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R

Rex L. Chisholm

northwestern university
H指数:63
被引数:2.9万

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Return of genome-informed risk-assessment results for common conditions to 23,840 adults and children: An eMERGE network study

将基于基因组信息的常见疾病风险评估结果反馈给23,840名成人和儿童:一项eMERGE网络研究

2026-03-230
PRE
The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessments

电子病历与基因组学研究:评估基因组信息风险评估影响的设计与分析框架

2026-03-230
OAAI
The Gene Ontology knowledgebase in 2026

2026年的基因本体知识库

2025-12-011
PRE
Advancing the science of genomic learning healthcare systems

推进基因组学习型医疗系统的科学

2025-07-230
OA
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing

临床测序可采取的单基因结果后医疗保健利用的前瞻性,多站点研究

2023-11-012
OAAI
Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores

教育和电子病历和基因组学网络,挑战和从使用多基因风险评分的大规模临床试验中吸取的教训

2023-09-015
OAAI
Returning integrated genomic risk and clinical recommendations: The eMERGE study

回归综合基因组风险和临床建议: eMERGE研究

2023-04-0145
OAAI
The Gene Ontology knowledgebase in 2023

基因本体知识库2023年

2023-03-03774
OAAI
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries

OAS1无意义介导的衰变的遗传调控与欧洲和非洲祖先患者的新型冠状病毒肺炎住院有关

2022-07-1466
OAAI
The Gene Ontology resource: enriching a GOld mine

基因本体论资源: 丰富一个金矿

2020-12-082.2K
OAAI
Frequency of genomic secondary findings among 21,915 eMERGE network participants
2020-09-0169
OAAI
A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies

通过全表型关联研究评估的多囊卵巢综合征的多基因和表型风险预测

2020-01-0939
OAAI
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network
2019-09-0187
OAAI
Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects
2018-03-30101
OAAI