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Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation
The Foundation Fighting Blindness is a 50‐year old 501c(3) non‐profit organization dedicated to supporting the development of treatments and cures for people affected by the inherited retinal diseases (IRD), a group of clinical diagnoses that include orphan diseases such as retinitis pigmentosa, Ush...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540299/ https://www.ncbi.nlm.nih.gov/pubmed/32783387 http://dx.doi.org/10.1002/ajmg.c.31825 |
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author | Mansfield, Brian C. Yerxa, Benjamin R. Branham, Kari H. |
author_facet | Mansfield, Brian C. Yerxa, Benjamin R. Branham, Kari H. |
author_sort | Mansfield, Brian C. |
collection | PubMed |
description | The Foundation Fighting Blindness is a 50‐year old 501c(3) non‐profit organization dedicated to supporting the development of treatments and cures for people affected by the inherited retinal diseases (IRD), a group of clinical diagnoses that include orphan diseases such as retinitis pigmentosa, Usher syndrome, and Stargardt disease, among others. Over $760 M has been raised and invested in preclinical and clinical research and resources. Key resources include a multi‐national clinical consortium, an international patient registry with over 15,700 members that is expanding rapidly, and an open access genetic testing program that provides no cost comprehensive genetic testing to people clinically diagnosed with an IRD living in the United States. These programs are described with particular focus on the challenges and outcomes of establishing the registry and genetic testing program. |
format | Online Article Text |
id | pubmed-7540299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75402992020-10-09 Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation Mansfield, Brian C. Yerxa, Benjamin R. Branham, Kari H. Am J Med Genet C Semin Med Genet Research Reviews The Foundation Fighting Blindness is a 50‐year old 501c(3) non‐profit organization dedicated to supporting the development of treatments and cures for people affected by the inherited retinal diseases (IRD), a group of clinical diagnoses that include orphan diseases such as retinitis pigmentosa, Usher syndrome, and Stargardt disease, among others. Over $760 M has been raised and invested in preclinical and clinical research and resources. Key resources include a multi‐national clinical consortium, an international patient registry with over 15,700 members that is expanding rapidly, and an open access genetic testing program that provides no cost comprehensive genetic testing to people clinically diagnosed with an IRD living in the United States. These programs are described with particular focus on the challenges and outcomes of establishing the registry and genetic testing program. John Wiley & Sons, Inc. 2020-08-11 2020-09 /pmc/articles/PMC7540299/ /pubmed/32783387 http://dx.doi.org/10.1002/ajmg.c.31825 Text en © 2020 The Authors. American Journal of Medical Genetics Part C: Seminars in Medical Genetics published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Reviews Mansfield, Brian C. Yerxa, Benjamin R. Branham, Kari H. Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation |
title | Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation |
title_full | Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation |
title_fullStr | Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation |
title_full_unstemmed | Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation |
title_short | Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation |
title_sort | implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation |
topic | Research Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540299/ https://www.ncbi.nlm.nih.gov/pubmed/32783387 http://dx.doi.org/10.1002/ajmg.c.31825 |
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