Bérengère Génin

486 total citations
7 papers, 270 citations indexed

About

Bérengère Génin is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Bérengère Génin has authored 7 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Oncology and 3 papers in Cancer Research. Recurrent topics in Bérengère Génin's work include Cancer Genomics and Diagnostics (2 papers), Autism Spectrum Disorder Research (2 papers) and Lung Cancer Treatments and Mutations (2 papers). Bérengère Génin is often cited by papers focused on Cancer Genomics and Diagnostics (2 papers), Autism Spectrum Disorder Research (2 papers) and Lung Cancer Treatments and Mutations (2 papers). Bérengère Génin collaborates with scholars based in France, United Kingdom and Switzerland. Bérengère Génin's co-authors include Florence Koeppel, Jacques Birraux, Claude Le Coultre, Giorgio C. La Scala, Cécile Jovelet, Ludovic Lacroix, Steven G. Blanchard, Emmanuel Martin, Samuel E. Taylor and P. Bugmann and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Annals of Oncology.

In The Last Decade

Bérengère Génin

7 papers receiving 256 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Bérengère Génin France	5	106	86	75	63	47	7	270
Lisa Müller Germany	13	27 0.3×	148 1.7×	18 0.2×	71 1.1×	10 0.2×	42	440
Sisi Wang China	10	29 0.3×	48 0.6×	60 0.8×	107 1.7×	8 0.2×	34	273
Christine Bruun Denmark	10	47 0.4×	259 3.0×	24 0.3×	159 2.5×	53 1.1×	14	475
Huaxiu Luo China	5	54 0.5×	11 0.1×	67 0.9×	119 1.9×	11 0.2×	7	224
Megumi Yamaguchi Japan	11	86 0.8×	63 0.7×	27 0.4×	71 1.1×	3 0.1×	36	328
K Nishioka Japan	5	44 0.4×	24 0.3×	45 0.6×	133 2.1×	25 0.5×	8	359
Eleonora Leggiero Italy	12	41 0.4×	24 0.3×	24 0.3×	172 2.7×	19 0.4×	16	325
Mustafa Gökhan Ertosun Türkiye	6	27 0.3×	31 0.4×	30 0.4×	106 1.7×	7 0.1×	18	200
Oana Herlea‐Pana United States	9	41 0.4×	24 0.3×	26 0.3×	128 2.0×	14 0.3×	13	325
Anthony Sandrasagra United States	8	52 0.5×	39 0.5×	20 0.3×	126 2.0×	7 0.1×	12	325

Countries citing papers authored by Bérengère Génin

Since Specialization

Citations

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

Fields of papers citing papers by Bérengère Génin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bérengère Génin

This figure shows the co-authorship network connecting the top 25 collaborators of Bérengère Génin. A scholar is included among the top collaborators of Bérengère Génin 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 Bérengère Génin. Bérengère Génin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Koeppel, Florence, Steven G. Blanchard, Cécile Jovelet, et al.. (2017). Whole exome sequencing for determination of tumor mutation load in liquid biopsy from advanced cancer patients. PLoS ONE. 12(11). e0188174–e0188174. 81 indexed citations

2.

Carayol, Jérôme, Gerard D. Schellenberg, Beth A. Dombroski, et al.. (2014). A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism. Frontiers in Genetics. 5. 33–33. 7 indexed citations

3.

Laurent‐Puig, Pierre, John Bridgewater, John Primrose, et al.. (2014). Mir-31-3P is a Predictive Biomarker of Cetuximab Effects in a Post-Hoc Analysis in the New Epoc Study. Annals of Oncology. 25. iv185–iv185. 1 indexed citations

4.

Laurent‐Puig, Pierre, John Bridgewater, John Primrose, et al.. (2014). Mir-31-3p as a predictive biomarker of cetuximab effects in a post hoc analysis of new EPOC phase III trial.. Journal of Clinical Oncology. 32(15_suppl). 3523–3523. 2 indexed citations

5.

Amiet, Claire, Isabelle Gourfinkel‐An, Claudine Laurent, et al.. (2013). Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?. Molecular Autism. 4(1). 47–47. 40 indexed citations

6.

Macé, Sandrine, Emmanuelle Cousin, Sylvain Ricard, et al.. (2004). ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease. Neurobiology of Disease. 18(1). 119–125. 79 indexed citations

7.

Bugmann, P., Samuel E. Taylor, Bérengère Génin, et al.. (1998). A silicone-coated nylon dressing reduces healing time in burned paediatric patients in comparison with standard sulfadiazine treatment: a prospective randomized trial. Burns. 24(7). 609–612. 60 indexed citations

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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