Projects per year
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Dive into the research topics where Laboratory of genomic and personalized medicine is active. These topic labels come from the works of this organisation's members. Together they form a unique fingerprint.
Collaborations and top research areas from the last five years
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Profiles
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Ulan Kozhamkulov, MD, Candidate of Medical Sciences
- Laboratory of genomic and personalized medicine - Leading Reseacher
Person: Staff
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Saule Rakhimova, MD, Candidate of Biological Sciences
- Laboratory of genomic and personalized medicine - Leading Reseacher
Person: Staff
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Identification and functional characterization of novel genetic mutations causing dilated cardiomyopathy in patients of Kazakhstan
Akilzhanova, A. (PI), Sarbassov, D. (Co-PI), Abdrakhmanov, A. (Co-PI), Loeys, B. (Other participant), Karazhanova, L. (Other participant), Bekbossynova, M. (Other Faculty/Researcher), Kairov, U. (Other Faculty/Researcher) & Rakhimova, S. (Other Faculty/Researcher)
1/1/24 → 12/31/26
Project: CRP
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Targeting KRAS mutant colorectal cancer by inducing a cytotoxic oxidative stress
Sarbassov, D. (PI), Akilzhanova, A. (Co-PI), Bersimbaev, R. (Co-PI), Yermekbayeva, B. (Other Faculty/Researcher), Utepbergenov, D. (Other Faculty/Researcher), Makishev, A. (Other Faculty/Researcher) & Kaidarova, D. (Other Faculty/Researcher)
1/1/21 → 12/31/25
Project: CRP
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Long non-coding RNA and microRNA identification in esophageal squamous cell carcinoma
Rakhimova, S. (PI), Sarbassov, D. (Co-PI) & Makishev, A. (Co-PI)
1/1/21 → 6/30/24
Project: CRP
Research output
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Enterococcus dysbiosis as a mediator of vitamin D deficiency-associated memory impairments
Vinogradova, E., Jarmukhanov, Z., Nurgaziyev, M., Kossumov, A., Nurgozhina, A., Mukhanbetzhanov, N., Sergazy, S., Chulenabyeva, L., Issilbayeva, A., Askarova, S., Kaiyrlykyzy, A., Rakhimova, S., Kozhamkulov, U., Kairov, U., Khassenbekova, Z., Tarzhanova, D., Akilzhanova, A., Lee, J. H., Terwilliger, J. & Sailybayeva, A. & 4 others, , Jan 30 2025, In: Heliyon. 11, 2, e41969.Research output: Contribution to journal › Article › peer-review
Open Access1 Citation (Scopus) -
Novel nonsense mutation in gene CHRNA2 identified by whole-genome sequencing in infant with epilepsy disorder: A case report
Makhmetov, S., Temirkhanova, K., Rakhimova, S., Satvaldina, N., Kalendar, R., Kozhamkulov, U., Bolatov, A., Bayanova, M., Bazenova, A., Nazarova, L., Akilzhanova, A. & Kairov, U., Jan 15 2025, In: Heliyon. 11, 1, e41484.Research output: Contribution to journal › Article › peer-review
Open Access -
The Impact of Genetic Polymorphism on Complication Development in Heart Failure Patients
Zhalbinova, M. R., Rakhimova, S. E., Kozhamkulov, U. A., Akilzhanov, K. R., Shaimardanov, N. K., Akilzhanova, G. A., Lee, J. H., Pya, Y. V., Bekbossynova, M. S. & Akilzhanova, A. R., Jan 2025, In: Journal of Clinical Medicine. 14, 1, 35.Research output: Contribution to journal › Article › peer-review
Open Access