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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: li j. 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.
The genetic predisposition to bronchopulmonary dysplasia.
Yu KH, Li J, Snyder M, Shaw GM, O'Brodovich HM. Yu KH, et al. Among authors: li j. Curr Opin Pediatr. 2016 Jun;28(3):318-23. doi: 10.1097/MOP.0000000000000344. Curr Opin Pediatr. 2016. PMID: 26963946 Free PMC article. Review.
Fetal de novo mutations and preterm birth.
Li J, Oehlert J, Snyder M, Stevenson DK, Shaw GM. Li J, et al. PLoS Genet. 2017 Apr 7;13(4):e1006689. doi: 10.1371/journal.pgen.1006689. eCollection 2017 Apr. PLoS Genet. 2017. PMID: 28388617 Free PMC article.
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. Cell. 2018 Sep 6;174(6):1361-1372.e10. doi: 10.1016/j.cell.2018.07.021. Cell. 2018. PMID: 30193110 Free article.
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