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

Genetic risk and polygenic risk score assessment of prediabetes and progression to type 2 diabetes

遗传风险和多基因风险评分评估糖尿病前期及进展为 2 型糖尿病

期刊:Diabetes Obesity & Metabolism
影响因子:5.7
doi:10.1111/dom.16490
Aliyu, Usama; Umlai, Umm-Kulthum Ismail; Al-Thani, Nayra M; Toor, Salman M; Abou-Samra, Abdul Badi; Albagha, Omar M E
糖尿病
代谢
发表日期：2025
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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

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms26199481
Hendi, Nagham Nafiz; Umlai, Umm-Kulthum; Albagha, Omar; Nemer, Georges
发表日期：2025
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A multi-ancestry genome-wide association study and evaluation of polygenic scores of LDL-C levels

一项多种族群全基因组关联研究及低密度脂蛋白胆固醇水平多基因评分评估

期刊:Journal of Lipid Research
影响因子:4.1
doi:10.1016/j.jlr.2025.100752
Ismail Umlai, Umm-Kulthum; Toor, Salman M; Al-Sarraj, Yasser A; Mohammed, Shaban; Al Hail, Moza S H; Ullah, Ehsan; Kunji, Khalid; El-Menyar, Ayman; Gomaa, Mohammed; Jayyousi, Amin; Saad, Mohamad; Qureshi, Nadeem; Al Suwaidi, Jassim M; Albagha, Omar M E
代谢
发表日期：2025
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Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol

全基因组关联研究和植物甾醇荟萃分析发现了一个新的血清菜油甾醇水平相关基因位点

期刊:Human Genomics
影响因子:4.3
doi:10.1186/s40246-024-00649-x
Alenbawi, Jamil; Al-Sarraj, Yasser A; Umlai, Umm-Kulthum I; Kadhi, Ayat; Hendi, Nagham N; Nemer, Georges; Albagha, Omar M E
发表日期：2024
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Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus

全基因组关联研究和跨种族荟萃分析确定了 2 型糖尿病的新易感基因位点

期刊:BMC Medical Genomics
影响因子:2.1
doi:10.1186/s12920-024-01855-1
Asma A Elashi, Salman M Toor, Umm-Kulthum Ismail Umlai, Yasser A Al-Sarraj, Shahrad Taheri, Karsten Suhre, Abdul Badi Abou-Samra, Omar M E Albagha
代谢
糖尿病
发表日期：2024
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Correction: Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus

更正：全基因组关联研究和跨种族荟萃分析发现了2型糖尿病的新易感基因位点

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-024-01903-w
Elashi, Asma A; Toor, Salman M; Umlai, Umm-Kulthum Ismail; Al-Sarraj, Yasser A; Taheri, Shahrad; Suhre, Karsten; Abou-Samra, Abdul Badi; Albagha, Omar M E
糖尿病
代谢
发表日期：2024
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Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene

印度一名男孩因GH1基因中一段6 kb的新型纯合缺失而患上严重的生长激素缺乏症

期刊:Journal of Clinical Research in Pediatric Endocrinology
影响因子:1.5
doi:10.4274/jcrpe.galenos.2022.2022-5-9
Haris, Basma; Mohammed, Idris; Ismail Umlai, Umm-Kulthum; Shirodkar, Diksha; Hussain, Khalid
免疫/内分泌
发表日期：2024
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Genetic determinants of Vitamin D deficiency in the Middle Eastern Qatari population: a genome-wide association study

中东卡塔尔人群维生素D缺乏症的遗传决定因素：一项全基因组关联研究

期刊:Frontiers in Nutrition
影响因子:5.1
doi:10.3389/fnut.2023.1242257
Hendi, Nagham Nafiz; Al-Sarraj, Yasser; Ismail Umlai, Umm-Kulthum; Suhre, Karsten; Nemer, Georges; Albagha, Omar
发表日期：2023
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A population study of clinically actionable genetic variation affecting drug response from the Middle East

一项针对中东地区影响药物反应的具有临床意义的基因变异的人群研究

期刊:npj Genomic Medicine
影响因子:4.8
doi:10.1038/s41525-022-00281-5
Jithesh, Puthen Veettil; Abuhaliqa, Mohammed; Syed, Najeeb; Ahmed, Ikhlak; El Anbari, Mohammed; Bastaki, Kholoud; Sherif, Shimaa; Umlai, Umm-Kulthum; Jan, Zainab; Gandhi, Geethanjali; Manickam, Chidambaram; Selvaraj, Senthil; George, Chinnu; Bangarusamy, Dhinoth; Abdel-Latif, Rania; Al-Shafai, Mashael; Tatari-Calderone, Zohreh; Estivill, Xavier; Pirmohamed, Munir
发表日期：2022
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Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly

病例报告：一例伴有身材矮小、语言发育迟缓和小头畸形的新型串联4q微重复病例的表型-基因相关性研究

期刊:Frontiers in Endocrinology
影响因子:4.6
doi:10.3389/fendo.2021.783235
Umlai, Umm-Kulthum Ismail; Haris, Basma; Hussain, Khalid; Jithesh, Puthen Veettil
发育与干细胞
发表日期：2021
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