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

Genetic Variants in Potassium Channel Genes and Their Clinical Implications in Kazakhstani Patients with Cardiac Arrhythmias

钾通道基因的遗传变异及其在哈萨克斯坦心律失常患者中的临床意义

期刊:Journal of Personalized Medicine
影响因子:3
doi:10.3390/jpm16020060
Chamoieva, Ayaulym; Rakhimova, Saule; Abilova, Zhannur; Akhmetova, Ainur; Akilzhanova, Gulbanu; Zhalbinova, Madina; Daniyarov, Asset; Akilzhanov, Kenes; Molkenov, Askhat; Kairov, Ulykbek; Kuanysheva, Anargul; Shaimardanov, Nurlan; Abdrakhmanov, Ayan; Bekbossynova, Makhabbat; Akilzhanova, Ainur
发表日期：2026
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Changes in Insulin Resistance with Different Weight Loss Methods in Patients with Type Two Diabetes Mellitus and Hypertension: A Comparative Clinical Trial

不同减肥方法对2型糖尿病合并高血压患者胰岛素抵抗的影响：一项比较临床试验

期刊:Journal of Clinical Medicine
影响因子:2.9
doi:10.3390/jcm15020546
Oshakbayev, Kuat; Durmanova, Aigul; Kuttymuratov, Gani; Bikhanov, Nurzhan; Nabiyev, Altay; Suleimenov, Timur; Idrissov, Alisher; Shakhmarova, Tomiris; Mirmanova, Zhanel; Rakhimova, Saule; Kozhamkulov, Ulan; Akilzhanova, Ainur
高血压
心血管
代谢
糖尿病
免疫/内分泌
发表日期：2026
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The association of VDR gene polymorphisms with serum vitamin D levels and injury predisposition in elite athletes of Kazakhstan

哈萨克斯坦精英运动员VDR基因多态性与血清维生素D水平和损伤易感性的关系

期刊:European Journal of Applied Physiology
影响因子:2.7
doi:10.1007/s00421-025-05976-y
Gabdulkayum, Aidana; Amangeldikyzy, Saya; Khassanova, Sayipzhamal; Yerezhepov, Adil; Akilzhanov, Kenes; Kozhamkulov, Ulan; Rakhimova, Saule; Kairov, Ulykbek; Yerezhepov, Dauren; Akilzhanova, Ainur
发表日期：2026
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Genomic landscape of the Great Steppe: Genetic variants in healthy Kazakh individuals

大草原的基因组图谱：健康哈萨克人的基因变异

期刊:Scientific Data
影响因子:6.9
doi:10.1038/s41597-025-05964-z
Serikzhan, Aygerim; Daniyarov, Asset; Molkenov, Askhat; Akhmetova, Ainur; Abilova, Zhannur; Sharip, Aigul; Yerezhepov, Dauren; Rakhimova, Saule; Kozhamkulov, Ulan; Kushugulova, Almagul; Askarova, Sholpan; Sarbassov, Dos; Akilzhanova, Ainur; Kairov, Ulykbek
发表日期：2025
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FokI Polymorphism of the VDR Gene Is Associated with Vitamin D Insufficiency in Elite Male Power Athletes of Kazakhstan

哈萨克斯坦精英男子力量型运动员中维生素D受体基因FokI多态性与维生素D缺乏症相关

期刊:Nutrients
影响因子:5
doi:10.3390/nu17203195
Gabdulkayum, Aidana; Amangeldikyzy, Saya; Yerezhepov, Adil; Khassanova, Sayipzhamal; Akilzhanov, Kenes R; Kozhamkulov, Ulan; Rakhimova, Saule; Kairov, Ulykbek; Akilzhanova, Ainur; Yerezhepov, Dauren
信号转导
发表日期：2025
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The Adaptation of Cancer Cells to Serum Deprivation Is Mediated by mTOR-Dependent Cholesterol Synthesis.

癌细胞对血清剥夺的适应是通过 mTOR 依赖性胆固醇合成介导的。

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms262210932
Ilyassova Bayansulu, Rakhimgerey Nargiz, Rakhimova Saule, Satvaldina Nazerke, Daniyarov Asset, Akilzhanova Ainur, Kairov Ulykbek, Begimbetova Dinara, Sarbassov Dos D
细胞生物学
MTOR
mTOR
发表日期：2025
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Correction: Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability

更正：对哈萨克斯坦早发性癫痫患儿进行全基因组测序，揭示了新的基因变异和表型变异

期刊:Molecular Neurobiology
影响因子:4.3
doi:10.1007/s12035-024-04544-3
Bayanova, Mirgul; Bolatov, Aidos K; Bazenova, Assiya; Nazarova, Lyazzat; Nauryzbayeva, Alissa; Tanko, Naanlep Matthew; Rakhimova, Saule; Satvaldina, Nazerke; Samatkyzy, Diana; Kozhamkulov, Ulan; Kairov, Ulykbek; Akilzhanova, Ainur; Sarbassov, Dos
癫痫
神经科学
发表日期：2025
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Enterococcus dysbiosis as a mediator of vitamin D deficiency-associated memory impairments

肠球菌菌群失调作为维生素D缺乏相关记忆障碍的介质

期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2025.e41969
Vinogradova, Elizaveta; Jarmukhanov, Zharkyn; Nurgaziyev, Madiyar; Kossumov, Alibek; Nurgozhina, Ayaulym; Mukhanbetzhanov, Nurislam; Sergazy, Shynggys; Chulenabyeva, Laura; Issilbayeva, Argul; Askarova, Sholpan; Kaiyrlykyzy, Aiym; Rakhimova, Saule; Kozhamkulov, Ulan; Kairov, Ulykbek; Khassenbekova, Zhanagul; Tarzhanova, Dinar; Akilzhanova, Ainur; Lee, Joseph H; Terwilliger, Joseph; Sailybayeva, Aliya; Bekbossynova, Makhabbat; Zhumadilov, Zhaxybay; Kozhakhmetov, Samat; Kushugulova, Almagul
微生物学
发表日期：2025
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Novel nonsense mutation in gene CHRNA2 identified by whole-genome sequencing in infant with epilepsy disorder: A case report

通过全基因组测序在患有癫痫症的婴儿中发现CHRNA2基因的新型无义突变：病例报告

期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2024.e41484
Makhmetov, Sultan; Temirkhanova, Kamila; Rakhimova, Saule; Satvaldina, Nazerke; Kalendar, Ruslan; Kozhamkulov, Ulan; Bolatov, Aidos; Bayanova, Mirgul; Bazenova, Assiya; Nazarova, Lyazzat; Akilzhanova, Ainur; Kairov, Ulykbek
癫痫
神经科学
发表日期：2025
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Targeted NGS Revealed Pathogenic Mutation in a 13-Year-Old Patient with Homozygous Familial Hypercholesterolemia: A Case Report

靶向NGS检测发现一名13岁纯合子家族性高胆固醇血症患者的致病突变：病例报告

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms252211882
Chamoieva, Ayaulym E; Mirmanova, Zhanel Z; Zhalbinova, Madina R; Rakhimova, Saule E; Daniyarov, Asset Z; Kairov, Ulykbek Y; Baigalkanova, Almira I; Mukarov, Murat A; Bekbossynova, Makhabbat S; Akilzhanova, Ainur R
代谢
发表日期：2024
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