Program areas at Hereditary Disease Foundation
The Hereditary Disease Foundation commemorates its 52nd year by making an even greater impact toward developing novel therapeutics and cures. We have put in place strategies and new grant funding programs to maximize our effectiveness. We have been funding catalytic and paradigm-changing research since our birth - including identifying the huntington's Disease marker in 1983 and the hd gene in 1993, and supporting gene silencing approaches since 2002. We want to continue to make an impact by funding research that pushes the envelope.the Hereditary Disease Foundation provides funding for research that advances the discovery and development of treatments for huntington's Disease and other brain disorders. We are (continue on schedule o) passionate about funding and the Foundation intends to use the endowment funds for its scientific activities which includes providing grants to fund scientific research to further the understanding of, and to develop diagnostics and therapeutics for neurodegenerative diseases, including huntington's Disease. The Hereditary Disease Foundation funds the most innovative, creative and paradigm-changing research possible. The data generated with hdf funding often allows researchers to get initial findings that help them apply successfully for larger, long-term funding from other funding agencies, including the national institutes of health. The Foundation's current focus is on:1) modifier studies - on dna repair pathways, protein degradation and other modifiers of phenotype and age of onset.2) research mechanisms of hd neurogeneration and biomarkers and therapy for hd-induced neurodegeneration.type of funding:the basic research grants program: supports projects contributing to identifying and understanding the fundamental defects in huntington's Disease. Postdoctoral fellowships: these postdoctoral fellowships are intended to cultivate interest in huntington's Disease research by bright young scientists. Fellowships are granted to those who possess imagination, rigor, creativity and spirit to push forward toward a cure for hd and ensure that these learning can be applied to other brain diseases.
Grants made by Hereditary Disease Foundation
Who funds Hereditary Disease Foundation
Grants from foundations and other nonprofits
Personnel at Hereditary Disease Foundation
Name | Title | Compensation | Date of data |
---|
Meghan Donaldson | Chief Executive Officer | $110,000 | 2024-10-14 |
Travis J. Carey | Chief Financial Officer | $11,516 | 2023-06-27 |
Julie Porter | Director of Administration | $103,600 | 2023-06-27 |
Sarah Hernandez | Director of Research Programs | | 2023-06-27 |
Nancy S. Wexler | Director / President | $0 | 2023-06-27 |
...and 7 more key personnel |
Financials for Hereditary Disease Foundation
Revenues | FYE 12/2022 | FYE 12/2021 | % Change |
---|
Total grants, contributions, etc. | $4,399,874 | $2,827,274 | 55.6% |
Program services | $0 | $0 | - |
Investment income and dividends | $270,807 | $245,544 | 10.3% |
Tax-exempt bond proceeds | $0 | $0 | - |
Royalty revenue | $0 | $0 | - |
Net rental income | $0 | $0 | - |
Net gain from sale of non-inventory assets | $-184,714 | $773,831 | -123.9% |
Net income from fundraising events | $0 | $0 | - |
Net income from gaming activities | $0 | $0 | - |
Net income from sales of inventory | $0 | $0 | - |
Miscellaneous revenues | $36,719 | $0 | 999% |
Total revenues | $4,522,686 | $3,846,649 | 17.6% |
Organizations like Hereditary Disease Foundation
Organization | Type | Location | Revenue |
---|
Cerebral Palsy Foundation (CPF) | 501(c)(3) | New York, NY | $4,021,273 |
Children's Tumor Foundation | 501(c)(3) | New York, NY | $16,990,325 |
Emily's Entourage | 501(c)(3) | Ardmore, PA | $2,799,957 |
International FOP Association | 501(c)(3) | North Kansas City, MO | $3,050,181 |
Foundation for Prader Willi Research (FPWR) | 501(c)(3) | Covina, CA | $5,083,937 |
Charcot-Marie-Tooth Association (CMTA) | 501(c)(3) | Glenolden, PA | $5,761,508 |
Cystic Fibrosis Research Institute | 501(c)(3) | Palo Alto, CA | $1,350,296 |
Parent Project Muscular Dystrophy (PPMD) | 501(c)(3) | Washington, DC | $13,881,085 |
Hemophilia of Indiana | 501(c)(3) | Indianapolis, IN | $1,184,923 |
The Cure Starts Now | 501(c)(3) | Cincinnati, OH | $5,080,693 |
Data update history
January 9, 2024
Posted financials
Added Form 990 for fiscal year 2022
January 8, 2024
Updated personnel
Identified 4 new personnel
December 27, 2023
Used new vendors
Identified 3 new vendors, including , , and
Nonprofit Types
Grantmaking organizationsDisease research fundraisersDisease-focused nonprofitsCharities
Issues
HealthDiseases and disorders
Characteristics
Provides grantsConducts researchFundraising eventsOperates internationallyEndowed supportGala fundraisersTax deductible donationsAccepts online donations
General information
- Address
- 601 W 168th St 54
- New York, NY 10032
- Metro area
- New York-Newark-Jersey City, NY-NJ-PA
- County
- New York County, NY
- Website URL
- hdfoundation.org/Â
- Phone
- (212) 981-2121
IRS details
- EIN
- 23-7376197
- Fiscal year end
- December
- Taxreturn type
- Form 990
- Year formed
- 1968
- Eligible to receive tax-deductible contributions (Pub 78)
- Yes
Categorization
- NTEE code, primary
- G20: Birth Defects and Genetic Diseases
- NAICS code, primary
- 813212: Health and Disease Research Fundraising Organizations
- Parent/child status
- Independent
California AB-488 details
- AB 488 status
- May Not Operate or Solicit for Charitable Purposes
- Charity Registration status
- Delinquent
- FTB status revoked
- Not revoked
- AG Registration Number
- 015979
- FTB Entity ID
- 0711794
- AB 488 data last updated ("as-of") date
- 2024-11-20
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