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Farid Radmanesh

Researcher at Harvard University

Publications -  36
Citations -  1838

Farid Radmanesh is an academic researcher from Harvard University. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 20, co-authored 34 publications receiving 1446 citations. Previous affiliations of Farid Radmanesh include Tehran University of Medical Sciences & University of Tehran.

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Ingrid E. Christophersen, +195 more
- 01 Jun 2017 - 
TL;DR: 12 new genetic loci that exceeded genome-wide significance, implicating genes involved in cardiac electrical and structural remodeling are identified, providing insights into the molecular basis of atrial fibrillation and may facilitate the identification of new potential targets for drug discovery.
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Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage

Daniel Woo, +84 more
TL;DR: A genome-wide association study of this condition that meta-analyzed data from six studies that enrolled individuals of European ancestry demonstrated biological heterogeneity across ICH subtypes and highlighted the importance of ascertaining ICH cases accordingly.
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Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

Ganesh Chauhan, +136 more
- 01 Jun 2016 - 
TL;DR: Empirical and experimental data suggest that FOXF2 mediates this association, potentially via differentiation defects of cerebral vascular mural cells, and further expression studies in appropriate human tissues are needed to fully understand the underlying mechanisms.
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Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.

Kristiina Rannikmäe, +51 more
- 03 Mar 2015 - 
TL;DR: The results indicate an association between common variation in the COL4A2 gene and symptomatic small vessel disease, particularly deep intracerebral hemorrhage, and merit replication studies, including in ethnic groups of non-European ancestry.