• Adult, Continuing Ed

• 37.

American Society for Genomic Medicine-Stefan University

STEMSCIENCETECHNOLOGY ENGINEERINGMATHEMATICS WisdomStefanUniversity.

• Private Grantmaking Foundations

• 38.

Hudson Foundation

Home Our Charitable PrivateFamily Foundation The Hudson Foundations philanthropic mission is to strengthen our communities through strategic monetary grants.

LICR FUND INC

We fund cutting-edge scientific research across multiple Branches and Centers to better understand cancer and eliminate the suffering caused by the disease.

• Research Institutes and/or Public Policy Analysis

• 40.

The Stanley Medical Research Institute

TO FIND THE CAUSE(S) OF AND BETTER PHARMACOLOGICAL TREATMENTS FOR SCHIZOPHRENIA AND BIPOLAR DISORDER.

• Birth Defects, Genetic Diseases Research

• 41.

Kate Foundation for Rett Syndrome Research Inc

The Kate Foundation is a 501(c)(3) organization dedicated to raising research funding for the reversal of Rett Syndrome and related disorders.

• Specifically Named Diseases

• 42.

Prion Alliance Inc

Non-profit organization devoted to funding scientific research towards a treatment or cure for human prion diseases.

• Professional Societies & Associations

• 43.

Molecular Psychiatry Association Inc

TO PROMOTE MOLECULAR PSYCHIATRY RESEARCH SAVE THE DATE 10TH BIENNIAL MOLECULAR PSYCHIATRY MEETING Registration and Submissions will open in May 2025.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

• Epilepsy Research

• 45.

Shay Emma Hammer Research Foundation

We’re working to document the first 1000 cases of SCN8A gene variants and connect families Advancing epilepsy awareness.