Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Rare coding variation provides insight into the genetic architecture and phenotypic context of autism have?

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism has 640 citations in the OpenAlex counts ScholarIQ stores.

When was Rare coding variation provides insight into the genetic architecture and phenotypic context of autism published?

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism has 2022 year in the ScholarIQ index.

What is the open-access status of Rare coding variation provides insight into the genetic architecture and phenotypic context of autism?

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism has green oa status in the ScholarIQ index.

What is the DOI of Rare coding variation provides insight into the genetic architecture and phenotypic context of autism?

The DOI for Rare coding variation provides insight into the genetic architecture and phenotypic context of autism is on the source record.

What is the PMID of Rare coding variation provides insight into the genetic architecture and phenotypic context of autism?

The PMID for Rare coding variation provides insight into the genetic architecture and phenotypic context of autism is on the source record.

What is the OpenAlex record for Rare coding variation provides insight into the genetic architecture and phenotypic context of autism?

The OpenAlex for Rare coding variation provides insight into the genetic architecture and phenotypic context of autism is on the source record.