Siddharth Srivastava

Department of Materials Science and Engineering, University of California Los Angeles

Affiliated withUniversity of California Los Angeles

Research Area

Biography

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title	2026

Other Publications

Article	Year
Neurobehavioral phenotype of autism spectrum disorder associated with germline heterozygous mutations in PTEN. Translational psychiatry\| PubMed ID: 31594918	2019
Brief Report: Role of Parent-Reported Executive Functioning and Anxiety in Insistence on Sameness in Individuals with Germline PTEN Mutations. Journal of autism and developmental disorders\| PubMed ID: 33595755	2022
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome medicine\| PubMed ID: 33874999	2021
A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statement. Clinical genetics\| PubMed ID: 34240408	2022
Toward better characterization of restricted and repetitive behaviors in individuals with germline heterozygous PTEN mutations. American journal of medical genetics. Part A\| PubMed ID: 34423884	2021
Psychiatric Characteristics Across Individuals With Mutations. Frontiers in psychiatry\| PubMed ID: 34489750	2021
Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms. Molecular genetics & genomic medicine\| PubMed ID: 34519438	2021
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants. Genetics in medicine : official journal of the American College of Medical Genetics\| PubMed ID: 36083290	2022
The Feasibility of Early Alzheimer's Disease Diagnosis Using a Neural Network Hybrid Platform. Biosensors\| PubMed ID: 36140138	2022
Longitudinal neurobehavioral profiles in children and young adults with PTEN hamartoma tumor syndrome and reliable methods for assessing neurobehavioral change. Journal of neurodevelopmental disorders\| PubMed ID: 36641436	2023
Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families. American journal of medical genetics. Part A\| PubMed ID: 37183572	2023
Heterozygous loss-of-function variants are associated with variable and incompletely penetrant growth and developmental features. medRxiv : the preprint server for health sciences\| PubMed ID: 37808847	2023
Controlling the Nucleation and Growth of Salt from Bodily Fluid for Enhanced Biosensing Applications. Biosensors\| PubMed ID: 38131777	2023
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features. HGG advances\| PubMed ID: 38297832	2024
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology\| PubMed ID: 38501559	2024
AI-Driven Spectral Decomposition: Predicting the Most Probable Protein Compositions from Surface Enhanced Raman Spectroscopy Spectra of Amino Acids. Bioengineering (Basel, Switzerland)\| PubMed ID: 38790349	2024
Label-free single-vesicle based surface enhanced Raman spectroscopy: A robust approach for investigating the biomolecular composition of small extracellular vesicles. PloS one\| PubMed ID: 38889139	2024
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes. American journal of human genetics\| PubMed ID: 39013459	2024
Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome-osteogenesis imperfecta. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research\| PubMed ID: 39088537	2024
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay. Molecular psychiatry\| PubMed ID: 39472663	2025
On the Feasibility of SERS-Based Monitoring of Drug Loading Efficiency in Exosomes for Targeted Delivery. Biosensors\| PubMed ID: 40136938	2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial Endpoints. American journal on intellectual and developmental disabilities\| PubMed ID: 40858308	2025