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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 3
2009 14
2010 35
2011 42
2012 53
2013 27
2014 30
2015 18
2016 6
2017 12
2018 4
2019 6
2020 3
2022 4
2024 1

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225 results

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Page 1
Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome.
Bainbridge MN, Mazumder A, Ogasawara D, Abou Jamra R, Bernard G, Bertini E, Burglen L, Cope H, Crawford A, Derksen A, Dure L, Gantz E, Koch-Hogrebe M, Hurst ACE, Mahida S, Marshall P, Micalizzi A, Novelli A, Peng H; Rady Children's Institute for Genomic Medicine; Rodriguez D, Robbins SL, Rutledge SL, Scalise R, Schließke S, Shashi V, Srivastava S, Thiffault I, Topol S; Undiagnosed Disease Network; Qebibo L, Wieczorek D, Cravatt B, Haricharan S, Torkamani A, Friedman J. Bainbridge MN, et al. Brain. 2022 Oct 21;145(10):3383-3390. doi: 10.1093/brain/awac223. Brain. 2022. PMID: 35737950 Free PMC article.
ATXN2 intermediate expansions in amyotrophic lateral sclerosis.
Glass JD, Dewan R, Ding J, Gibbs JR, Dalgard C, Keagle PJ, Shankaracharya, García-Redondo A, Traynor BJ, Chia R, Landers JE. Glass JD, et al. Brain. 2022 Aug 27;145(8):2671-2676. doi: 10.1093/brain/awac167. Brain. 2022. PMID: 35521889 Free PMC article.
Impact of polygenic risk communication: an observational mobile application-based coronary artery disease study.
Muse ED, Chen SF, Liu S, Fernandez B, Schrader B, Molparia B, León AN, Lee R, Pubbi N, Mejia N, Ren C, El-Kalliny A, Prado Montes de Oca E, Aguilar H, Ghoshal A, Dias R, Evans D, Chen KY, Zhang Y, Wineinger NE, Spencer EG, Topol EJ, Torkamani A. Muse ED, et al. NPJ Digit Med. 2022 Mar 11;5(1):30. doi: 10.1038/s41746-022-00578-w. NPJ Digit Med. 2022. PMID: 35277577 Free PMC article.
Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease.
Bandres-Ciga S, Saez-Atienzar S, Kim JJ, Makarious MB, Faghri F, Diez-Fairen M, Iwaki H, Leonard H, Botia J, Ryten M, Hernandez D, Gibbs JR, Ding J, Gan-Or Z, Noyce A, Pihlstrom L, Torkamani A, Soltis AR, Dalgard CL; American Genome Center; Scholz SW, Traynor BJ, Ehrlich D, Scherzer CR, Bookman M, Cookson M, Blauwendraat C, Nalls MA, Singleton AB; International Parkinson Disease Genomics Consortium. Bandres-Ciga S, et al. Acta Neuropathol. 2020 Sep;140(3):341-358. doi: 10.1007/s00401-020-02181-3. Epub 2020 Jun 29. Acta Neuropathol. 2020. PMID: 32601912 Free PMC article.
Novel exomic rare variants associated with venous thrombosis.
Deguchi H, Shukla M, Hayat M, Torkamani A, Elias DJ, Griffin JH. Deguchi H, et al. Br J Haematol. 2020 Sep;190(5):783-786. doi: 10.1111/bjh.16613. Epub 2020 Mar 30. Br J Haematol. 2020. PMID: 32232851 Free PMC article.
225 results