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.
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
3.
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
4.
Polymicrogyria is Associated With Pathogenic Variants in PTEN.
Ann Neurol
; 88(6): 1153-1164, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32959437
5.
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
6.
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
7.
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
8.
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
9.
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
10.
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
11.
Landmarks of human embryonic development inscribed in somatic mutations.
Science
; 371(6535): 1249-1253, 2021 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33737485
12.
MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutations.
BMC Med Genomics
; 14(1): 47, 2021 02 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33579278
13.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-33432195
14.
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions.
Neuron
; 109(20): 3239-3251.e7, 2021 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34478631
15.
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder.
Sci Rep
; 10(1): 14045, 2020 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32820185
16.
Micromanipulation reveals an XO-XX sex determining system in the orb-weaving spider Neoscona arabesca (Walckenaer).
Hereditas
; 146(4): 180-2, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19765098
17.
Rare De Novo and Inherited Genes in Familial and Nonfamilial Pediatric Attention-Deficit/Hyperactivity Disorder.
JAMA Pediatr
; 178(1): 81-84, 2024 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37983059
18.
Recessive gene disruptions in autism spectrum disorder.
Nat Genet
; 51(7): 1092-1098, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31209396
19.
Postnatal changes in epigenetic modifications of neutrophils of foals are associated with increased ROS function and regulation of neutrophil function.
Dev Comp Immunol
; 87: 182-187, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29958850
20.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-37644260