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

Screening for Maternally Inherited Diabetes and Deafness in Large Cohorts of Hearing Impaired and Diabetic Patients

在大样本听力障碍和糖尿病患者队列中筛查母系遗传性糖尿病和耳聋

期刊:Ear and Hearing
影响因子:2.8
doi:10.1097/AUD.0000000000001780
Varga, Lukas; Borecka, Silvia; Skopkova, Martina; Rambani, Vibhuti; Sklenar, Marek; Cipkova, Klaudia; Kickova, Terezia; Ugorova, Diana; Kabatova, Zuzana; Stanik, Juraj; Profant, Milan; Gasperikova, Daniela
糖尿病
代谢
发表日期：2026
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Genetic heterogeneity in patients with enlarged vestibular aqueduct and Pendred syndrome.

前庭导水管扩大和彭德雷德综合征患者的遗传异质性

期刊:Molecular Medicine
影响因子:6.4
doi:10.1186/s10020-025-01262-x
Sklenar Marek, Borecka Silvia, Varga Lukas, Bernardinelli Emanuele, Stanik Juraj, Skopkova Martina, Sabo Miroslav, Ugorova Diana, Dossena Silvia, Gasperikova Daniela
发表日期：2025
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Separation of halide oxidation and substrate halogenation chemistries rationalizes site-selective vanadium dependent haloperoxidase catalysis

卤化物氧化和底物卤化化学的分离解释了位点选择性钒依赖性卤过氧化物酶催化的合理性

期刊:
影响因子:
doi:10.1101/2025.10.24.684477
Baumgartner, Jackson T; Varga, Lukas A; Calhoun, Jackson T; Serrão, Vitor H Balasco; Loerch, Sarah; McKinnie, Shaun M K
发表日期：2025
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Vanadium haloperoxidases as noncanonical terpene synthases

钒卤过氧化物酶作为非典型萜烯合酶

期刊:Methods in Enzymology
影响因子:
doi:10.1016/bs.mie.2024.03.024
Baumgartner, Jackson T; Lozano Salazar, Lia I; Varga, Lukas A; Lefebre, Gabriel H; McKinnie, Shaun M K
发表日期：2024
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Slovak Translation and Cross-Cultural Validation of the Eating Assessment Tool (EAT10(®))

饮食评估工具 (EAT10(®)) 的斯洛伐克语翻译和跨文化验证

期刊:Journal of Clinical Medicine
影响因子:2.9
doi:10.3390/jcm11195966
Frajkova, Zofia; Paouris, Dimitrios; Nado, Ladislav; Vyrvova, Ivana; Fabianova, Adelaida; Printza, Athanasia; Varga, Lukas; Tedla, Miroslav
发表日期：2022
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Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss

中频感音神经性听力损失的综合分子遗传学分析

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-021-01876-1
Pavlenkova, Zuzana; Varga, Lukas; Borecka, Silvia; Karhanek, Miloslav; Huckova, Miloslava; Skopkova, Martina; Profant, Milan; Gasperikova, Daniela
发表日期：2021
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Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant

MANBA基因的c.2158-2A>G变异是捷克和斯洛伐克罗姆人遗传性听力损失和β-甘露糖苷酶缺乏症的重要且常见的病因——这是新的种族特异性变异的证据。

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-020-01508-3
Safka Brozkova, Dana; Varga, Lukas; Uhrova Meszarosova, Anna; Slobodova, Zuzana; Skopkova, Martina; Soltysova, Andrea; Ficek, Andrej; Jencik, Jan; Lastuvkova, Jana; Gasperikova, Daniela; Seeman, Pavel
发表日期：2020
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Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report.

斯洛伐克家族中发现一种新的EYA4变异，导致晚发性常染色体显性遗传性听力损失：病例报告

期刊:BMC Medical Genetics
影响因子:
doi:10.1186/s12881-019-0806-y
Varga Lukas, Danis Daniel, Skopkova Martina, Masindova Ivica, Slobodova Zuzana, Demesova Lucia, Profant Milan, Gasperikova Daniela
发表日期：2019
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Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss.

MARVELD2 的分子遗传学和巴基斯坦和斯洛伐克家族中 DFNB49 听力损失的临床表型

期刊:Human Genetics
影响因子:3.6
doi:10.1007/s00439-015-1532-y
Nayak Gowri, Varga Lukas, Trincot Claire, Shahzad Mohsin, Friedman Penelope L, Klimes Iwar, Greinwald John H Jr, Riazuddin S Amer, Masindova Ivica, Profant Milan, Khan Shaheen N, Friedman Thomas B, Ahmed Zubair M, Gasperikova Daniela, Riazuddin Sheikh, Riazuddin Saima
其它
发表日期：2015
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