The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families, and other concerned parties. Their ultimate goal is finding a cure.

Angelman Syndrome Foundation

Angelman Syndrome Foundation Call for Proposals

Hope for Hypothalamic Hamartomas (Hope for HH) is a volunteer-based nonprofit organization aimed at driving education, support, and research for hypothalamic hamartomas. The organization is dedicated to the early detection, improved treatments, and management of hypothalamic hamartomas as a complex medical syndrome with the ultimate goal of finding a cure.

Hope for Hypothalamic Hamartomas

HH Research Grant

The CHARGE Syndrome Foundation aims to discover the causes and improve the management of CHARGE syndrome through research and education, support individuals with CHARGE syndrome and their families, and promote awareness among professionals and the public.

CHARGE Syndrome Foundation

CHARGE Syndrome Foundation: Clinical Research Grant Program

The Brain & Behavior Research Foundation is committed to alleviating the suffering caused by mental illness by awarding grants that will lead to advances and breakthroughs in scientific research.

Brain & Behavior Research Foundation

Patricia Goldman-Rakic Prize Cognitive Neuroscience Research

The Pediatric Brain Tumor Foundation aims to accelerate the discovery and development of more effective treatments for children with brain tumors. This involves working closely with the global scientific community to identify and fill critical gaps in pediatric brain tumor research.

Pediatric Brain Tumor Foundation of the United States, Inc.

Pediatric Brain Tumor Research Funding Proposals

Pediatric Low-grade Glioma and Astrocytoma Research Fund (PLGG/PLGA Grant)

Our mission is to find better treatments and a cure for Fanconi anemia and to provide education and support services to affected families worldwide. The Fanconi Anemia Research Fund (FARF) is the world leader in advancing research for better treatments and a cure for Fanconi anemia, having supported over 260 grants to more than 202 investigators worldwide with $33 million in research projects since its founding in 1989 by parents Lynn and David Frohnmayer.

Fanconi Anemia Research Fund Inc

Fanconi Anemia Research Fund: Research Grant Awards

The mission of the Hereditary Disease Foundation is to fund the most promising, innovative, and paradigm-changing research aimed at curing Huntington’s disease. This genetic brain disorder causes irreversible declines in mood, memory, and movement control, with no current cure or treatment available. By focusing on this single-gene disorder, the foundation hopes to unlock potential cures for other brain disorders such as Parkinson’s, Alzheimer’s, and Lou Gehrig’s (ALS) diseases.

Hereditary Disease Foundation

Hereditary Disease Foundation: Transformative Research Award

Apraxia Kids is dedicated to funding high-quality scientific research on childhood apraxia of speech (CAS) that will lead to peer-reviewed publications and have clinical applications. They aim to cover a wide range of topics related to CAS, prioritizing research that encompasses diverse populations and factors like race/ethnicity, socio-economic status, language, age, and comorbidity.

Childhood Apraxia of Speech Association of North America

Apraxia Kids Research Grants: Undergraduate/Masters Student Clinical Research Grant

The mission of the Koolen-de Vries Syndrome Foundation (KdVSF) is to accelerate the development of therapeutics for the treatment of Koolen-de Vries Syndrome (KdVS), aiming to improve the lives of those living with KdVS.

Koolen-de Vries Syndrome Foundation

KdVSF Investigator Grant

The North American Spine Society (NASS) is a leading multidisciplinary medical society dedicated to promoting the highest quality ethical, value-based, and evidence-based spine care. With nearly 8,000 members worldwide, NASS focuses on fostering excellence in spine care through education, research, and advocacy. Its members come from various spine-related specialties, including orthopedics, neurosurgery, physiatry, and pain management. NASS is committed to being a prominent supporter of spine research, having funded over $4.6 million in spine-related studies since 1989, aiming to improve patient care and understanding of spinal disorders.

Angelman Syndrome Foundation Call for Proposals

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