日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Global trajectories of polygenic risk score research: a systematic bibliometric review of precision medicine, equity, and clinical translation

多基因风险评分研究的全球发展轨迹:精准医学、公平性和临床转化方面的系统性文献计量学综述

Bitar, Fouad; Zareef, Rana; Abou-Karam, Roukoz; Nemer, Georges; Bitar, Fadi F; Fahed, Akl C; Sater, Zahi Abdul

Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome Sequencing

利用全外显子组测序对一例家族性Goldenhar综合征病例进行特征分析

Bejaoui, Yosra; Al-Sarraj, Yasser; Al-Hage, Jana; Bitar, Fadi F; El Hajj, Nady; Nemer, Georges; Kurban, Mazen

Targeting ceramide metabolism to restore hypoxia-induced apoptosis in p53-deficient colon cancer cells.

通过靶向神经酰胺代谢来恢复 p53 缺陷型结肠癌细胞中缺氧诱导的细胞凋亡。

Mechleb Karen, Hourani Nancy, Fakhry Maya, Alyamani Osama A, Hage-Sleiman Rouba, Younes Hicham, Fayad Antoine Abou, Soudani Nadia, Sakr Amer, Darwiche Nadine, Nemer Georges, Saab Raya, Mrad Marguerite, Dbaibo Ghassan

Genome-Wide Association Study for Resting Electrocardiogram in the Qatari Population Identifies 6 Novel Genes and Validates Novel Polygenic Risk Scores

卡塔尔人群静息心电图全基因组关联研究发现6个新基因并验证了新的多基因风险评分

Khan, Nahin; Shaar, Abdullah; Kunji, Khalid; Khan, Atlas; Elshrif, Mohamed; Bashir, Mohammed; Ali, Mohammed Thamer; Al Haj Zen, Ayman; Kiryluk, Krzysztof; Nemer, Georges; Fahed, Akl C; Saad, Mohamad

Rare-Variant Genome-Wide Association and Polygenic Score Assessment of Vitamin D Status in a Middle Eastern Population

中东人群维生素D状态的罕见变异全基因组关联分析和多基因评分评估

Hendi, Nagham Nafiz; Umlai, Umm-Kulthum; Albagha, Omar; Nemer, Georges

SDR42E1 modulates vitamin D absorption and cancer pathogenesis: insights from an in vitro model.

SDR42E1 调节维生素 D 吸收和癌症发病机制:来自体外模型的启示

Hendi Nagham Nafiz, Nemer Georges

Case Report: Novel combinatorial factors in the WNT pathway in a pediatric case of valvular aortic stenosis from Lebanon: a brief report

病例报告:黎巴嫩一例儿童主动脉瓣狭窄病例中WNT通路的新型组合因素:简要报告

Ataya, Wiam; Mohammed, Fathima; Arabi, Mariam; Bitar, Fadi; Nemer, Georges

Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature Review

一种与注意力缺陷多动障碍和神经发育异常相关的新型纯合METTL5变异的功能解释:病例报告和文献综述

Hashem, Sheema; Elhag, Saba F; Bhat, Ajaz A; Aamer, Waleed; Al-Maraghi, Aljazi; Alhaboub, Hala; Abuthaher, Dalya; Akil, Ammira S Al-Shabeeb; Haris, Mohammad; Fakhro, Khalid; Nemer, Georges; Kamal, Madeeha

Repositioning of moxidectin: a promising approach in cutaneous leishmaniasis therapy.

莫昔克汀的重新定位:皮肤利什曼病治疗中一种有前景的方法

Al Samra Lynn, El Nahas Mohamad, Mneimneh Ilham, Tokajian Sima, Nemer Georges, Sinno Aia, Rahy Kelven, Thoumi Sergio, Zibara Zahraa, El Khatib Ahmad, Sabbagh Dalal, Guillot Jacques, Karam Louna, Ali Lazo, Baghdadi Ruqaya, Al Khoury Charbel

Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region

遗传性皮肤病中的双基因遗传:来自中东和北非(MENA)地区黎巴嫩参考中心两例近亲结婚病例的启示

Kadhi, Ayat; Hamie, Lamiaa; Eid, Edward; Nemer, Georges; Kurban, Mazen