Julian Martinez-Agosto

Has grant

Associate Professor (with tenure)

David Geffen School of Medicine at UCLA

United States

Research Interests

Explore related searches

Professors in United States Professors in Medical Science Medical Science professors in United States

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Julian Martinez-Agosto is an Associate Professor (with tenure) at the University of California Los Angeles David Geffen School of Medicine, USA. His research focuses on autism, neurodevelopmental disorders, and genetic mutations, as evidenced by his recent publications examining topics such as the collaborative data platforms for autism research and the epigenetic aging in Bloom syndrome patients. He also explores the characterization of behavioral phenotypes associated with genetic variants, contributing to a deeper understanding of developmental delays and psychiatric conditions.

Recent Grants

Grant: Close

Genetic analysis of growth

Open Date:

Close Date:

Articles (10)

Year:

2024

Year:

2023

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Collaborators (4)

Mirko Uljarević

Stanford University

UNITED STATES

View details

Steve Horvath

University of California, Los Angeles

UNITED STATES

View details

Ina Amarillo

Director (Cytogenetics and Molecular Pathology Lab); Associate Professor (Pathology and Lab Medicine)

UNITED STATES

View details

Aaron Besterman

Assistant Professor

University of California, San Diego

UNITED STATES

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Julian Martinez-Agosto

Research Interests

Explore related searches

Contact this professor

About

Recent Grants

Articles (10)

Enhancing multi‐site autism research through the development of a collaborative data platform

Bloom syndrome patients and mice display accelerated epigenetic aging

Mosaic de novo SNRPN gene variant associated with Prader-Willi syndrome

Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autism

Toward better characterization of restricted and repetitive behaviors in individuals with germline heterozygous PTEN mutations

14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and language delay in three unrelated patients

5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulation

Expansion of NEUROD2 phenotypes to include developmental delay without seizures

Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization

The Feasibility and Outcomes of Genetic Testing for Autism and Neurodevelopmental Disorders on an Inpatient Child and Adolescent Psychiatry Service

Collaborators (4)

Mirko Uljarević

Steve Horvath

Ina Amarillo

Aaron Besterman

Make your next move.