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1.
Somatic genomic changes in single Alzheimer's disease neurons.
Nature
; 604(7907): 714-722, 2022 04.
Article
in English
| MEDLINE | ID: mdl-35444284
2.
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features.
Genet Med
; 23(6): 1158-1162, 2021 06.
Article
in English
| MEDLINE | ID: mdl-33531666
3.
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.
bioRxiv
; 2023 Nov 06.
Article
in English
| MEDLINE | ID: mdl-37986891
4.
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Nat Neurosci
; 24(2): 176-185, 2021 02.
Article
in English
| MEDLINE | ID: mdl-33432195
5.
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions.
Neuron
; 109(20): 3239-3251.e7, 2021 10 20.
Article
in English
| MEDLINE | ID: mdl-34478631
6.
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Nat Neurosci
; 26(10): 1833, 2023 Oct.
Article
in English
| MEDLINE | ID: mdl-37644260
7.
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Nat Neurosci
; 24(4): 611, 2021 Apr.
Article
in English
| MEDLINE | ID: mdl-33753946
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