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

Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population

全基因组图谱分析揭示了阿拉伯人群代谢性状的新关联信号

Hebbar, Prashantha; Abubaker, Jehad Ahmed; Abu-Farha, Mohamed; Alsmadi, Osama; Elkum, Naser; Alkayal, Fadi; John, Sumi Elsa; Channanath, Arshad; Iqbal, Rasheeba; Pitkaniemi, Janne; Tuomilehto, Jaakko; Sladek, Robert; Al-Mulla, Fahd; Thanaraj, Thangavel Alphonse

MC4R Variant rs17782313 Associates With Increased Levels of DNAJC27, Ghrelin, and Visfatin and Correlates With Obesity and Hypertension in a Kuwaiti Cohort

MC4R 变异体 rs17782313 与 DNAJC27、胃饥饿素和内脏脂肪素水平升高相关,并与科威特人群的肥胖和高血压相关

Hammad, Maha M; Abu-Farha, Mohamed; Hebbar, Prashantha; Cherian, Preethi; Al Khairi, Irina; Melhem, Motasem; Alkayal, Fadi; Alsmadi, Osama; Thanaraj, Thangavel Alphonse; Al-Mulla, Fahd; Abubaker, Jehad

Higher Levels of ANGPTL5 in the Circulation of Subjects With Obesity and Type 2 Diabetes Are Associated With Insulin Resistance.

肥胖和 2 型糖尿病患者血液循环中 ANGPTL5 水平较高与胰岛素抵抗有关

Alghanim Ghazi, Qaddoumi Mohamed G, Alhasawi Nouf, Cherian Preethi, Al-Khairi Irina, Nizam Rasheeba, Alkayal Fadi, Alanbaei Muath, Tuomilehto Jaakko, Abubaker Jehad, Abu-Farha Mohamed, Al-Mulla Fahd

FTO Variant rs1421085 Associates With Increased Body Weight, Soft Lean Mass, and Total Body Water Through Interaction With Ghrelin and Apolipoproteins in Arab Population.

FTO 变异体 rs1421085 与阿拉伯人群中通过与生长素释放肽和载脂蛋白的相互作用而增加体重、瘦体重和总体液量

Hebbar Prashantha, Abu-Farha Mohamed, Mohammad Anwar, Alkayal Fadi, Melhem Motasem, Abubaker Jehad, Al-Mulla Fahd, Thanaraj Thangavel Alphonse

Investigation of genetic variation and lifestyle determinants in vitamin D levels in Arab individuals

对阿拉伯人群维生素D水平的遗传变异和生活方式决定因素进行研究

Mezzavilla, Massimo; Tomei, Sara; Alkayal, Fadi; Melhem, Motasem; Ali, Maisa M; Al-Arouj, Monira; Bennakhi, Abdullah; Alsmadi, Osama; Elkum, Naser

Response to leptin and nitric oxide in blood pressure regulation in humans

瘦素和一氧化氮在人体血压调节中的作用

Alsmadi, Osama; Melhem, Motasem; Hebbar, Prashantha; Channanath, Arshad; Thareja, Gaurav; John, Sumi E; Alkayal, Fadi; Behbehani, Kazem; Thanaraj, Thangavel Alphonse

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)

由成纤维细胞生长因子 3 (FGF3) 基因的新型同源突变引起的综合征性先天性感觉神经性耳聋、小耳畸形和小牙畸形

Alsmadi, Osama; Meyer, Brian F; Alkuraya, Fowzan; Wakil, Salma; Alkayal, Fadi; Al-Saud, Haya; Ramzan, Khushnooda; Al-Sayed, MoeenAldeen