Grégory Raux

3.6k citations

27 papers · 2.3k · 2 hit papers · h-index 19

Impact in

Physiology top 2%
- Alzheimer's disease research and treatments
Neurology top 5%

Papers in

Molecular Biology 10
Pathology and Forensic Medicine 9
- Autoimmune Bullous Skin Diseases 5
- Genetic factors in colorectal cancer 3

Co-authors: Thierry Frébourg (16 shared papers)Dominique Campion (11 shared papers)Didier Hannequin (6 shared papers)Alexis Brice (6 shared papers)Cécile Dumanchin (3 shared papers)Anne Rovelet‐Lecrux (2 shared papers)Nathalie Le Meur (1 shared paper)Annie Laquerrière (1 shared paper)
Journals: Neurology (3 papers)Human Mutation (3 papers)Molecular Psychiatry (3 papers)Genes and Immunity (2 papers)European Journal of Medical Genetics (1 paper)
Partner nations: France Belgium China

In The Last Decade

Grégory Raux

27 papers receiving 2.3k citations

Grégory Raux's Hit Papers

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy 2005 · 877 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2005 Nature Genetics
1999 The American Journal of Human Genetics

Peers

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-authors

The 25 scholars most cited alongside Grégory Raux, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Grégory Raux Line = papers co-authored together Grégory Raux links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy Nature Genetics ·Anne Rovelet‐Lecrux, Didier Hannequin, Grégory Raux, Nathalie Le Meur, Annie Laquerrière, Anne Vital, Cécile Dumanchin, Sébastien Feuillette, Alexis Brice, Martine Vercelletto, Frédéric Dubas, Thierry Frébourg, Dominique Campion Hit paper breakdown →	2005	877
2	Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum The American Journal of Human Genetics ·Dominique Campion, Cécile Dumanchin, Didier Hannequin, Bruno Dubois, Serge Belliard, Michèle Puel, Catherine Thomas-Antérion, Agnès Michon, Cosette Martin, Françoise Charbonnier, Grégory Raux, Agnès Camuzat, Christiane Penet, Valérie Mesnage, María Martínez, Françoise Clerget‐Darpoux, Alexis Brice, Thierry Frébourg Hit paper breakdown →	1999	544
3	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 ·F. Charbonnier, Grégory Raux, Qing Wang, Nathalie Drouot, Florence Cordier, Jean‐Marc Limacher, Jean‐Christophe Saurin, Alain Puisieux, Sylviane Olschwang, Thierry Frébourg	2000	144
4	Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation Neurology ·Grégory Raux, René Gantier, C. Thomas-Antérion, J Boulliat, Patrice Verpillat, Didier Hannequin, Alexis Brice, Thierry Frébourg, Dominique Campion	2000	104
5	Hyperprolinemia is a risk factor for schizoaffective disorder Molecular Psychiatry ·Hélène Jacquet, Caroline Demily, (unknown), B. Hecketsweiler, (unknown), Grégory Raux, Jérôme Lerond, Gabrielle Allio, Sadeq Haouzir, A Tillaux, C Bellegou, Gaël Fouldrin, Pascal Delamillieure, J.F. Ménard, Sonia Dollfus, Thierry d’Amato, M. Petit, Florence Thibaut, Thierry Frébourg, Dominique Campion	2004	79
6	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 ·Grégory Raux, Frédérique Bonnet‐Brilhault, Sandy Louchart, (unknown), René Gantier, D. Levillain, Gabrielle Allio, Sadeq Haouzir, Marie‐Agnès Petit, María Martínez, Thierry Frébourg, Florence Thibaut, Dominique Campion	2002	77
7	Distribution ofENG andACVRL1 (ALK1) mutations in French HHT patients Human Mutation ·Gaëtan Lesca, Nelly Burnichon, Grégory Raux, Mario Tosi, S. Pinson, Marie‐Jeanne Marion, E. Babin, Brigitte Gilbert‐Dussardier, Sophie Rivière, Cyril Goizet, Laurence Faivre, Henri Plauchu, Thierry Frébourg, Alain Calender, Sophie Giraud, (unknown)	2006	74
8	The promoter −194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit Molecular Psychiatry ·(unknown), Grégory Raux, Florence Thibaut, Angélique Belmont, Caroline Demily, Gabrielle Allio, Sadeq Haouzir, Gaël Fouldrin, Marie‐Agnès Petit, Thierry Frébourg, Dominique Campion	2003	54
9	Screening for TP53 rearrangements in families with the Li–Fraumeni syndrome reveals a complete deletion of the TP53 gene Oncogene ·Gaëlle Bougeard, Laurence Brugières, Agnès Chompret, Paul Gesta, Françoise Charbonnier, Alexander Valent, Cosette Martin, Grégory Raux, Jean Feunteun, Brigitte Bressac–de Paillerets, Thierry Frébourg	2003	50
10	Variations in the APP gene promoter region and risk of Alzheimer disease Neurology ·Lucie Guyant‐Maréchal, Anne Rovelet‐Lecrux, Louisa Goumidi, Emmanuelle Cousin, Didier Hannequin, Grégory Raux, Christiane Penet, Sylvain Ricard, Sandrine Macé, Philippe Amouyel, J.-F. Deleuze, Thierry Frébourg, Alexis Brice, Jean‐Charles Lambert, Dominique Campion	2007	44
