Catherine Bourgain

2.2k total citations · 1 hit paper
58 papers, 1.4k citations indexed

About

Catherine Bourgain is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Catherine Bourgain has authored 58 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 15 papers in Molecular Biology and 7 papers in Rheumatology. Recurrent topics in Catherine Bourgain's work include Genetic Associations and Epidemiology (17 papers), Genetic Mapping and Diversity in Plants and Animals (8 papers) and Genetic and phenotypic traits in livestock (6 papers). Catherine Bourgain is often cited by papers focused on Genetic Associations and Epidemiology (17 papers), Genetic Mapping and Diversity in Plants and Animals (8 papers) and Genetic and phenotypic traits in livestock (6 papers). Catherine Bourgain collaborates with scholars based in France, United States and Italy. Catherine Bourgain's co-authors include Emmanuelle Génin, Françoise Clerget‐Darpoux, Carole Ober, Mary Sara McPeek, Hadi Quesneville, Karen Walker, Lori Steiner, Sabine Hoffjan, Rebecca Reynolds and Dina L. Newman and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Catherine Bourgain

54 papers receiving 1.3k 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.

Adopt a moratorium on heritable genome editing

2019 251 citations Eric S. Lander, Françoise Βaylis et al. Nature profile →

Peers

Countries citing papers authored by Catherine Bourgain

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Bourgain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Bourgain

