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2023


117 publication(s):

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

International refereed journal articles

51 - 
Hepatitis E Virus Infection in Pediatric Oncology
Anna Lenglart, Celine Chappe, Isabelle Grulois, Francoise Herve, Virginie Gandemer, Guillaume Robert
Journal of Pediatric Hematology/Oncology, 2023, 45 (1), pp.E150-E153.
DOI : https://doi.org/10.1097/MPH.0000000000002539
Pubmed : 36598968
 Reprint request: Subject to availability
52 - 
Studying Muscle Transcriptional Dynamics at Single-molecule Scales in Drosophila
Emma Leroux, Nourhene Ammar, Savannah Moinet, Thierry Pecot, Hadi Boukhatmi
Studying Muscle Transcriptional Dynamics at Single-molecule Scales in Drosophila. Journal of visualized experiments : JoVE, 2023, 199,
DOI : https://doi.org/10.3791/65713
Pubmed : 37747217
PDF file
 Reprint request: Subject to availability
53 - 
Genomic Diversity and Runs of Homozygosity in Bernese Mountain Dogs
Anna Letko, Benoit Hedan, Anna Snell, A Harris, Vidhya Jagannathan, Göran Andersson, B Holst, Elaine A.. Ostrander, Pascale Quignon, Catherine André, Tosso Leeb
Genes, 2023, 14 (3),
DOI : https://doi.org/10.3390/genes14030650
Pubmed : 36980922
PDF file
 Reprint request: Subject to availability
54 - 
Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study group
Lucille Lew-Derivry, Alice Marceau-Renaut, Laurène Fenwarth, Wendy Cuccuini, Paola Ballerini, Maxime Ferreboeuf, Audrey Guilmatre, Arnaud Petit, Virginie Gandemer, Fanny Rialland, Pascale Schneider, Bruno Gérard, Michel, B.G.M. Robert, Yves Bertrand et al.
Leukemia, 2023, 37 (8), pp.1723-1726.
DOI : https://doi.org/10.1038/s41375-023-01931-y
Pubmed : 37328541
PDF file
 Reprint request: Subject to availability
55 - 
Genome-wide DNA methylation analysis identifies potent CpG signature for temzolomide response in non-G-CIMP glioblastomas with unmethylated MGMT promoter: MGMT-dependent roles of GPR81
Bao-Bao Liang, Yu-Hong Wang, Jingjing Huang, Shuai Lin, Guo-Chao Mao, Zhangjian Zhou, Wan-Jun Yan, Chang-You Shan, Hui-Zi Wu, Amandine Etcheverry, Ya-Long He, Fangfang Liu, Hua-Feng Kang, An-An Yin, Shu-Qun Zhang et al.
CNS Neuroscience & Therapeutics, 2023,
DOI : https://doi.org/10.1111/cns.14465
Pubmed : 37830163
 Reprint request: Subject to availability
56 - 
Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples
L. Mary, M. Fradin, L. Pasquier, C. Quélin, P. Loget, M. Le Lous, G. Le Bouar, S Nivot-Adamiak, A. Lokchine, Christèle Dubourg, V. Jauffret, B. Nouyou, C Henry, E. Launay, S. Odent et al.
European Journal of Medical Genetics, 2023, 66 (6), pp.104748.
DOI : https://doi.org/10.1016/j.ejmg.2023.104748
Pubmed : 36948288
PDF file
 Reprint request: Subject to availability
57 - 
Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing
Laura Mary, Delphine Leclerc, Audrey Labalme, Pascale Bellaud, Séverine Mazaud-Guittot, Stéphane Dreano, Bertrand Evrard, Antoine Bigand, Aurélie Cauchoix, Philippe Loget, Anna Lokchine, Laurence Cluzeau, David Gilot, Marc-Antoine Belaud-Rotureau, Sylvie Jaillard et al.
Genes, 2023, 14 (2), pp.273.
DOI : https://doi.org/10.3390/genes14020273
Pubmed : 36833200
PDF file
 Reprint request: Subject to availability
58 - 
Classification of PRSS1 variants responsible for chronic pancreatitis: An expert perspective from the Franco-Chinese GREPAN Study Group
Emmanuelle Masson, Wen-Bin Zou, Na Pu, Vinciane Rebours, Emmanuelle Génin, Hao Wu, Jin-Huan Lin, Yuan-Chen Wang, Zhao-Shen Li, David Cooper, Claude Férec, Zhuan Liao, Jian-Min Chen, Thomas Grainville, Astrid Lièvre et al.
Pancreatology, 2023, 23 (5), pp.491-506.
DOI : https://doi.org/10.1016/j.pan.2023.04.004
PDF file
 Reprint request: Subject to availability
59 - 
Update of the UMD-VHL database: classification of 164 challenging variants based on genotype–phenotype correlation among 605 entries Mise à jour de la base de données UMD-VHL : classification de 164 variants difficiles sur la base de la corrélation génotype-phénotype parmi 605 entrées
Gregory Mougel, Amira Mohamed, Nelly Burnichon, Sophie Giraud, Pascal Pigny, Brigitte Bressac-de Paillerets, Delphine Mirebeau-Prunier, Alexandre Buffet, Frédérique Savagner, Pauline Romanet, Yannick Arlot-Bonnemains, Betty Gardie, Anne-Paule Gimenez-Roqueplo, Christophe Beroud, Stephane Richard et al.
Update of the UMD-VHL database: classification of 164 challenging variants based on genotype–phenotype correlation among 605 entries: Cancer genetics. Journal of Medical Genetics, In press, J Med Chem,
DOI : https://doi.org/10.1136/jmg-2023-109550
Pubmed : 37979962
PDF file
 Reprint request: Subject to availability
60 - 
Editorial: Chromatin structure and function
Laxmi Narayan Mishra, Christophe Thiriet, Dileep Vasudevan
Frontiers in Genetics, 2023, 14,
DOI : https://doi.org/10.3389/fgene.2023.1140534
Pubmed : 36824440
PDF file
 Reprint request: Subject to availability


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