Pariser A - Search Results

1

The national economic burden of rare disease in the United States in 2019.

Yang G, Cintina I, Pariser A, Oehrlein E, Sullivan J, Kennedy A. Yang G, et al. Among authors: pariser a. Orphanet J Rare Dis. 2022 Apr 12;17(1):163. doi: 10.1186/s13023-022-02299-5. Orphanet J Rare Dis. 2022. PMID: 35414039 Free PMC article.

2

From scientific discovery to treatments for rare diseases - the view from the National Center for Advancing Translational Sciences - Office of Rare Diseases Research.

Kaufmann P, Pariser AR, Austin C. Kaufmann P, et al. Orphanet J Rare Dis. 2018 Nov 6;13(1):196. doi: 10.1186/s13023-018-0936-x. Orphanet J Rare Dis. 2018. PMID: 30400963 Free PMC article. Review.

3

The IDeaS initiative: pilot study to assess the impact of rare diseases on patients and healthcare systems.

Tisdale A, Cutillo CM, Nathan R, Russo P, Laraway B, Haendel M, Nowak D, Hasche C, Chan CH, Griese E, Dawkins H, Shukla O, Pearce DA, Rutter JL, Pariser AR. Tisdale A, et al. Among authors: pariser ar. Orphanet J Rare Dis. 2021 Oct 22;16(1):429. doi: 10.1186/s13023-021-02061-3. Orphanet J Rare Dis. 2021. PMID: 34674728 Free PMC article.

4

Scientific evidence based rare disease research discovery with research funding data in knowledge graph.

Zhu Q, Nguyễn ÐT, Sheils T, Alyea G, Sid E, Xu Y, Dickens J, Mathé EA, Pariser A. Zhu Q, et al. Among authors: pariser a. Orphanet J Rare Dis. 2021 Nov 18;16(1):483. doi: 10.1186/s13023-021-02120-9. Orphanet J Rare Dis. 2021. PMID: 34794473 Free PMC article.

5

Towards the international interoperability of clinical research networks for rare diseases: recommendations from the IRDiRC Task Force.

Nabbout R, Zanello G, Baker D, Black L, Brambilla I, Buske OJ, Conklin LS, Davies EH, Julkowska D, Kim Y, Klopstock T, Nakamura H, Nielsen KG, Pariser AR, Pastor JC, Scarpa M, Smith M, Taruscio D, Groft S. Nabbout R, et al. Among authors: pariser ar. Orphanet J Rare Dis. 2023 May 9;18(1):109. doi: 10.1186/s13023-023-02650-4. Orphanet J Rare Dis. 2023. PMID: 37161573 Free PMC article.

6

Leveraging the UMLS As a Data Standard for Rare Disease Data Normalization and Harmonization.

Zhu Q, Nguyen DT, Sid E, Pariser A. Zhu Q, et al. Among authors: pariser a. Methods Inf Med. 2020 Aug;59(4-05):131-139. doi: 10.1055/s-0040-1718940. Epub 2020 Nov 4. Methods Inf Med. 2020. PMID: 33147635

7

An integrative knowledge graph for rare diseases, derived from the Genetic and Rare Diseases Information Center (GARD).

Zhu Q, Nguyen DT, Grishagin I, Southall N, Sid E, Pariser A. Zhu Q, et al. Among authors: pariser a. J Biomed Semantics. 2020 Nov 12;11(1):13. doi: 10.1186/s13326-020-00232-y. J Biomed Semantics. 2020. PMID: 33183351 Free PMC article.

8

Artificial Intelligence in Medical Imaging and its Impact on the Rare Disease Community: Threats, Challenges and Opportunities.

Hasani N, Farhadi F, Morris MA, Nikpanah M, Rhamim A, Xu Y, Pariser A, Collins MT, Summers RM, Jones E, Siegel E, Saboury B. Hasani N, et al. Among authors: pariser a. PET Clin. 2022 Jan;17(1):13-29. doi: 10.1016/j.cpet.2021.09.009. PET Clin. 2022. PMID: 34809862 Free PMC article. Review.

9

Phenotypically Similar Rare Disease Identification from an Integrative Knowledge Graph for Data Harmonization: Preliminary Study.

Zhu Q, Nguyen DT, Alyea G, Hanson K, Sid E, Pariser A. Zhu Q, et al. Among authors: pariser a. JMIR Med Inform. 2020 Oct 2;8(10):e18395. doi: 10.2196/18395. JMIR Med Inform. 2020. PMID: 33006565 Free PMC article.

10

Global Regulatory and Public Health Initiatives to Advance Pediatric Drug Development for Rare Diseases.

Epps C, Bax R, Croker A, Green D, Gropman A, Klein AV, Landry H, Pariser A, Rosenman M, Sakiyama M, Sato J, Sen K, Stone M, Takeuchi F, Davis JM. Epps C, et al. Among authors: pariser a. Ther Innov Regul Sci. 2022 Nov;56(6):964-975. doi: 10.1007/s43441-022-00409-w. Epub 2022 Apr 26. Ther Innov Regul Sci. 2022. PMID: 35471559 Free PMC article. Review.

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