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Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity.
Zhang S, Cooper-Knock J, Weimer AK, Harvey C, Julian TH, Wang C, Li J, Furini S, Frullanti E, Fava F, Renieri A, Pan C, Song J, Billing-Ross P, Gao P, Shen X, Timpanaro IS, Kenna KP; VA Million Veteran Program; GEN-COVID Network; Davis MM, Tsao PS, Snyder MP. Zhang S, et al. medRxiv [Preprint]. 2021 Jun 21:2021.06.15.21258703. doi: 10.1101/2021.06.15.21258703. medRxiv. 2021. Update in: Cell Syst. 2022 Aug 17;13(8):598-614.e6. doi: 10.1016/j.cels.2022.05.007 PMID: 34189540 Free PMC article. Updated. Preprint.
Decoding the Genomics of Abdominal Aortic Aneurysm.
Li J, Pan C, Zhang S, Spin JM, Deng A, Leung LLK, Dalman RL, Tsao PS, Snyder M. Li J, et al. Among authors: zhang s. Cell. 2018 Sep 6;174(6):1361-1372.e10. doi: 10.1016/j.cell.2018.07.021. Cell. 2018. PMID: 30193110 Free article.
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene.
Cooper-Knock J, Zhang S, Kenna KP, Moll T, Franklin JP, Allen S, Nezhad HG, Iacoangeli A, Yacovzada NY, Eitan C, Hornstein E, Elhaik E, Celadova P, Bose D, Farhan S, Fishilevich S, Lancet D, Morrison KE, Shaw CE, Al-Chalabi A; Project MinE ALS Sequencing Consortium; Veldink JH, Kirby J, Snyder MP, Shaw PJ. Cooper-Knock J, et al. Among authors: zhang s. Cell Rep. 2020 Dec 1;33(9):108456. doi: 10.1016/j.celrep.2020.108456. Cell Rep. 2020. PMID: 33264630 Free PMC article.
Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene.
Cooper-Knock J, Zhang S, Kenna KP, Moll T, Franklin JP, Allen S, Nezhad HG, Iacoangeli A, Yacovzada NY, Eitan C, Hornstein E, Elhaik E, Celadova P, Bose D, Farhan S, Fishilevich S, Lancet D, Morrison KE, Shaw CE, Al-Chalabi A; Project MinE ALS Sequencing Consortium; Veldink JH, Kirby J, Snyder MP, Shaw PJ. Cooper-Knock J, et al. Among authors: zhang s. Cell Rep. 2021 Feb 2;34(5):108730. doi: 10.1016/j.celrep.2021.108730. Cell Rep. 2021. PMID: 33535055 Free PMC article. No abstract available.
Physical exercise is a risk factor for amyotrophic lateral sclerosis: Convergent evidence from Mendelian randomisation, transcriptomics and risk genotypes.
Julian TH, Glascow N, Barry ADF, Moll T, Harvey C, Klimentidis YC, Newell M, Zhang S, Snyder MP, Cooper-Knock J, Shaw PJ. Julian TH, et al. Among authors: zhang s. EBioMedicine. 2021 Jun;68:103397. doi: 10.1016/j.ebiom.2021.103397. Epub 2021 May 26. EBioMedicine. 2021. PMID: 34051439 Free PMC article.
Advances in the genetic classification of amyotrophic lateral sclerosis.
Cooper-Knock J, Harvey C, Zhang S, Moll T, Timpanaro IS, Kenna KP, Iacoangeli A, Veldink JH. Cooper-Knock J, et al. Among authors: zhang s. Curr Opin Neurol. 2021 Oct 1;34(5):756-764. doi: 10.1097/WCO.0000000000000986. Curr Opin Neurol. 2021. PMID: 34343141 Free PMC article. Review.
A review of Mendelian randomization in amyotrophic lateral sclerosis.
Julian TH, Boddy S, Islam M, Kurz J, Whittaker KJ, Moll T, Harvey C, Zhang S, Snyder MP, McDermott C, Cooper-Knock J, Shaw PJ. Julian TH, et al. Among authors: zhang s. Brain. 2022 Apr 29;145(3):832-842. doi: 10.1093/brain/awab420. Brain. 2022. PMID: 34791088 Free PMC article. Review.
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