Géraldine Mathonnet

2.2k total citations
20 papers, 1.5k citations indexed

About

Géraldine Mathonnet is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Géraldine Mathonnet has authored 20 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Géraldine Mathonnet's work include DNA Repair Mechanisms (5 papers), Acute Lymphoblastic Leukemia research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Géraldine Mathonnet is often cited by papers focused on DNA Repair Mechanisms (5 papers), Acute Lymphoblastic Leukemia research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Géraldine Mathonnet collaborates with scholars based in Canada, United States and United Kingdom. Géraldine Mathonnet's co-authors include Nahum Sonenberg, Daniel Sinnett, Thomas F. Duchaîne, Marc R. Fabian, Yuri V. Svitkin, Witold Filipowicz, Armen Parsyan, Damian Labuda, Maja Krajinović and Edward Darżynkiewicz and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Molecular Cell.

In The Last Decade

Géraldine Mathonnet

19 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Géraldine Mathonnet Canada	16	1.1k	563	259	154	114	20	1.5k
George Xinarianos United Kingdom	24	1.5k 1.3×	474 0.8×	262 1.0×	186 1.2×	49 0.4×	35	2.2k
Neeme Tõnisson Estonia	16	937 0.8×	241 0.4×	305 1.2×	97 0.6×	33 0.3×	38	1.3k
Marta Kulis Spain	13	1.5k 1.3×	480 0.9×	251 1.0×	63 0.4×	44 0.4×	29	1.9k
Fides D. Lay United States	16	1.8k 1.6×	374 0.7×	306 1.2×	104 0.7×	33 0.3×	20	2.1k
Brian Rhees United States	12	716 0.6×	569 1.0×	249 1.0×	232 1.5×	31 0.3×	26	1.3k
Atsuya Nishiyama Japan	16	1.4k 1.2×	242 0.4×	242 0.9×	48 0.3×	91 0.8×	29	1.6k
Eric M. Kallin United States	13	2.0k 1.8×	349 0.6×	279 1.1×	89 0.6×	51 0.4×	16	2.4k
Jacob M. Zahn United States	13	943 0.8×	160 0.3×	222 0.9×	356 2.3×	45 0.4×	14	2.0k
Jozef Madžo United States	20	1.0k 0.9×	201 0.4×	174 0.7×	118 0.8×	226 2.0×	52	1.5k
Nongluk Plongthongkum United States	12	1.4k 1.2×	354 0.6×	192 0.7×	48 0.3×	26 0.2×	18	1.7k

Countries citing papers authored by Géraldine Mathonnet

Since Specialization

Citations

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

Fields of papers citing papers by Géraldine Mathonnet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Géraldine Mathonnet

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Laramée, Louise, Marieke Rozendaal, Henrique Bittencourt, et al.. (2024). The impact of comparative genomic hybridization/single‐nucleotide polymorphism microarray in risk stratification of pediatric acute lymphoblastic leukemia. Pediatric Blood & Cancer. 71(9). e31129–e31129.

Huguet, Guillaume, Catherine Schramm, Élise Douard, et al.. (2018). Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples. JAMA Psychiatry. 75(5). 447–447. 45 indexed citations

Chénier, Sébastien, Grace Yoon, Bob Argiropoulos, et al.. (2014). CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems. Journal of Neurodevelopmental Disorders. 6(1). 9–9. 63 indexed citations

Mathonnet, Géraldine, Raouf Fetni, Sonia Nizard, et al.. (2014). SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay. BMC Medical Genomics. 7(1). 70–70. 12 indexed citations

Hamdan, Fadi F., et al.. (2013). De novo deletion of FMN2 in a girl with mild non-syndromic intellectual disability. European Journal of Medical Genetics. 56(12). 686–688. 15 indexed citations

Fortier, Amanda, Raouf Fetni, Géraldine Mathonnet, et al.. (2013). Diagnostic utility of molecular and cytogenetic analysis in lipoblastoma: a study of two cases and review of the literature. Histopathology. 64(5). 731–740. 15 indexed citations

