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Research Abr. 15, 2024

Dr. Sameer Sheth and a Rice University team develop and demonstrate a miniature brain stimulator in humans

Research Abr. 01, 2024

YKT6 gene variants cause a new genetic disorder finds a new study

Research Mar. 25, 2024

Study finds sensory changes are more severe in MECP2 duplication disorder patients than Rett patients

Research Mar. 12, 2024

FRYL gene variants linked to a new neurological disorder

Research Feb. 29, 2024

Dissecting the roles for excitatory and inhibitory neurons in STXBP1 encephalopathy

Research Feb. 28, 2024

Texas Children’s Hospital and Baylor College of Medicine researchers develop a new toolkit in fruit flies to study Zika virus

Research Feb. 22, 2024

TMEM208 variants cause a new developmental disorder

Research Feb. 20, 2024

The molecular signatures of a common brain tumor found to be similar in dogs and humans

Research Feb. 06, 2024

A new deep-learning tool developed to analyze RNA dynamics on a large scale

Research Ene. 31, 2024

Dr. Sameer Sheth And Collaborators Develop A Holographic Tool To Facilitate Interactive Surgical Planning

Research Ene. 12, 2024

Dr. King invited to serve as Chair of NIH study section (Jul 12, 2023)

Research Ene. 12, 2024

Texas Children’s Cancer Center researchers receive grants

Carl Allen and Phillip Lupo
Research Ene. 12, 2024

Allen, Lupo earn pediatric cancer grants

Research Ene. 12, 2024

Gene mutation underlies neurodevelopmental disorders (Aug 4, 2023)

Research Ene. 12, 2024

Rouce Team Awarded $1.2 Million National Cancer Institute Grant

Research Ene. 04, 2024

Variants in PPFIA3, a synaptic scaffolding protein, discovered to be the cause of a newly recognized syndromic neurodevelopmental disorder

Research Nov. 27, 2023

How neurotransmitters work together to detect and distinguish odors

Research Nov. 13, 2023

A new biomarker can better predict clinical outcomes after radiation for meningiomas

Research Oct. 27, 2023

Novel Rett syndrome variant shines light on new screening strategies for therapies

Research Oct. 13, 2023

DOT1L gene variants associated with a new neurological disorder