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Eleonora Khlebus
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Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels
E Khlebus, V Kutsenko, A Meshkov, A Ershova, A Kiseleva, A Shevtsov, ...
PLoS One 14 (5), e0217620, 2019
152019
Возможности фармакогенетического тестирования в кардиологии на основе данных экзомного секвенирования
НВ Щербакова, АИ Ершова, АА Суворова, ЭЮ Хлебус, АН Мешков, ...
Рациональная фармакотерапия в кардиологии 10 (6), 646-650, 2014
132014
A data-driven approach to carrier screening for common recessive diseases
AV Kiseleva, MV Klimushina, EA Sotnikova, MG Divashuk, AI Ershova, ...
Journal of Personalized Medicine 10 (3), 140, 2020
122020
Cystic Fibrosis Polymorphic Variants in a Russian Population
A Kiseleva, M Klimushina, E Sotnikova, O Skirko, M Divashuk, O Kurilova, ...
Pharmacogenomics and Personalized Medicine, 679-686, 2020
102020
Изучение влияния курения как фактора риска атеросклероза на уровень метилирования ДНК
АВ Киселева, ЭЮ Хлебус, АИ Ершова, ПГ Шахнович, КН Ткаченко, ...
Профилактическая медицина 18 (6), 66-70, 2015
72015
Identification of pathogenic variant burden and selection of optimal diagnostic method is a way to improve carrier screening for autosomal recessive diseases
EA Sotnikova, AV Kiseleva, VA Kutsenko, AA Zharikova, VE Ramensky, ...
Journal of Personalized Medicine 12 (7), 1132, 2022
42022
ПОКАЗАТЕЛИ ЛИПИДНОГО СПЕКТРА И ГЕНЕТИЧЕСКИЕ МАРКЕРЫ, АССОЦИИРОВАННЫЕС УРОВНЕМ ОКИСЛИТЕЛЬНО МОДИФИЦИРОВАННЫХ ЛИПОПРОТЕИДОВ НИЗКОЙ ПЛОТНОСТИ
Российский кардиологический журнал 10, 49-54, 2017
42017
Modern probabilistic and statistical approaches to search for nucleotide sequence options associated with integrated diseases
AI Rytova, EY Khlebus, AE Shevtsov, VA Kutsenko, NV Shcherbakova, ...
Russian journal of genetics 53, 1091-1104, 2017
32017
Lipid profile and genetic markers associated with the level of oxidized low density lipoproteides
EY Khlebus, AN Meshkov, VZ Lankin, AA Orlovsky, AV Kiseleva, ...
Russian Journal of Cardiology 150 (10), 49-54, 2017
22017
Дифференциальная диагностика наследственного синдрома гипохолестеринемии с применением экзомного секвенирования
АИ Ершова, НВ Щербакова, АА Суворова, ЭЮ Хлебус, ИВ Сидонец, ...
Рациональная фармакотерапия в кардиологии 10 (5), 509-512, 2014
22014
Comparative Tumor Microenvironment Analysis of Primary and Recurrent Ovarian Granulosa Cell Tumors
E Khlebus, VK Vuttaradhi, T Welte, N Khurana, J Celestino, HC Beird, ...
Molecular Cancer Research 21 (5), 483-494, 2023
12023
The Frequency of Heterozygous Carriage of the PAH Gene Nucleotide Sequence Variants Associated with the Development of Phenylketonuria in the ESSE-Vologda Population-Based …
OV Kurilova, MV Klimushina, AV Kiseleva, AI Ershova, EA Sotnikova, ...
Molecular Genetics, Microbiology and Virology 36 (2), 92-99, 2021
12021
The frequency of heterozygous carriage of CFTR gene mutations causing the development of cystic fibrosis in a population-based cohort study (ESSE-Vologda)
EA Sotnikova, MV Klimushina, AV Kiseleva, OP Skirko, OV Kurilova, ...
Medical Genetics 19 (7), 64-65, 2020
12020
Abstract B057: Oncogenic Foxl2 directs enhancer reprogramming and changes in 3D genome structure in ovarian granulosa cell tumors
VK Vuttaradhi, E Khlebus, T Welte, B Lawson, RT Hillman
Cancer Research 84 (5_Supplement_2), B057-B057, 2024
2024
13 Glucocorticoids promote granulosa cell tumor growth and antagonize paclitaxel via a FOXL2 c. C402G-dependent mechanism
RT Hillman, T Welte, V Vuttaradhi, E Khlebus, J Li
Gynecologic Oncology Reports 48, S7-S8, 2023
2023
Tumor microenvironment composition correlates with relapse in ovarian granulosa cell tumors
E Khlebus, VK Vuttaradhi, T Welte, N Khurana, J Celestino, HC Beird, ...
Cancer Research 83 (7_Supplement), 2503-2503, 2023
2023
Targeting FOXL2C402Gvulnerabilities in adult type ovarian granulosa cell tumors
T Welte, V Vuttaradhi, E Khlebus, B Lawson, RT Hillman, N Nguyen, ...
Cancer Research 83 (7_Supplement), 453-453, 2023
2023
Comparative Transcriptomic Analysis of Primary and Recurrent Ovarian Granulosa Cell Tumors
E Khlebus, VK Vuttaradhi, T Welte, N Khurana, J Celestino, HC Beird, ...
2022
Oncogenic Foxl2 is a chromatin-remodeling pioneer transcription factor in adult-type ovarian granulosa cell tumors
VK Vuttaradhi, E Khlebus, T Welte, N Khurana, RT Hillman
2022
QuantStudio 12k flex Real-Time PCR system for screening phenylalanine hydroxylase (PAH) gene mutations
OV Kurilova, MV Klimushina, AV Kiseleva, OP Skirko, EA Sotnikova, ...
Medical Genetics 19 (7), 71-72, 2020
2020
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