Karit Reinson

1.0k total citations
14 papers, 198 citations indexed

About

Karit Reinson is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karit Reinson has authored 14 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Clinical Biochemistry, 8 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karit Reinson's work include Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (4 papers) and Neonatal Health and Biochemistry (3 papers). Karit Reinson is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (4 papers) and Neonatal Health and Biochemistry (3 papers). Karit Reinson collaborates with scholars based in Estonia, United States and Netherlands. Karit Reinson's co-authors include Katrin Õunap, Sander Pajusalu, Eve Õiglane‐Shlik, Sanna Puusepp, Inga Talvik, Kai Muru, Rita Teek, Richard J. Rodenburg, Mari‐Anne Vals and Ulvi Vaher and has published in prestigious journals such as EMBO Molecular Medicine, European Journal of Human Genetics and Journal of Inherited Metabolic Disease.

In The Last Decade

Karit Reinson

13 papers receiving 197 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karit Reinson Estonia 8 122 80 67 36 29 14 198
Omar Hikmat Norway 9 234 1.9× 128 1.6× 26 0.4× 37 1.0× 18 0.6× 20 281
Mara Lúcia Schmitz Ferreira Santos Brazil 8 101 0.8× 57 0.7× 23 0.3× 31 0.9× 28 1.0× 37 276
Ilya Kanivets Russia 7 91 0.7× 29 0.4× 61 0.9× 11 0.3× 10 0.3× 39 162
Bregje Jaeger Netherlands 9 80 0.7× 95 1.2× 16 0.2× 19 0.5× 57 2.0× 22 216
Clara D. van Karnebeek Netherlands 9 97 0.8× 53 0.7× 60 0.9× 18 0.5× 11 0.4× 23 174
Cheuk Wing Fung China 9 67 0.5× 29 0.4× 54 0.8× 21 0.6× 7 0.2× 18 177
Anne Dieux‐Coëslier France 7 99 0.8× 25 0.3× 39 0.6× 22 0.6× 12 0.4× 12 156
Naomi Meeks United States 8 86 0.7× 64 0.8× 50 0.7× 9 0.3× 13 0.4× 16 169
Chiemi Hayakawa Japan 10 145 1.2× 94 1.2× 119 1.8× 23 0.6× 15 0.5× 20 350
Roberta Solazzi Italy 8 55 0.5× 19 0.2× 91 1.4× 31 0.9× 13 0.4× 20 162

Countries citing papers authored by Karit Reinson

Since Specialization
Citations

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

Fields of papers citing papers by Karit Reinson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karit Reinson

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

All Works

14 of 14 papers shown
1.
Reinson, Karit, Kai Muru, Tiia Reimand, et al.. (2025). Exploratory analysis of epilepsy biomarkers using untargeted metabolomics across multiple cohorts. Frontiers in Neurology. 16. 1684456–1684456.
2.
Reinson, Karit, Marcello Bellusci, Julien H. Park, et al.. (2024). Current global vitamin and cofactor prescribing practices for primary mitochondrial diseases: Results of a European reference network survey. Journal of Inherited Metabolic Disease. 48(1). e12805–e12805. 2 indexed citations
3.
4.
Puusepp, Sanna, Karit Reinson, Sander Pajusalu, et al.. (2020). Atypical presentation of Arts syndrome due to a novel hemizygous loss-of-function variant in the PRPS1 gene. Molecular Genetics and Metabolism Reports. 25. 100677–100677. 10 indexed citations
5.
Reinson, Karit & Katrin Õunap. (2020). Complex I deficiency and Leigh syndrome through the eyes of a clinician. EMBO Molecular Medicine. 12(11). e13187–e13187. 4 indexed citations
6.
Kahre, Tiina, Riina Žordania, Karit Reinson, et al.. (2019). A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016. European Journal of Human Genetics. 27(11). 1649–1658. 17 indexed citations
7.
Reinson, Karit, et al.. (2019). The evaluation of phenylalanine levels in Estonian phenylketonuria patients during eight years by electronic laboratory records. Molecular Genetics and Metabolism Reports. 19. 100467–100467. 4 indexed citations
8.
Muru, Kai, Karit Reinson, Zahra Nochi, et al.. (2019). FLAD1‐associated multiple acyl‐CoA dehydrogenase deficiency identified by newborn screening. Molecular Genetics & Genomic Medicine. 7(9). e915–e915. 13 indexed citations
9.
Puusepp, Sanna, Karit Reinson, Sander Pajusalu, et al.. (2018). Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia. Molecular Genetics and Metabolism Reports. 15. 80–89. 30 indexed citations
10.
Reinson, Karit, et al.. (2018). High incidence of low vitamin B12 levels in Estonian newborns. Molecular Genetics and Metabolism Reports. 15. 1–5. 21 indexed citations
11.
Reinson, Karit, Réka Kovács-Nagy, Eve Õiglane‐Shlik, et al.. (2018). Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11. European Journal of Medical Genetics. 62(11). 103572–103572. 23 indexed citations
12.
13.
Reinson, Karit, Eve Õiglane‐Shlik, Inga Talvik, et al.. (2016). Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy. American Journal of Medical Genetics Part A. 170(8). 2173–2176. 62 indexed citations
14.

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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