E. Passage
Impact in
- Immunology and Allergy top 5%
- Cell Adhesion Molecules Research
-
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Papers in
-
- RNA Research and Splicing 7
- Glycosylation and Glycoproteins Research 4
- Genomics and Chromatin Dynamics 3
- Genetics 11
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 3
- 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)J F Pellissier (1 shared paper)Andrée Robaglia‐Schlupp (1 shared paper)
- Journals
- Human Genetics (10 papers)Genomics (5 papers)Mammalian Genome (1 paper)Gene (1 paper)Nature Medicine (1 paper)
- Partner nations
- FranceBelgiumUnited States
In The Last Decade
E. Passage
34 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 85
- Immunology and Allergy 151
- Cellular and Molecular Neuroscience 407
- Genetics 435
- Developmental Neuroscience 57
- Neurology 102
Countries citing papers authored by E. Passage
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
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.
All Works
Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 304 | |
| 2 | 2004 | 279 | |
| 3 | Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen. | 1988 | 134 |
| 4 | Human elastin gene: new evidence for localization to the long arm of chromosome 7. | 1991 | 83 |
| 5 | 1989 | 77 | |
| 6 | 1988 | 64 | |
| 7 | 1986 | 63 | |
| 8 | 1991 | 59 | |
| 9 | 2000 | 44 | |
| 10 | 2001 | 38 | |
| 11 | 1987 | 38 | |
| 12 | Human nidogen: cDNA cloning, cellular expression, and mapping of the gene to chromosome Iq43. | 1989 | 36 |
| 13 | 1985 | 35 | |
| 14 | 1993 | 35 | |
| 15 | 2007 | 32 | |
| 16 | 1989 | 25 | |
| 17 | 1995 | 24 | |
| 18 | 1995 | 23 | |
| 19 | 1988 | 22 | |
| 20 | [MICROTECHNIC FOR THE STUDY OF HUMAN CHROMOSOMES FROM A HUMAN LEUKOCYTE CULTURE]. | 1964 | 22 |
About E. Passage
E. Passage is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Immunology and Allergy and Neurology, having authored 34 papers that have together received 1.6k 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), Glycosylation and Glycoproteins Research (4 papers), Cell Adhesion Molecules Research (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Botulinum Toxin and Related Neurological Disorders (3 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Immunology and Allergy (151 citations), Cellular and Molecular Neuroscience (407 citations), Genetics (435 citations), Developmental Neuroscience (57 citations) and Neurology (102 citations). E. Passage has collaborated with scholars based in France, Belgium and United States. Frequent co-authors include Marie‐Geneviève Mattéi, J. F. Mattéi, Michel Fontés, N. Philip, Jean‐Louis Mandel, Jean‐Paul Moisan, J F Pellissier, Andrée Robaglia‐Schlupp, Xavier Thirion and Rupert Timpl. Their work appears in journals such as Human Genetics, Genomics, Mammalian Genome, 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.