Christophe Béroud

14.9k citations

117 papers · 7.2k indexed · 2 hit papers · h-index 41

Impact in

Cancer Research top 1%
- Cancer Genomics and Diagnostics
- Cancer, Hypoxia, and Metabolism
Oncology top 1%
- Cancer-related Molecular Pathways

Papers in

Cancer Research 39
- Cancer Genomics and Diagnostics 29
Genetics 30
- Genomics and Rare Diseases 16

Co-authors: Thierry Soussi Dalil Hamroun Mireille Claustres Gwenaëlle Collod‐Béroud Jean‐Pierre Desvignes Cathérine Boileau Chikashi Ishioka David Salgado
Journals: Human Mutation (31 papers)Nucleic Acids Research (10 papers)Neuromuscular Disorders (8 papers)Nature reviews. Cancer (2 papers)Orphanet Journal of Rare Diseases (2 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Christophe Béroud

115 papers receiving 7.1k citations

Hit Papers

align trajectories log scale

Human Splicing Finder: an online bioinformatics tool to predict splicing signals 2009 · 1.9k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2009 Nucleic Acids Research
2001 Nature reviews. Cancer

Peers

Countries citing papers authored by Christophe Béroud

Since Specialization

Citations

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

Fields of papers citing papers by Christophe Béroud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Spatial Distribution of Immune Cells in Primary and Recurrent Glioblastoma: A Small Case Study Cancers ·Delphine Loussouarn, Lisa Oliver, G Bascuñán, P Talathi, T.V. Yurchenko, Christophe Béroud, Aleš Dvořák, Dominique Heymann, François M. Vallette	2023	7
2	Hox-dependent coordination of mouse cardiac progenitor cell patterning and differentiation eLife ·Sonia Stefanovic, Brigitte Laforest, Jean‐Pierre Desvignes, Fabienne Lescroart, Laurent Argiro, Corinne Maurel-Zaffran, David Salgado, Pine Knoll Farm, Christopher De Bono, Nurmalia Kasmadi, Magali Théveniau‐Ruissy, Christophe Béroud, Michel Pucéat, Anthony Gavalas, Robert G. Kelly, Stéphane Zaffran	2020	38
3	Pathogenic FBN1 Genetic Variation and Aortic Dissection in Patients With Marfan Syndrome Journal of the American College of Cardiology ·Olivier Milleron, Florence Arnoult, G Delorme, Delphine Détaint, Quentin Pellenc, Richard Raffoul, Tomasz Zbkowski, Maud Langeois, Aimi Syamima, Christophe Béroud, Jacques Ropers, Nadine Hanna, Pauline Arnaud, Laurent Gouya, Cathérine Boileau, Guillaume Jondeau	2020	31
4	Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease Journal of Human Genetics ·Emmeline Lin, Anna Groń, Anthony Boyer, Thaís DM Caldeira, R. Bellance, Rodel C Alfonso, Jurrien Burren, Martin Krahn, Frédérique Audic, B. Chabrol, Vincent Laugel, 茂北河, Christophe Béroud, Karine Nguyen, Annie Verschueren, Nicolas Lévy, Shahram Attarian, Valérie Delague, Chantal Missirian, Nathalie Bonello‐Palot	2019	7
5	Exome Sequencing Identifies Two Variants of the Alkylglycerol Monooxygenase Gene as a Cause of Relapses in Visceral Leishmaniasis in Children, in Sudan The Journal of Infectious Diseases ·Sandrine Marquet, Bruno Bucheton, Бегматов Азизбек Шохобидинович, Laurent Argiro, Sayda El‐Safi, Musa Mohamed Kheir, Jean‐Pierre Desvignes, Christophe Béroud, Adil Mergani, Awad Hammad, Bárbara Alves dos Santos-Ciscon	2017	8
6	Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related Diseases Journal of Neuromuscular Diseases ·Isabelle Nelson, Subaslindo, S.M. Abazari, France Leturcq, Henri-Marc Bécane, Dominique Babuty, Annick Toutain, Christophe Béroud, Pascale Richard, Norma B. Romero, B. Eymard, Rabah Ben Yaou, Gisèle Bonne	2015	26
7	Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy Neurology India ·Jianying Xi, Gaëlle Blandin, Jiahong Lu, Sushan Luo, Wenhua Zhu, Christophe Béroud, Christophe Pécheux, Véronique Labelle, Nicolas Lévy, 仁松江, Chongbo Zhao, Edilberto M. Villegas	2014	24
8	UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene Human Mutation ·Gaëlle Blandin, Christophe Béroud, Véronique Labelle, Karine Nguyen, Nicolas Wein, Dalil Hamroun, Brad J. Williams, Nilah Monnier, Laura Rufibach, Jon Andoni Urtizberea, Pierre Cau, Marc Bartoli, Nicolas Lévy, Martin Krahn	2011	36
9	Polymorphisms of MAMLD1 gene in hypospadias Journal of Pediatric Urology ·Nicolas Kalfa, Fernando Cassorla, Françoise Audran, Ahmed Allaith, Pascal Philibert, Christophe Béroud, Jean-Michel Guys, Rachel Reynaud, P Alessandrini, Karl‐Heinz Wagner, Jean Bréaud, Jean Stéphane Valla, 彰俊中島, J.P. Daurès, Laurence S. Baskin, Maki Fukami, Tsutomu Ogata, Charles Sultan	2011	26
