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Ángel Carracedo

universidade de santiago de compostela
H指数:107
被引数:6.1万

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Runs of Homozygosity and Signatures of Positive Selection in Colombian Native American Populations: Genetic Architecture and Demographic History

纯合连续片段和正向选择的信号在哥伦比亚土著美洲人群中的遗传架构与人口历史

2026-09-290
PRE
Polygenic Risk Modelling in Periodontitis: Insights From a Feasibility Study of 4243 European Cases and Current Limitations

牙周炎的多基因风险建模:来自4243例欧洲病例可行性与当前局限性的研究

2026-08-250
OAAI
Expanding CIRdb, a comprehensive catalog of whole-exome sequencing data of Canary Islanders

扩展CIRdb,加那利群岛全外显子组测序数据的综合目录

2026-08-100
OAAI
Advancing Personalized Medicine in Psychiatry: A Descriptive Pilot Study Integrating Pharmacogenetics and Pharmacokinetics in Long-Acting Antipsychotic Treatment

推进精神科个性化医学:一项整合药代动力学和药代动力学在长效抗精神病药物治疗中的描述性试点研究

2026-08-050
OA
Polygenic liability to loneliness increases psychosis risk through adolescent loneliness: evidence from the EU-GEI study

多基因易感性增加孤独症风险,通过青少年孤独:来自EU-GEI研究的证据

2026-07-280
OA
A New Patient With SPOUT1-Related Neurodevelopmental Disorder Identified by Genomic Data Re-Analysis: Novel Phenotypic Features and Literature Review

通过基因组数据再分析鉴定的一例新发SPOUT1相关神经发育障碍患者:新的表型特征及文献综述

2026-03-010
PRE
Splicing Predictions, Splicing Assays, and Variant Classification Using ACMG/AMP Guidelines: Challenges Observed with BRCA1 and BRCA2 Variants

使用ACMG/AMP指南进行剪接预测、剪接检测和变异分类:在BRCA1和BRCA2变异中观察到的挑战

2026-01-010
PRE
Identifying sepsis susceptibility genes in post-surgical patients using an artificial intelligence approach

使用人工智能方法识别术后患者脓毒症易感基因

2025-12-150
OAAI
Cell type-specific methylome-wide association studies of childhood ADHD symptoms

细胞类型特异性全甲基组关联研究儿童ADHD症状

2025-10-260
OAAI
Genome-wide association study of susceptibility to acute respiratory distress syndrome

急性呼吸窘迫综合征易感性的全基因组关联研究

2025-09-300
OAAI
Exploring the sensory profile and pharmacogenetic biomarkers in child and youth ADHD patients undergoing methylphenidate (MPH) treatment: a systematic review conducted in European studies

探索接受哌甲酯(MPH)治疗的儿童和青少年ADHD患者的感官特征和药物遗传学生物标志物:一项在欧洲研究中进行的系统综述

2025-09-020
PREAI
A Lack of Complete Linkage Disequilibrium Between c.1236G>A and c.1129-5923C>G HapB3 Variants of DPYD: A Call to Revise European Pharmacogenetic Guidelines

DPYD基因c.1236G>A与c.1129-5923C>G HapB3变异之间的完全连锁不平衡缺失:呼吁修订欧洲药物基因组学指南

2025-08-220
PRE