Jérôme Toutain

Université de Bordeaux — France

Medicine · Health Sciences

21h-index1.8kcitations66works1.02yr avg
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Research Topics

Prenatal Screening and Diagnostics(17), Genomic variations and chromosomal abnormalities(15), CRISPR and Genetic Engineering(6), Congenital heart defects research(6), Genetic Syndromes and Imprinting(6)

Publications66 total

Single-cell multiplex approaches deeply map ON-target CRISPR-genotoxicity and reveal its mitigation by palbociclib and long-term engraftment
Nature Communications·2026Open Access
Targeted versus whole-brain radiotherapy: systematic multiparametric and longitudinal investigations in the adult rat
Lab Animal·2025
Single-cell multiplex approaches deeply map ON-target CRISPR-genotoxicity and reveal its mitigation by palbociclib and long-term engraftment
2025· 1 citedOpen Access
Single-cell SNP-DNA sequencing precisely maps genotoxic events in CRISPR-edited primary cells
2025Open Access
Table of Contents, Volume 194A, Number 4, April 2024
American Journal of Medical Genetics Part A·2024Open Access
<i>In vivo</i> biodistribution and tumor uptake of [<sup>64</sup>Cu]-FAU nanozeolite <i>via</i> positron emission tomography Imaging
Nanoscale·2024· 5 citedOpen Access
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases
American Journal of Medical Genetics Part A·2023· 10 citedOpen Access
Effets non-ciblés de l’irradiation globale du cerveau chez le rat : focus sur les muscles squelettiques
SPIRE - Sciences Po Institutional REpository·2022
Investigating the effects of proton therapy versus X-rays on circulating leukocytes in a context of brain irradiation: a preclinical study
HAL (Le Centre pour la Communication Scientifique Directe)·2022
Assisted reproductive technology outcomes of infertile men carrying balanced chromosomal rearrangements or Y-chromosome microdeletions – Retrospective study
Annales de biologie clinique·2021
Modulation of the intrinsic chromatin binding property of HIV-1 integrase by LEDGF/p75
Nucleic Acids Research·2021· 18 citedOpen Access
CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
Nature Communications·2021· 83 citedOpen Access
Critical role of Aquaporin-1 and telocytes in infantile hemangioma response to propranolol beta blockade
Proceedings of the National Academy of Sciences·2021· 38 citedOpen Access
Analysis of the intrinsic chromatin binding property of HIV-1 integrase and its regulation by LEDGF/p75 using human chromosomes spreads
2020Open Access
Mutation-Specific Guide RNA for Compound Heterozygous Porphyria On-target Scarless Correction by CRISPR/Cas9 in Stem Cells
Stem Cell Reports·2020· 9 citedOpen Access
Kinetics of radiation-induced motor and cognitive impairments in the adult rat model
HAL (Le Centre pour la Communication Scientifique Directe)·2019
Type 3 confined placental mosaicisms excluding trisomies 16 are also associated with adverse pregnancy outcomes
Genetics in Medicine·2019· 12 citedOpen Access
Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders
Journal of Medical Genetics·2019· 79 citedOpen Access
CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations
Nature Communications·2019· 460 citedOpen Access
Fetal phenotype of Rubinstein‐Taybi syndrome caused by <i>CREBBP</i> mutations
Clinical Genetics·2019· 15 cited
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Frequent Co-authors

Robert Saura(17), Caroline Rooryck(16), J. Horovitz(16), Didier Lacombe(15), Benoı̂t Arveiler(12), Dorothée Cailley(7), Julie Bouron(6), Laurence Taine(6), Myriam Bernaudin(5), David Cappellen(5), Marie‐Laure Vuillaume(5), Julian Boutin(4), Isabelle Lamrissi‐Garcia(4), Sandrine Dabernat(4), François Moreau‐Gaudry(4), Aurélie Bedel(4), Jean‐Philippe Merlio(4), Fanny Morice‐Picard(4), Sébastien Moutton(4), Sophie Naudion(4)