Tag: genome-wide association study

March 06, 2023

A new approach to analyzing genomic association data finds convergence of both rare and common genetic influences on autism at chromosome 16p By Azra Jaferi

May 09, 2022

Characterizing the convergent molecular mechanisms of common and rare autism-associated genetic variation

December 01, 2020

Defining the regulatory landscape of autism susceptibility genes in human neurons

April 29, 2020

Progress in understanding the genetic basis of mental health

May 30, 2019

SFARI fall 2018 science meeting highlighted recent findings in autism research By Serena Bianchi

Image of Dora Angelaki (New York University) presented her research on multisensory integration in autism

March 19, 2019

Largest genome-wide association study yields common variants associated with risk of autism

A graph of the main ASD scan, with combined results from the replication sample marked in yellow. Genome-wide significant clusters are marked in green. The x axis shows genomic position (chromosomes 1–22) and the y axis shows statistical significance as –log10(P) of z statistics. The cutoff for statistical significance is marked by the horizontal red line.

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