Detalhe da pesquisa
1.
Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior.
Cell
; 167(2): 341-354.e12, 2016 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27667684
2.
Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex.
Cell
; 166(5): 1147-1162.e15, 2016 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-27565344
3.
Evolutionary Changes in Transcriptional Regulation: Insights into Human Behavior and Neurological Conditions.
Annu Rev Neurosci
; 41: 185-206, 2018 07 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29986162
4.
Pathologic characterization of canine multiple system degeneration in the Ibizan hound.
Vet Pathol
; 59(1): 132-137, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34490804
5.
Polymicrogyria is Associated With Pathogenic Variants in PTEN.
Ann Neurol
; 88(6): 1153-1164, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32959437
6.
Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial.
Epilepsia
; 62(6): 1416-1428, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33949696
7.
Co-segregation of sex chromosomes in the male black widow spider Latrodectus mactans (Araneae, Theridiidae).
Chromosoma
; 126(5): 645-654, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28233057
8.
Identification of a Candidate Mutation in the COL1A2 Gene of a Chow Chow With Osteogenesis Imperfecta.
J Hered
; 109(3): 308-314, 2018 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29036614
9.
TMEM184b Promotes Axon Degeneration and Neuromuscular Junction Maintenance.
J Neurosci
; 36(17): 4681-9, 2016 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27122027
10.
Nutritional programming of accelerated puberty in heifers: alterations in DNA methylation in the arcuate nucleus.
Biol Reprod
; 96(1): 174-184, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28395339
11.
Prevention of vincristine-induced peripheral neuropathy by genetic deletion of SARM1 in mice.
Brain
; 139(Pt 12): 3092-3108, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27797810
12.
Identification of copy number variants in horses.
Genome Res
; 22(5): 899-907, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22383489
13.
Dock1 acts cell-autonomously in Schwann cells to regulate the development, maintenance, and repair of peripheral myelin.
bioRxiv
; 2023 Oct 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37961336
14.
Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk.
medRxiv
; 2023 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37790480
15.
Somatic Mosaicism in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Reveals Widespread Degeneration from Focal Mutations.
bioRxiv
; 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38077003
16.
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.
bioRxiv
; 2023 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37986891
17.
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.
JAMA Neurol
; 80(9): 980-988, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37486637
18.
Whole-genome sequencing and genetic variant analysis of a Quarter Horse mare.
BMC Genomics
; 13: 78, 2012 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22340285
19.
Rates and Patterns of Clonal Oncogenic Mutations in the Normal Human Brain.
Cancer Discov
; 12(1): 172-185, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34389641
20.
Landmarks of human embryonic development inscribed in somatic mutations.
Science
; 371(6535): 1249-1253, 2021 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33737485