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Bourgain. A scholar is included among the top collaborators of Catherine Bourgain 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 Catherine Bourgain. Catherine Bourgain 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	Les félicités du capital en santé: Épanouissement, épreuves et tensions critiques des industries pharmaceutiques aux Nords et aux Suds 2021 ·HAL (Le Centre pour la Communication Scientifique Directe) ·Catherine Bourgain, Maurice Cassier, Jean‐Paul Gaudillière, (unknown)	1
2	Genomic susceptibility in practice: The regulatory trajectory of non-rare thrombophilia (NRT) genetic tests in the clinical management of venous thrombo-embolism (VTE) 2020 ·Social Science & Medicine ·Mauro Turrini, Catherine Bourgain	5
3	Adopt a moratorium on heritable genome editing breakdown → 2019 ·Nature ·Eric S. Lander, Françoise Βaylis, Feng Zhang, Emmanuelle Charpentier, Paul R. Berg, Catherine Bourgain, Bärbel Friedrich, J. Keith Joung, Jinsong Li, David Liu, Luigi Naldini, Jing‐Bao Nie, Qiu Renzong, Bettina Schöne-Seifert, Feng Shao, Sharon F. Terry, Wensheng Wei, Ernst‐Ludwig Winnacker	251
4	Imperfect biomarkers for adjuvant chemotherapy in early stage breast cancer with good prognosis 2019 ·Social Science & Medicine ·Catherine Bourgain, (unknown), Chafika Mazouni, Martine Bungener, Julia Bonastre	6
5	Génomique, de la recherche à la clinique 2014 ·médecine/sciences ·Catherine Bourgain	2
6	Genetic and Environmental Factors Influencing the Placental Growth Factor (PGF) Variation in Two Populations 2012 ·PLoS ONE ·Rossella Sorice, Daniela Ruggiero, Teresa Nutile, (unknown), (unknown), Allan Linneberg, Catherine Bourgain, Anne‐Louise Leutenegger, Marina Ciullo	12
7	Genetics of VEGF Serum Variation in Human Isolated Populations of Cilento: Importance of VEGF Polymorphisms 2011 ·PLoS ONE ·Daniela Ruggiero, Cyril Dalmasso, Teresa Nutile, Rossella Sorice, Laura Dionisi, (unknown), Philippe Broët, Anne‐Louise Leutenegger, Catherine Bourgain, Marina Ciullo	61
8	Comprehensive Linkage and Association Analyses Identify Haplotype, Near to the TNFSF15 Gene, Significantly Associated with Spondyloarthritis 2009 ·PLoS Genetics ·Elena Zinovieva, Catherine Bourgain, Amir Kadi, Franck Letourneur, Brigitte Izac, Roula Said‐Nahal, Nicolas Lebrun, Nicolas Cagnard, (unknown), Sébastien Jacques, Corinne Miceli‐Richard, Henri‐Jean Garchon, Simon Heath, Céline Charon, Delphine Bacq, Anne Boland, Diana Zélénika, Gilles Chiocchia, Maxime Bréban	46
9	Linkage Analysis with Dense SNP Maps in Isolated Populations 2009 ·Human Heredity ·Céline Bellenguez, Carole Ober, Catherine Bourgain	15
10	Epidemiology, Pathology, and Genetics of Histiocytic Sarcoma in the Bernese Mountain Dog Breed 2009 ·Journal of Heredity ·Jérôme Abadie, Benoît Hédan, Édouard Cadieu, (unknown), Patrick Devauchelle, Catherine Bourgain, Heidi G. Parker, Amaury Vaysse, Patricia Margaritte‐Jeannin, Francis Galibert, Elaine A. Ostrander, Catherine André	84
11	Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis 2007 ·Lara D. Veeken ·Kim W. Carter, Anna Pluzhnikov, Andrew E. Timms, Corinne Miceli‐Richard, Catherine Bourgain, B P Wordsworth, Hélène Jean‐Pierre, Nancy J. Cox, Lyle J. Palmer, Maxime Bréban, John D. Reveille, Matthew A. Brown	50
12	New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate 2006 ·Human Molecular Genetics ·Marina Ciullo, Céline Bellenguez, Vincenza Colonna, Teresa Nutile, (unknown), (unknown), (unknown), Bruno Trimarco, Catherine Bourgain, M. Graziella Persico	35
13	Detection of susceptibility loci by genome-wide linkage analysis 2005 ·BMC Genetics ·Marie‐Claude Babron, Catherine Bourgain, Anne‐Louise Leutenegger, Françoise Clerget‐Darpoux	5
14	Impact of the diagnosis definition on linkage detection 2005 ·BMC Genetics ·Marie‐Hélène Dizier, Emmanuelle Génin, Marie‐Claude Babron, Catherine Bourgain	1
15	Modeling the effect of a genetic factor for a complex trait in a simulated population 2005 ·BMC Genetics ·Mathieu Bourgey, Anne‐Louise Leutenegger, Emmanuelle Cousin, Catherine Bourgain, Marie‐Claude Babron, Françoise Clerget‐Darpoux	1
16	Comparing strategies for association mapping in samples with related individuals 2005 ·BMC Genetics ·Catherine Bourgain	9
17	Are common disease susceptibility alleles the same in outbred and founder populations? 2004 ·European Journal of Human Genetics ·Dina L. Newman, Sabine Hoffjan, Catherine Bourgain, Mark Abney, Raluca Nicolae, (unknown), Michael Grow, Karen Walker, Lori Steiner, Rodney Parry, Rebecca Reynolds, Mary Sara McPeek, Suzanne Cheng, Carole Ober	21
18	Missing data in haplotype analysis: a study on the MILC method 2002 ·Annals of Human Genetics ·Catherine Bourgain, Emmanuelle Génin, Carole Ober, Françoise Clerget‐Darpoux	21
19	Use of Closely Related Affected Individuals for the Genetic Study of Complex Diseases in Founder Populations 2001 ·The American Journal of Human Genetics ·Catherine Bourgain, Emmanuelle Génin, P. Holopainen, K. Mustalahti, Markku Mäki, Jukka Partanen, Françoise Clerget‐Darpoux	39
20	Search for multifactorial disease susceptibility genes in founder populations 2000 ·Annals of Human Genetics ·Catherine Bourgain, Emmanuelle Génin, Hadi Quesneville, Françoise Clerget‐Darpoux	63

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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