Detalhe da pesquisa
1.
Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly.
Cell
; 172(5): 897-909.e21, 2018 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29474918
2.
Ultrasound Blood-Brain Barrier Opening and Aducanumab in Alzheimer's Disease.
N Engl J Med
; 390(1): 55-62, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38169490
3.
TWO-SIGMA-G: a new competitive gene set testing framework for scRNA-seq data accounting for inter-gene and cell-cell correlation.
Brief Bioinform
; 23(3)2022 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35325048
4.
Pleiotropic loci for cannabis use disorder severity in multi-ancestry high-risk populations.
Mol Cell Neurosci
; 125: 103852, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37061172
5.
SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection.
Brief Bioinform
; 22(3)2021 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32591778
6.
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction.
Prenat Diagn
; 42(5): 567-573, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34265090
7.
Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing.
BMC Bioinformatics
; 22(1): 374, 2021 Jul 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34284719
8.
Projected t-SNE for batch correction.
Bioinformatics
; 36(11): 3522-3527, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32176244
9.
Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations.
Addict Biol
; 26(1): e12877, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32027075
10.
Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice.
Genet Med
; 22(8): 1426, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32555414
11.
An approach to integrating exome sequencing for fetal structural anomalies into clinical practice.
Genet Med
; 22(5): 954-961, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31974414
12.
Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity.
Alcohol Clin Exp Res
; 42(12): 2349-2359, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30276832
13.
Whole genome sequence study of cannabis dependence in two independent cohorts.
Addict Biol
; 23(1): 461-473, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28111843
14.
Integration of expression quantitative trait loci and pleiotropy identifies a novel psoriasis susceptibility gene, PTPN1.
J Gene Med
; 19(1-2)2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27976820
15.
Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Genet Med
; 19(11): 1207-1216, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28518170
16.
Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence.
Alcohol Clin Exp Res
; 41(10): 1695-1704, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28815635
17.
A Novel Tobacco Use Phenotype Suggests the 15q25 and 19q13 Loci May be Differentially Associated With Cigarettes per Day and Tobacco-Related Problems.
Nicotine Tob Res
; 19(4): 426-434, 2017 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27663783
18.
Genetic Complexity of Mitral Valve Prolapse Revealed by Clinical and Genetic Evaluation of a Large Family.
J Heart Valve Dis
; 26(5): 569-580, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29762926
19.
Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations.
Twin Res Hum Genet
; 20(3): 197-207, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28262088
20.
Genetic Influences on Evening Preference Overlap with Those for Bipolar Disorder in a Sample of Mexican Americans and American Indians.
Twin Res Hum Genet
; 20(6): 499-510, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29192581