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Géraldine Mathonnet · SciRah

Researcher profile · Semantic Scholar

Géraldine Mathonnet

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Géraldine Mathonnet — researcher profile on SciRah

h-index: 18
Works: 26
Citations: 2,310

Most-cited papers

MicroRNA Inhibition of Translation Initiation in Vitro by Targeting the Cap-Binding Complex eIF4F
Géraldine Mathonnet, M. Fabian, Y. Svitkin, A. Parsyan +9 more
2007Science614 citations Open access
Semantic Scholar
Mammalian miRNA RISC Recruits CAF1 and PABP to Affect PABP-Dependent Deadenylation
M. Fabian, Géraldine Mathonnet, Thomas R. Sundermeier, Hansruedi Mathys +13 more
2009Molecules and Cells432 citations Open access
Semantic Scholar
Polymorphisms in genes encoding drugs and xenobiotic metabolizing enzymes, DNA repair enzymes, and response to treatment of childhood acute lymphoblastic leukemia.
M. Krajinovic, D. Labuda, Géraldine Mathonnet, M. Labuda +3 more
2002Clinical Cancer Research157 citations
Semantic Scholar
The helicase protein DHX29 promotes translation initiation, cell proliferation, and tumorigenesis
A. Parsyan, D. Shahbazian, Y. Martineau, E. Petroulakis +8 more
2009Proceedings of the National Academy of Sciences of the United States of America122 citations Open access
Semantic Scholar
Risk of childhood leukemia associated with diagnostic irradiation and polymorphisms in DNA repair genes.
C. Infante-Rivard, Géraldine Mathonnet, D. Sinnett
2000Environmental Health Perspectives120 citations Open access
Semantic Scholar
Pervasive and Cooperative Deadenylation of 3’UTRs by Embryonic MicroRNA Families
Edlyn Wu, Caroline Thivierge, M. Flamand, Géraldine Mathonnet +5 more
2010Molecules and Cells112 citations Open access
Semantic Scholar
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems
S. Chénier, G. Yoon, B. Argiropoulos, J. Lauzon +14 more
2014Journal of Neurodevelopmental Disorders100 citations Open access
Semantic Scholar
Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples
G. Huguet, C. Schramm, E. Douard, Lai Jiang +16 more
2018JAMA psychiatry97 citations Open access
Semantic Scholar
Mutations in TMEM231 cause Joubert syndrome in French Canadians
M. Srour, F. Hamdan, J. Schwartzentruber, L. Patry +16 more
2012Journal of Medical Genetics81 citations Open access
Semantic Scholar
Whole‐genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype
G. D'Amours, Z. Kibar, Géraldine Mathonnet, Raouf Fetni +5 more
2012Clinical Genetics78 citations
Semantic Scholar
UV wavelength-dependent regulation of transcription-coupled nucleotide excision repair in p53-deficient human cells
Géraldine Mathonnet, C. Léger, J. Desnoyers, R. Drouin +2 more
2003Proceedings of the National Academy of Sciences of the United States of America60 citations Open access
Semantic Scholar
Genome wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability
G. Huguet, C. Schramm, E. Douard, P. Tamer +35 more
2021Molecular Psychiatry59 citations Open access
Semantic Scholar
Role of DNA mismatch repair genetic polymorphisms in the risk of childhood acute lymphoblastic leukaemia
Géraldine Mathonnet, M. Krajinovic, D. Labuda, D. Sinnett
2003British Journal of Haematology52 citations
Semantic Scholar
Expression of hepatitis B virus X oncoprotein inhibits transcription-coupled nucleotide excision repair in human cells.
Géraldine Mathonnet, S. Lachance, M. Alaoui-Jamali, E. Drobetsky
2004Mutation research51 citations
Semantic Scholar
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).
U. Brockstedt, M. Krajinovic, Chantal Richer, Géraldine Mathonnet +3 more
2002Mutation research47 citations
Semantic Scholar
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
M. Uddin, G. Pellecchia, B. Thiruvahindrapuram, L. D’Abate +25 more
2016Scientific Reports39 citations Open access
Semantic Scholar
SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay
G. D'Amours, Mathieu Langlois, Géraldine Mathonnet, Raouf Fetni +6 more
2014BMC Medical Genomics25 citations Open access
Semantic Scholar
De novo deletion of FMN2 in a girl with mild non-syndromic intellectual disability.
Mohammed Almuqbil, F. Hamdan, Géraldine Mathonnet, B. Rosenblatt +1 more
2013European Journal of Medical Genetics22 citations
Semantic Scholar
Diagnostic utility of molecular and cytogenetic analysis in lipoblastoma: a study of two cases and review of the literature
J. Choi, Dorothée Bouron-Dal Soglio, Amanda L. Fortier, Raouf Fetni +6 more
2014Histopathology18 citations
Semantic Scholar
Variable continental distribution of polymorphisms in the coding regions of DNA-repair genes
Géraldine Mathonnet, D. Labuda, C. Meloche, T. Wambach +2 more
2003Journal of Human Genetics9 citations
Semantic Scholar
by Targeting the Cap-Binding Complex eIF4F MicroRNA Inhibition of Translation Initiation in Vitro
Géraldine Mathonnet
20086 citations
Semantic Scholar
The impact of comparative genomic hybridization/single‐nucleotide polymorphism microarray in risk stratification of pediatric acute lymphoblastic leukemia
A. Gourmel, Héloïse Perrault, Marie-Laure Colaiacovo, L. Laramée +13 more
2024Pediatric Blood & Cancer4 citations
Semantic Scholar
Genome wide analysis of gene dosage in 24,092 individuals shows that 10,000 genes modulate cognitive ability
G. Huguet, C. Schramm, E. Douard, Tamer Petra +35 more
2020bioRxiv4 citations Open access
Semantic Scholar
MG-120 Chorionic villus sampling: 3 cases with discrepancies between ifish, array-cgh and karyotype
F. Léveillé, S. Nizard, Géraldine Mathonnet, E. Lemyre +1 more
20150 citations
Semantic Scholar
MG-122 Cytogenetic characterisation of 3 small supernumerary chromosomal markers in a 1 year-old girl
F. Léveillé, Géraldine Mathonnet, R. Laframboise, E. Lemyre +2 more
20150 citations
Semantic Scholar
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems
S. Chénier, G. Yoon, B. Argiropoulos, J. Lauzon +14 more
2014Journal of Neurodevelopmental Disorders0 citations Open access
Semantic Scholar

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