Sabine Grønborg

1.6k total citations
25 papers, 330 citations indexed

About

Sabine Grønborg is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Sabine Grønborg has authored 25 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 4 papers in Physiology. Recurrent topics in Sabine Grønborg's work include Metabolism and Genetic Disorders (8 papers), Peroxisome Proliferator-Activated Receptors (6 papers) and Lysosomal Storage Disorders Research (4 papers). Sabine Grønborg is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Peroxisome Proliferator-Activated Receptors (6 papers) and Lysosomal Storage Disorders Research (4 papers). Sabine Grønborg collaborates with scholars based in Denmark, United States and Germany. Sabine Grønborg's co-authors include Sven Thoms, Jutta Gärtner, Peter Uldall, Mari Mori, Sarah B. Mulkey, Andrea M. Lewis, David A. Koolen, Bruria Ben‐Zeev, Phillip L. Pearl and Maurizio Taglialatela and has published in prestigious journals such as Human Molecular Genetics, Epilepsia and Movement Disorders.

In The Last Decade

Sabine Grønborg

22 papers receiving 328 citations

Peers

Sabine Grønborg

GENET

PHYSI

PMH

Charlotte Thiels Germany

Aziza Chedrawi Saudi Arabia

Martino Montomoli Italy

Isabel Fineza Portugal

Thatjana Gardeitchik Netherlands

Anna Marcé‐Grau Spain

Magdalena Pajdowska Poland

Heiko Brennenstuhl Germany

Hana Vlášková Czechia

Jaina Patel Canada

Charlotte Thiels Germany

Sabine Grønborg

225 ×1.1

40 ×0.5

46 ×0.7

GENET

66 ×1.0

PHYSI

27 ×0.4

PMH

Citations per year, relative to Sabine Grønborg Sabine Grønborg (= 1×) peers Charlotte Thiels

Countries citing papers authored by Sabine Grønborg

Since Specialization

Citations

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

Fields of papers citing papers by Sabine Grønborg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Grønborg

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Gao, Qian, Adnan Mujahid Khan, Mette Christensen, et al.. (2025). A diagnostic algorithm for inherited metabolic disorders using untargeted metabolomics. Metabolomics. 21(4). 101–101.

Zabel, Claus, et al.. (2025). A Novel Mutation in CNTNAP1 Gene Causes Disorganization of Axonal Domains, Hypomyelination and Severe Neurological Deficits. Journal of Neuroscience Research. 103(4). e70040–e70040.

Mochel, Fanny, Laura Adang, Jaap Jan Boelens, et al.. (2024). Inventory of current practices regarding hematopoietic stem cell transplantation in metachromatic leukodystrophy in Europe and neighboring countries. Orphanet Journal of Rare Diseases. 19(1). 46–46. 2 indexed citations

Grønborg, Sabine, et al.. (2024). Psychological Impact of Presymptomatic X-Linked ALD Diagnosis and Surveillance: A Small Qualitative Study of Patient and Parent Experiences. International Journal of Neonatal Screening. 10(4). 73–73.

Hock, Daniella H., Nicole J. Lake, Sarah E. Calvo, et al.. (2023). Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease. Human Molecular Genetics. 32(15). 2441–2454. 13 indexed citations

Petersen, Esben Thade, Christina Fenger, Mette Cathrine Ørngreen, et al.. (2023). X-linked creatine transporter (SLC6A8) deficiency in females: Difficult to recognize, but a potentially treatable disease. Molecular Genetics and Metabolism. 140(3). 107694–107694. 5 indexed citations

Melgaard, Lars, et al.. (2023). Newborn screening for adrenoleukodystrophy: International experiences and challenges. Molecular Genetics and Metabolism. 140(4). 107734–107734. 4 indexed citations

Beerepoot, Shanice, Laura Adang, Annette Bley, et al.. (2022). Modified Delphi procedure-based expert consensus on endpoints for an international disease registry for Metachromatic Leukodystrophy: The European Metachromatic Leukodystrophy initiative (MLDi). Orphanet Journal of Rare Diseases. 17(1). 48–48. 13 indexed citations

Tseng, Laura A., José E. Abdenur, Ashley Andrews, et al.. (2022). Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy. Molecular Genetics and Metabolism. 135(4). 350–356. 17 indexed citations

10.

Bak, Mads, et al.. (2021). Case report: ‘AARS2 leukodystrophy’. Molecular Genetics and Metabolism Reports. 28. 100782–100782. 5 indexed citations

11.

Witters, Peter, Rita Barone, Katrin Õunap, et al.. (2020). Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG. Genetics in Medicine. 22(6). 1102–1107. 56 indexed citations

12.

Diness, Birgitte Rode, Hanne Hove, Henning Bundgaard, et al.. (2020). Expanding the cerebrovascular phenotype of the p.R258H variant in ACTA2 related hereditary thoracic aortic disease (HTAD). Journal of the Neurological Sciences. 415. 116897–116897. 2 indexed citations

13.

Grønborg, Sabine, Lotte Risom, Jakob Ek, et al.. (2018). A Faroese founder variant in TBCD causes early onset, progressive encephalopathy with a homogenous clinical course. European Journal of Human Genetics. 26(10). 1512–1520. 12 indexed citations

14.

Mulkey, Sarah B., Bruria Ben‐Zeev, Joost Nicolai, et al.. (2017). Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain‐of‐function variants R201C and R201H. Epilepsia. 58(3). 436–445. 71 indexed citations

15.

Grønborg, Sabine, Niklas Darín, María J. Miranda, et al.. (2016). Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling. JIMD Reports. 33. 69–77. 19 indexed citations

16.

Grønborg, Sabine & Peter Uldall. (2013). Mortality and causes of death in children referred to a tertiary epilepsy center. European Journal of Paediatric Neurology. 18(1). 66–71. 16 indexed citations

17.

Grønborg, Sabine, Ralph Krätzner, Hendrik Rosewich, & Jutta Gärtner. (2011). Lymphoblastoid Cell Lines for Diagnosis of Peroxisome Biogenesis Disorders. JIMD Reports. 1. 29–36. 2 indexed citations

18.

Thoms, Sven, et al.. (2011). Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients. BMC Medical Genetics. 12(1). 109–109. 2 indexed citations

19.

Grønborg, Sabine, Ralph Krätzner, Juliane Spiegler, et al.. (2010). Typical cMRI pattern as diagnostic clue for D‐bifunctional protein deficiency without apparent biochemical abnormalities in plasma. American Journal of Medical Genetics Part A. 152A(11). 2845–2849. 13 indexed citations

20.

Thoms, Sven, Sabine Grønborg, & Jutta Gärtner. (2009). Organelle interplay in peroxisomal disorders. Trends in Molecular Medicine. 15(7). 293–302. 46 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