11	Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu) Neurology ·F. Portet, Yves Dauvilliers, Dominique Campion, Grégory Raux, J J Hauw, O. Lyon‐Caen, William Camu, J. Touchon	2003	35
12	Severe myoclonus‐dystonia syndrome associated with a novel epsilon‐sarcoglycan gene truncating mutation American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Lucie Maréchal, Grégory Raux, Cécile Dumanchin, Guillaume Lefebvre, Emmanuelle Deslandre, Carole Girard, Dominique Campion, D. Parain, Thierry Frébourg, Didier Hannequin	2003	33
13	APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population European Journal of Human Genetics ·Laurence Zurutuza, Patrice Verpillat, Grégory Raux, Didier Hannequin, Michèle Puel, Serge Belliard, Agnès Michon, Yolaine Pothin, Agnès Camuzat, Christiane Penet, Cozette Martin, Alexis Brice, Dominique Campion, Françoise Clerget‐Darpoux, Thierry Frébourg	2000	30
14	Acd, a peptidoglycan hydrolase of Clostridium difficile with N-acetylglucosaminidase activity Microbiology ·Anne Dhalluin, Ingrid Bourgeois, Martine Pestel‐Caron, Émilie Camiade, Grégory Raux, Pascal Courtin, Marie‐Pierre Chapot‐Chartier, Jean-Louis Pons	2005	27
15	Deleterious mutations in exon 1 of MECP2 in Rett syndrome European Journal of Medical Genetics ·Aline Quenard, Saliha Yılmaz, Hervé Fontaine, Thierry Bienvenu, Anne Moncla, Vincent des Portes, François Rivier, Michèle Mathieu, Grégory Raux, Philippe Jonveaux, Christophe Philippe	2005	24
16	Analysis of the allele-specific expression of the mismatch repair geneMLH1using a simple DHPLC-Based Method Human Mutation ·Isabelle Tournier, Grégory Raux, Frédéric FIORE, Isabelle Maréchal, Carole Leclerc, Cosette Martin, Qing Wang, Marie‐Pierre Buisine, Dominique Stoppa‐Lyonnet, Sylviane Olschwang, Thierry Frébourg, Mario Tosi	2004	24
17	Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients Leukemia ·Christian Bastard, Grégory Raux, Christophe Fruchart, F Parmentier, Dominique Vaur, Dominique Penther, Xavier Troussard, D Nagib, Stéphane Leprêtre, Mario Tosi, Thierry Frébourg, Hervé Tilly	2007	20
18	A Simple Method for the Routine Detection of Somatic Quantitative Genetic Alterations in Colorectal Cancer Gastroenterology ·Audrey Killian, Frédéric FIORE, Florence Le Pessot, France Blanchard, Aude Lamy, Grégory Raux, Jean‐Michel Flaman, B Paillot, Pierre Michel, Jean‐Christophe Sabourin, Jean–Jacques Tuech, F Michot, Jean‐Pierre Kerckaert, Richard Sesboüé, Thierry Frébourg	2006	18
19	A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease Genes and Immunity ·Philippe Martel, D. Gilbert, Laurent Drouot, C. Prost, Grégory Raux, E. Delaporte, P. Joly, François Tron	2001	18
20	A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease Human Mutation ·Grégory Raux, René Gantier, Cosette Martin, Yolaine Pothin, Alexis Brice, Thierry Frébourg, Dominique Campion	2000	17

About Grégory Raux

Grégory Raux is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Genetics, Physiology and Genetics, having authored 27 papers that have together received 2.3k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (6 papers), Autoimmune Bullous Skin Diseases (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers), Genetic factors in colorectal cancer (3 papers), Cholinesterase and Neurodegenerative Diseases (2 papers) and Computational Drug Discovery Methods (2 papers). The work is most often cited by research in Physiology (1.0k citations), Neurology (190 citations), Biological Psychiatry (49 citations), Genetics (506 citations) and Cellular and Molecular Neuroscience (288 citations). Grégory Raux has collaborated with scholars based in France, Belgium and China. Frequent co-authors include Thierry Frébourg, Dominique Campion, Didier Hannequin, Alexis Brice, Cécile Dumanchin, Anne Rovelet‐Lecrux, Nathalie Le Meur, Annie Laquerrière, Martine Vercelletto and Anne Vital. Their work appears in journals such as Neurology, Human Mutation, Molecular Psychiatry, Genes and Immunity and European Journal of Medical Genetics.

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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In The Last Decade

Grégory Raux

Grégory Raux's Hit Papers

Peers

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Fields of papers citing papers by Grégory Raux

All Works

About Grégory Raux

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