E. Passage

1.9k citations

34 papers · 1.5k indexed · h-index 21

Impact in

Immunology and Allergy top 5%
- Cell Adhesion Molecules Research
Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases

Papers in ⓘ

Immunology and Allergy 4
- Cell Adhesion Molecules Research 4
Genetics 11
- Genomic variations and chromosomal abnormalities 5

Co-authors: Marie‐Geneviève Mattéi (22 shared papers)J. F. Mattéi (6 shared papers)Michel Fontés (7 shared papers)N. Philip (2 shared papers)Jean‐Louis Mandel (1 shared paper)Jean‐Paul Moisan (1 shared paper)Xavier Thirion (1 shared paper)Andrée Robaglia‐Schlupp (1 shared paper)
Journals: Human Genetics (10 papers)Cytogenetic and Genome Research (5 papers)Genomics (5 papers)Gene (1 paper)Nature Medicine (1 paper)
Partner nations: France United States Belgium

In The Last Decade

E. Passage

34 papers receiving 1.5k citations

Peers

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-authors

The 25 scholars most cited alongside E. Passage, 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 E. Passage Line = papers co-authored together E. Passage links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome Human Genetics ·Marie‐Geneviève Mattéi, N. Philip, E. Passage, Jean‐Paul Moisan, Jean‐Louis Mandel, J. F. Mattéi	1985	302
2	Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease Nature Medicine ·E. Passage, Jean Chrétien Norreel, Pauline Noack-Fraissignes, Véronique Sanguedolce, Josette Pizant, Xavier Thirion, Andrée Robaglia‐Schlupp, J F Pellissier, Michel Fontés	2004	262
3	Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen. PubMed ·Dominique Weil, Marie‐Geneviève Mattéi, E. Passage, Công Văn Nguyến, Dorothy Pribula-Conway, Karlheinz Mann, Rainer Deutzmann, Rupert Timpl, Mon‐Li Chu	1988	125
4	Human elastin gene: new evidence for localization to the long arm of chromosome 7. PubMed ·Michael Fazio, Marie‐Geneviève Mattéi, E. Passage, M. L. Chu, D. N. Black, E. Solomon, J. M. Davidson, Jouni Uitto	1991	76
5	Human plasma inter‐α‐trypsin inhibitor is encoded by four genes on three chromosomes European Journal of Biochemistry ·Maryam DIARRA‐MEHRPOUR, Jeannette Bourguignon, Richard Sesboüé, Marie‐Geneviève Mattéi, E. Passage, Jean‐Philippe Salier, Jean‐Pierre Martin	1989	75
6	Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor Genomics ·Frédérick Libert, E. Passage, Marc Parmentier, Marie-Jeanne Simons, G Vassart, Marie‐Geneviève Mattéi	1991	56
7	The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome Human Genetics ·Marie‐Geneviève Mattéi, Patrick M. Alliel, A. Dautigny, E. Passage, Danielle Pham-Dinh, J. F. Mattéi, P. Jollès	1986	54
8	Molecular and cytogenetic evidence for the location of Tdy and Hya on the mouse Y chromosome short arm. Proceedings of the National Academy of Sciences ·C.J. Roberts, Andreas Weith, E. Passage, J.-L. Michot, Marie‐Geneviève Mattéi, Colin E. Bishop	1988	53
9	Molecular dissection of the Schwann cell specific promoter of the PMP22 gene Gene ·Délara Sabéran‐Djoneidi, Véronique Sanguedolce, Zahra Assouline, Nicolas Lévy, E. Passage, Michel Fontés	2000	41
10	Localization of human thyrotropin receptor gene to chromosome region 14q31 by in situ hybridization Cytogenetic and Genome Research ·F. Libert, E. Passage, Anne Lefort, Gilbert Vassart, Marie‐Geneviève Mattéi	1990	36
11	Behavioural profiling of a murine Charcot–Marie–Tooth disease type 1A model European Journal of Neuroscience ·Jean Chrétien Norreel, Marc Jamon, George R. Riviere, E. Passage, Michel Fontés, F. Clarac	2001	34
