E. Passage

1.9k total citations
34 papers, 1.5k citations indexed

About

E. Passage is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, E. Passage has authored 34 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in E. Passage's work include RNA Research and Splicing (7 papers), Hereditary Neurological Disorders (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). E. Passage is often cited by papers focused on RNA Research and Splicing (7 papers), Hereditary Neurological Disorders (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). E. Passage collaborates with scholars based in France, United States and Belgium. E. Passage's co-authors include Marie‐Geneviève Mattéi, J. F. Mattéi, Michel Fontés, N. Philip, Jean‐Louis Mandel, Jean‐Paul Moisan, Xavier Thirion, Andrée Robaglia‐Schlupp, J F Pellissier and Dominique Weil and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Human Molecular Genetics.

In The Last Decade

E. Passage

34 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Passage France 21 834 444 402 184 159 34 1.5k
Julia Rankin United Kingdom 21 1.1k 1.3× 314 0.7× 560 1.4× 258 1.4× 282 1.8× 39 1.7k
Kumi Kawai Japan 22 1.0k 1.2× 218 0.5× 202 0.5× 179 1.0× 54 0.3× 36 1.8k
H.J.M. Smeets Netherlands 30 1.5k 1.8× 501 1.1× 290 0.7× 100 0.5× 121 0.8× 63 2.4k
Saïd Akli United States 24 1.0k 1.2× 562 1.3× 287 0.7× 238 1.3× 104 0.7× 40 1.8k
Fatima Banine United States 15 914 1.1× 180 0.4× 254 0.6× 509 2.8× 243 1.5× 23 1.8k
Randall D. McKinnon United States 20 1.3k 1.5× 180 0.4× 691 1.7× 221 1.2× 90 0.6× 36 2.2k
Ruud A. Wolterman Netherlands 15 658 0.8× 122 0.3× 604 1.5× 188 1.0× 397 2.5× 24 1.5k
Tatyana V. Taksir United States 17 1.0k 1.2× 242 0.5× 241 0.6× 164 0.9× 334 2.1× 24 1.9k
Katharine L. Sugars United Kingdom 12 838 1.0× 116 0.3× 560 1.4× 65 0.4× 163 1.0× 12 1.3k

Countries citing papers authored by E. Passage

Since Specialization
Citations

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

Fields of papers citing papers by E. Passage

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Passage

This figure shows the co-authorship network connecting the top 25 collaborators of E. Passage. A scholar is included among the top collaborators of E. Passage 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 E. Passage. E. Passage 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.
Burtey, Stéphane, Marta Riera, Petra Pennekamp, et al.. (2007). Overexpression of PKD2 in the mouse is associated with renal tubulopathy. Nephrology Dialysis Transplantation. 23(4). 1157–1165. 32 indexed citations
2.
Passage, E., et al.. (2004). Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease. Nature Medicine. 10(4). 396–401. 262 indexed citations
3.
Jamon, Marc, et al.. (2001). Behavioural profiling of a murine Charcot–Marie–Tooth disease type 1A model. European Journal of Neuroscience. 13(8). 1625–1634. 34 indexed citations
4.
Sabéran‐Djoneidi, Délara, et al.. (2000). Molecular dissection of the Schwann cell specific promoter of the PMP22 gene. Gene. 248(1-2). 223–231. 41 indexed citations
5.
Briault, Sylvain, Laurent Villard, Ute C. Rogner, et al.. (2000). Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]?. American Journal of Medical Genetics. 95(2). 178–181. 18 indexed citations
6.
Hugnot, Jean‐Philippe, Florence Pédeutour, Josiane Grosgeorge, et al.. (1997). The Human Inward Rectifying K+Channel Kir 2.2 (KCNJ12) Gene: Gene Structure, Assignment to Chromosome 17p11.1, and Identification of a Simple Tandem Repeat Polymorphism. Genomics. 39(1). 113–116. 18 indexed citations
7.
Chevillard, Christophe, Denis Le Paslier, E. Passage, et al.. (1993). Relationship between Charcot - Marie-Tooth 1A and Smith - Magenis regions. snU3 may be a candidate gene for the Smith - Magenis syndrome. Human Molecular Genetics. 2(8). 1235–1243. 33 indexed citations
8.
Parmentier, Marc, E. Passage, Gilbert Vassart, & Marie‐Geneviève Mattéi. (1991). The human calbindin D28k (CALB1) and calretinin (CALB2) genes are located at 8q21.3→q22.1 and 16q22→q23, respectively, suggesting a common duplication with the carbonic anhydrase isozyme loci. Cytogenetic and Genome Research. 57(1). 41–43. 26 indexed citations
9.
Parmentier, Marc, E. Passage, Marie‐Geneviève Mattéi, & Gilbert Vassart. (1991). A new human hypervariable locus (K29) maps to the q37.3 region of chromosome 2 and reveals a fingerprint. Genomics. 11(3). 760–762. 1 indexed citations
10.
Mazan, Sylvie, Marie‐Geneviève Mattéi, E. Passage, & Jean‐Pierre Bachellerie. (1991). Composition and chromosomal localization of the small multigene family encoding mouse U3B nucleolar RNA. Cytogenetic and Genome Research. 56(1). 18–22. 14 indexed citations
11.
Libert, F., E. Passage, Anne Lefort, Gilbert Vassart, & Marie‐Geneviève Mattéi. (1990). Localization of human thyrotropin receptor gene to chromosome region 14q31 by in situ hybridization. Cytogenetic and Genome Research. 54(1-2). 82–83. 36 indexed citations
12.
Lefort, Anne, E. Passage, F. Libert, et al.. (1990). Localization of human calcyphosine gene (CAPS) to the p13.3 region of chromosome 19 by in situ hybridization. Cytogenetic and Genome Research. 54(3-4). 154–155. 3 indexed citations
13.
Mattéi, Marie‐Geneviève, et al.. (1990). In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13. Human Genetics. 84(2). 210–2. 8 indexed citations
14.
Pol, Stanislas, Frédérique Bulle, E. Passage, et al.. (1989). Chromosomal localization of human aspartate aminotransferase genes by in situ hybridization. Human Genetics. 83(2). 159–164. 8 indexed citations
15.
Mattéi, Marie‐Geneviève, et al.. (1989). Human laminin a chain (LAMA) gene: Chromosomal mapping to locus 18p11.3. Genomics. 5(4). 932–935. 23 indexed citations
16.
Mattéi, Marie‐Geneviève, Patrick M. Alliel, Fabrice Bonnet, et al.. (1989). Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridization. Human Genetics. 82(1). 87–88. 8 indexed citations
17.
Bourguignon, Jeannette, et al.. (1989). Human plasma inter‐α‐trypsin inhibitor is encoded by four genes on three chromosomes. European Journal of Biochemistry. 179(1). 147–154. 75 indexed citations
18.
Mattéi, Marie‐Geneviève, A. Dautigny, Danielle Pham-Dinh, et al.. (1988). The gene encoding the large human neurofilament subunit (NF-H) maps to the q121–q131 region on human chromosome 22. Human Genetics. 80(3). 293–295. 16 indexed citations
19.
Mattéi, Marie‐Geneviève, Dominique Weil, Michael P. Bernard, et al.. (1988). cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31. Human Genetics. 79(3). 235–241. 21 indexed citations
20.
Philip, N., et al.. (1988). Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization. Human Genetics. 80(3). 277–281. 17 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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