Grégory Raux

3.6k total citations · 2 hit papers
27 papers, 2.3k citations indexed

About

Grégory Raux is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Grégory Raux has authored 27 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Pathology and Forensic Medicine and 6 papers in Genetics. Recurrent topics in Grégory Raux's work include Alzheimer's disease research and treatments (6 papers), Autoimmune Bullous Skin Diseases (5 papers) and Urticaria and Related Conditions (3 papers). Grégory Raux is often cited by papers focused on Alzheimer's disease research and treatments (6 papers), Autoimmune Bullous Skin Diseases (5 papers) and Urticaria and Related Conditions (3 papers). Grégory Raux collaborates with scholars based in France, Belgium and China. Grégory Raux's co-authors include Thierry Frébourg, Dominique Campion, Didier Hannequin, Alexis Brice, Cécile Dumanchin, Anne Rovelet‐Lecrux, Annie Laquerrière, Anne Vital, Frédéric Dubas and Martine Vercelletto and has published in prestigious journals such as Nature Genetics, Blood and Gastroenterology.

In The Last Decade

Grégory Raux

27 papers receiving 2.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

2005 871 citations Anne Rovelet‐Lecrux, Didier Hannequin et al. Nature Genetics profile →
Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

1999 544 citations Dominique Campion, Cécile Dumanchin et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Grégory Raux France	19	1.1k	1.1k	562	319	270	27	2.3k
Kouzin Kamino Japan	26	1.0k 0.9×	1.2k 1.2×	247 0.4×	289 0.9×	172 0.6×	70	2.3k
Christer Möller Sweden	27	992 0.9×	1.0k 1.0×	320 0.6×	341 1.1×	298 1.1×	61	2.9k
Cécile Dumanchin France	12	1.4k 1.3×	988 0.9×	414 0.7×	378 1.2×	322 1.2×	17	2.2k
Henne Holstege Netherlands	26	620 0.5×	1.3k 1.2×	600 1.1×	158 0.5×	88 0.3×	72	2.8k
Anne Rovelet‐Lecrux France	20	1.2k 1.0×	804 0.8×	448 0.8×	288 0.9×	193 0.7×	38	2.1k
Nikolai D. Belyaev United Kingdom	27	686 0.6×	1.6k 1.6×	445 0.8×	414 1.3×	226 0.8×	38	2.5k
Daniel R. Premkumar United States	27	648 0.6×	956 0.9×	141 0.3×	152 0.5×	111 0.4×	44	1.9k
Andrea Caricasole Italy	34	701 0.6×	2.2k 2.0×	516 0.9×	1.1k 3.4×	207 0.8×	71	3.2k
Nathalie Brouwers Belgium	26	1.6k 1.4×	1.2k 1.1×	364 0.6×	263 0.8×	255 0.9×	46	2.6k
Angela Hodges United Kingdom	26	844 0.7×	1.6k 1.5×	339 0.6×	244 0.8×	78 0.3×	40	2.9k

Countries citing papers authored by Grégory Raux

Since Specialization

Citations

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

Fields of papers citing papers by Grégory Raux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Grégory Raux

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

All Works

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20 of 20 papers shown

Bastard, Christian, Grégory Raux, Christophe Fruchart, et al.. (2007). Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients. Leukemia. 21(7). 1460–1463. 20 indexed citations

Lesca, Gaëtan, Nelly Burnichon, Grégory Raux, et al.. (2006). Distribution ofENG andACVRL1 (ALK1) mutations in French HHT patients. Human Mutation. 27(6). 598–598. 74 indexed citations

Killian, Audrey, Frédéric Di Fiore, Florence Le Pessot, et al.. (2006). A Simple Method for the Routine Detection of Somatic Quantitative Genetic Alterations in Colorectal Cancer. Gastroenterology. 132(2). 645–653. 18 indexed citations

Rovelet‐Lecrux, Anne, Didier Hannequin, Grégory Raux, et al.. (2005). APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nature Genetics. 38(1). 24–26. 871 indexed citations breakdown →

Yılmaz, Saliha, Thierry Bienvenu, Anne Moncla, et al.. (2005). Deleterious mutations in exon 1 of MECP2 in Rett syndrome. European Journal of Medical Genetics. 49(4). 313–322. 24 indexed citations

Jacquet, Hélène, Caroline Demily, B. Hecketsweiler, et al.. (2004). Hyperprolinemia is a risk factor for schizoaffective disorder. Molecular Psychiatry. 10(5). 479–485. 79 indexed citations

Tournier, Isabelle, Grégory Raux, Frédéric Di Fiore, et al.. (2004). Analysis of the allele-specific expression of the mismatch repair geneMLH1using a simple DHPLC-Based Method. Human Mutation. 23(4). 379–384. 24 indexed citations

Raux, Grégory, Cécile Dumanchin, Guillaume Lefebvre, et al.. (2003). Severe myoclonus‐dystonia syndrome associated with a novel epsilon‐sarcoglycan gene truncating mutation. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 119B(1). 114–117. 32 indexed citations

Raux, Grégory, Florence Thibaut, Angélique Belmont, et al.. (2003). The promoter −194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit. Molecular Psychiatry. 9(3). 320–322. 55 indexed citations

10.

Dauvilliers, Yves, Dominique Campion, Grégory Raux, et al.. (2003). Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu). Neurology. 61(8). 1136–1137. 35 indexed citations

11.

Zitouni, M., Philippe Martel, M. Ben Ayed, et al.. (2002). Pemphigus is not associated with allotypic markers of immunoglobulin kappa. Genes and Immunity. 3(1). 50–52. 7 indexed citations

12.

Raux, Grégory, Frédérique Bonnet‐Brilhault, Sandy Louchart, et al.. (2002). The −2 bp deletion in exon 6 of the ‘alpha 7-like’ nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit. Molecular Psychiatry. 7(9). 1006–1011. 77 indexed citations

13.

Martel, Philippe, D. Gilbert, Laurent Drouot, et al.. (2001). A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease. Genes and Immunity. 2(1). 41–43. 18 indexed citations

14.

Raux, Grégory, Danièle Gilbert, P. Joly, et al.. (2001). IGHV3-Associated Restriction Fragment Length Polymorphisms Confer Susceptibility to Bullous Pemphigoid. PubMed. 18(2). 59–66. 3 indexed citations

15.

Raux, Grégory, René Gantier, Cosette Martin, et al.. (2000). A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease. Human Mutation. 16(1). 95–95. 17 indexed citations

16.

Raux, Grégory, Danièle Gilbert, P. Joly, et al.. (2000). Association of KM Genotype with Bullous Pemphigoid. Journal of Autoimmunity. 14(1). 79–82. 5 indexed citations

17.

Charbonnier, F., Grégory Raux, Qing Wang, et al.. (2000). Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments.. PubMed. 60(11). 2760–3. 144 indexed citations

18.

Campion, Dominique, Cécile Dumanchin, Didier Hannequin, et al.. (1999). Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum. The American Journal of Human Genetics. 65(3). 664–670. 544 indexed citations breakdown →

19.

Koutouzov, Sophie, et al.. (1997). Comparison of Structural Characteristics of Antisubnucleosome and Anti‐DNA Monoclonal Antibodies Derived from Lupus Mice^a. Annals of the New York Academy of Sciences. 815(1). 327–330. 9 indexed citations

20.

Raux, Grégory, et al.. (1996). Immunoglobin Variable-Region mRNA Direct Sequencing: A Method to Bypass Aberrant Myeloma Light-Chain Transcripts. BioTechniques. 21(4). 576–580. 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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