Dominique Campion

54.6k total citations · 2 hit papers
164 papers, 6.8k citations indexed

About

Dominique Campion is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Dominique Campion has authored 164 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Physiology, 65 papers in Molecular Biology and 57 papers in Genetics. Recurrent topics in Dominique Campion's work include Alzheimer's disease research and treatments (71 papers), Genetics and Neurodevelopmental Disorders (22 papers) and Genetic Associations and Epidemiology (19 papers). Dominique Campion is often cited by papers focused on Alzheimer's disease research and treatments (71 papers), Genetics and Neurodevelopmental Disorders (22 papers) and Genetic Associations and Epidemiology (19 papers). Dominique Campion collaborates with scholars based in France, United States and Australia. Dominique Campion's co-authors include Thierry Frébourg, Didier Hannequin, Alexis Brice, Cécile Dumanchin, Anne Rovelet‐Lecrux, Grégory Raux, Sébastien Feuillette, María Martínez, Martine Vercelletto and Anne Vital and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Dominique Campion

160 papers receiving 6.6k citations

Hit Papers

align trajectories sort by overperformance

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 Didier Hannequin, Grégory Raux et al. profile →
Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

1999 544 citations Dominique Campion, Cécile Dumanchin et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dominique Campion France	45	3.2k	2.7k	1.4k	1.4k	1.2k	164	6.8k
Kristel Sleegers Belgium	49	4.2k 1.3×	2.9k 1.1×	1.1k 0.8×	1.6k 1.1×	904 0.7×	135	7.4k
Ellen Nemens United States	15	4.5k 1.4×	2.6k 1.0×	781 0.5×	862 0.6×	1.1k 0.9×	20	5.6k
David Nochlin United States	45	4.0k 1.2×	3.0k 1.1×	568 0.4×	1.5k 1.1×	1.2k 1.0×	92	6.6k
Ekaterina Rogaeva Canada	53	3.4k 1.1×	3.6k 1.3×	938 0.7×	3.4k 2.5×	1.6k 1.3×	188	8.3k
Caroline Graff Sweden	40	3.2k 1.0×	3.1k 1.1×	543 0.4×	730 0.5×	883 0.7×	159	6.5k
John B. Kwok Australia	41	1.9k 0.6×	2.4k 0.9×	930 0.7×	1.8k 1.3×	699 0.6×	136	6.3k
Patrick M. Sullivan United States	51	3.5k 1.1×	3.3k 1.2×	956 0.7×	654 0.5×	1.4k 1.2×	107	8.5k
Jordi Pérez‐Tur Spain	37	3.5k 1.1×	2.2k 0.8×	524 0.4×	1.7k 1.2×	1.3k 1.0×	91	5.6k
Rohan de Silva United Kingdom	36	3.3k 1.0×	1.9k 0.7×	614 0.4×	2.7k 2.0×	1.5k 1.2×	80	6.2k
Jordi Clarimón Spain	41	2.2k 0.7×	1.5k 0.6×	703 0.5×	1.8k 1.3×	891 0.7×	122	4.9k

Countries citing papers authored by Dominique Campion

Since Specialization

Citations

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

Fields of papers citing papers by Dominique Campion

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dominique Campion

This figure shows the co-authorship network connecting the top 25 collaborators of Dominique Campion. A scholar is included among the top collaborators of Dominique Campion 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 Dominique Campion. Dominique Campion 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

Charon, Céline, Audrey Guilmatre, Patrick Vourc’h, et al.. (2013). Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families. Behavior Genetics. 43(2). 132–140. 7 indexed citations

Miguel, Laëtitia, et al.. (2011). Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila. Neurobiology of Aging. 33(5). 1008.e1–1008.e15. 45 indexed citations

Feuillette, Sébastien, Laëtitia Miguel, Thierry Frébourg, Dominique Campion, & Magalie Lecourtois. (2010). Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein. Journal of Neurochemistry. 113(4). 895–903. 64 indexed citations

Hannequin, Didier, Lucie Guyant‐Maréchal, Isabelle Le Ber, et al.. (2009). Démences du sujet jeune : démarche diagnostique. Revue Neurologique. 2 indexed citations

Goumidi, Louisa, Frédéric Flamant, Corinne Lendon, et al.. (2009). Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease. Neurobiology of Aging. 32(4). 624–630. 14 indexed citations

Laumet, Geoffroy, Franck Hansmannel, Julien Chapuis, et al.. (2009). A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease. Neuroscience Letters. 468(1). 1–2. 12 indexed citations

Martinaud, Olivier, A. Laquérrière, Lucie Guyant‐Maréchal, et al.. (2005). Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family. Acta Neuropathologica. 110(1). 84–92. 18 indexed citations

Ménard, Jean-François, Gabrielle Allio, Sadeq Haouzir, et al.. (2005). P50 inhibitory gating deficit is correlated with the negative symptomatology of schizophrenia. Psychiatry Research. 136(1). 27–34. 54 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

10.

Cousin, Emmanuelle, Didier Hannequin, Sylvain Ricard, et al.. (2003). A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism. Neuroscience Letters. 342(1-2). 5–8. 12 indexed citations

11.

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

12.

Hannequin, Didier, Dominique Campion, Cécile Dumanchin, et al.. (1998). Génétique de la maladie d'Alzheimer. Revue Neurologique. 154. 1 indexed citations

13.

Thibaut, Florence, Didier Hannequin, Cosette Martin, et al.. (1998). No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients. Schizophrenia Research. 30(2). 149–153. 22 indexed citations

14.

Martínez, María, Dominique Campion, Alexis Brice, et al.. (1998). Apolipoprotein E ϵ4 Allele and Familial Aggregation of Alzheimer Disease. Archives of Neurology. 55(6). 810–810. 45 indexed citations

15.

Frébourg, Thierry, Cécile Dumanchin, & Dominique Campion. (1997). Formes autosomiques dominantes. 3(5). 1 indexed citations

16.

Didierjean, Olivier, María Martínez, Dominique Campion, et al.. (1997). No effect of the alpha 1-antichymotrypsin A allele in Alzheimer's disease. Journal of Neurology Neurosurgery & Psychiatry. 63(1). 103–105. 14 indexed citations

17.

Hannequin, Didier, Dominique Campion, Alexis Brice, et al.. (1996). Génétique de la maladie d'Alzheimer. La Revue de Médecine Interne. 17(7). 545–550.

18.

Campion, Dominique, Cosette Martin, Roland Heilig, et al.. (1995). The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease. Genomics. 26(2). 254–257. 79 indexed citations

19.

Campion, Dominique, Thierry d’Amato, Christian Bastard, et al.. (1994). Genetic study of dopamine D1, D2, and D4 receptors in schizophrenia. Psychiatry Research. 51(3). 215–230. 36 indexed citations

20.

Carter, Dee, Dominique Campion, Thierry d’Amato, et al.. (1993). No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients. Human Molecular Genetics. 2(3). 321–321. 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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