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

Great Bolgar's historical genetics: a genomic study of individuals from burials close to the Greek Chamber in the 14th century

大博尔加的历史遗传学:对14世纪希腊墓室附近墓葬个体的基因组研究

Andreeva, T V; Soshkina, A D; Kunizheva, S S; Manakhov, A D; Pezhemsky, D V; Rogaev, E I

Mitogenomic analysis of a representative of the Chernyakhov culture in the Middle Dniester and their genetic relationship with the Slavs in the context of paleoanthropological data

对德涅斯特河中游切尔尼亚霍夫文化代表人物的线粒体基因组分析及其与斯拉夫人的遗传关系(基于古人类学数据)

Rozhdestvenskikh, E V; Andreeva, T V; Malyarchuk, A B; Adrianova, I Yu; Khodyreva, D S; Evteev, A A; Buzhilova, A P; Rogaev, E I

Unconventional animal models to study the role of telomeres in aging and longevity.

利用非常规动物模型研究端粒在衰老和长寿中的作用

Simoroz E V, Vasilevska J, Arakelyan N A, Manakhov A D, Rogaev E I

The Effects of Assisted Reproductive Technologies on De Novo Mutations

辅助生殖技术对新生突变的影响

Arakelyan, N A; Vasilevska, J; Rogaev, E I

An Analysis of Genetic Predisposition to Hereditary Catalepsy in a Mouse Model of Neuropsychiatric Disorders Using Whole-Genome Sequencing Data

利用全基因组测序数据分析神经精神疾病小鼠模型中遗传性僵直症的遗传易感性

Andreeva, T V; Gusev, F E; Sinyakova, N A; Kulikov, A V; Grigorenko, A P; Adrianova, I Yu; Bazovkina, D V; Rogaev, E I

Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases

人类神经退行性疾病和肿瘤疾病中Y染色体的嵌合性缺失

Kuznetsova, I L; Uralsky, L I; Tyazhelova, T V; Andreeva, T V; Rogaev, E I

Quantifying human genome parameters in aging

量化衰老过程中人类基因组参数

Volobaev, V P; Kunizheva, S S; Uralsky, L I; Kupriyanova, D A; Rogaev, E I

Current Trends and Approaches to the Search for Genetic Determinants of Aging and Longevity

当前寻找衰老和长寿遗传决定因素的趋势和方法

Kunizheva, S S; Volobaev, V P; Plotnikova, M Yu; Kupriyanova, D A; Kuznetsova, I L; Tyazhelova, T V; Rogaev, E I

Classification and monomer-by-monomer annotation dataset of suprachromosomal family 1 alpha satellite higher-order repeats in hg38 human genome assembly

人类基因组组装hg38中超染色体家族1α卫星高阶重复序列的分类和单体注释数据集

Uralsky, L I; Shepelev, V A; Alexandrov, A A; Yurov, Y B; Rogaev, E I; Alexandrov, I A

Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies

全外显子组测序将牙源性肿瘤与ANO5基因的常染色体显性突变联系起来,该突变与颌骨干发育不良和肌肉营养不良有关。

Andreeva, T V; Tyazhelova, T V; Rykalina, V N; Gusev, F E; Goltsov, A Yu; Zolotareva, O I; Aliseichik, M P; Borodina, T A; Grigorenko, A P; Reshetov, D A; Ginter, E K; Amelina, S S; Zinchenko, R A; Rogaev, E I