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

Year Number of Results
1993 1
2003 4
2004 1
2005 5
2007 1
2008 3
2009 4
2010 7
2011 6
2012 5
2013 4
2014 3
2015 7
2016 13
2017 10
2018 9
2019 13
2020 9
2021 4
2022 2
2023 4
2024 0

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99 results

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Page 1
Neurotransmitters: The Critical Modulators Regulating Gut-Brain Axis.
Mittal R, Debs LH, Patel AP, Nguyen D, Patel K, O'Connor G, Grati M, Mittal J, Yan D, Eshraghi AA, Deo SK, Daunert S, Liu XZ. Mittal R, et al. Among authors: yan d. J Cell Physiol. 2017 Sep;232(9):2359-2372. doi: 10.1002/jcp.25518. Epub 2017 Apr 10. J Cell Physiol. 2017. PMID: 27512962 Free PMC article. Review.
Current concepts in the pathogenesis and treatment of chronic suppurative otitis media.
Mittal R, Lisi CV, Gerring R, Mittal J, Mathee K, Narasimhan G, Azad RK, Yao Q, Grati M, Yan D, Eshraghi AA, Angeli SI, Telischi FF, Liu XZ. Mittal R, et al. Among authors: yan d. J Med Microbiol. 2015 Oct;64(10):1103-1116. doi: 10.1099/jmm.0.000155. Epub 2015 Aug 5. J Med Microbiol. 2015. PMID: 26248613 Free PMC article. Review.
Review of Genotype-Phenotype Correlations in Usher Syndrome.
Nisenbaum E, Thielhelm TP, Nourbakhsh A, Yan D, Blanton SH, Shu Y, Koehler KR, El-Amraoui A, Chen Z, Lam BL, Liu X. Nisenbaum E, et al. Among authors: yan d. Ear Hear. 2022 Jan/Feb;43(1):1-8. doi: 10.1097/AUD.0000000000001066. Ear Hear. 2022. PMID: 34039936 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.
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. Among authors: yan d. Dis Markers. 2015;2015:127013. doi: 10.1155/2015/127013. Epub 2015 May 24. Dis Markers. 2015. PMID: 26089585 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. Among authors: yan d. Front Neurol. 2021 Feb 5;12:633207. doi: 10.3389/fneur.2021.633207. eCollection 2021. Front Neurol. 2021. PMID: 33613440 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: yan d. 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.
Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2.
Dinh CT, Nisenbaum E, Chyou D, Misztal C, Yan D, Mittal R, Young J, Tekin M, Telischi F, Fernandez-Valle C, Liu XZ. Dinh CT, et al. Among authors: yan d. Otol Neurotol. 2020 Jun;41(5):e529-e537. doi: 10.1097/MAO.0000000000002613. Otol Neurotol. 2020. PMID: 32150022 Free PMC article. Review.
99 results