Fabienne Wavrant DeVriéze

1.2k total citations
6 papers, 432 citations indexed

About

Fabienne Wavrant DeVriéze is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Fabienne Wavrant DeVriéze has authored 6 papers receiving a total of 432 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Cellular and Molecular Neuroscience and 2 papers in Neurology. Recurrent topics in Fabienne Wavrant DeVriéze's work include Alzheimer's disease research and treatments (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers) and Genomics and Rare Diseases (1 paper). Fabienne Wavrant DeVriéze is often cited by papers focused on Alzheimer's disease research and treatments (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers) and Genomics and Rare Diseases (1 paper). Fabienne Wavrant DeVriéze collaborates with scholars based in United States, United Kingdom and Spain. Fabienne Wavrant DeVriéze's co-authors include John Hardy, M. Axel Wollmer, Roger M. Nitsch, Randall T. Moon, G. Ferrari, Christopher M. Morris, Katia Sáez, Andreas Papassotiropoulos, Travis L. Biechele and Michael B. Major and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Movement Disorders and Neuroscience Letters.

In The Last Decade

Fabienne Wavrant DeVriéze

6 papers receiving 424 citations

Peers

Fabienne Wavrant DeVriéze

MB

PHYSI

NEURO

CMN

GENET

Yunlan Du China

Talisha A. Hunter United States

Veerle Bogaerts Belgium

Stefano Cattaneo Italy

Karunya Ramasamy United States

Luis M. Guisasola Spain

Farah Bardai United States

Julia van der Hoven Australia

Shahzad S. Khan United States

Anikó Gál Hungary

Yunlan Du China

Fabienne Wavrant DeVriéze

168 ×0.7

MB

123 ×0.7

PHYSI

154 ×1.1

NEURO

128 ×0.9

CMN

37 ×0.3

GENET

Citations per year, relative to Fabienne Wavrant DeVriéze Fabienne Wavrant DeVriéze (= 1×) peers Yunlan Du

Countries citing papers authored by Fabienne Wavrant DeVriéze

Since Specialization

Citations

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

Fields of papers citing papers by Fabienne Wavrant DeVriéze

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fabienne Wavrant DeVriéze. 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 Fabienne Wavrant DeVriéze. The network helps show where Fabienne Wavrant DeVriéze may publish in the future.

Co-authorship network of co-authors of Fabienne Wavrant DeVriéze

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

All Works

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6 of 6 papers shown

1.

Hollingworth, Paul, Marian L. Hamshere, Peter Holmans, et al.. (2007). Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 841–848. 32 indexed citations

2.

Ferrari, G., Andreas Papassotiropoulos, Travis L. Biechele, et al.. (2007). Common genetic variation within the Low-Density Lipoprotein Receptor-Related Protein 6 and late-onset Alzheimer's disease. Proceedings of the National Academy of Sciences. 104(22). 9434–9439. 224 indexed citations

3.

Hernández, Dena, Anthony Crawley, Roneil G. Malkani, et al.. (2005). The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases. Neuroscience Letters. 389(3). 137–139. 77 indexed citations

4.

Clark, Lorraine N., Helen Mejia‐Santana, Juliette Harris, et al.. (2004). Analysis of an early‐onset Parkinson's disease cohort for DJ‐1 mutations. Movement Disorders. 19(7). 796–800. 56 indexed citations

5.

Compton, Danielle, Fabienne Wavrant DeVriéze, Ronald C. Petersen, et al.. (2002). Possible association between genetic variability at the apolipoprotein(a) locus and Alzheimer's disease in apolipoprotein E2 carriers. Neuroscience Letters. 331(1). 60–62. 11 indexed citations

6.

Baker, Matt, Fabienne Wavrant DeVriéze, Caroline Graff, et al.. (2000). No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease. Neuroscience Letters. 285(2). 147–149. 32 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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