Detalhe da pesquisa
1.
Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.
Am J Hum Genet
; 110(4): 575-591, 2023 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37028392
2.
Elevated Levels of the Cytokine LIGHT in Pediatric Crohn's Disease.
J Immunol
; 210(5): 590-594, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36688686
3.
Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing.
Hum Mol Genet
; 31(22): 3769-3776, 2022 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35642741
4.
Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes.
J Hepatol
; 79(6): 1385-1395, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37572794
5.
DeepCNV: a deep learning approach for authenticating copy number variations.
Brief Bioinform
; 22(5)2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33429424
6.
Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients.
Mol Psychiatry
; 27(3): 1469-1478, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34997195
7.
Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population.
Respir Res
; 23(1): 116, 2022 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35524249
8.
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB gene.
Am J Med Genet A
; 188(2): 618-623, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34636138
9.
MONTAGE: a new tool for high-throughput detection of mosaic copy number variation.
BMC Genomics
; 22(1): 133, 2021 Feb 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33627065
10.
Association of novel rare coding variants with juvenile idiopathic arthritis.
Ann Rheum Dis
; 80(5): 626-631, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33408077
11.
Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters.
Int J Mol Sci
; 22(7)2021 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33805976
12.
Common variants at 5q33.1 predispose to migraine in African-American children.
J Med Genet
; 55(12): 831-836, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30266756
13.
Leveraging electronic health records to assess the role of ADRB2 single nucleotide polymorphisms in predicting exacerbation frequency in asthma patients.
Pharmacogenet Genomics
; 28(11): 256-259, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30334910
14.
Identification of Four Novel Loci in Asthma in European American and African American Populations.
Am J Respir Crit Care Med
; 195(4): 456-463, 2017 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27611488
15.
Genetic correlations among psychiatric and immune-related phenotypes based on genome-wide association data.
Am J Med Genet B Neuropsychiatr Genet
; 177(7): 641-657, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30325587
16.
Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy.
Hum Mutat
; 38(5): 507-510, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28150392
17.
Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy.
J Immunol
; 195(4): 1599-607, 2015 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26188062
18.
The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth.
Neuroimage
; 124(Pt B): 1115-1119, 2016 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25840117
19.
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Hum Mol Genet
; 22(7): 1457-64, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23263863
20.
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.
Hum Mol Genet
; 22(12): 2529-38, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23446634