Author

Hajar Amini

University of California, DavisORCID 0000-0001-9364-7839Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Agnieszka SłowikiD· 1 shared Alejandro BustamanteiD· 1 shared Alejandro Hornick· 1 shared Alessandro A. Viana Oliveira Souza· 1 shared Alonso GutiérreziD· 1 shared Andria L. FordiD· 1 shared Antoni DávalosiD· 1 shared Antonio AraúziD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Agnieszka SłowikORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineBrainPeer-reviewedFeb 24, 2022

MULTI-ANCESTRY GENETIC STUDY IN 5,876 PATIENTS IDENTIFIES AN ASSOCIATION BETWEEN EXCITOTOXIC GENES AND EARLY OUTCOMES AFTER ACUTE ISCHEMIC STROKE

Laura Ibáñez, Laura Heitsch, Caty Carrera…·Carlos Cruchaga

This paper identifies seven genome-wide significant loci associated with early neurological instability after acute ischemic stroke, linking excitotoxic genes to poor outcomes.

51 citationstop 2%

humanGWAS summary statistics

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BioinformaticsBioinformaticsPeer-reviewedMar 29, 2019

Discovery of tandem and interspersed segmental duplications using high throughput sequencing

Arda Söylev, Thong Minh Le, Hajar Amini…·Fereydoun Hormozdiari

The paper develops TARDIS, a tool for accurately detecting complex structural variations, including tandem and interspersed segmental duplications, using short-read whole genome sequencing data.

40 citationstop 4%

humanwhole-genome sequencing

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