Dustin L. Gable
Neurology
6201 Greenleigh Ave
Middle River, MD 21220
Middle River, MD 21220
Last Updated: 09/26/2026
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Found 14 publications
ADAT3 variants disrupt the activity of the ADAT tRNA deaminase complex and impair neuronal migration.
Journal: Brain : a journal of neurology
Published: November 06, 2024
Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders.
Journal: Annals of clinical and translational neurology
Published: July 20, 2023
Familial Clonal Hematopoiesis in a Long Telomere Syndrome.
Journal: The New England journal of medicine
Published: May 04, 2023
T cell immune deficiency rather than chromosome instability predisposes patients with short telomere syndromes to squamous cancers.
Journal: Cancer cell
Published: October 15, 2022
Upper motor neuron signs and early onset gait abnormalities in young children with bi-allelic VWA1 variants.
Journal: American journal of medical genetics. Part A
Published: March 25, 2022
Mendelian etiologies identified with whole exome sequencing in cerebral palsy.
Journal: Annals of clinical and translational neurology
Published: November 16, 2021
ZCCHC8, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation.
Journal: Genes & development
Published: April 19, 2019
Short telomere syndromes cause a primary T cell immunodeficiency.
Journal: The Journal of clinical investigation
Published: February 05, 2018
Germline Mutations in DNA Repair Genes in Lung Adenocarcinoma.
Journal: Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
Published: July 14, 2017
Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema.
Journal: Science translational medicine
Published: April 03, 2016
Erratum. Radiation sensitivity and radiation necrosis in the short telomere syndromes.
Journal: International journal of radiation oncology, biology, physics
Published: February 09, 2016
A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex.
Journal: American journal of human genetics
Published: September 22, 2015
Last Updated: 09/26/2026