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ATHAR KHALIL
ATHAR KHALIL
Verified email at case.edu
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Cited by
Cited by
Year
AutoDock and AutoDockTools for protein-ligand docking: beta-site amyloid precursor protein cleaving enzyme 1 (BACE1) as a case study
N El-Hachem, B Haibe-Kains, A Khalil, FH Kobeissy, G Nemer
Neuroproteomics: Methods and Protocols, 391-403, 2017
1172017
Thalidomide-revisited: are COVID-19 patients going to be the latest victims of yet another theoretical drug-repurposing?
A Khalil, A Kamar, G Nemer
Frontiers in immunology 11, 549261, 2020
502020
The Lebanese COVID-19 cohort; a challenge for the ABO blood group system
A Khalil, R Feghali, M Hassoun
Frontiers in Medicine 7, 585341, 2020
462020
A HAND to TBX5 explains the link between thalidomide and cardiac diseases
A Khalil, R Tanos, N El-Hachem, M Kurban, P Bouvagnet, F Bitar, ...
Scientific Reports 7 (1), 1416, 2017
322017
The digenic causality in familial hypercholesterolemia: Revising the genotype–phenotype correlations of the disease
A Kamar, A Khalil, G Nemer
Frontiers in Genetics 11, 572045, 2021
222021
TBX2 subfamily suppression in lung cancer pathogenesis: a high-potential marker for early detection
AA Khalil, S Sivakumar, FA San Lucas, T McDowell, W Lang, K Tabata, ...
Oncotarget 8 (40), 68230, 2017
212017
Epigenetic Suppression of the T-box Subfamily 2 (TBX2) in Human Non-Small Cell Lung Cancer
E Nehme, Z Rahal, A Sinjab, A Khalil, H Chami, G Nemer, H Kadara
International journal of molecular sciences 20 (5), 1159, 2019
192019
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans
G Nemer, N El‐Hachem, E Eid, L Hamie, T Bardawil, S Khalil, I El‐Rassy, ...
Clinical Genetics 98 (2), 116-125, 2020
172020
A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the …
A Khalil, C Al-Haddad, H Hariri, K Shibbani, F Bitar, M Kurban, G Nemer, ...
Frontiers in Cardiovascular Medicine 4, 58, 2017
162017
Questioning the sex-specific differences in the association of smoking on the survival rate of hospitalized COVID-19 patients
A Khalil, R Dhingra, J Al-Mulki, M Hassoun, N Alexis
PLoS One 16 (8), e0255692, 2021
142021
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes
A Khalil, B Dekmak, F Boulos, J Kantrowitz, A Spira, J Fujimoto, H Kadara, ...
Frontiers in Oncology 8, 482, 2018
142018
Founder mutation in N terminus of cardiac troponin I causes malignant hypertrophic cardiomyopathy
AC Fahed, G Nemer, FF Bitar, S Arnaout, AB Abchee, M Batrawi, A Khalil, ...
Circulation: Genomic and Precision Medicine 13 (5), 444-452, 2020
102020
A cautious note on thalidomide usage in cancer treatment: genetic profiling of the TBX2 sub-family gene expression is required
G Nemer, A Khalil
Drug Research 69 (09), 512-518, 2019
102019
Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases
MM Refaat, S Hassanieh, JA Ballout, P Zakka, M Hotait, A Khalil, F Bitar, ...
BMC Medical Genomics 12, 1-11, 2019
82019
Congenital heart disease in Syrian refugee children: the experience at a tertiary care center in a developing country
H Mostafa, M Rashed, M Azzo, A Tabbakh, O El Sedawi, HB Hussein, ...
Pediatric Cardiology 42, 1010-1017, 2021
52021
Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis
H Hariri, M Kurban, C Al-Haddad, AC Fahed, S Poladian, A Khalil, ...
Journal of Dermatological Science 92 (3), 237-244, 2018
52018
Weekly nowcasting of new COVID-19 cases using past viral load measurements
A Khalil, K Al Handawi, Z Mohsen, A Abdel Nour, R Feghali, ...
Viruses 14 (7), 1414, 2022
42022
Thalidomide-Revisited: Are COVID-19 Patients Going to Be the Latest Victims of Yet Another Theoretical Drug-Repurposing? Front Immunol. 2020; 11: 1248
A Khalil, A Kamar, G Nemer
42020
The potential oncogenic role of the RAS-like GTP-binding gene RIT1 in glioblastoma
A Khalil, G Nemer
Cancer Biomarkers 29 (4), 509-519, 2020
42020
Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
A Khalil, SB Karroum, R Barake, G Dunya, S Abou-Rizk, A Kamar, ...
BMC Medical Genetics 21, 1-8, 2020
32020
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