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Zhanel Z. Mirmanova

Observed names: Z. Mirmanova, Zh. Mirmanova, Zh.Zh. Mirmanova, Zhanel Mirmanova, Ж.Ж. Мирманова
Observed institution: Nazarbayev University
ORCID: 0000-0002-0284-3891
Observed ORCID: 0000-0002-0284-3891
OpenAlex ID: A5095372901
Changes in Insulin Resistance with Different Weight Loss Methods in Patients with Type Two Diabetes Mellitus and Hypertension: A Comparative Clinical Trial
2026 · Kuat Oshakbayev, Aigul Durmanova, et al. · Journal of Clinical Medicine · 1
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Targeted NGS Revealed Pathogenic Mutation in a 13-Year-Old Patient with Homozygous Familial Hypercholesterolemia: A Case Report
2024 · Ayaulym E. Chamoieva, Zhanel Z. Mirmanova, et al. · International Journal of Molecular Sciences · 1
Sudden Cardiac Death: The Utility of Genetic Screening Using NGS in Kazakhstan
2024 · A. Akilzhanova, M. Zhalbinova, et al. · The Journal of Heart and Lung Transplantation · 1
Whole-exome Sequencing of Monozygotic Twins With Epilepsy and Autism Spectrum Disorder in a Kazakhstani Family: a Case Report
2026 · A.K. Gabdulkayum, Zh.Zh. Mirmanova, et al. · Eurasian journal of applied biotechnology
Genetic Insights Into А Kazakhstani Family With Multiple Neurological Conditions: a Case Report
2026 · A. Gabdulkayum, Zh. Mirmanova, et al. · Eurasian journal of applied biotechnology
Early-Onset and Syndromic Pediatric Epilepsy in Kazakhstan: Clinical, Molecular, and Phenotypic Spectrum
2026 · Mirgul Bayanova, Lyazzat Nazarova, et al. · Journal of Clinical Medicine
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Prenatal genetic testing for NDUFV1gene-related mitochondrial complex Ideficiency in a Kazakhstani family
2026 · Aidana Gabdulkayum, Zhanel Mirmanova, et al. · Astana Medical Journal
Prenatal Genetic Testing for Multiple Mitochondrial Dysfunction Syndrome Caused by Iba57 Gene Mutation Kazakhstani Family: a Case Report
2026 · A. Gabdulkayum, Z. Mirmanova, et al. · Experimental biology
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Prevalence of damaging genetic variants in genes of lipid metabolism pathway in Kazakhstani atherosclerosis cohort
2025 · Zhanel Mirmanova, Madina Zhalbinova, et al. · Eurasian journal of applied biotechnology
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Whole Exome Sequencing Identifies Rare NR1H3 Variants Linked to Fatty Liver and Atherosclerosis
2025 · Rassul Shokenov, Zhanel Mirmanova, et al. · Eurasian journal of applied biotechnology
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Role of genetic polymorphisms in preventing complications development in heart failure patients
2025 · Madina Zhalbinova, Saule Rakhimova, et al. · Eurasian journal of applied biotechnology
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Clonal Hematopoiesis of Indeterminate Potential Mutations and Cardiovascular Risk in Kazakhstani Cohort
2025 · Tomiris Shakhmarova, Zhanel Mirmanova, et al. · Eurasian journal of applied biotechnology
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Genetic spectrum of channelopathies in Kazakhstani patients revealed by targeted NGS panel
2025 · Ayaulym Chamoieva, Zhanel Mirmanova, et al. · Eurasian journal of applied biotechnology
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Comparative Genetic Analysis of Cardiac Ion Channel Genes in Sudden Cardiac Death Victims and Cardiac Patients Using Targeted Next-generation Sequencing
2024 · A. Chamoieva, M Zhalbinova, et al. · Eurasian journal of applied biotechnology
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Targeted Sequencing Reveal Two Pathogenic Mutations in Ldlr and Apoe Genes in Patient With Family Hypercholesterolemia: Case Report
2024 · Zh. Mirmanova, M. Zhalbinova, et al. · Eurasian journal of applied biotechnology
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Exploring the Role of Ngs in Genetic Profiling for Understanding Non-violent Sudden Cardiac Death in Astana
2024 · T. Shakhmarova, A. Chamoieva, et al. · Eurasian journal of applied biotechnology
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Клональный Гемопоэз С Неопределенным Потенциалом И Риск Развития Ишемической Болезни Сердца
2023 · Т.К. Шахмарова, М.Р. Жалбинова, et al. · Ġylym men densaulyķ saķtau.
Mutations in Cardiac Ion Channel Genes in Kazakhstani Patients With Long Qt Syndrome
· Ayaulym E. Chamoieva, Madina R. Zhalbinova, et al. · CyberLeninK (CyberLeninka)
Works count: 18
Citation count: 3
H-index: 1
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