Srour, Myriam, Fadi F. Hamdan, Jeremy Schwartzentruber, et al.. (2012). Mutations in TMEM231 cause Joubert syndrome in French Canadians. Journal of Medical Genetics. 49(10). 636–641. 49 indexed citations

Kibar, Zoha, Géraldine Mathonnet, Raouf Fetni, et al.. (2011). Whole‐genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype. Clinical Genetics. 81(2). 128–141. 65 indexed citations

Thivierge, Caroline, Mathieu N. Flamand, Géraldine Mathonnet, et al.. (2010). Pervasive and Cooperative Deadenylation of 3′UTRs by Embryonic MicroRNA Families. Molecular Cell. 40(4). 558–570. 88 indexed citations

10.

Fabian, Marc R., Géraldine Mathonnet, Thomas R. Sundermeier, et al.. (2009). Mammalian miRNA RISC Recruits CAF1 and PABP to Affect PABP-Dependent Deadenylation. Molecular Cell. 35(6). 868–880. 305 indexed citations

11.

Parsyan, Armen, David Shahbazian, Yvan Martineau, et al.. (2009). The helicase protein DHX29 promotes translation initiation, cell proliferation, and tumorigenesis. Proceedings of the National Academy of Sciences. 106(52). 22217–22222. 93 indexed citations

12.

Mathonnet, Géraldine, Marc R. Fabian, Yuri V. Svitkin, et al.. (2007). MicroRNA Inhibition of Translation Initiation in Vitro by Targeting the Cap-Binding Complex eIF4F. Science. 317(5845). 1764–1767. 403 indexed citations

13.

Mathonnet, Géraldine, S Lachance, Moulay A. Alaoui‐Jamali, & Elliot Drobetsky. (2004). Expression of hepatitis B virus X oncoprotein inhibits transcription-coupled nucleotide excision repair in human cells. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 554(1-2). 305–318. 37 indexed citations

14.

Mathonnet, Géraldine, Maja Krajinović, Damian Labuda, & Daniel Sinnett. (2003). Role of DNA mismatch repair genetic polymorphisms in the risk of childhood acute lymphoblastic leukaemia. British Journal of Haematology. 123(1). 45–48. 39 indexed citations

15.

Mathonnet, Géraldine, et al.. (2003). Variable continental distribution of polymorphisms in the coding regions of DNA-repair genes. Journal of Human Genetics. 48(12). 659–664. 7 indexed citations

16.

Mathonnet, Géraldine, et al.. (2003). UV wavelength-dependent regulation of transcription-coupled nucleotide excision repair in p53-deficient human cells. Proceedings of the National Academy of Sciences. 100(12). 7219–7224. 45 indexed citations

17.

Krajinović, Maja, Chantal Richer, Géraldine Mathonnet, et al.. (2002). Analyses of bulky DNA adduct levels in human breast tissue and genetic polymorphisms of cytochromes P450 (CYPs), myeloperoxidase (MPO), quinone oxidoreductase (NQO1), and glutathione S-transferases (GSTs). Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 516(1-2). 41–47. 35 indexed citations

18.

Krajinović, Maja, Damian Labuda, Géraldine Mathonnet, et al.. (2002). Polymorphisms in genes encoding drugs and xenobiotic metabolizing enzymes, DNA repair enzymes, and response to treatment of childhood acute lymphoblastic leukemia.. PubMed. 8(3). 802–10. 119 indexed citations

19.

Infante‐Rivard, Claire, Géraldine Mathonnet, & Daniel Sinnett. (2000). Risk of childhood leukemia associated with diagnostic irradiation and polymorphisms in DNA repair genes.. Environmental Health Perspectives. 108(6). 495–498. 89 indexed citations

20.

Infante‐Rivard, Claire, Géraldine Mathonnet, & Daniel Sinnett. (2000). Risk of Childhood Leukemia Associated with Diagnostic Irradiation and Polymorphisms in DNA Repair Genes. Environmental Health Perspectives. 108(6). 495–495. 5 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.

Explore authors with similar magnitude of impact