Detalhe da pesquisa
1.
Genome sequencing data analysis for rare disease gene discovery.
Brief Bioinform
; 23(1)2022 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34498682
2.
Therapeutic targeting of the TPX2/TTK network in colorectal cancer.
Cell Commun Signal
; 21(1): 265, 2023 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37770979
3.
Artificial Intelligence for the Prediction and Early Diagnosis of Pancreatic Cancer: Scoping Review.
J Med Internet Res
; 25: e44248, 2023 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37000507
4.
Seven novel glucose-6-phosphate dehydrogenase (G6PD) deficiency variants identified in the Qatari population.
Hum Genomics
; 15(1): 61, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34620237
5.
Genome sequencing unveils mutational landscape of the familial Mediterranean fever: Potential implications of IL33/ST2 signalling.
J Cell Mol Med
; 24(19): 11294-11306, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32853466
6.
Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome.
J Clin Immunol
; 40(6): 807-819, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32572726
7.
Integrated omics profiling reveals novel patterns of epigenetic programming in cancer-associated myofibroblasts.
Carcinogenesis
; 40(4): 500-512, 2019 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30624614
8.
Monoallelic expression in melanoma.
J Transl Med
; 17(1): 112, 2019 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30953523
9.
Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome.
BMC Genet
; 18(1): 3, 2017 01 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28103792
10.
Total proteome analysis identifies migration defects as a major pathogenetic factor in immunoglobulin heavy chain variable region (IGHV)-unmutated chronic lymphocytic leukemia.
Mol Cell Proteomics
; 14(4): 933-45, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25645933
11.
Distinct miRNA profiles in normal and gastric cancer myofibroblasts and significance in Wnt signaling.
Am J Physiol Gastrointest Liver Physiol
; 310(9): G696-704, 2016 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26939869
12.
Depletion of Human DNA in Spiked Clinical Specimens for Improvement of Sensitivity of Pathogen Detection by Next-Generation Sequencing.
J Clin Microbiol
; 54(4): 919-27, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26763966
13.
Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome: one clinical entity?
BMC Med Genet
; 17(1): 42, 2016 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27282200
14.
Forging the path to precision medicine in Qatar: a public health perspective on pharmacogenomics initiatives.
Front Public Health
; 12: 1364221, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38550311
15.
Identification of a potential DNA methyltransferase (DNMT) inhibitor.
J Biomol Struct Dyn
; : 1-15, 2023 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37424222
16.
Protegrin-2, a potential inhibitor for targeting SARS-CoV-2 main protease Mpro.
Comput Struct Biotechnol J
; 21: 3665-3671, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37576748
17.
Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing.
Front Psychiatry
; 14: 1251884, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38025430
18.
Erratum to: Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome.
BMC Genet
; 18(1): 9, 2017 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28148224
19.
Human leukocyte antigen class II gene diversity tunes antibody repertoires to common pathogens.
Front Immunol
; 13: 856497, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36003377
20.
A population study of clinically actionable genetic variation affecting drug response from the Middle East.
NPJ Genom Med
; 7(1): 10, 2022 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35169154