Publications by:
Shan Dong, PhD

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Nr2f1 enhancers have distinct functions in controlling Nr2f1 expression during cortical development.

Sunday, September 22nd, 2024

Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants.

Tuesday, July 20th, 2021

Prenatal exposure to paternal smoking and likelihood for autism spectrum disorder.

Tuesday, April 20th, 2021

Whole-Exome Sequencing in Fetuses with Congenital Diaphragmatic Hernias: Known and Novel Genetic Mutation

Thursday, October 1st, 2020

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.

Tuesday, April 7th, 2020

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.

Friday, December 14th, 2018