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Julien Bryois
Julien Bryois
在 roche.com 的电子邮件经过验证
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Single-nucleus and spatial transcriptomic profiling of human temporal cortex and white matter reveals novel associations with AD pathology
P Gaur, J Bryois, D Calini, L Foo, JJM Hoozemans, D Malhotra, V Menon
bioRxiv, 2024
2024
Machine learning methods for predicting guide RNA effects in CRISPR epigenome editing experiments
W Mu, T Luo, A Barrera, LR Bounds, TS Klann, M Weele, J Bryois, ...
bioRxiv, 2024.04. 18.590188, 2024
2024
Leveraging polygenic enrichments for risk gene prioritisation from GWAS summary statistics
T Dupuis, W Macnair, A Brown, M Ebeling, J Bryois
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 661-661, 2024
2024
scMetaBrain: federated single-cell consortium for cell-type specific eQTL analysis of neurological disease variants
M Vochteloo, R Oelen, D Neavin, R Warmerdam, U Vosa, M Korshevniuk, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 726-727, 2024
2024
Cellular and molecular mapping of human adult hippocampal neurogenesis in Alzheimer’s disease
G Tosoni, A Penning, D Ayyildiz, S Snoeck, SK Poovathingal, K Davie, ...
Alzheimer's & Dementia 19, e074691, 2023
2023
A structured evaluation of cryopreservation in generating single-cell transcriptomes from cerebrospinal fluid
H Touil, T Roostaei, D Calini, C Diaconu, S Epstein, C Raposo, ...
Cell Reports Methods 3 (7), 2023
22023
Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability
X Wang, A Walker, JA Revez, G Ni, MJ Adams, AM McIntosh, NR Wray, ...
The American Journal of Human Genetics 110 (7), 1207-1215, 2023
82023
Mapping human adult hippocampal neurogenesis with single-cell transcriptomics: Reconciling controversy or fueling the debate?
G Tosoni, D Ayyildiz, J Bryois, W Macnair, CP Fitzsimons, PJ Lucassen, ...
Neuron 111 (11), 1714-1731. e3, 2023
232023
Single-cell Mendelian randomisation identifies cell-type specific genetic effects on human brain disease and behaviour
A Haglund, V Zuber, Y Yang, M Abouzeid, R Feleke, JH Ko, A Nott, ...
bioRxiv, 2022.11. 28.517913, 2022
52022
Dysregulation of synaptic and developmental transcriptomic/proteomic profiles upon depletion of MUNC18-1
AA Van Berkel, F Koopmans, MA Gonzalez-Lozano, HCA Lammertse, ...
Eneuro 9 (6), 2022
32022
Single nuclei RNA sequencing stratifies multiple sclerosis patients into three distinct white matter glia responses
D Calini, W McNair, E Agirre, J Bryois, S Jaekel, P Kukanja, N Stokar, ...
MULTIPLE SCLEROSIS JOURNAL 28 (3_ SUPPL), 504-505, 2022
2022
Cell-type specific cis-eQTLs in eight brain cell-types identify novel risk genes for human brain disorders
J Bryois, D Calini, W MacNair, L Foo, E Urich, W Ortmann, VA Iglesias, ...
Nature Neuroscience, 2022
22022
Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders
J Bryois, D Calini, W Macnair, L Foo, E Urich, W Ortmann, VA Iglesias, ...
Nature neuroscience 25 (8), 1104-1112, 2022
1132022
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ...
Nature 604 (7906), 502-508, 2022
12022022
Single nuclei RNAseq stratifies multiple sclerosis patients into distinct white matter glial responses
W Macnair, D Calini, E Agirre, J Bryois, S Jäkel, P Kukanja, N Stokar, V Ott, ...
BioRxiv, 2022.04. 06.487263, 2022
122022
Identifying the common genetic basis of antidepressant response
O Pain, K Hodgson, V Trubetskoy, S Ripke, VS Marshe, MJ Adams, ...
Biological psychiatry global open science 2 (2), 115-126, 2022
472022
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Biological psychiatry 91 (3), 313-327, 2022
1452022
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (vol 11, 1872, 2021)
M Halvorsen, R Huh, N Oskolkov, J Wen, S Netotea, P Giusti-Rodriguez, ...
NATURE COMMUNICATIONS 13 (1), 2022
2022
Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia
M Halvorsen, R Huh, N Oskolkov, J Wen, S Netotea, P Giusti-Rodriguez, ...
Nature Communications 13, 2022
12022
Sex-dependent shared and nonshared genetic architecture across mood and psychotic disorders
GAM Blokland, J Grove, CY Chen, C Cotsapas, S Tobet, R Handa, ...
Biological psychiatry 91 (1), 102-117, 2022
812022
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