Detalhe da pesquisa
1.
Biallelic variants in HECT E3 paralogs, HECTD4 and UBE3C, encoding ubiquitin ligases cause neurodevelopmental disorders that overlap with Angelman syndrome.
Genet Med
; 25(2): 100323, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36401616
2.
Prognostic value of TP53 expression and MGMT methylation in glioblastoma patients treated with temozolomide combined with other chemotherapies.
J Neurooncol
; 152(3): 541-549, 2021 May.
Artigo
Inglês
| MEDLINE | ID: mdl-33661424
3.
Leptin Protein Expression and Promoter Methylation in Ovarian Cancer: A Strong Prognostic Value with Theranostic Promises.
Int J Mol Sci
; 22(23)2021 Nov 28.
Artigo
Inglês
| MEDLINE | ID: mdl-34884678
4.
MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia.
BMC Med Genet
; 20(1): 144, 2019 08 20.
Artigo
Inglês
| MEDLINE | ID: mdl-31429705
5.
Membranous or Cytoplasmic HER2 Expression in Colorectal Carcinoma: Evaluation of Prognostic Value Using Both IHC & BDISH.
Cancer Invest
; 36(2): 129-140, 2018 Feb 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29504811
6.
Comprehensive molecular biomarker identification in breast cancer brain metastases.
J Transl Med
; 15(1): 269, 2017 12 29.
Artigo
Inglês
| MEDLINE | ID: mdl-29287594
7.
The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlights.
BMC Genomics
; 17(Suppl 9): 747, 2016 10 17.
Artigo
Inglês
| MEDLINE | ID: mdl-27766952
8.
Clinical significance of frequent somatic mutations detected by high-throughput targeted sequencing in archived colorectal cancer samples.
J Transl Med
; 14(1): 118, 2016 05 04.
Artigo
Inglês
| MEDLINE | ID: mdl-27146902
9.
Utilization of amplicon-based targeted sequencing panel for the massively parallel sequencing of sporadic hearing impairment patients from Saudi Arabia.
BMC Med Genet
; 17(Suppl 1): 67, 2016 Oct 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27766948
10.
Identification of novel genetic variations affecting osteoarthritis patients.
BMC Med Genet
; 17(Suppl 1): 68, 2016 Oct 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27766954
11.
Prognostic value of HER2 status in bladder transitional cell carcinoma revealed by both IHC and BDISH techniques.
BMC Cancer
; 16: 653, 2016 08 19.
Artigo
Inglês
| MEDLINE | ID: mdl-27539085
12.
Exome Sequencing of Normal and Isogenic Transformed Human Colonic Epithelial Cells (HCECs) Reveals Novel Genes Potentially Involved in the Early Stages of Colorectal Tumorigenesis.
BMC Genomics
; 16 Suppl 1: S8, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25923178
13.
Transcriptomics profiling study of breast cancer from Kingdom of Saudi Arabia revealed altered expression of Adiponectin and Fatty Acid Binding Protein4: Is lipid metabolism associated with breast cancer?
BMC Genomics
; 16 Suppl 1: S11, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25923423
14.
Characterization of familial breast cancer in Saudi Arabia.
BMC Genomics
; 16 Suppl 1: S3, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25923920
15.
Frequent methylation of the KLOTHO gene and overexpression of the FGFR4 receptor in invasive ductal carcinoma of the breast.
Tumour Biol
; 36(12): 9677-83, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26152288
16.
High fibroblast growth factor 19 (FGF19) expression predicts worse prognosis in invasive ductal carcinoma of breast.
Tumour Biol
; 35(3): 2817-24, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-24248542
17.
Identification of a novel SBF2 missense mutation associated with a rare case of thrombocytopenia using whole-exome sequencing.
J Thromb Thrombolysis
; 36(4): 501-6, 2013 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-23334996
18.
Five novel glucose-6-phosphate dehydrogenase deficiency haplotypes correlating with disease severity.
J Transl Med
; 10: 199, 2012 Sep 24.
Artigo
Inglês
| MEDLINE | ID: mdl-23006493
19.
A paediatric dysembryoplastic neuroepithelial tumour (DNET) with deregulated stem cell markers: a case report.
Transl Pediatr
; 11(6): 1040-1049, 2022 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-35800288
20.
The Diagnostic Value of Pan-Trk Expression to Detect Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusion in CNS Tumours: A Study Using Next-Generation Sequencing Platform.
Pathol Oncol Res
; 28: 1610233, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35295612