scispace - formally typeset
J

Jason Chiang

Researcher at St. Jude Children's Research Hospital

Publications -  49
Citations -  751

Jason Chiang is an academic researcher from St. Jude Children's Research Hospital. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 11, co-authored 32 publications receiving 397 citations. Previous affiliations of Jason Chiang include University of Pittsburgh.

Papers
More filters
Journal ArticleDOI

Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic features.

TL;DR: This study proposes an additional molecular layer to the current histopathological classification of DLGNT, of particular use for cases without typical morphological or radiological characteristics, such as diffuse growth and radiologic leptomeningeal dissemination.
Journal ArticleDOI

Inflammatory Reaction in Neurological Diseases

TL;DR: Findings suggest that patients with and without ARD were found to have similar risks of developing dementia and the Longitudinal Health Insurance Database 2000 to investigate and compare the risk of dementia between patients clinically diagnosed with autoimmune rheumatic diseases and non-ARD patients during a 5-year follow-up period.
Journal ArticleDOI

Structure and evolution of double minutes in diagnosis and relapse brain tumors

TL;DR: The results suggest that double minutes readily evolve, increasing tumor heterogeneity rapidly, and understanding patterns of double minute evolution can shed light on future therapeutic solutions to brain tumors carrying such variants.
Journal ArticleDOI

Molecular pathology of paediatric central nervous system tumours.

TL;DR: Molecular genetic alterations in paediatric CNS tumours, including those in low‐grade and high‐grade gliomas, ependymomas, and embryonal tumours are reviewed.
Journal ArticleDOI

Cell-surface antigen profiling of pediatric brain tumors: B7-H3 is consistently expressed and can be targeted via local or systemic CAR T-cell delivery.

TL;DR: The importance of studying target antigen and HLA class-I expression in PDOX samples for the future design of immunotherapies is highlighted, and active preclinical and clinical exploration of B7-H3-targeted CAR T-cell therapies for a broad spectrum of pediatric brain tumors are supported.