F Kyle Satterstrom

14PUBLICATIONS
114CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Infant and child healthDevelopmental genetics (incl. sex determination)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (14)

|May 30, 2026
Identification of moderate effect size genes in autism spectrum disorder through a novel gene pairing approach.

|Nov 12, 2025
Rare genetic variants confer a high risk of ADHD and implicate neuronal biology.

Ditte Demontis, Jinjie Duan, Yu-Han H Hsu

|May 03, 2024
Contribution of autosomal rare and de novo variants to sex differences in autism.

Mahmoud Koko, F Kyle Satterstrom, Varun Warrier

|Jul 27, 2023
Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders.

Alfredo M Valencia, Akshay Sankar, Pleuntje J van der Sluijs

|Mar 01, 2023
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.

Ditte Demontis, G Bragi Walters, Georgios Athanasiadis

|Jan 26, 2023
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.

Ditte Demontis, G Bragi Walters, Georgios Athanasiadis

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Frequent Collaborators

10 joint publications

Mark J Daly

7 joint publications

Ditte Demontis

7 joint publications

Jonas Bybjerg-Grauholm

7 joint publications

Jakob Grove