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M

Mark I. Rees

swansea university
H指数:54
被引数:8,527

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Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy

遗传性全身性癫痫患者中多基因风险评分与临床表型的相关性

2026-09-100
OAAI
The role of copy number variants in the genetic architecture of common familial epilepsies
2024-01-201
PRE
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

超过29,000名癫痫患者的ghis荟萃分析确定了26个风险基因座和亚型特异性遗传结构

2023-08-3143
OAAI
Sex-specific disease modifiers in juvenile myoclonic epilepsy
2022-02-2126
OAAI
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

亚基因不耐受,ClinVar和癫痫: 29,165个人的全外显子组测序研究

2021-06-0143
OAAI
Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy
2021-01-0122
OAAI
Trait impulsivity in Juvenile Myoclonic Epilepsy
2020-12-0231
OAAI
Ten-year Mortality, Disease Progression, and Treatment-related Side Effects in Men with Localised Prostate Cancer from the ProtecT Randomised Controlled Trial According to Treatment Received
2020-03-01116
OAAI
Quantitative analysis of phenotypic elements augments traditional electroclinical classification of common familial epilepsies
2019-10-170
OAAI
Clinical spectrum of STX1B-related epileptic disorders
2019-03-1246
OAAI