Detalhe da pesquisa
1.
Pleiotropy and genetically inferred causality linking multisite chronic pain to substance use disorders.
Mol Psychiatry
; 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38355787
2.
Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population.
Mol Psychiatry
; 2023 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36882501
3.
Investigation of convergent and divergent genetic influences underlying schizophrenia and alcohol use disorder.
Psychol Med
; 53(4): 1196-1204, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34231451
4.
Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci.
Mol Psychiatry
; 27(10): 3970-3979, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35879402
5.
Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank.
Genet Med
; 24(3): 601-609, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906489
6.
Ancestral haplotype reconstruction in endogamous populations using identity-by-descent.
PLoS Comput Biol
; 17(2): e1008638, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33635861
7.
Genetic liability for substance use associated with medical comorbidities in electronic health records of African- and European-ancestry individuals.
Addict Biol
; 27(1): e13099, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34611967
8.
Association of APOL1 Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program.
Circulation
; 140(12): 1031-1040, 2019 09 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31337231
9.
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.
Circulation
; 140(1): 42-54, 2019 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31216868
10.
Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways.
Kidney Int
; 97(5): 1032-1041, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32247630
11.
A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes.
Genet Med
; 22(1): 102-111, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31383942
12.
Differentiating Types of Self-Reported Alcohol Abstinence.
AIDS Behav
; 24(2): 655-665, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31435887
13.
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Genet Med
; 21(4): 816-825, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30190612
14.
Patterns and Correlates of Prescription Opioid Receipt Among US Veterans: A National, 18-Year Observational Cohort Study.
AIDS Behav
; 23(12): 3340-3349, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31317364
15.
Increased burden of deleterious variants in essential genes in autism spectrum disorder.
Proc Natl Acad Sci U S A
; 113(52): 15054-15059, 2016 12 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27956632
16.
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry.
JAMA
; 322(22): 2191-2202, 2019 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31821430
17.
Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate.
PLoS Genet
; 10(3): e1004229, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24625924
18.
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder.
BMC Genet
; 16: 27, 2015 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25887117
19.
Application of polygenic scores to a deeply phenotyped sample enriched for substance use disorders reveals extensive pleiotropy with psychiatric and medical traits.
medRxiv
; 2024 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38343859
20.
Divergent gene expression patterns in alcohol and opioid use disorders lead to consistent alterations in functional networks within the Dorsolateral Prefrontal Cortex.
bioRxiv
; 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38746311