Detalhe da pesquisa
1.
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations.
Hum Mol Genet
; 32(6): 907-916, 2023 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36168886
2.
Integrated epigenome, whole genome sequence and metabolome analyses identify novel multi-omics pathways in type 2 diabetes: a Middle Eastern study.
BMC Med
; 21(1): 347, 2023 09 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37679740
3.
Genome-wide association study identifies genetic variants which predict the response of bone mineral density to teriparatide therapy.
Ann Rheum Dis
; 82(7): 985-991, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36941031
4.
Identification of a Gene Panel Predictive of Triple-Negative Breast Cancer Response to Neoadjuvant Chemotherapy Employing Transcriptomic and Functional Validation.
Int J Mol Sci
; 23(18)2022 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36142814
5.
The Genetic Spectrum of Maturity-Onset Diabetes of the Young (MODY) in Qatar, a Population-Based Study.
Int J Mol Sci
; 24(1)2022 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36613572
6.
Circulating MicroRNA Profiling Identifies Distinct MicroRNA Signatures in Acute Ischemic Stroke and Transient Ischemic Attack Patients.
Int J Mol Sci
; 24(1)2022 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36613546
7.
Identification of Novel Circulating miRNAs in Patients with Acute Ischemic Stroke.
Int J Mol Sci
; 23(6)2022 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35328807
8.
Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.
Ann Rheum Dis
; 77(3): 378-385, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29170203
9.
Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone.
Hum Mol Genet
; 24(11): 3286-95, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25701875
10.
Assessing the contribution of 38 genetic loci to the risk of type 2 diabetes in the Saudi Arabian Population.
Clin Endocrinol (Oxf)
; 80(4): 532-7, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23448427
11.
Genetics of Paget's disease of bone.
Curr Osteoporos Rep
; 12(3): 263-71, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24988994
12.
Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus.
BMC Med Genomics
; 17(1): 115, 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38685053
13.
The genetic landscape of autism spectrum disorder in the Middle Eastern population.
Front Genet
; 15: 1363849, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38572415
14.
Identification of PCSK9-like human gene knockouts using metabolomics, proteomics, and whole-genome sequencing in a consanguineous population.
Cell Genom
; 3(1): 100218, 2023 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36777185
15.
Transcriptome profiling and network enrichment analyses identify subtype-specific therapeutic gene targets for breast cancer and their microRNA regulatory networks.
Cell Death Dis
; 14(7): 415, 2023 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37438342
16.
Epigenetic DNA Methylation Signatures Associated With the Severity of Paget's Disease of Bone.
Front Cell Dev Biol
; 10: 903612, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35769265
17.
The Paget's disease of bone risk gene PML is a negative regulator of osteoclast differentiation and bone resorption.
Dis Model Mech
; 15(4)2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35229101
18.
The Prevalence and Genetic Spectrum of Familial Hypercholesterolemia in Qatar Based on Whole Genome Sequencing of 14,000 Subjects.
Front Genet
; 13: 927504, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35910211
19.
Ratios of Acetaminophen Metabolites Identify New Loci of Pharmacogenetic Relevance in a Genome-Wide Association Study.
Metabolites
; 12(6)2022 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35736429
20.
Metabolic and proteomic signatures of type 2 diabetes subtypes in an Arab population.
Nat Commun
; 13(1): 7121, 2022 11 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36402758