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

Year Number of Results
2002 1
2003 4
2004 6
2005 8
2006 17
2007 11
2008 14
2009 13
2010 12
2011 11
2012 14
2013 9
2014 17
2015 10
2016 12
2017 11
2018 13
2019 12
2020 18
2021 23
2022 26
2023 35
2024 9

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267 results

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Page 1
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
Fu F, Li R, Yu Q, Wang D, Deng Q, Li L, Lei T, Chen G, Nie Z, Yang X, Han J, Pan M, Zhen L, Zhang Y, Jing X, Li F, Li F, Zhang L, Yi C, Li Y, Lu Y, Zhou H, Cheng K, Li J, Xiang L, Zhang J, Tang S, Fang P, Li D, Liao C. Fu F, et al. Among authors: liao c. Genome Med. 2022 Oct 28;14(1):123. doi: 10.1186/s13073-022-01130-x. Genome Med. 2022. PMID: 36307859 Free PMC article.
PDIA2 variant associated with vitiligo.
Li F, Liao C, Li R, Zhang Y, Jing X, Li D, Deng W. Li F, et al. Among authors: liao c. Skin Health Dis. 2023 Aug 16;3(5):e278. doi: 10.1002/ski2.278. eCollection 2023 Oct. Skin Health Dis. 2023. PMID: 37799362 Free PMC article.
Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion.
Wang Y, Zhou H, Fu F, Cheng K, Yu Q, Huang R, Lei T, Yang X, Li D, Liao C. Wang Y, et al. Among authors: liao c. Genes (Basel). 2022 Dec 8;13(12):2315. doi: 10.3390/genes13122315. Genes (Basel). 2022. PMID: 36553582 Free PMC article.
Differential effects of macrophage subtypes on SARS-CoV-2 infection in a human pluripotent stem cell-derived model.
Lian Q, Zhang K, Zhang Z, Duan F, Guo L, Luo W, Mok BW, Thakur A, Ke X, Motallebnejad P, Nicolaescu V, Chen J, Ma CY, Zhou X, Han S, Han T, Zhang W, Tan AY, Zhang T, Wang X, Xu D, Xiang J, Xu A, Liao C, Huang FP, Chen YW, Na J, Randall G, Tse HF, Chen Z, Chen Y, Chen HJ. Lian Q, et al. Among authors: liao c. Nat Commun. 2022 Apr 19;13(1):2028. doi: 10.1038/s41467-022-29731-5. Nat Commun. 2022. PMID: 35440562 Free PMC article.
Exome sequencing improves genetic diagnosis of congenital orofacial clefts.
Yan S, Fu F, Li R, Yu Q, Li F, Zhou H, Wang Y, Huang R, Ma C, Guo F, Wang D, Yang X, Han J, Lei T, Li D, Liao C. Yan S, et al. Among authors: liao c. Front Genet. 2023 Sep 7;14:1252823. doi: 10.3389/fgene.2023.1252823. eCollection 2023. Front Genet. 2023. PMID: 37745857 Free PMC article.
Whole exome sequencing improves genetic diagnosis of fetal clubfoot.
Huang R, Zhou H, Ma C, Fu F, Cheng K, Wang Y, Li R, Lei T, Yu Q, Wang D, Yan S, Yang X, Li D, Liao C. Huang R, et al. Among authors: liao c. Hum Genet. 2023 Mar;142(3):407-418. doi: 10.1007/s00439-022-02516-y. Epub 2022 Dec 25. Hum Genet. 2023. PMID: 36566310
Genetic diagnosis of fetal microcephaly at a single tertiary center in China.
Wang Y, Fu F, Lei T, Zhen L, Deng Q, Zhou H, Ma C, Cheng K, Huang R, Li R, Yu Q, Li L, Han J, Yang X, Li D, Liao C. Wang Y, et al. Among authors: liao c. Front Genet. 2023 May 9;14:1112153. doi: 10.3389/fgene.2023.1112153. eCollection 2023. Front Genet. 2023. PMID: 37229200 Free PMC article.
267 results