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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.
Artículo
en Inglés
| MEDLINE | ID: mdl-29474918
2.
Pleiotropic loci for cannabis use disorder severity in multi-ancestry high-risk populations.
Mol Cell Neurosci
; 125: 103852, 2023 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-37061172
3.
SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection.
Brief Bioinform
; 22(3)2021 05 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-32591778
4.
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction.
Prenat Diagn
; 42(5): 567-573, 2022 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-34265090
5.
Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing.
BMC Bioinformatics
; 22(1): 374, 2021 Jul 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-34284719
6.
Projected t-SNE for batch correction.
Bioinformatics
; 36(11): 3522-3527, 2020 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32176244
7.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-32027075
8.
Whole genome sequence study of cannabis dependence in two independent cohorts.
Addict Biol
; 23(1): 461-473, 2018 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28111843
9.
Integration of expression quantitative trait loci and pleiotropy identifies a novel psoriasis susceptibility gene, PTPN1.
J Gene Med
; 19(1-2)2017 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-27976820
10.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-28815635
11.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-27663783
12.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-29762926
13.
Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations.
Twin Res Hum Genet
; 20(3): 197-207, 2017 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28262088
14.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-29192581
15.
Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population.
Am J Med Genet B Neuropsychiatr Genet
; 174(4): 435-450, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28436151
16.
Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence.
Am J Med Genet B Neuropsychiatr Genet
; 174(5): 557-567, 2017 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-28440896
17.
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.
Genet Med
; 18(5): 467-75, 2016 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26270767
18.
Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population.
J Psychiatry Neurosci
; 41(6): 413-421, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27091718
19.
The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review.
Am J Med Genet A
; 167A(9): 2176-81, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-25920937
20.
Variants Near CCK Receptors are Associated With Electrophysiological Responses to Pre-pulse Startle Stimuli in a Mexican American Cohort.
Twin Res Hum Genet
; 18(6): 727-37, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26608796