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Submission declined on 18 May 2026 by Devonian Wombat (talk). This draft reads like an advertisement. Wikipedia is an encyclopedia, not a platform for promotion or marketing. Drafts that are exclusively promotional may be deleted without notice.
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Declined by Devonian Wombat 2 months ago.
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Submission declined on 19 December 2025 by Pythoncoder (talk). Resubmitted without changes; previous decline still stands. Declined by Pythoncoder 7 months ago. |
Submission declined on 1 December 2025 by Pythoncoder (talk). This draft appears to contain text generated by a large language model (such as ChatGPT). You cannot use LLMs to generate article content.
Declined by Pythoncoder 8 months ago.LLM-generated pages with certain obvious signs of being machine generated may be deleted without notice. Instead, only summarize in your own words a range of independent, reliable, published sources that discuss the subject. See the advice page on large language models for more information. |
Submission declined on 20 November 2025 by Pythoncoder (talk). Resubmitted without improvement; previous decline still stands. Declined by Pythoncoder 8 months ago. |
This draft's references do not show that the subject meets Wikipedia's criteria for inclusion for organizations and companies. The draft requires multiple published secondary sources that:
Declined by Cabrils 9 months ago.
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Answer ALS is a United States-based research consortium and nonprofit focused on amyotrophic lateral sclerosis (ALS). It has enrolled more than 1,500 participants and created a resource that links longitudinal clinical data with multi-omics from induced pluripotent stem cell (iPSC) derived motor neurons. Data and matched biospecimens are made available to researchers through the Neuromine Data Portal and an iPSC repository operated with Cedars-Sinai.[1][2][3][4]
Answer ALS grew out of the Team Gleason ALS Summit held in 2013, organized by former NFL player and New Orlean Saint Steve Gleason and his foundation, which convened researchers, clinicians, and advocates to draft a coordinated research plan.[5][6] At the time, Answer ALS was described as a multi-year, 20-million-dollar research project involving Johns Hopkins, Cedars-Sinai, Massachusetts General Hospital and other centers.[7][AI-retrieved source] Gleason publicly announced the “Answer ALS” initiative in June 2014, calling it “the single largest effort to end ALS in the history of the disease.”[8] The nonprofit Answer ALS Foundation received U.S. tax-exempt status in 2015 and is headquartered in New Orleans, Louisiana.[9]
Enrollments and data collection were coordinated across eight U.S. ALS clinics beginning in 2016. The design of the cohort, longitudinal measures and multi-omics paired with patient-derived neurons were outlined in a 2022 Nature Neuroscience resource paper.[10] The enrolling clinics listed in the Nature Neuroscience paper are Johns Hopkins University; Massachusetts General Hospital, Healey & AMG Center for ALS; Ohio State University Wexner Medical Center; Emory University; Washington University in St. Louis; Northwestern University, Les Turner ALS Center; Cedars-Sinai Medical Center; and Texas Neurology in Dallas.[10]
In November 2018, Microsoft announced a one million dollar contribution and Azure cloud support.[11] In November 2024, Answer ALS and Cedars-Sinai reported public availability of a large patient-based ALS iPSC and biodata repository, with access via the Cedars-Sinai Biomanufacturing Center and the Neuromine portal.[12][13][14][15]
The core Answer ALS cohort combines longitudinal in-clinic assessments with iPSC derived spinal motor neurons generated from participant blood cells. The associated multi-omics include whole-genome sequencing, RNA sequencing, proteomics, and epigenomics such as ATAC-seq, linked to matched biofluids and cell lines available to outside laboratories.[10]
Answer ALS operates Neuromine, a data portal that provides controlled access to de-identified clinical data and multi-omics, with tools for cohort definition and visualization.[16] In March 2024, ALS Therapy Development Institute announced a data sharing collaboration to incorporate ALS TDI datasets into Neuromine.[17]
In late 2024, Answer ALS and Cedars-Sinai announced public availability of a patient-based iPSC and ALS biodata repository, with access through the Cedars-Sinai Biomanufacturing Center and Neuromine.[12][13][14][15]
Large-scale differentiation and characterization of iPSC derived spinal motor neurons from ALS and control donors were reported in Neuron, 19 Apr 2023.[18] Chromatin accessibility in more than 500 iPSC derived motor neuron lines and prediction of clinical progression rates were reported in Nature Communications, 2 May 2024[19]. MIT News summarized the epigenomic analysis and implications on 2 May 2024.[20]
In August 2025, Answer ALS, ALS Therapy Development Institute, and Augie's Quest announced Champion Insights,[21] [22]a remote participation study intended to investigate why athletes, military service members, and other high-performing groups show elevated incidences of ALS, with data planned for open sharing through the Neuromine Data Portal.[23][24][25] The combined dataset and cell bank is one of the largest resources for ALS research, with over 1,800 iPSC lines distributed to more than 130 institutions worldwide.[26]
Jeffrey D. Rothstein is co-founder and executive director of the research program in institutional profiles and reporting.[27][28] Clare Durrett serves as managing director.[12][29][30]
Answer ALS is a 501(c)(3) organization with tax-exempt status since 2015.[9]
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