Search details
1.
A cross-disorder dosage sensitivity map of the human genome.
Cell
; 185(16): 3041-3055.e25, 2022 08 04.
Article
in English
| MEDLINE | ID: mdl-35917817
2.
DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data.
PLoS Comput Biol
; 16(4): e1007522, 2020 04.
Article
in English
| MEDLINE | ID: mdl-32282793
3.
Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci.
Mult Scler
; 24(14): 1815-1824, 2018 12.
Article
in English
| MEDLINE | ID: mdl-28933650
4.
PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population.
PLoS Comput Biol
; 11(3): e1004139, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25735005
5.
Genome-wide association study of lung function phenotypes in a founder population.
J Allergy Clin Immunol
; 133(1): 248-55.e1-10, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-23932459
6.
Effects of Smilaxchinoside A and Smilaxchinoside C, two steroidal glycosides from Smilax riparia, on hyperuricemia in a mouse model.
Phytother Res
; 28(12): 1822-8, 2014 Dec.
Article
in English
| MEDLINE | ID: mdl-25098402
7.
Physical Activity and Incident Obesity Across the Spectrum of Genetic Risk for Obesity.
JAMA Netw Open
; 7(3): e243821, 2024 Mar 04.
Article
in English
| MEDLINE | ID: mdl-38536175
8.
Integrating Electronic Health Records and Polygenic Risk to Identify Genetically Unrelated Comorbidities of Schizophrenia That May Be Modifiable.
Biol Psychiatry Glob Open Sci
; 4(3): 100297, 2024 May.
Article
in English
| MEDLINE | ID: mdl-38645405
9.
Interoperability of phenome-wide multimorbidity patterns: a comparative study of two large-scale EHR systems.
medRxiv
; 2024 May 27.
Article
in English
| MEDLINE | ID: mdl-38585743
10.
Genome-Wide Association Study of Treatment-Resistant Depression: Shared Biology With Metabolic Traits.
Am J Psychiatry
; : appiajp20230247, 2024 May 15.
Article
in English
| MEDLINE | ID: mdl-38745458
11.
Quantifying physical activity needed to mitigate genetic risk for obesity.
Res Sq
; 2023 Jun 08.
Article
in English
| MEDLINE | ID: mdl-37333237
12.
Identifying modifiable comorbidities of schizophrenia by integrating electronic health records and polygenic risk.
medRxiv
; 2023 Jun 05.
Article
in English
| MEDLINE | ID: mdl-37333378
13.
Evaluating the impact of modeling choices on the performance of integrated genetic and clinical models.
medRxiv
; 2023 Nov 01.
Article
in English
| MEDLINE | ID: mdl-37961557
14.
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies.
Cell Genom
; 3(4): 100277, 2023 Apr 12.
Article
in English
| MEDLINE | ID: mdl-37082147
15.
Identity by descent estimation with dense genome-wide genotype data.
Genet Epidemiol
; 35(6): 557-67, 2011 Sep.
Article
in English
| MEDLINE | ID: mdl-21769932
16.
Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing.
Nat Med
; 27(6): 1097-1104, 2021 06.
Article
in English
| MEDLINE | ID: mdl-34083811
17.
Genome-wide evaluation for quantitative trait loci under the variance component model.
Genetica
; 138(9-10): 1099-109, 2010 Oct.
Article
in English
| MEDLINE | ID: mdl-20835884
18.
Functional annotation of rare structural variation in the human brain.
Nat Commun
; 11(1): 2990, 2020 06 12.
Article
in English
| MEDLINE | ID: mdl-32533064
19.
Using matrix of thresholding partial correlation coefficients to infer regulatory network.
Biosystems
; 91(1): 158-65, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-17919808
20.
Editorial: Statistical methods, computing, and resources for genome-wide association studies, Volume II.
Front Genet
; 13: 1040022, 2022.
Article
in English
| MEDLINE | ID: mdl-36338957