Matthew A. Deardorff

University of Southern California — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

51h-index11.0kcitations242works0.42yr avg
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Research Topics

Genomics and Chromatin Dynamics(39), Genomic variations and chromosomal abnormalities(38), Genomics and Rare Diseases(38), Genetic Syndromes and Imprinting(32), Genetics and Neurodevelopmental Disorders(24)

Publications235 total

Lipid transport is necessary for neocortical lamination
2025Open Access
Isolated lateralized overgrowth and the need for tumor screening: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2025Open Access
Opioid-Related Pharmacogenomic Variants in a Retrospective Cohort of High-Risk Hospitalized Infants
The Journal of Pediatrics·2025· 1 cited
Correction: Clinical impact of pharmacogenomics in pediatric care: insights extracted from clinical exome sequencing
Frontiers in Genetics·2025Open Access
Contributors
Elsevier eBooks·2025
Survival of an Infant With PTPRQ Deletion With Congenital Absence of the Anterior Chest Wall
American Journal of Respiratory and Critical Care Medicine·2025
16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome
Genes·2025· 1 citedOpen Access
P796: Vanishing copy number gains: causative chromosomal changes or unstable findings of unknown consequence?
Genetics in Medicine Open·2025Open Access
P564: Parental perspectives on pediatric genomic testing, research, and data management in a multicultural population
Genetics in Medicine Open·2025Open Access
Identifying Opioid-Related Pharmacogenomic Variants in High-Risk Hospitalized Infants: A Pilot Study
2024Open Access
Increased Expression of <i>ZFPM2</i> Bypasses <i>SRY</i> to Drive 46,XX Testicular Development: A New Mechanism of 46,XX DSD
2024Open Access
Autonomous drone behavior via MCDM of UFOMap layers
2024· 1 cited
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features
Human Genetics and Genomics Advances·2024· 3 citedOpen Access
P562: A model for genetic counselor result triage in a busy pediatric neurology division
Genetics in Medicine Open·2024Open Access
54. VMD4Kids: A highly sensitive NGS panel to detect low-level mosaic variants in vascular anomalies and overgrowth disorders
Cancer Genetics·2023
Heterozygous loss-of-function <i>SMC3</i> variants are associated with variable and incompletely penetrant growth and developmental features
2023Open Access
Frame Selection Strategies for Real-Time Structure-from-Motion from an Aerial Platform
2023· 2 cited
Improving Real-Time Aerial 3D Reconstruction: Towards Fusion of a Hand-Crafted SfM Algorithm with a Data-Driven Deep Neural Network
2023· 1 cited
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, <scp>genotype–phenotype</scp> correlations and common mechanisms
American Journal of Medical Genetics Part A·2023· 37 citedOpen Access
Simulated gold-standard for quantitative evaluation of monocular vision algorithms
2023· 8 cited
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Frequent Co-authors

Ian D. Krantz(16), Elaine H. Zackai(10), Dinah Clark(10), Maninder Kaur(8), Antonie D. Kline(8), Laura K. Conlin(8), Nancy B. Spinner(8), Håkon Håkonarson(7), Peter S. Klein(6), Laird G. Jackson(6), Juan Pié(5), Victoria Mok Siu(5), Feliciano J. Ramos(5), A. Micheil Innes(5), Alisha Wilkens(5), Leslie G. Biesecker(4), Change Tan(4), Holly Dubbs(4), Gregory M. Cooper(3), Antonio Musio(3)