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

Year Number of Results
1989 1
1990 4
1991 6
1992 6
1993 6
1994 4
1995 7
1996 10
1997 4
1999 1
2000 6
2001 4
2002 7
2003 2
2004 4
2005 4
2006 4
2007 3
2008 3
2009 6
2010 13
2011 14
2012 9
2013 5
2014 9
2015 9
2016 14
2017 7
2018 8
2019 11
2020 7
2021 7
2022 2
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Article attribute
Article type
Publication date

Search Results

194 results
Results by year
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Page 1
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. Among authors: blanton sh. 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.
Precision medicine in hearing loss.
Rudman JR, Mei C, Bressler SE, Blanton SH, Liu XZ. Rudman JR, et al. Among authors: blanton sh. J Genet Genomics. 2018 Feb 20;45(2):99-109. doi: 10.1016/j.jgg.2018.02.004. Epub 2018 Feb 16. J Genet Genomics. 2018. PMID: 29500086 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. Among authors: blanton sh. Front Neurol. 2021 Feb 5;12:633207. doi: 10.3389/fneur.2021.633207. eCollection 2021. Front Neurol. 2021. PMID: 33613440 Free PMC article. Review.
Peripheral vestibular system: Age-related vestibular loss and associated deficits.
Coto J, Alvarez CL, Cejas I, Colbert BM, Levin BE, Huppert J, Rundek T, Balaban C, Blanton SH, Lee DJ, Loewenstein D, Hoffer M, Liu XZ. Coto J, et al. Among authors: blanton sh. J Otol. 2021 Oct;16(4):258-265. doi: 10.1016/j.joto.2021.06.001. Epub 2021 Jun 11. J Otol. 2021. PMID: 34548873 Free PMC article. Review.
Next-generation sequencing in genetic hearing loss.
Yan D, Tekin M, Blanton SH, Liu XZ. Yan D, et al. Among authors: blanton sh. 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.
The genetic basis of deafness in populations of African descent.
Rudman JR, Kabahuma RI, Bressler SE, Feng Y, Blanton SH, Yan D, Liu XZ. Rudman JR, et al. Among authors: blanton sh. J Genet Genomics. 2017 Jun 20;44(6):285-294. doi: 10.1016/j.jgg.2017.03.008. Epub 2017 May 6. J Genet Genomics. 2017. PMID: 28642064 Review.
Whole-exome sequencing and its impact in hereditary hearing loss.
Atik T, Bademci G, Diaz-Horta O, Blanton SH, Tekin M. Atik T, et al. Among authors: blanton sh. Genet Res (Camb). 2015 Mar 31;97:e4. doi: 10.1017/S001667231500004X. Genet Res (Camb). 2015. PMID: 25825321 Free PMC article. Review.
COVID19: A Systematic Approach to Early Identification and Healthcare Worker Protection.
Zhao Y, Cui C, Zhang K, Liu J, Xu J, Nisenbaum E, Huang Y, Qin G, Chen B, Hoffer M, Blanton SH, Telischi F, Hare JM, Daunert S, Shukla B, Pahwa SG, Jayaweera DT, Farmer PE, Del Rio C, Liu X, Shu Y. Zhao Y, et al. Among authors: blanton sh. Front Public Health. 2020 May 19;8:205. doi: 10.3389/fpubh.2020.00205. eCollection 2020. Front Public Health. 2020. PMID: 32574296 Free PMC article. Review.
194 results