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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

PaperCitations, authors & open-access status

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data have?

ScholarIQcitation count

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data has 365 citations in the OpenAlex counts ScholarIQ stores.

When was Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data published?

ScholarIQyear

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data has 2022 year in the ScholarIQ index.

What is the open-access status of Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data?

ScholarIQoa status

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data has green oa status in the ScholarIQ index.

What is the DOI of Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data?

ScholarIQdoi

The DOI for Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data is on the source record.

What is the PMID of Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data?

ScholarIQpmid

The PMID for Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data is on the source record.

What is the OpenAlex record for Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data?

ScholarIQopenalex

The OpenAlex for Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data is on the source record.

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