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G. Nemer · SciRah

Researcher profile · Semantic Scholar

G. Nemer

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G. Nemer — researcher profile on SciRah

h-index: 30
Works: 153
Citations: 4,890

Most-cited papers

Retinoids: a journey from the molecular structures and mechanisms of action to clinical uses in dermatology and adverse effects
S. Khalil, T. Bardawil, Carla Stephan, N. Darwiche +4 more
2017Journal of dermatological treatment (Print)190 citations
Semantic Scholar
AutoDock and AutoDockTools for Protein-Ligand Docking: Beta-Site Amyloid Precursor Protein Cleaving Enzyme 1(BACE1) as a Case Study.
N. El-Hachem, Benjamin Haibe-Kains, Athar Khalil, F. Kobeissy +1 more
2017Methods in molecular biology173 citations
Semantic Scholar
BRCA1 and BRCA2 mutations in ethnic Lebanese Arab women with high hereditary risk breast cancer.
N. E. El Saghir, N. Zgheib, H. Assi, Katia E. Khoury +17 more
2015The Oncologist60 citations Open access
Semantic Scholar
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis
Y. Shigehara, S. Okuda, G. Nemer, A. Chedraoui +10 more
201754 citations Open access
Semantic Scholar
SuPAR, an emerging biomarker in kidney and inflammatory diseases
L. Hamie, G. Daoud, G. Nemer, T. Nammour +5 more
2018Postgraduate medical journal44 citations
Semantic Scholar
NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity
Ossama K. Abou Hassan, A. Fahed, Manal Batrawi, M. Arabi +6 more
2015Scientific Reports41 citations Open access
Semantic Scholar
Thalidomide-Revisited: Are COVID-19 Patients Going to Be the Latest Victims of Yet Another Theoretical Drug-Repurposing?
Athar Khalil, Amina Kamar, G. Nemer
2020Frontiers in Immunology40 citations Open access
Semantic Scholar
A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases
Athar Khalil, Rachel S. Tanos, N. El-Hachem, M. Kurban +3 more
2017Scientific Reports34 citations Open access
Semantic Scholar
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient
K. Kassab, Hadla Hariri, L. Gharibeh, A. Fahed +6 more
2015Molecular Genetics & Genomic Medicine28 citations Open access
Semantic Scholar
SLURP‐1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene
C. Bergqvist, H. Kadara, L. Hamie, G. Nemer +9 more
2018International Journal of Dermatology26 citations
Semantic Scholar
Linezolid Toxicity and Mitochondrial Susceptibility: A Novel Neurological Complication in a Lebanese Patient
Ossama K. Abou Hassan, Mohamad Karnib, R. El-Khoury, G. Nemer +2 more
2016Frontiers in Pharmacology25 citations Open access
Semantic Scholar
Three novel genes tied to mandibular prognathism in eastern Mediterranean families.
Pamela G. Genno, G. Nemer, Savo Bou Zeineddine, Anthony T. Macari +1 more
2019American Journal of Orthodontics and Dentofacial Orthopedics24 citations
Semantic Scholar
Identification of Several Mutations in ATP2C1 in Lebanese Families: Insight into the Pathogenesis of Hailey-Hailey Disease
Waed Btadini, Ossama K. Abou Hassan, D. Saadeh, O. Abbas +6 more
2015PLoS ONE22 citations Open access
Semantic Scholar
In Vitro Activity of Beauvericin against All Developmental Stages of Sarcoptes scabiei
C. Al Khoury, N. Nemer, G. Nemer, M. Kurban +3 more
2019Antimicrobial Agents and Chemotherapy21 citations Open access
Semantic Scholar
Epigenetic Suppression of the T-box Subfamily 2 (TBX2) in Human Non-Small Cell Lung Cancer
Eliana Nehme, Zahraa Rahal, Ansam Sinjab, Athar Khalil +3 more
2019International Journal of Molecular Sciences21 citations Open access
Semantic Scholar
Clinical and genetic characteristics of pulmonary arterial hypertension in Lebanon
