Eric Seboun

5.9k total citations · 2 hit papers
24 papers, 3.9k citations indexed

About

Eric Seboun is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Eric Seboun has authored 24 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Genetics and 8 papers in Immunology. Recurrent topics in Eric Seboun's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), RNA regulation and disease (5 papers) and Sexual Differentiation and Disorders (5 papers). Eric Seboun is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), RNA regulation and disease (5 papers) and Sexual Differentiation and Disorders (5 papers). Eric Seboun collaborates with scholars based in United States, France and Canada. Eric Seboun's co-authors include Alain Vignal, Gàbor Gyapay, Philippe Millasseau, Jean Morissette, Delphine Samson, Jean Weissenbach, Sabine Fauré, Cécile Fizames, Mark Lathrop and Nathalie Drouot and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Eric Seboun

24 papers receiving 3.8k citations

Hit Papers

align trajectories

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.

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1996 2.4k citations Colette Dib, Sabine Fauré et al. Nature profile →
Interferon-γ –Receptor Deficiency in an Infant with Fatal Bacille Calmette–Guérin Infection

1996 657 citations Emmanuelle Jouanguy, Frédéric Altare et al. New England Journal of Medicine profile →

Peers

Countries citing papers authored by Eric Seboun

Since Specialization

Citations

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

Fields of papers citing papers by Eric Seboun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Seboun

