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Analysis of clinically relevant variants from ancestrally diverse Asian genomes

PaperCitations, authors & open-access status

Analysis of clinically relevant variants from ancestrally diverse Asian genomes is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Analysis of clinically relevant variants from ancestrally diverse Asian genomes have?

ScholarIQcitation count

Analysis of clinically relevant variants from ancestrally diverse Asian genomes has 82 citations in the OpenAlex counts ScholarIQ stores.

When was Analysis of clinically relevant variants from ancestrally diverse Asian genomes published?

ScholarIQyear

Analysis of clinically relevant variants from ancestrally diverse Asian genomes has 2022 year in the ScholarIQ index.

What is the open-access status of Analysis of clinically relevant variants from ancestrally diverse Asian genomes?

ScholarIQoa status

Analysis of clinically relevant variants from ancestrally diverse Asian genomes has gold oa status in the ScholarIQ index.

What is the DOI of Analysis of clinically relevant variants from ancestrally diverse Asian genomes?

ScholarIQdoi

The DOI for Analysis of clinically relevant variants from ancestrally diverse Asian genomes is on the source record.

What is the PMID of Analysis of clinically relevant variants from ancestrally diverse Asian genomes?

ScholarIQpmid

The PMID for Analysis of clinically relevant variants from ancestrally diverse Asian genomes is on the source record.

What is the OpenAlex record for Analysis of clinically relevant variants from ancestrally diverse Asian genomes?

ScholarIQopenalex

The OpenAlex for Analysis of clinically relevant variants from ancestrally diverse Asian genomes is on the source record.

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