Detalhe da pesquisa
1.
Distinct molecular profiles of skull bone marrow in health and neurological disorders.
Cell
; 186(17): 3706-3725.e29, 2023 08 17.
Artigo
Inglês
| MEDLINE | ID: mdl-37562402
2.
KBTBD4-mediated reduction of MYC is critical for hematopoietic stem cell expansion upon UM171 treatment.
Blood
; 143(10): 882-894, 2024 Mar 07.
Artigo
Inglês
| MEDLINE | ID: mdl-38207291
3.
Continued dysfunction of capillary pericytes promotes no-reflow after experimental stroke in vivo.
Brain
; 147(3): 1057-1074, 2024 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38153327
4.
Nonclassical Nucleation and Crystallization of LiNbO3 Nanoparticles from the Aqueous Solvothermal Alkoxide Route.
Small
; 20(13): e2306417, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-37968253
5.
Pathways linking aging and atheroprotection in Mif-deficient atherosclerotic mice.
FASEB J
; 37(3): e22752, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36794636
6.
Global characterization of copy number variants in epilepsy patients from whole genome sequencing.
PLoS Genet
; 14(4): e1007285, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29649218
7.
Testing association of rare genetic variants with resistance to three common antiseizure medications.
Epilepsia
; 61(4): 657-666, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32141622
8.
Human copy number variants are enriched in regions of low mappability.
Nucleic Acids Res
; 46(14): 7236-7249, 2018 08 21.
Artigo
Inglês
| MEDLINE | ID: mdl-30137632
9.
Impact of Paternal Age at Conception on Human Health.
Clin Chem
; 65(1): 146-152, 2019 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30602478
10.
Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Clin Genet
; 96(3): 199-206, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31038196
11.
Optical porosimetry of weakly absorbing porous materials.
Opt Express
; 27(16): 22983-22993, 2019 Aug 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31510583
12.
Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males.
Am J Med Genet B Neuropsychiatr Genet
; 180(6): 335-340, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-30378261
13.
UBAP2L is amplified in a large subset of human lung adenocarcinoma and is critical for epithelial lung cell identity and tumor metastasis.
FASEB J
; 31(11): 5012-5018, 2017 11.
Artigo
Inglês
| MEDLINE | ID: mdl-28754713
14.
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.
Hum Mol Genet
; 24(5): 1363-73, 2015 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-25343993
15.
Genome-wide association study in essential tremor identifies three new loci.
Brain
; 139(Pt 12): 3163-3169, 2016 12.
Artigo
Inglês
| MEDLINE | ID: mdl-27797806
16.
Polygenic risk score for atopic dermatitis in the Canadian population.
J Allergy Clin Immunol
; 147(1): 406-409, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32439431
17.
UBAP2L is a novel BMI1-interacting protein essential for hematopoietic stem cell activity.
Blood
; 124(15): 2362-9, 2014 Oct 09.
Artigo
Inglês
| MEDLINE | ID: mdl-25185265
18.
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans.
PLoS Genet
; 9(9): e1003815, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-24086152
19.
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
PLoS Genet
; 9(10): e1003864, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-24204291
20.
Exome sequencing identifies FUS mutations as a cause of essential tremor.
Am J Hum Genet
; 91(2): 313-9, 2012 Aug 10.
Artigo
Inglês
| MEDLINE | ID: mdl-22863194