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

#	Work	Indexed citations
1	Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III 2010 ·The American Journal of Human Genetics ·Ruth Belostotsky, Eric Seboun, (unknown), Dawn S. Milliner, Rachel Becker‐Cohen, Choni Rinat, Carla G. Monico, Sofia Feinstein, Efrat Ben‐Shalom, Daniella Magen, Irith Weissman, Céline Charon, Yaacov Frishberg	162
2	Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy 2005 ·The American Journal of Human Genetics ·Kazuhiko Nakabayashi, (unknown), Yan Ren, Ulpu Saarialho‐Kere, Nili Avidan, S. Gentles, Jeffrey R. MacDonald, Erik G. Puffenberger, Angela M. Christiano, Amalia Martı́nez-Mir, Julio C. Salas‐Alanís, Renata Rizzo, Esther Vamos, Anja Raams, Clifford Les, Eric Seboun, Nicolaas G.J. Jaspers, J. Beckmann, Charles E. Jackson, Stephen W. Scherer	55
3	Amish brittle hair syndrome gene maps to 7p14.1 2005 ·American Journal of Medical Genetics Part A ·Eric Seboun, Arnaud Lemainque, Charles E. Jackson	4
4	Myotilin is not the Causative Gene for Vocal Cord and Pharyngeal Weakness with Distal Myopathy (VCPDM) 2005 ·Annals of Human Genetics ·Sean M. Garvey, Jan Senderek, J. Beckmann, Eric Seboun, Charles E. Jackson, Michael A. Hauser	4
5	Vacuoliting Megalencephalic Leukoencephalopathy with Subcortical Cysts, Mapped to Chromosome 22qtel 2000 ·The American Journal of Human Genetics ·Meral Topçu, Corine Gartioux, Florence Ribiérre, Cengiz Yalçınkaya, (unknown), (unknown), J. Beckmann, Meral Özgüç, Eric Seboun	60
6	Vocal Cord and Pharyngeal Weakness with Autosomal Dominant Distal Myopathy: Clinical Description and Gene Localization to 5q31 1998 ·The American Journal of Human Genetics ·Howard Feit, Alice K. Silbergleit, (unknown), J. Antonio Gutierrez, (unknown), Cécile Réyès, (unknown), Bernard Brais, Charles E. Jackson, J. Beckmann, Eric Seboun	97
7	Gene Sequence, Localization, and Evolutionary Conservation ofDAZLA,a Candidate Male Sterility Gene 1997 ·Genomics ·Eric Seboun, Sandrine Barbaux, Thomas Bourgeron, Shinya Nishi, (unknown), (unknown), (unknown), Colin E. Bishop, Marc Fellous, Ken McElreavey, Masanori Kasahara	86
8	Genetics of Demyelinating Diseases 1996 ·Brain Pathology ·Scott S. Zamvil, Eric Seboun, Stephen L. Hauser	34
9	A comprehensive genetic map of the human genome based on 5,264 microsatellites breakdown → 1996 ·Nature ·Colette Dib, Sabine Fauré, Cécile Fizames, Delphine Samson, Nathalie Drouot, Alain Vignal, Philippe Millasseau, (unknown), (unknown), Eric Seboun, Mark Lathrop, Gàbor Gyapay, Jean Morissette, Jean Weissenbach	2444
10	Interferon-γ –Receptor Deficiency in an Infant with Fatal Bacille Calmette–Guérin Infection breakdown → 1996 ·New England Journal of Medicine ·Emmanuelle Jouanguy, Frédéric Altare, Salma Lamhamedi, Patrick Revy, Jean‐François Emile, Melanie J. Newport, Michael Levin, Stéphane Blanche, Eric Seboun, Alain Fischer, Jean‐Laurent Casanova	657
11	Segregation of immunoglobulin heavy chain constant region genes in multiple sclerosis sibling pairs 1993 ·Journal of Neuroimmunology ·John S. Yu, Janardan P. Pandey, Luca Massacesi, Robin Lincoln, Koichiro Usuku, Eric Seboun, Stephen L. Hauser	10
12	Unusual organization of the human T-cell receptor beta-chain gene complex is linked to recombination hotspots. 1993 ·Proceedings of the National Academy of Sciences ·Eric Seboun, Lesley A. Houghton, Charles J. Hatem, Robin Lincoln, Stephen L. Hauser	7
13	Haplotypic origin of ?-chain genes expressed by human T-cell clones 1992 ·Immunogenetics ·Eric Seboun, Narendra Joshi, (unknown)	4
14	Genetic mapping of a male germ cell-expressed gene Tpx-2 to mouse chromosome 17 1991 ·Immunogenetics ·Masanori Kasahara, Eric Seboun, Marc Fellous, (unknown)	2
15	Fos RNA accumulation in multiple sclerosis white matter tissue 1991 ·Journal of the Neurological Sciences ·John S. Yu, Tatsuhiko Hayashi, Eric Seboun, R. Sklar, Teresa H. Doolittle, Stephen L. Hauser	10
16	Insertion/deletion-related polymorphisms in the human T cell receptor beta gene complex. 1989 ·The Journal of Experimental Medicine ·Eric Seboun, Mary Ann Robinson, Thomas J. Kindt, Stephen L. Hauser	42
17	A susceptibility locus for multiple sclerosis is linked to the T cell receptor β chain complex 1989 ·Cell ·Eric Seboun, Mary Ann Robinson, Teresa H. Doolittle, Thomas A. Ciulla, Thomas J. Kindt, Stephen L. Hauser	193
18	Molecular Genotypes of the T‐Cell Receptor Beta Chain in Families with Multiple Sclerosisa 1988 ·Annals of the New York Academy of Sciences ·Thomas A. Ciulla, Mary Ann Robinson, Eric Seboun, Teresa H. Doolittle, Takaharu Hayashi, Thomas J. Kindt, S L Hauser	4
19	Testis-specific transcripts detected by a human Y-DNA-derived probe 1987 ·Development ·Pascale Leroy, Eric Seboun, Marie‐Geneviève Mattéi, Marc Fellous, Colin E. Bishop	14
20	Prenatal identification of a Y‐chromosome deletion by Y‐specific single copy DNA probes 1986 ·Prenatal Diagnosis ·S Gilgenkrantz, P. Droullé, Eric Seboun, M Casanova, Morton D. Schweitzer, (unknown), Marc Fellous	1

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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