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure. Orphanet Journal of Rare Diseases. 17(1). 379–379. 30 indexed citations
10.
Derks, Terry G. J., David Rodriguez‐Buritica, Ayesha Ahmad, et al.. (2021). Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs. Nutrients. 13(11). 3828–3828. 35 indexed citations
11.
Schmitt, Johannes, Michael Wurm, Karl Otfried Schwab, et al.. (2021). Glycogen storage disease type I patients with hyperlipidemia have no signs of early vascular dysfunction and premature atherosclerosis. Nutrition Metabolism and Cardiovascular Diseases. 31(12). 3384–3392. 3 indexed citations
12.
Grünert, Sarah C., Anke Schumann, Allan M. Lund, et al.. (2021). Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease. Biochimie. 183. 55–62. 9 indexed citations
13.
Grünert, Sarah C., Anke Schumann, Federico Baronio, et al.. (2021). Evidence for a Genotype–Phenotype Correlation in Patients with Pathogenic GLUT2 (SLC2A2) Variants. Genes. 12(11). 1785–1785. 5 indexed citations
14.
Eckenweiler, Matthias, Johannes A. Mayr, Sarah C. Grünert, Angela Abicht, & Rudolf Korinthenberg. (2020). Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants. Neuropediatrics. 52(2). 123–125. 6 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.
Schmitt, Johannes, Michael Wurm, Karl Otfried Schwab, et al.. (2020). Elevated Plasma Vitamin B12 in Patients with Hepatic Glycogen Storage Diseases. Journal of Clinical Medicine. 9(8). 2326–2326. 6 indexed citations
17.
Landolt, Markus A., Annet M. Bosch, Sarah C. Grünert, et al.. (2019). Reducing complexity: explaining inborn errors of metabolism and their treatment to children and adolescents. Orphanet Journal of Rare Diseases. 14(1). 248–248. 9 indexed citations
18.
Hannibal, Luciana, Vegard Lysne, Anne‐Lise Bjørke‐Monsen, et al.. (2016). Biomarkers and Algorithms for the Diagnosis of Vitamin B12 Deficiency. Frontiers in Molecular Biosciences. 3. 27–27. 230 indexed citations
19.
Grünert, Sarah C., Pablo Villavicencio‐Lorini, Ekkehart Lausch, et al.. (2015). Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening. BMC Medical Genetics. 16(1). 56–56. 15 indexed citations
20.
Grünert, Sarah C., Brian Fowler, Andrea Superti‐Furga, Jörn Oliver Sass, & Karl Otfried Schwab. (2010). Hyperpyrexia resulting in encephalopathy in a 14-month-old patient with cblC disease. Brain and Development. 33(5). 432–436. 2 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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