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

Year Number of Results
2009 3
2010 1
2013 2
2015 4
2016 4
2017 1
2018 6
2019 4
2020 7
2021 10
2022 6
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41 results
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Page 1
Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes.
Yap ZY, Park YH, Wortmann SB, Gunning AC, Ezer S, Lee S, Duraine L, Wilichowski E, Wilson K, Mayr JA, Wagner M, Li H, Kini U, Black ED, Monaghan KG, Lupski JR, Ellard S, Westphal DS, Harel T, Yoon WH. Yap ZY, et al. Genome Med. 2021 Apr 12;13(1):55. doi: 10.1186/s13073-021-00873-3. Genome Med. 2021. PMID: 33845882 Free PMC article.
Waste Mineral Wool and Its Opportunities-A Review.
Yap ZS, Khalid NHA, Haron Z, Mohamed A, Tahir MM, Hasyim S, Saggaff A. Yap ZS, et al. Materials (Basel). 2021 Oct 2;14(19):5777. doi: 10.3390/ma14195777. Materials (Basel). 2021. PMID: 34640174 Free PMC article. Review.
Experimental parameters defining ultra-low biomass bioaerosol analysis.
Luhung I, Uchida A, Lim SBY, Gaultier NE, Kee C, Lau KJX, Gusareva ES, Heinle CE, Wong A, Premkrishnan BNV, Purbojati RW, Acerbi E, Kim HL, Junqueira ACM, Longford S, Lohar SR, Yap ZH, Panicker D, Koh Y, Kushwaha KK, Ang PN, Putra A, Drautz-Moses DI, Schuster SC. Luhung I, et al. Among authors: yap zh. NPJ Biofilms Microbiomes. 2021 Apr 16;7(1):37. doi: 10.1038/s41522-021-00209-4. NPJ Biofilms Microbiomes. 2021. PMID: 33863892 Free PMC article.
Glaucoma related retinal oximetry: a technology update.
Yap ZL, Verma S, Lee YF, Ong C, Mohla A, Perera SA. Yap ZL, et al. Clin Ophthalmol. 2018 Jan 4;12:79-84. doi: 10.2147/OPTH.S128459. eCollection 2018. Clin Ophthalmol. 2018. PMID: 29379268 Free PMC article. Review.
Long-term outcomes of abdominal paraganglioma.
Choi HR, Yap Z, Choi SM, Choi SH, Kim JK, Lee CR, Lee J, Jeong JJ, Nam KH, Chung WY, Kang SW. Choi HR, et al. Among authors: yap z. Ann Surg Treat Res. 2020 Dec;99(6):315-319. doi: 10.4174/astr.2020.99.6.315. Epub 2020 Nov 26. Ann Surg Treat Res. 2020. PMID: 33304858 Free PMC article.
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia.
Yap ZY, Efthymiou S, Seiffert S, Vargas Parra K, Lee S, Nasca A, Maroofian R, Schrauwen I, Pendziwiat M, Jung S, Bhoj E, Striano P, Mankad K, Vona B, Cuddapah S, Wagner A, Alvi JR, Davoudi-Dehaghani E, Fallah MS, Gannavarapu S, Lamperti C, Legati A, Murtaza BN, Nadeem MS, Rehman MU, Saeidi K, Salpietro V, von Spiczak S, Sandoval A, Zeinali S, Zeviani M, Reich A; SYNaPS Study Group; University of Washington Center for Mendelian Genomics, Jang C, Helbig I, Barakat TS, Ghezzi D, Leal SM, Weber Y, Houlden H, Yoon WH. Yap ZY, et al. Am J Hum Genet. 2021 Dec 2;108(12):2368-2384. doi: 10.1016/j.ajhg.2021.11.003. Epub 2021 Nov 19. Am J Hum Genet. 2021. PMID: 34800363 Free PMC article.
41 results