Last Updated: 09/26/2026
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Found 13 publications
Abstract word dropout and cross-speaker misalignment of word concreteness are features of conversation in aging.
Journal: Cortex; a journal devoted to the study of the nervous system and behavior
Published: March 11, 2025
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.
Journal: American journal of human genetics
Published: March 03, 2023
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.
Journal: American journal of human genetics
Published: April 15, 2022
Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders.
Journal: American journal of human genetics
Published: January 15, 2021
COVID-19: neonatal-perinatal perspectives.
Journal: Journal of perinatology : official journal of the California Perinatal Association
Published: June 24, 2020
De novo variants in MPP5 cause global developmental delay and behavioral changes.
Journal: Human molecular genetics
Published: May 29, 2020
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects.
Journal: American journal of human genetics
Published: April 24, 2020
Alkylglycerol monooxygenase, a heterotaxy candidate gene, regulates left-right patterning via Wnt signaling.
Journal: Developmental biology
Published: December 10, 2018
RAPGEF5 Regulates Nuclear Translocation of β-Catenin.
Journal: Developmental cell
Published: March 16, 2017
Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy.
Journal: Seminars in cell & developmental biology
Published: November 29, 2015
Last Updated: 09/26/2026