Dustin Baldridge
Overview
Explore the profile of Dustin Baldridge including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
38
Citations
891
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Cole J, Williams J, Sellitto A, Baratta L, Huecker J, Baldridge D, et al.
Neurology
. 2025 Feb;
104(5):e210275.
PMID: 39937999
Background And Objectives: Genetic testing is critical for optimal diagnosis and management of pediatric neurology patients, but access is challenging. We investigated whether social determinants of health (SDOH) were associated...
2.
Zerafati-Jahromi G, Oxman E, Hoang H, Charng W, Kotla T, Yuan W, et al.
Am J Hum Genet
. 2025 Jan;
112(3):537-553.
PMID: 39879987
Dysregulation of genes encoding the homologous to E6AP C-terminus (HECT) E3 ubiquitin ligases has been linked to cancer and structural birth defects. One member of this family, the HECT-domain-containing protein...
3.
Kraft F, Rodriguez-Aliaga P, Yuan W, Franken L, Zajt K, Hasan D, et al.
Science
. 2024 Oct;
386(6721):516-525.
PMID: 39480921
Malformations of the brain are common and vary in severity, from negligible to potentially fatal. Their causes have not been fully elucidated. Here, we report pathogenic variants in the core...
4.
Kohler J, Legro N, Baldridge D, Shin J, Bowman A, Ugur B, et al.
Genet Med
. 2024 May;
26(9):101166.
PMID: 38767059
Purpose: The function of FAM177A1 and its relationship to human disease is largely unknown. Recent studies have demonstrated FAM177A1 to be a critical immune-associated gene. One previous case study has...
5.
Baldridge D, Kaster L, Sancimino C, Srivastava S, Molholm S, Gupta A, et al.
J Neurodev Disord
. 2024 Apr;
16(1):17.
PMID: 38632549
Monogenic disorders account for a large proportion of population-attributable risk for neurodevelopmental disabilities. However, the data necessary to infer a causal relationship between a given genetic variant and a particular...
6.
Chopra M, Savatt J, Bingaman T, Good M, Morgan A, Cooney C, et al.
Genet Med
. 2023 Dec;
26(3):101035.
PMID: 38059438
Purpose: Clinically ascertained variants are under-utilized in neurodevelopmental disorder research. We established the Brain Gene Registry (BGR) to coregister clinically identified variants in putative brain genes with participant phenotypes. Here,...
7.
Marom R, Zhang B, Washington M, Song I, Burrage L, Rossi V, et al.
PLoS Genet
. 2023 Nov;
19(11):e1011005.
PMID: 37934770
Background: Kinesin motor proteins transport intracellular cargo, including mRNA, proteins, and organelles. Pathogenic variants in kinesin-related genes have been implicated in neurodevelopmental disorders and skeletal dysplasias. We identified de novo,...
8.
Koop K, Yuan W, Tessadori F, Rodriguez-Polanco W, Grubbs J, Zhang B, et al.
Hum Mol Genet
. 2023 Aug;
32(21):3063-3077.
PMID: 37552066
Rab GTPases are important regulators of intracellular vesicular trafficking. RAB5C is a member of the Rab GTPase family that plays an important role in the endocytic pathway, membrane protein recycling...
9.
Ebstein F, Kury S, Most V, Rosenfelt C, Scott-Boyer M, van Woerden G, et al.
Sci Transl Med
. 2023 May;
15(698):eabo3189.
PMID: 37256937
A critical step in preserving protein homeostasis is the recognition, binding, unfolding, and translocation of protein substrates by six AAA-ATPase proteasome subunits (ATPase-associated with various cellular activities) termed PSMC1-6, which...
10.
Sheppard S, Bryant L, Wickramasekara R, Vaccaro C, Robertson B, Hallgren J, et al.
Sci Adv
. 2023 Mar;
9(10):eade1463.
PMID: 36897941
Pathogenic variants in , a lysine methyltransferase, are associated with global developmental delay, macrocephaly, autism, and congenital anomalies (OMIM 617788). Given the relatively recent discovery of this disorder, it has...