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M Fu

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Nature Medicine|March 30, 2026

Deleterious coding variation associated with autism is shared across ancestriesMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.

Nature Genetics|August 18, 2022

Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.

Biorxiv : the Preprint Server for Biology|September 16, 2024

A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective mannerToni A Boltz, Benjamin B Chu, Calwing Liao, et al.

The New England Journal of Medicine|June 5, 2024

Genome Sequencing for Diagnosing Rare DiseasesMonica H Wojcik, Gabrielle Lemire, Eva Berger, et al.

Nature Genetics|July 8, 2026

A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective mannerToni A Boltz, Benjamin B Chu, Matthew DeFelice, et al.

Medrxiv : the Preprint Server for Health Sciences|March 3, 2023

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.

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Search research articles

Showing results (771-780 of 776) with videos related to

Sort By:

Pageof 78

You have reached the last page of results.This site can display upto 776 results.

Nature Medicine|March 30, 2026

Deleterious coding variation associated with autism is shared across ancestriesMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.

Nature Genetics|August 18, 2022

Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.

Biorxiv : the Preprint Server for Biology|September 16, 2024

A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective mannerToni A Boltz, Benjamin B Chu, Calwing Liao, et al.

The New England Journal of Medicine|June 5, 2024

Genome Sequencing for Diagnosing Rare DiseasesMonica H Wojcik, Gabrielle Lemire, Eva Berger, et al.

Nature Genetics|July 8, 2026

A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective mannerToni A Boltz, Benjamin B Chu, Matthew DeFelice, et al.

Medrxiv : the Preprint Server for Health Sciences|March 3, 2023

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.

Pageof 78