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Nadine Jalkh

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Articles 37
Citations 417
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Recent Articles
1.
Kourie H, Zouein J, Succar B, Mardirossian A, Ahmadieh N, Chouery E, et al.
Oncol Rev . 2023 Nov; 17:10603. PMID: 38025894
Bladder cancer (BC) has been associated with genetic susceptibility. Single peptide polymorphisms (SNPs) can modulate BC susceptibility. A literature search was performed covering the period between January 2000 and October...
2.
Feghaly I, Kourie H, Moubarak M, Chouery E, Mehawej C, Jalkh N, et al.
Int J Gynaecol Obstet . 2023 May; 162(3):1027-1032. PMID: 37185951
Objective: To assess the molecular profile of borderline ovarian tumors (BOT) in the Lebanese population by whole-exome sequencing and to correlate the results with the patients' clinical profiles. Methods: We...
3.
Kourie H, Succar B, Chouery E, Mehawej C, Ahmadieh N, Zouein J, et al.
BMC Med Genomics . 2022 Oct; 15(1):217. PMID: 36253817
Background: Bladder cancer (BC) is the 10 most frequent tumor worldwide. Evidence shows an association between elevated risk of BC and various single nucleotide polymorphisms (SNP). BC incidence was the...
4.
El Hadi C, Ayoub G, Bachir Y, Haykal M, Jalkh N, Kourie H
Expert Rev Mol Diagn . 2022 Apr; 22(4):427-438. PMID: 35400274
Introduction: Diseases were initially thought to be the consequence of a single gene mutation. Advances in DNA sequencing tools and our understanding of gene behavior have revealed that complex diseases,...
5.
Rammal S, Kourie H, Jalkh N, Mehawej C, Chouery E, Moujaess E, et al.
Pharmacogenomics . 2021 Aug; 22(12):791-803. PMID: 34410147
Among all cancer types, pulmonary cancer has the highest mortality rate. Tobacco consumption remains the major risk factor for the development of lung cancer. However, many studies revealed a correlation...
6.
Abi Karam M, Kourie H, Jalkh N, Mehawej C, Kesrouani C, Haddad F, et al.
BMC Med Genomics . 2021 Jul; 14(1):187. PMID: 34284772
Background: Basal cell carcinoma (BCC) represents by far the most common non-melanoma skin cancer (NMSC) in the world with an increasing incidence of 3% to 10% per year, especially in...
7.
Hamdan N, Mehawej C, Sebaaly G, Jalkh N, Corbani S, Abou-Ghoch J, et al.
Clin Genet . 2020 Jun; 98(3):288-292. PMID: 32578875
Intellectual disability (ID) is a neurodevelopmental disorder characterized by limitations in both intellectual and behavioral functioning. It can occur in non-syndromic and syndromic forms involving multiple organs. While the majority...
8.
Jalkh N, Mehawej C, Chouery E
Front Genet . 2020 Apr; 11:208. PMID: 32231684
The expanded use of NGS tests in genetic diagnosis enables the massive generation of data related to each individual, among which some findings are of medical value. Over the last...
9.
Haidar Z, Jalkh N, Corbani S, Abou-Ghoch J, Fawaz A, Mehawej C, et al.
Mov Disord . 2020 Mar; 35(5):896-899. PMID: 32196122
No abstract available.
10.
Gutierrez-Rodrigues F, Masri N, Chouery E, Diamond C, Jalkh N, Vicente A, et al.
Hum Genet . 2019 Nov; 138(11-12):1323-1330. PMID: 31677132
Phenotypic heterogeneity is often observed in patients with telomeropathies caused by pathogenic variants in telomere biology genes. However, the roles of recessive variants in these different phenotypes are not fully...