Publications by authors named "Emily Magness"

Claim this Profile
A
Autosomal dominant -related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder.
Bobby G Ng, Erik A Eklund, Jill A Rosenfeld, Abdallah F Elias, Aya Abu-El-Haija, Emily C Magness

Genet Med Open· March 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.
Alinoë Lavillaureix, Paul Rollier, Artem Kim, Veranika Panasenkava, Marie De Tayrac, Emily Magness

Genet Med· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Improving access to exome sequencing in a medically underserved population through the Texome Project.
Blake Vuocolo, Ryan J German, Seema R Lalani, Chaya N Murali, Carlos A Bacino, Emily Magness

Genet Med· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Therapeutic Potential of a Small-Molecule STAT3 Inhibitor in a Mouse Model of Colitis.
Prema Robinson, Kelsey Montoya, Emily Magness, Emma Rodriguez, Viviana Villalobos

Cancers (Basel)· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic and Small-Molecule Modulation of Stat3 in a Mouse Model of Crohn's Disease.
Prema Robinson, Emily Magness, Kelsey Montoya, Nikita Engineer, Thomas K Eckols

J Clin Med· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Characterization of genetic counselor practices in inpatient care settings.
Emily Magness, Pilar Magoulas, Tia Moscarello, Daria Ma, Benjamin M Helm

J Genet Couns· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis