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

Year Number of Results
1977 1
2003 1
2006 1
2007 2
2008 2
2009 2
2010 5
2011 10
2012 8
2013 6
2014 12
2015 11
2016 16
2017 30
2018 24
2019 27
2020 19
2021 32
2022 37
2023 31
2024 14

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248 results

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Page 1
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis.
Zhang S, Cooper-Knock J, Weimer AK, Shi M, Moll T, Marshall JNG, Harvey C, Nezhad HG, Franklin J, Souza CDS, Ning K, Wang C, Li J, Dilliott AA, Farhan S, Elhaik E, Pasniceanu I, Livesey MR, Eitan C, Hornstein E, Kenna KP; Project MinE ALS Sequencing Consortium; Veldink JH, Ferraiuolo L, Shaw PJ, Snyder MP. Zhang S, et al. Among authors: farhan s. Neuron. 2022 Mar 16;110(6):992-1008.e11. doi: 10.1016/j.neuron.2021.12.019. Epub 2022 Jan 18. Neuron. 2022. PMID: 35045337 Free PMC article.
Matrin3: Disorder and ALS Pathogenesis.
Salem A, Wilson CJ, Rutledge BS, Dilliott A, Farhan S, Choy WY, Duennwald ML. Salem A, et al. Among authors: farhan s. Front Mol Biosci. 2022 Jan 10;8:794646. doi: 10.3389/fmolb.2021.794646. eCollection 2021. Front Mol Biosci. 2022. PMID: 35083279 Free PMC article. Review.
DnaJC7 in Amyotrophic Lateral Sclerosis.
Dilliott AA, Andary CM, Stoltz M, Petropavlovskiy AA, Farhan SMK, Duennwald ML. Dilliott AA, et al. Among authors: farhan smk. Int J Mol Sci. 2022 Apr 7;23(8):4076. doi: 10.3390/ijms23084076. Int J Mol Sci. 2022. PMID: 35456894 Free PMC article. Review.
Rare neurovascular genetic and imaging markers across neurodegenerative diseases.
Dilliott AA, Berberian SA, Sunderland KM, Binns MA, Zimmer J, Ozzoude M, Scott CJM, Gao F, Lang AE, Breen DP, Tartaglia MC, Tan B, Swartz RH, Rogaeva E, Borrie M, Finger E, Fischer CE, Frank A, Freedman M, Kumar S, Pasternak S, Pollock BG, Rajji TK, Tang-Wai DF, Abrahao A, Turnbull J, Zinman L, Casaubon L, Dowlatshahi D, Hassan A, Mandzia J, Sahlas D, Saposnik G, Grimes D, Marras C, Steeves T, Masellis M, Farhan SMK, Bartha R, Symons S, Hegele RA, Black SE, Ramirez J; ONDRI Investigators. Dilliott AA, et al. Among authors: farhan smk. Alzheimers Dement. 2023 Dec;19(12):5583-5595. doi: 10.1002/alz.13316. Epub 2023 Jun 5. Alzheimers Dement. 2023. PMID: 37272523
Clinical testing panels for ALS: global distribution, consistency, and challenges.
Dilliott AA, Al Nasser A, Elnagheeb M, Fifita J, Henden L, Keseler IM, Lenz S, Marriott H, Mccann E, Mesaros M, Opie-Martin S, Owens E, Palus B, Ross J, Wang Z, White H, Al-Chalabi A, Andersen PM, Benatar M, Blair I, Cooper-Knock J, Harrington EA, Heckmann J, Landers J, Moreno C, Nel M, Rampersaud E, Roggenbuck J, Rouleau G, Traynor B, Van Blitterswijk M, Van Rheenen W, Veldink J, Weishaupt J, Drury L, Harms MB, Farhan SMK; Amyotrophic lateral sclerosis spectrum disorders Gene Curation Expert Panel. Dilliott AA, et al. Among authors: farhan smk. Amyotroph Lateral Scler Frontotemporal Degener. 2023 Aug;24(5-6):420-435. doi: 10.1080/21678421.2023.2173015. Epub 2023 Mar 10. Amyotroph Lateral Scler Frontotemporal Degener. 2023. PMID: 36896705 Review.
Everolimus-Eluting Bioresorbable Scaffolds Versus Everolimus-Eluting Metallic Stents.
Sorrentino S, Giustino G, Mehran R, Kini AS, Sharma SK, Faggioni M, Farhan S, Vogel B, Indolfi C, Dangas GD. Sorrentino S, et al. Among authors: farhan s. J Am Coll Cardiol. 2017 Jun 27;69(25):3055-3066. doi: 10.1016/j.jacc.2017.04.011. Epub 2017 Apr 12. J Am Coll Cardiol. 2017. PMID: 28412389 Free article. Review.
Platelet function variability and non-genetic causes.
Tentzeris I, Siller-Matula J, Farhan S, Jarai R, Wojta J, Huber K. Tentzeris I, et al. Among authors: farhan s. Thromb Haemost. 2011 May;105 Suppl 1:S60-6. doi: 10.1160/THS11-01-0025. Epub 2011 Apr 14. Thromb Haemost. 2011. PMID: 21491057 Review.
248 results