V. Ramaekers

4.6k total citations
74 papers, 3.1k citations indexed

About

V. Ramaekers is a scholar working on Rheumatology, Molecular Biology and Genetics. According to data from OpenAlex, V. Ramaekers has authored 74 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Rheumatology, 20 papers in Molecular Biology and 19 papers in Genetics. Recurrent topics in V. Ramaekers's work include Folate and B Vitamins Research (18 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Metabolism and Genetic Disorders (9 papers). V. Ramaekers is often cited by papers focused on Folate and B Vitamins Research (18 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Metabolism and Genetic Disorders (9 papers). V. Ramaekers collaborates with scholars based in Germany, United States and Belgium. V. Ramaekers's co-authors include Nenad Blau, Edward V. Quadros, Jeffrey M. Sequeira, Martin Häusler, J.M. Sequeira, Thomas Opladen, G. Heimann, E. Quadros, Paul Casaer and Richard P. Lifton and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and SHILAP Revista de lepidopterología.

In The Last Decade

V. Ramaekers

72 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Ramaekers Germany 32 999 783 718 561 545 74 3.1k
Edward V. Quadros United States 31 1.3k 1.3× 1.7k 2.2× 736 1.0× 709 1.3× 514 0.9× 105 3.4k
Pierangelo Veggiotti Italy 39 996 1.0× 396 0.5× 915 1.3× 674 1.2× 854 1.6× 182 4.7k
Roberta Battini Italy 29 1.2k 1.2× 230 0.3× 441 0.6× 213 0.4× 555 1.0× 178 2.9k
Pirkko Santavuori Finland 42 2.6k 2.6× 708 0.9× 486 0.7× 153 0.3× 192 0.4× 133 5.7k
Makiko Ōsawa Japan 36 2.4k 2.4× 370 0.5× 818 1.1× 321 0.6× 351 0.6× 196 4.9k
Nardo Nardocci Italy 34 1.2k 1.2× 484 0.6× 387 0.5× 201 0.4× 529 1.0× 144 4.0k
Aída Ormazábal Spain 28 729 0.7× 422 0.5× 372 0.5× 157 0.3× 865 1.6× 86 1.8k
Bruria Ben‐Zeev Israel 33 1.3k 1.3× 104 0.1× 994 1.4× 530 0.9× 264 0.5× 105 3.4k
Niklas Darín Sweden 36 3.2k 3.2× 196 0.3× 463 0.6× 334 0.6× 1.3k 2.3× 105 4.8k
Ki Joong Kim South Korea 28 892 0.9× 375 0.5× 407 0.6× 236 0.4× 217 0.4× 199 3.0k

Countries citing papers authored by V. Ramaekers

Since Specialization
Citations

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

Fields of papers citing papers by V. Ramaekers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Ramaekers

This figure shows the co-authorship network connecting the top 25 collaborators of V. Ramaekers. A scholar is included among the top collaborators of V. Ramaekers 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 V. Ramaekers. V. Ramaekers 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.
Han, Xiao, Xuanye Cao, Robert M. Cabrera, et al.. (2022). KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology. 12(1). 74–74. 4 indexed citations
2.
Ramaekers, V., et al.. (2021). Folate Receptor Alpha Autoantibodies in Autism Spectrum Disorders: Diagnosis, Treatment and Prevention. Journal of Personalized Medicine. 11(8). 710–710. 28 indexed citations
3.
Cao, Xuanye, Annika Wolf, Sung‐Eun Kim, et al.. (2020). CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression. Journal of Medical Genetics. 58(7). 484–494. 18 indexed citations
4.
Ramaekers, V., et al.. (2019). Improving Outcome in Infantile Autism with Folate Receptor Autoimmunity and Nutritional Derangements: A Self-Controlled Trial. SHILAP Revista de lepidopterología. 2019. 1–12. 26 indexed citations
5.
Ramaekers, V., Karin Segers, J.M. Sequeira, et al.. (2018). Genetic assessment and folate receptor autoantibodies in infantile-onset cerebral folate deficiency (CFD) syndrome. Molecular Genetics and Metabolism. 124(1). 87–93. 18 indexed citations
6.
Ramaekers, V., J.M. Sequeira, & Edward V. Quadros. (2016). The basis for folinic acid treatment in neuro-psychiatric disorders. Biochimie. 126. 79–90. 29 indexed citations
7.
Ramaekers, V., Beat Thöny, J.M. Sequeira, et al.. (2014). Folinic acid treatment for schizophrenia associated with folate receptor autoantibodies. Molecular Genetics and Metabolism. 113(4). 307–314. 44 indexed citations
8.
Küry, Sébastien, V. Ramaekers, Stéphane Bezieau, & Barry Wolf. (2012). Clinical utility gene card for: Biotinidase deficiency. European Journal of Human Genetics. 20(5). 4–4. 7 indexed citations
9.
Scholl, Ute I., Murim Choi, V. Ramaekers, et al.. (2009). Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10. Proceedings of the National Academy of Sciences. 106(14). 5842–5847. 354 indexed citations
10.
Ramaekers, V., et al.. (2007). Mitochondrial Complex I Encephalomyopathy and Cerebral 5-Methyltetrahydrofolate Deficiency. Neuropediatrics. 38(4). 184–187. 42 indexed citations
11.
Ramaekers, V. & Nenad Blau. (2004). Cerebral folate deficiency. Developmental Medicine & Child Neurology. 46(12). 843–851. 150 indexed citations
12.
Wenzl, Tobias G., Ulrich Merz, V. Ramaekers, et al.. (2002). Functional Upper Airway Obstruction in a Child with Freeman-Sheldon Syndrome. ORL. 64(1). 53–56. 7 indexed citations
13.
Ramaekers, V., Jan Senderek, Martin Häusler, et al.. (2001). A Novel Neurodevelopmental Syndrome Responsive to 5-Hydroxytryptophan and Carbidopa. Molecular Genetics and Metabolism. 73(2). 179–187. 13 indexed citations
14.
Abicht, Angela, Rolf Stucka, Veronika Karcagi, et al.. (1999). A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology. 53(7). 1564–1564. 77 indexed citations
15.
Ramaekers, V., Johannes M. H. M. Reul, G. Kusenbach, A. Thron, & G. Heimann. (1997). Central Pontme Myelinolysis Associated with Acquired Folate Depletion. Neuropediatrics. 28(2). 126–130. 14 indexed citations
16.
Ramaekers, V., et al.. (1997). Increased plasma malondialdehyde associated with cerebellar structural defects. Archives of Disease in Childhood. 77(3). 231–234. 10 indexed citations
17.
Jaeken, Jaak, Paul De Cock, Helena Stibler, et al.. (1993). Carbohydrate‐deficient glycoprotein syndrome type II. Journal of Inherited Metabolic Disease. 16(6). 1041–1041. 35 indexed citations
18.
Ramaekers, V., Paul Casaer, Johannes M. A. Daniels, & G Marchal. (1992). The influence of blood transfusion on brain blood flow autoregulation among stable preterm infants. Early Human Development. 30(3). 211–220. 12 indexed citations
19.
Ramaekers, V., Paul Casaer, Johannes M. A. Daniels, & Guy Marchal. (1990). Upper limits of brain blood flow autoregulation in stable infants of various conceptional age. Early Human Development. 24(3). 249–258. 39 indexed citations
20.
Ramaekers, V., et al.. (1988). THE EFFECT OF BLOOD TRANSFUSION ON CEREBRAL BLOOD‐FLOW IN PRETERM INFANTS: A DOPPLER STUDY. Developmental Medicine & Child Neurology. 30(3). 334–341. 24 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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