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2022


37 publication(s):

Note: when necessary, only the first 15 authors are displayed.

International refereed journal articles

1 - 
Therapeutic approach and outcome of children with Philadelphia chromosome-positive acute lymphoblastic leukemia at first relapse in the era of tyrosine kinase inhibitors: An SFCE retrospective study
L. Aubert, A. Petit, Y. Bertrand, A.-F. Ray-Lunven, M. Angoso, C. Pluchart, F. Millot, P. Saultier, N. Cheikh, I. Pellier, D. Plantaz, A. Sirvent, S. Thouvenin-Doublet, J. Valduga, G. Plat et al.
Pediatric Blood and Cancer, Wiley, 2022, 69 (2), pp.e29441.
DOI : https://doi.org/10.1002/pbc.29441
Pubmed : 34854546
 Reprint request: Subject to availability
2 - 
Neural network fast‐classifies biological images through features selecting to power automated microscopy
M. Balluet, F. Sizaire, Y. E. Habouz, T. Walter, J. Pont, B. Giroux, O. Bouchareb, M. Tramier, J. Pecreaux
Journal of Microscopy, Wiley, 2022, 285 (1), pp.3-19.
DOI : https://doi.org/10.1111/jmi.13062
Pubmed : 34623634
PDF file
 Reprint request: Subject to availability
3 - 
Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy
C. Bar, D. Breuillard, M. Kuchenbuch, M. Jennesson, G. Le Guyader, H. Isnard, A. Rolland, D. Doummar, J. Fluss, A. Afenjar, P. Berquin, A. de Saint Martin, S. Dupont, A. Goldenberg, D. Lederer et al.
Epilepsy & Behavior, [San Diego CA]: Elsevier B.V., 2022, 126, pp.108471.
DOI : https://doi.org/10.1016/j.yebeh.2021.108471
Pubmed : 34915430
PDF file
 Reprint request: Subject to availability
4 - 
Genome sequencing for genetics diagnosis of patients with intellectual disability: the DEFIDIAG study
C. Binquet, C. Lejeune, L. Faivre, M. Bouctot, M.-L. Asensio, A. Simon, J.-F. Deleuze, A. Boland, F. Guillemin, V. Seror, C. Delmas, H. Esperou, Y. Duffourd, S. Lyonnet, S. Odent et al.
Frontiers in Genetics, Frontiers, 2022, 12, pp.766964.
DOI : https://doi.org/10.3389/fgene.2021.766964
Pubmed : 35178068
PDF file
 Reprint request: Subject to availability
5 - 
MiR-31-3p do not predict anti-EGFR efficacy in first-line therapy of RAS wild-type metastatic right-sided colon cancer
E. Boisteau, A. Lespagnol, M. de Tayrac, S. Corre, A. Perrot, N. Rioux-Leclercq, S. Martin-Lannerée, P. Artru, P. Chalabreysse, P.-G. Poureau, L. Doucet, D. Coupez, J. Bennouna, C. Bossard, R. Coriat et al.
Clinics and Research in Hepatology and Gastroenterology, Elsevier, 2022, pp.101888.
DOI : https://doi.org/10.1016/j.clinre.2022.101888
Pubmed : 35189426
PDF file
 Reprint request: Subject to availability
6 - 
Cofilin regulates actin network homeostasis and microvilli length in mouse oocytes
A. Bourdais, B. Dehapiot, G. Halet
Journal of Cell Science, Company of Biologists, 2022, 134 (24), pp.jcs259237.
DOI : https://doi.org/10.1242/jcs.259237
Pubmed : 34841429
PDF file
 Reprint request: Subject to availability
7 - 
Quality of life and mental health of adolescents and adults with Silver-Russell syndrome
M. Burgevin, A. Lacroix, K. Bourdet, R. Coutant, B. Donadille, L. Faivre, S. Manouvrier-Hanu, F. Petit, C. Thauvin-Robinet, A. Toutain, I. Netchine, S. Odent
European Journal of Medical Genetics, Elsevier, 2022, 65 (5), pp.104482.
DOI : https://doi.org/10.1016/j.ejmg.2022.104482
Pubmed : 35304302
PDF file
 Reprint request: Subject to availability
8 - 
Trans-Translation Is an Appealing Target for the Development of New Antimicrobial Compounds
R. Campos-Silva, G. d'Urso, O. Delalande, E. Giudice, A. J. Macedo, R. Gillet
Microorganisms, MDPI, 2022, 10 (1), pp.3.
DOI : https://doi.org/10.3390/microorganisms10010003
Pubmed : 35056452
PDF file
 Reprint request: Subject to availability
9 - 
DNA methylation episignature in Gabriele-de Vries syndrome
F. Cherik, J. Reilly, J. Kerkhof, M. Levy, H. Mcconkey, M. Barat-Houari, K. M. Butler, C. Coubes, J. A. Lee, G. Le Guyader, R. J. Louie, W. G. Patterson, M. L. Tedder, M. Bak, T. B. Hammer et al.
Genetics in Medicine, Nature Publishing Group, 2022,
DOI : https://doi.org/10.1016/j.gim.2021.12.003
Pubmed : 35027293
 Reprint request: Subject to availability
10 - 
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients
B. Chesneau, M. Aubert-Mucca, F. Fremont, J. Pechmeja, V. Soler, B. Isidor, M. Nizon, H. Dollfus, J. Kaplan, L. Fares-Taie, J.-M. Rozet, T. Busa, D. Lacombe, S. Naudion, J. Amiel et al.
Clinical Genetics, Wiley, 2022,
DOI : https://doi.org/10.1111/cge.14123
Pubmed : 35170016
PDF file
 Reprint request: Subject to availability


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