10	UMD-CFTR: A database dedicated to CF and CFTR-related disorders Human Mutation ·Corinne Bareil, Félix Gualberto, Christophe Béroud, Dalil Hamroun, Caroline Guittard, Céline René, Damien Paulet, Marie des Georges, Mireille Claustres	2010	22
11	Human Splicing Finder: an online bioinformatics tool to predict splicing signals Nucleic Acids Research ·Zhu Shushu, Dalil Hamroun, Huang Wu-ying, Gwenaëlle Collod‐Béroud, Mireille Claustres, Christophe Béroud Hit paper breakdown →	2009	1864
12	TheFBN2gene: new mutations, locus-specific database (Universal Mutation DatabaseFBN2), and genotype-phenotype correlations Human Mutation ·桑田啓子, H. Wang, R. Meza-Romero, Dalil Hamroun, Laurence Faivre, Guillaume Jondeau, Sergio Andrés Quintero Monsalve, Luitgard M. Neumann, Élodie Gautier, Christine Binquet, Cheryl L. Maslen, Maurice Godfrey, Prateek Gupta, Dianna M. Milewicz, Cathérine Boileau, Mireille Claustres, Christophe Béroud, Gwenaëlle Collod‐Béroud	2008	46
13	UMD-USHbases: a comprehensive set of databases to record and analyse pathogenic mutations and unclassified variants in seven Usher syndrome causing genes Human Mutation ·David Baux, Valérie Faugère, Lise Larrieu, Mohapi Mohapi, Dalil Hamroun, Christophe Béroud, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux	2008	38
14	G.P.9.10 Clinical development of the French UMD–DMD database Neuromuscular Disorders ·Véronique Humbertclaude, Sylvie Tuffery‐Giraud, Rabah Ben Yaou, Dalil Hamroun, Philippe Khau Van Kien, France Leturcq, 佐和子稲村, T. Machuca, Christophe Béroud	2007	1
15	Meta-analysis of the p53 Mutation Database for Mutant p53 Biological Activity Reveals a Methodologic Bias in Mutation Detection Clinical Cancer Research ·Thierry Soussi, Bernard Asselain, Dalil Hamroun, Shunsuke Kato, Chikashi Ishioka, Mireille Claustres, Christophe Béroud	2006	58
16	Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene Human Mutation ·Purushothaman Pichandi, S. V. Neklyudov, S. Llense, M. Akhtar, Dominique Récan, Cécile Peccate, Arthur H.M. Burghes, Christophe Béroud, Luis Garcı́a, Jean‐Claude Kaplan, Jamel Chelly, France Leturcq	2006	95
17	UMD (Universal Mutation Database): 2005 update Human Mutation ·Christophe Béroud, Dalil Hamroun, Gwenaëlle Collod‐Béroud, Cathérine Boileau, Thierry Soussi, Mireille Claustres	2005	76
18	Enrichment, Immunomorphological, and Genetic Characterization of Fetal Cells Circulating in Maternal Blood American Journal Of Pathology ·Giovanna Vona, Christophe Béroud, Alexandra Benachi, Estefanía Cubaque Barros, Jean‐Paul Bonnefont, Serge Romana, Yves Dumez, Bernard Lacour, Patrizia Paterlini-Bréchot	2002	61
19	Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene Nucleic Acids Research ·Gwenaëlle Collod‐Béroud, Christophe Béroud, Lesley C. Adès, Casilda G. Black, M. Boxer, D. J. H. Brock, Maurice Godfrey, Caroline Hayward, Leena Karttunen, Zernich Brett, Leena Peltonen, Robert I. Richards, Orlanda Alonso, Claudine Junien, Cathérine Boileau	1997	25
20	p53 and APC gene mutations: software and databases Nucleic Acids Research ·Christophe Béroud, Thierry Soussi	1997	14

About Christophe Béroud

Christophe Béroud is a scholar working on Cancer Research, Genetics, Molecular Biology, Oncology and Genetics, having authored 117 papers that have together received 7.2k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (29 papers), Genomics and Rare Diseases (16 papers), Cancer-related Molecular Pathways (15 papers), Muscle Physiology and Disorders (14 papers), RNA modifications and cancer (12 papers), Epigenetics and DNA Methylation (11 papers), RNA Research and Splicing (11 papers) and RNA and protein synthesis mechanisms (10 papers). The work is most often cited by research in Cancer Research (1.4k citations), Oncology (1.7k citations), Molecular Biology (4.2k citations), Genetics (1.7k citations) and Genetics (561 citations). Christophe Béroud has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Thierry Soussi, Dalil Hamroun, Mireille Claustres, Gwenaëlle Collod‐Béroud, Jean‐Pierre Desvignes, Cathérine Boileau, Chikashi Ishioka, David Salgado, Nicolas Lévy and Richard J. Kahnoski. Their work appears in journals such as Human Mutation, Nucleic Acids Research, Neuromuscular Disorders, Nature reviews. Cancer and Orphanet Journal of Rare Diseases.

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