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

Year Number of Results
1998 1
1999 1
2000 1
2001 2
2002 2
2003 1
2004 1
2005 2
2006 1
2007 1
2008 5
2009 6
2010 8
2011 6
2012 6
2013 4
2014 5
2015 6
2016 15
2017 4
2018 5
2019 9
2020 4
2021 9
2022 1
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Search Results

96 results
Results by year
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Page 1
Stem Cells and Gene Therapy in Progressive Hearing Loss: the State of the Art.
Nourbakhsh A, Colbert BM, Nisenbaum E, El-Amraoui A, Dykxhoorn DM, Koehler KR, Chen ZY, Liu XZ. Nourbakhsh A, et al. J Assoc Res Otolaryngol. 2021 Apr;22(2):95-105. doi: 10.1007/s10162-020-00781-0. Epub 2021 Jan 28. J Assoc Res Otolaryngol. 2021. PMID: 33507440 Free PMC article. Review.
Next-generation sequencing in genetic hearing loss.
Yan D, Tekin M, Blanton SH, Liu XZ. Yan D, et al. Genet Test Mol Biomarkers. 2013 Aug;17(8):581-7. doi: 10.1089/gtmb.2012.0464. Epub 2013 Jun 5. Genet Test Mol Biomarkers. 2013. PMID: 23738631 Free PMC article. Review.
Genetics of hearing and deafness.
Angeli S, Lin X, Liu XZ. Angeli S, et al. Anat Rec (Hoboken). 2012 Nov;295(11):1812-29. doi: 10.1002/ar.22579. Epub 2012 Oct 8. Anat Rec (Hoboken). 2012. PMID: 23044516 Free PMC article. Review.
Genetics and the Individualized Therapy of Vestibular Disorders.
Mei C, Dong H, Nisenbaum E, Thielhelm T, Nourbakhsh A, Yan D, Smeal M, Lundberg Y, Hoffer ME, Angeli S, Telischi F, Nie G, Blanton SH, Liu X. Mei C, et al. Front Neurol. 2021 Feb 5;12:633207. doi: 10.3389/fneur.2021.633207. eCollection 2021. Front Neurol. 2021. PMID: 33613440 Free PMC article. Review.
A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder.
Jang MW, Oh DY, Yi E, Liu X, Ling J, Kim N, Sharma K, Kim TY, Lee S, Kim AR, Kim MY, Kim MA, Lee M, Han JH, Han JJ, Park HR, Kim BJ, Lee SY, Woo DH, Oh J, Oh SJ, Du T, Koo JW, Oh SH, Shin HW, Seong MW, Lee KY, Kim UK, Shin JB, Sang S, Cai X, Mei L, He C, Blanton SH, Chen ZY, Chen H, Liu X, Nourbakhsh A, Huang Z, Kang KW, Park WY, Feng Y, Lee CJ, Choi BY. Jang MW, et al. Proc Natl Acad Sci U S A. 2021 Jun 1;118(22):e2019681118. doi: 10.1073/pnas.2019681118. Proc Natl Acad Sci U S A. 2021. PMID: 34050020 Free PMC article.
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.
Dai P, Huang LH, Wang GJ, Gao X, Qu CY, Chen XW, Ma FR, Zhang J, Xing WL, Xi SY, Ma BR, Pan Y, Cheng XH, Duan H, Yuan YY, Zhao LP, Chang L, Gao RZ, Liu HH, Zhang W, Huang SS, Kang DY, Liang W, Zhang K, Jiang H, Guo YL, Zhou Y, Zhang WX, Lyu F, Jin YN, Zhou Z, Lu HL, Zhang X, Liu P, Ke J, Hao JS, Huang HM, Jiang D, Ni X, Long M, Zhang L, Qiao J, Morton CC, Liu XZ, Cheng J, Han DM. Dai P, et al. Am J Hum Genet. 2019 Oct 3;105(4):803-812. doi: 10.1016/j.ajhg.2019.09.003. Epub 2019 Sep 26. Am J Hum Genet. 2019. PMID: 31564438 Free PMC article.
Association of PRPS1 Mutations with Disease Phenotypes.
Mittal R, Patel K, Mittal J, Chan B, Yan D, Grati M, Liu XZ. Mittal R, et al. Dis Markers. 2015;2015:127013. doi: 10.1155/2015/127013. Epub 2015 May 24. Dis Markers. 2015. PMID: 26089585 Free PMC article. Review.
Role of innate immunity in the pathogenesis of otitis media.
Mittal R, Kodiyan J, Gerring R, Mathee K, Li JD, Grati M, Liu XZ. Mittal R, et al. Int J Infect Dis. 2014 Dec;29:259-67. doi: 10.1016/j.ijid.2014.10.015. Epub 2014 Nov 5. Int J Infect Dis. 2014. PMID: 25447732 Free PMC article. Review.
96 results