Ossama K. Abou Hassan, Wiam Haidar, G. Nemer, H. Skouri +2 more
2018BMC Medical Genetics21 citations Open access
Semantic Scholar
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 +8 more
2020Clinical Genetics20 citations
Semantic Scholar
Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia
A. Fahed, K. Shibbani, Rabih R. Andary, M. Arabi +7 more
2017Cholesterol20 citations Open access
Semantic Scholar
The Digenic Causality in Familial Hypercholesterolemia: Revising the Genotype–Phenotype Correlations of the Disease
Amina Kamar, Athar Khalil, G. Nemer
2021Frontiers in Genetics19 citations Open access
Semantic Scholar
Variable expressivity and co‐occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy
A. Fahed, R. Khalaf, Rony H. Salloum, Rabih R. Andary +6 more
2016Molecular Genetics & Genomic Medicine19 citations Open access
Semantic Scholar
Beauvericin potentiates the activity of pesticides by neutralizing the ATP-binding cassette transporters in arthropods
C. Al Khoury, N. Nemer, G. Nemer
2021Scientific Reports18 citations Open access
Semantic Scholar
Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature
M. Chakhtoura, M. S. Ramnitz, N. Khoury, G. Nemer +7 more
2018Osteoporosis International18 citations
Semantic Scholar
Genome-Wide Gene Expression Changes in the Normal-Appearing Airway during the Evolution of Smoking-Associated Lung Adenocarcinoma
J. Kantrowitz, Ansam Sinjab, Li Xu, T. McDowell +13 more
2018Cancer Prevention Research18 citations Open access
Semantic Scholar
TBX2 subfamily suppression in lung cancer pathogenesis: a high-potential marker for early detection
Athar Khalil, S. Sivakumar, F. A. S. Lucas, T. McDowell +8 more
2017OncoTarget18 citations Open access
Semantic Scholar
In silico evidence of beauvericin antiviral activity against SARS-CoV-2
C. Al Khoury, Z. Bashir, S. Tokajian, N. Nemer +2 more
2021Comput. Biol. Medicine17 citations Open access
Semantic Scholar
Inherited Cardiomyopathies and the Role of Mutations in Non-coding Regions of the Genome
Oday Salman, H. El-Rayess, Charbel Abi Khalil, G. Nemer +1 more
2018Frontiers in Cardiovascular Medicine17 citations Open access
Semantic Scholar
Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy
A. Fahed, G. Nemer, F. Bitar, S. Arnaout +10 more
2020Circulation Genomic and Precision Medicine16 citations Open access
Semantic Scholar
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 Phenotypic Variations
Athar Khalil, Christiane Al-Haddad, Hadla Hariri, K. Shibbani +4 more
2017Frontiers in Cardiovascular Medicine16 citations Open access
Semantic Scholar
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis.
Y. Shigehara, S. Okuda, G. Nemer, A. Chedraoui +10 more
2016Human Molecular Genetics16 citations
Semantic Scholar
Integrative Transcriptome Analyses Empower the Anti-COVID-19 Drug Arsenal
N. El-Hachem, E. Eid, G. Nemer, G. Dbaibo +9 more
2020iScience15 citations Open access
Semantic Scholar
Understanding the phenotypic similarities between IFAP and Olmsted syndrome from a molecular perspective: the interaction of MBTPS2 and TRPV3
G. Nemer, R. Safi, F. Kreidieh, J. Usta +8 more
2017Archives of Dermatological Research15 citations
Semantic Scholar
Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous form
T. Bardawil, A. Rebeiz, M. Châabouni, J. El Halabi +8 more
2017EJD. European journal of dermatology15 citations
Semantic Scholar
Pharmacogenomics Variability of Lipid-Lowering Therapies in Familial Hypercholesterolemia
N. Hindi, Jamil Alenbawi, G. Nemer
2021Journal of Personalized Medicine14 citations Open access
Semantic Scholar