12	Relationship between Charcot - Marie-Tooth 1A and Smith - Magenis regions. snU3 may be a candidate gene for the Smith - Magenis syndrome Human Molecular Genetics ·Christophe Chevillard, Denis Le Paslier, E. Passage, Pierre Ougen, Alain Billault, Sylvie Boyer, Sylvie Mazan, Jean Pierre Bachellerie, Alain Vignal, Daniel Cohen, Michel Fontés	1993	33
13	Overexpression of PKD2 in the mouse is associated with renal tubulopathy Nephrology Dialysis Transplantation ·Stéphane Burtey, Marta Riera, Émilie Ribe, Petra Pennekamp, E. Passage, Roselyne J. Rance, Bernd Dworniczak, Michel Fontés	2007	32
14	Human nidogen: cDNA cloning, cellular expression, and mapping of the gene to chromosome Iq43. PubMed ·David R. Olsen, T Nagayoshi, Michael Fazio, Marie‐Geneviève Mattéi, E. Passage, Dominique Weil, Rupert Timpl, Mon‐Li Chu, Jouni Uitto	1989	32
15	Localization of the thyroglobulin gene by in situ hybridization to human chromosomes Human Genetics ·Jean-Louis Berg�-Lefranc, G Cartouzou, Marie-Genevi�ve Matt�i, E. Passage, Christiane Malezet‐Desmoulins, Serge Lissitzky	1985	32
16	Assignment of the human gamma-glutamyl transferase gene to the long arm of chromosome 22 Human Genetics ·Frédérique Bulle, Marie‐Geneviève Mattéi, Sylvie Siegrist, André Pawlak, E. Passage, Marie-Noële Chobert, Yannick Laperche, Georges Guellañ	1987	30
17	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 ·Marc Parmentier, E. Passage, Gilbert Vassart, Marie‐Geneviève Mattéi	1991	26
18	Human laminin a chain (LAMA) gene: Chromosomal mapping to locus 18p11.3 Genomics ·T Nagayoshi, Marie‐Geneviève Mattéi, E. Passage, Knowlton Robert, M. L. Chu, Jouni Uitto	1989	23
19	Assignment of microsatellite sequences to the region duplicated in CMT1A (17p12): a useful tool for diagnosis. Journal of Medical Genetics ·Claire Cudrey, Christophe Chevillard, Denis Le Paslier, Alain Vignal, E. Passage, Michel Fontés	1995	23
20	cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31 Human Genetics ·Marie‐Geneviève Mattéi, Dominique Weil, Dorothy Pribula-Conway, Michael P. Bernard, E. Passage, N. Van Cong, Rupert Timpl, Mon‐Li Chu	1988	21

About E. Passage

E. Passage is a scholar working on Immunology and Allergy, Genetics, Molecular Biology, Cellular and Molecular Neuroscience and Developmental Neuroscience, having authored 34 papers that have together received 1.5k indexed citations. Recurring topics across this work include RNA Research and Splicing (7 papers), Hereditary Neurological Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Cell Adhesion Molecules Research (4 papers), Glycosylation and Glycoproteins Research (4 papers), Botulinum Toxin and Related Neurological Disorders (3 papers), Genomics and Chromatin Dynamics (3 papers) and RNA regulation and disease (3 papers). The work is most often cited by research in Immunology and Allergy (147 citations), Cellular and Molecular Neuroscience (402 citations), Genetics (444 citations), Developmental Neuroscience (54 citations) and Neurology (104 citations). E. Passage has collaborated with scholars based in France, United States and Belgium. Frequent 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 Mon‐Li Chu. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Genomics, Gene and Nature Medicine.

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.

Explore authors with similar magnitude of impact