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Yann Loe-Mie
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Two independent modes of chromatin organization revealed by cohesin removal
W Schwarzer, N Abdennur, A Goloborodko, A Pekowska, G Fudenberg, ...
Nature 551 (7678), 51-56, 2017
10582017
Cnidarian cell type diversity and regulation revealed by whole-organism single-cell RNA-Seq
A Sebé-Pedrós, B Saudemont, E Chomsky, F Plessier, MP Mailhé, ...
Cell 173 (6), 1520-1534. e20, 2018
2922018
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome
AM Lepagnol-Bestel, A Zvara, G Maussion, F Quignon, B Ngimbous, ...
Human molecular genetics 18 (8), 1405-1414, 2009
1562009
Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors
S Haziza, N Mohan, Y Loe-Mie, AM Lepagnol-Bestel, S Massou, ...
Nature nanotechnology 12 (4), 322-328, 2017
1412017
A cross-talk between CAR T cell subsets and the tumor microenvironment is essential for sustained cytotoxic activity
M Boulch, M Cazaux, Y Loe-Mie, R Thibaut, B Corre, F Lemaître, ...
Science immunology 6 (57), eabd4344, 2021
1232021
SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution
Y Loe-Mie, AM Lepagnol-Bestel, G Maussion, A Doron-Faigenboim, ...
Human molecular genetics 19 (14), 2841-2857, 2010
1032010
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism
G Maussion, J Carayol, AM Lepagnol-Bestel, F Tores, Y Loe-Mie, ...
Human molecular genetics 17 (16), 2541-2551, 2008
912008
H Haering C, Mirny L, Spitz F. 2017. Two independent modes of chromatin organization revealed by cohesin removal
W Schwarzer, N Abdennur, A Goloborodko, A Pekowska, G Fudenberg, ...
Nature 551 (7678), 51-56, 0
48
instaGRAAL: chromosome-level quality scaffolding of genomes using a proximity ligation-based scaffolder
L Baudry, N Guiglielmoni, H Marie-Nelly, A Cormier, M Marbouty, K Avia, ...
Genome Biology 21, 1-22, 2020
432020
HENA, heterogeneous network-based data set for Alzheimer’s disease
E Sügis, J Dauvillier, A Leontjeva, P Adler, V Hindie, T Moncion, V Collura, ...
Scientific data 6 (1), 151, 2019
402019
Somatostatin-IRES-Cre mice: between knockout and wild-type?
C Viollet, A Simon, V Tolle, A Labarthe, D Grouselle, Y Loe-Mie, ...
Frontiers in endocrinology 8, 131, 2017
302017
BIN1 genetic risk factor for Alzheimer is sufficient to induce early structural tract alterations in entorhinal cortex-dentate gyrus pathway and related hippocampal multi-scale …
R Daudin, D Marechal, Q Wang, Y Abe, N Bourg, M Sartori, Y Loe-Mie, ...
BioRxiv, 437228, 2018
142018
Primate-accelerated evolutionary genes: novel routes to drug discovery in psychiatric disorders
JM Moalic, Y Le Strat, AM Lepagnol-Bestel, N Ramoz, Y Loe-Mie, ...
Current medicinal chemistry 17 (13), 1300-1316, 2010
112010
Transient suppression of SUMOylation in embryonic stem cells generates embryo-like structures
JC Cossec, T Traboulsi, S Sart, Y Loe-Mie, M Guthmann, IA Hendriks, ...
Cell Reports 42 (4), 2023
42023
Chr21 protein–protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer’s disease
J Viard, Y Loe-Mie, R Daudin, M Khelfaoui, C Plancon, A Boland, ...
Life science alliance 5 (12), 2022
32022
A major role for CD4+ T cells in driving cytokine release syndrome during CAR T cell therapy
M Boulch, M Cazaux, A Cuffel, M Ruggiu, V Allain, B Corre, Y Loe-Mie, ...
Cell Reports Medicine 4 (9), 2023
22023
Single cell atlas of Xenoturbella bocki highlights the limited cell-type complexity of a non-vertebrate deuterostome lineage
HE Robertson, A Sebe-Pedros, B Saudemont, Y Loe Mie, A Zakrzewski, ...
Biorxiv, 2022.08. 18.504214, 2022
22022
TATTOO-seq delineates spatial and cell type–specific regulatory programs in the developing limb
S Bastide, E Chomsky, B Saudemont, Y Loe-Mie, S Schmutz, S Novault, ...
Science advances 8 (50), eadd0695, 2022
12022
AUTS2 gene dosage affects synaptic AMPA receptors via a local dendritic spine AUTS2-TTC3-AKT-mTORC1 signaling dysfunction
AM Lepagnol-Bestel, A Duchon, J Viard, M Kvajo, R Daudin, M Khelfaoui, ...
bioRxiv, 2022.12. 01.518705, 2022
12022
Multi-hit autism genomic architecture evidenced from consanguineous families with involvement of FEZF2 and mutations in high-risk genes
M Bensaid, Y Loe-Mie, AM Lepagnol-Bestel, W Han, G Santpere, T Klarić, ...
bioRxiv, 759480, 2019
12019
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