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes
Athar Khalil, Batoul Dekmak, F. Boulos, J. Kantrowitz +5 more
2018Frontiers in Oncology14 citations Open access
Semantic Scholar
The Genetic Pathways Underlying Immunotherapy in Dilated Cardiomyopathy
Ayat Kadhi, F. Mohammed, G. Nemer
2021Frontiers in Cardiovascular Medicine12 citations Open access
Semantic Scholar
Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
A. Hanna, S. Sanjad, R. Andary, G. Nemer +1 more
2018JDR Clinical & Translational Research11 citations Open access
Semantic Scholar
A X‐linked nonsense APOO/MIC26 variant causes a lethal mitochondrial disease with progeria‐like phenotypes
Leon Peifer-Weiß, M. Kurban, C. David, Melissa Lubeck +4 more
2023Clinical Genetics10 citations Open access
Semantic Scholar
Loss of ferrochelatase is protective against colon cancer cells: ferrochelatase a possible regulator of the long noncoding RNA H19.
R. Safi, Tala Mohsen‐Kanson, G. Nemer, Batoul Dekmak +7 more
2019Journal of Gastrointestinal Oncology10 citations Open access
Semantic Scholar
A Cautious Note on Thalidomide Usage in Cancer Treatment: Genetic Profiling of the TBX2 Sub-Family Gene Expression is Required
G. Nemer, Athar Khalil
2019Drug Research10 citations Open access
Semantic Scholar
Expression analysis of the genes involved in the virulence of Beauveria bassiana
C. Al Khoury, G. Nemer, J. Guillot, A. Abdel Nour +1 more
201910 citations
Semantic Scholar
Use of Topical Glycolic Acid Plus a Lovastatin-Cholesterol Combination Cream for the Treatment of Autosomal Recessive Congenital Ichthyoses
S. Khalil, T. Bardawil, Serena Saade, A. Chedraoui +6 more
2018JAMA dermatology10 citations Open access
Semantic Scholar
A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects
Amina Kamar, A. Fahed, K. Shibbani, N. El-Hachem +9 more
2017Frontiers in Genetics10 citations Open access
Semantic Scholar
Statins Modulate Cyclooxygenase‐2 and Microsomal Prostaglandin E Synthase‐1 in Human Hepatic Myofibroblasts
Charbel A. Mouawad, May F. Mrad, Ghewa A. El-Achkar, A. Abdul-Sater +4 more
2016Journal of Cellular Biochemistry10 citations
Semantic Scholar
Genetics of inherited cardiocutaneous syndromes: a review
T. Bardawil, S. Khalil, C. Bergqvist, O. Abbas +4 more
2016Open Heart10 citations Open access
Semantic Scholar
Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension
Ossama K. Abou Hassan, Wiam Haidar, M. Arabi, H. Skouri +3 more
2019BMC Medical Genetics9 citations Open access
Semantic Scholar
A novel mutation in the RSPO4 gene in a patient with autosomal recessive anonychia
S. Khalil, R. Hayashi, L. Daou, S. A. Staiteieh +5 more
2017Clincal and Experimental Dermatology9 citations
Semantic Scholar
Absolute quantification of gene expression in drug discovery using RT-qPCR: Case of a drug used in the treatment of leishmaniasis.
C. Al Khoury, G. Nemer, J. Guillot, S. Tokajian
2022Research in Veterinary Science8 citations Open access
Semantic Scholar
Interleukin-37: A Link Between COVID-19, Diabetes, and the Black Fungus
S. Tokajian, Georgi Merhi, C. Al Khoury, G. Nemer
2022Frontiers in Microbiology8 citations Open access
Semantic Scholar
Consanguinity rates among Syrian refugees in Lebanon: a study on genetic awareness.
Malak El Sabeh, M. Kassir, Paola Ghanem, Omran Saifi +8 more
2020Journal of Biosocial Science8 citations
Semantic Scholar
A Novel Somatic Variant in HEY2 Unveils an Alternative Splicing Isoform Linked to Ventricular Septal Defect
Manal M. Fardoun, Hassan Dehaini, Amina Kamar, F. Bitar +4 more
2019Pediatric Cardiology8 citations
Semantic Scholar

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