Valérie Race

2.0k total citations
45 papers, 929 citations indexed

About

Valérie Race is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Valérie Race has authored 45 papers receiving a total of 929 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 14 papers in Genetics and 13 papers in Genetics. Recurrent topics in Valérie Race's work include Biochemical and Molecular Research (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Iron Metabolism and Disorders (8 papers). Valérie Race is often cited by papers focused on Biochemical and Molecular Research (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Iron Metabolism and Disorders (8 papers). Valérie Race collaborates with scholars based in Belgium, Democratic Republic of the Congo and United States. Valérie Race's co-authors include Gert Matthijs, Koenraad Devriendt, Jaak Jaeken, François Foulquier, Emile Van Schaftingen, Philip Van Damme, Hilde Van Esch, Daisy Rymen, Claire Rosnoblet and Wim Robberecht and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Valérie Race

44 papers receiving 919 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valérie Race Belgium 18 545 220 137 130 112 45 929
Ginat Narkis Israel 14 528 1.0× 127 0.6× 107 0.8× 88 0.7× 62 0.6× 23 836
Sandra Meulemans Belgium 19 470 0.9× 201 0.9× 267 1.9× 29 0.2× 81 0.7× 29 1.0k
Jinmin Miao United States 13 578 1.1× 408 1.9× 90 0.7× 25 0.2× 130 1.2× 22 1.1k
Pengfei Lin China 19 445 0.8× 54 0.2× 105 0.8× 73 0.6× 88 0.8× 66 872
Mei-Yao Lin United States 12 695 1.3× 68 0.3× 147 1.1× 52 0.4× 186 1.7× 14 1.2k
Emma L. Baple United Kingdom 18 547 1.0× 373 1.7× 137 1.0× 37 0.3× 36 0.3× 59 902
Alexandre Janer Canada 15 842 1.5× 67 0.3× 138 1.0× 41 0.3× 86 0.8× 20 1.1k
Ruilin Tian China 14 1.1k 2.0× 101 0.5× 273 2.0× 38 0.3× 261 2.3× 30 1.5k
Keunmyoung Lee United States 11 638 1.2× 204 0.9× 109 0.8× 38 0.3× 123 1.1× 11 1.0k
Leonarda Ianzano Italy 21 696 1.3× 702 3.2× 61 0.4× 87 0.7× 234 2.1× 26 1.4k

Countries citing papers authored by Valérie Race

Since Specialization
Citations

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

Fields of papers citing papers by Valérie Race

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valérie Race

This figure shows the co-authorship network connecting the top 25 collaborators of Valérie Race. A scholar is included among the top collaborators of Valérie Race 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 Valérie Race. Valérie Race 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.
Lumaka, Aimé, Valérie Race, Gert Matthijs, et al.. (2023). Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa. SHILAP Revista de lepidopterología. 4(3). 595–601. 3 indexed citations
2.
Moisse, Matthieu, Valérie Race, Liesbeth Keldermans, et al.. (2021). RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvement. European Journal of Neurology. 29(1). 345–349. 6 indexed citations
3.
Race, Valérie, et al.. (2020). Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutation. Neuromuscular Disorders. 30(9). 709–718. 7 indexed citations
4.
Race, Valérie, et al.. (2019). Challenges in molecular diagnosis of X-linked Intellectual disability. British Medical Bulletin. 133(1). 36–48. 13 indexed citations
5.
Blommaert, Eline, Romain Péanne, Н. А. Черепанова, et al.. (2019). Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype. Proceedings of the National Academy of Sciences. 116(20). 9865–9870. 61 indexed citations
6.
Ardui, Simon, Valérie Race, Thomy de Ravel, et al.. (2018). Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience. Frontiers in Genetics. 9. 150–150. 27 indexed citations
7.
Lukusa-Tshilobo, Prosper, Michel Ntetani Aloni, Aimé Lumaka, et al.. (2017). Protective BCL11A and HBS1L‐MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia. Journal of Clinical Laboratory Analysis. 32(1). 3 indexed citations
8.
Ardui, Simon, Valérie Race, Matthew S. Hestand, et al.. (2016). Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing. Human Mutation. 38(3). 324–331. 31 indexed citations
9.
Mehta, Nitesh R., Valérie Race, François Foulquier, et al.. (2015). Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDG. Glycobiology. 25(6). 669–682. 30 indexed citations
10.
Matthijs, Gert, Mariëlle Alders, Peter Bauer, et al.. (2014). EuroGentest guidelines for diagnostic next generation sequencing. European Journal of Human Genetics. 22. 566–566. 3 indexed citations
11.
Debray, Sarah, Valérie Race, Gert Matthijs, et al.. (2013). Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study. Neurobiology of Aging. 34(12). 2890.e7–2890.e12. 30 indexed citations
12.
Foulquier, François, Mustapha Amyere, Jaak Jaeken, et al.. (2012). TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation. The American Journal of Human Genetics. 91(1). 15–26. 163 indexed citations
13.
Esch, Hilde Van, et al.. (2008). Very early premature ovarian failure in two sisters compound heterozygous for the FMR1 premutation. European Journal of Medical Genetics. 52(1). 37–40. 12 indexed citations
14.
Debeer, Philippe, Valérie Race, Marc Gewillig, Koenraad Devriendt, & Jean‐Pierre Frijns. (2007). Novel TBX5 Mutations in Patients with Holt-Oram Syndrome. Clinical Orthopaedics and Related Research. 462. 20–26. 23 indexed citations
15.
Race, Valérie, Younès Achouri, Elsa Wiame, et al.. (2007). Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway. The American Journal of Human Genetics. 80(5). 931–937. 89 indexed citations
16.
Smal, Caroline, Luc Bertrand, Eric Van Den Neste, et al.. (2004). New Evidences for a Regulation of Deoxycytidine Kinase Activity by Reversible Phosphorylation. Nucleosides Nucleotides & Nucleic Acids. 23(8-9). 1363–1365. 7 indexed citations
17.
Race, Valérie, Sandrine Marie, Pascal Kienlen‐Campard, et al.. (2004). Adenylosuccinate Lyase Deficiency: Study of Physiopathologic Mechanism(s). Nucleosides Nucleotides & Nucleic Acids. 23(8-9). 1227–1229. 2 indexed citations
18.
Race, Valérie. (2000). Clinical, biochemical and molecular genetic correlations in adenylosuccinate lyase deficiency. Human Molecular Genetics. 9(14). 2159–2165. 45 indexed citations
19.
Liacini, Abdelhamid, Sandrine Marie, Valérie Race, M. F. Vincent, & Greet Van den Berghe. (1999). Isozymes of adenylosuccinate lyase in human tissues. Cellular & Molecular Biology Letters. 4(3). 1 indexed citations
20.
Marie, Sandrine, Valérie Race, Marie‐Cécile Nassogne, Marie Vincent, & Greet Van den Berghe. (1999). A mutation in the 5'UTR of the ADSL gene in a patient with adenylosuccinate lyase deficiency. Cellular & Molecular Biology Letters. 4(3). 3 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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