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

PaperCitations, authors & open-access status

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

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

PICO Portalcitation count

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

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

PICO Portalyear

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

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

PICO Portaloa status

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

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

PICO Portaldoi

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?

PICO Portalpmid

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?

PICO Portalopenalex

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

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