Georges Nemer

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 16

Top Venues

BMC medical genetics

Metabolites

Nutrients

Journal of fungi (Basel, Switzerland)

Hamad Bin Khalifa University

Universite de Montreal (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hamad Bin Khalifa University Sep 29 2019

Qatar

Professor :: College of Health and Life Sciences

American University of Beirut Faculty of Medicine Sep 01 2015

Lebanon

Professor :: Biochemistry and Molecular Genetics

Education History

Universite de Montreal Jan 01 1994 - Dec 01 2002

Canada

PHD :: Pharmacology

Publications

Charbel Al Khoury, Sima Tokajian, Nabil Nemer, Georges Nemer, Kelven Rahy, Sergio Thoumi, Lynn Al Samra, Aia Sinno
Computational Applications: Beauvericin from a Mycotoxin into a Humanized Drug. Metabolites 14 (4) (2024)
Charbel Al Khoury, Sima Tokajian, Nabil Nemer, Georges Nemer, Kelven Rahy, Sergio Thoumi, Lynn Al Samra, Aia Sinno
Computational Applications: Beauvericin from a Mycotoxin into a Humanized Drug. Metabolites 14 (4) (2024)
Charbel Al Khoury, Sima Tokajian, Nabil Nemer, Georges Nemer, Kelven Rahy, Sergio Thoumi, Lynn Al Samra, Aia Sinno
Computational Applications: Beauvericin from a Mycotoxin into a Humanized Drug. Metabolites 14 (4) (2024)
Nagham Nafiz Hindi, Georges Nemer
Epigenetic regulation of vitamin D deficiency. Epigenomics (2023)
Nagham Nafiz Hindi, Marlene Chakhtoura, Yasser Al-Sarraj, Dania Saleh Basha, Omar M E Albagha, Ghada El-Hajj Fuleihan, Georges Nemer
The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association Study. Nutrients 15 (14) (2023)
Ayat Kadhi, Lamiaa Hamie, Christel Tamer, Georges Nemer, Mazen Kurban
A Novel Pathogenic CDH3 Variant underlying Heredity Hypotrichosis Simplex detected by Whole-Exome Sequencing (WES)-A Case Report. Cold Spring Harbor molecular case studies (2022)
Perla Gerges, Tania Bitar, Frederic Laumonnier, Sylviane Marouillat, Georges Nemer, Christian R Andres, Walid Hleihel
Identification of Novel Gene Variants for Autism Spectrum Disorders in the Lebanese Population Using Whole-Exome Sequencing. Genes 13 (2) (2022)
Charbel Al Khoury, Georges Nemer, Richard Humber, Nehme El-Hachem, Jacques Guillot, Racha Chehab, Elise Noujeim, Yara El Khoury, Wadih Skaff, Nathalie Estephan, Nabil Nemer
Bioexploration and Phylogenetic Placement of Entomopathogenic Fungi of the Genus Beauveria in Soils of Lebanon Cedar Forests. Journal of fungi (Basel, Switzerland) 7 (11) (2021)
Nagham N Hindi, Jamil Alenbawi, Georges Nemer
Pharmacogenomics Variability of Lipid-Lowering Therapies in Familial Hypercholesterolemia. Journal of personalized medicine 11 (9) (2021)
Athar Khalil, Samer Bou Karroum, Rana Barake, Gabriel Dunya, Samer Abou-Rizk, Amina Kamar, Georges Nemer, Marc Bassim
Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF. BMC medical genetics 21 (1) (2020)
Georges Nemer, Nehme El-Hachem, Edward Said Eid, Lamiaa Hamie, Tara Bardawil, Samar Khalil, Inaam El-Rassy, Remi Safi, Athar Khalil, Ossama Abbas, Yutaka Shimomura, Mazen Kurban
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans. Clinical genetics 98 (2) (2020)
Eliana Nehme, Zahraa Rahal, Ansam Sinjab, Athar Khalil, Hassan Chami, Georges Nemer, Humam Kadara
Epigenetic Suppression of the T-box Subfamily 2 (TBX2) in Human Non-Small Cell Lung Cancer. International journal of molecular sciences 20 (5) (2019)
Ossama K Abou Hassan, Wiam Haidar, Mariam Arabi, Hadi Skouri, Fadi Bitar, Georges Nemer, Imad Bou Akl
Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension. BMC medical genetics 20 (1) (2019)
Ossama K Abou Hassan, Wiam Haidar, Georges Nemer, Hadi Skouri, Fadi Haddad, Imad BouAkl
Clinical and genetic characteristics of pulmonary arterial hypertension in Lebanon. BMC medical genetics 19 (1) (2018)
Rabih Andary, Abdul-Karim El-Hage-Sleiman, Theresa Farhat, Sami Sanjad, Georges Nemer
Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes. Journal of pediatric endocrinology & metabolism : JPEM 30 (4) (2017)
Akl C Fahed, Kamel Shibbani, Rabih R Andary, Mariam T Arabi, Robert H Habib, Denis D Nguyen, Fady F Haddad, Elie Moubarak, Georges Nemer, Sami T Azar, Fadi F Bitar
Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia. Cholesterol 2017 (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Georges Nemer