Detalhe da pesquisa
1.
Inference of putative cell-type-specific imprinted regulatory elements and genes during human neuronal differentiation.
Hum Mol Genet
; 32(3): 402-416, 2023 01 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35994039
2.
Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis.
Am J Hum Genet
; 108(9): 1647-1668, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34416157
3.
Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain.
Science
; 384(6698): eadh0829, 2024 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38781368
4.
Genetic variants for head size share genes and pathways with cancer.
Cell Rep Med
; 5(5): 101529, 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38703765
5.
Inferring cell-type-specific causal gene regulatory networks during human neurogenesis.
Genome Biol
; 24(1): 130, 2023 05 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37254169
6.
Genetics of cell-type-specific post-transcriptional gene regulation during human neurogenesis.
bioRxiv
; 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37693528
7.
MicroRNA-eQTLs in the developing human neocortex link miR-4707-3p expression to brain size.
Elife
; 122023 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36629315
8.
Cellular Genome-wide Association Study Identifies Common Genetic Variation Influencing Lithium-Induced Neural Progenitor Proliferation.
Biol Psychiatry
; 93(1): 8-17, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36307327
9.
Wnt activity reveals context-specific genetic effects on gene regulation in neural progenitors.
bioRxiv
; 2023 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36798360
10.
Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brain.
medRxiv
; 2023 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36945630
11.
Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation.
Nat Neurosci
; 24(7): 941-953, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34017130
12.
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.
Transl Psychiatry
; 10(1): 265, 2020 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32747698
13.
Sexual dimorphism of microglia and synapses during mouse postnatal development.
Dev Neurobiol
; 78(6): 618-626, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29239126