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Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.
Yin X, Tan K, Vajta G, Jiang H, Tan Y, Zhang C, Chen F, Chen S, Zhang C, Pan X, Gong C, Li X, Lin C, Gao Y, Liang Y, Yi X, Mu F, Zhao L, Peng H, Xiong B, Zhang S, Cheng D, Lu G, Zhang X, Lin G, Wang W. Yin X, et al. Among authors: peng h. Biol Reprod. 2013 Mar 21;88(3):69. doi: 10.1095/biolreprod.112.106211. Print 2013 Mar. Biol Reprod. 2013. PMID: 23349234
Genomic Sequencing as a First-Tier Screening Test and Outcomes of Newborn Screening.
Chen T, Fan C, Huang Y, Feng J, Zhang Y, Miao J, Wang X, Li Y, Huang C, Jin W, Tang C, Feng L, Yin Y, Zhu B, Sun M, Liu X, Xiang J, Tan M, Jia L, Chen L, Huang H, Peng H, Sun X, Gu X, Peng Z, Zhu B, Zou H, Han L. Chen T, et al. Among authors: peng h, peng z. JAMA Netw Open. 2023 Sep 5;6(9):e2331162. doi: 10.1001/jamanetworkopen.2023.31162. JAMA Netw Open. 2023. PMID: 37656460 Free PMC article.
Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples.
Qian Y, Sun Y, Guo X, Song L, Sun Y, Gao X, Liu B, Xu Y, Chen N, Chen M, Luo Y, Qiao Z, Fan L, Man J, Zhang K, Wang X, Rong T, Wang Z, Liu F, Zhao J, Wei X, Chen M, Peng Z, Peng H, Sun J, Dong M. Qian Y, et al. Among authors: peng h, peng z. J Med Genet. 2023 Oct;60(10):933-938. doi: 10.1136/jmg-2022-109112. Epub 2023 Apr 3. J Med Genet. 2023. PMID: 37012053
Non-invasive prediction of preeclampsia using the maternal plasma cell-free DNA profile and clinical risk factors.
Yu Y, Xu W, Zhang S, Feng S, Feng F, Dai J, Zhang X, Tian P, Wang S, Zhao Z, Zhao W, Guan L, Qiu Z, Zhang J, Peng H, Lin J, Zhang Q, Chen W, Li H, Zhao Q, Xiao G, Li Z, Zhou S, Peng C, Xu Z, Zhang J, Zhang R, He X, Li H, Li J, Ruan X, Zhao L, He J. Yu Y, et al. Among authors: peng c, peng h. Front Med (Lausanne). 2024 Apr 17;11:1254467. doi: 10.3389/fmed.2024.1254467. eCollection 2024. Front Med (Lausanne). 2024. PMID: 38695016 Free PMC article.
T cell receptor β repertoires as novel diagnostic markers for systemic lupus erythematosus and rheumatoid arthritis.
Liu X, Zhang W, Zhao M, Fu L, Liu L, Wu J, Luo S, Wang L, Wang Z, Lin L, Liu Y, Wang S, Yang Y, Luo L, Jiang J, Wang X, Tan Y, Li T, Zhu B, Zhao Y, Gao X, Wan Z, Huang C, Fang M, Li Q, Peng H, Liao X, Chen J, Li F, Ling G, Zhao H, Luo H, Xiang Z, Liao J, Liu Y, Yin H, Long H, Wu H, Yang H, Wang J, Lu Q. Liu X, et al. Among authors: peng h. Ann Rheum Dis. 2019 Aug;78(8):1070-1078. doi: 10.1136/annrheumdis-2019-215442. Epub 2019 May 17. Ann Rheum Dis. 2019. PMID: 31101603
Test development, optimization and validation of a WGS pipeline for genetic disorders.
Yang Z, Yang X, Sun Y, Wang Y, Song L, Qiao Z, Fang Z, Wang Z, Liu L, Chen Y, Yan S, Guo X, Zhang J, Fan C, Liu F, Peng Z, Peng H, Sun J, Chen W. Yang Z, et al. Among authors: peng h, peng z. BMC Med Genomics. 2023 Apr 5;16(1):74. doi: 10.1186/s12920-023-01495-x. BMC Med Genomics. 2023. PMID: 37020281 Free PMC article.
Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma.
Guo G, Gui Y, Gao S, Tang A, Hu X, Huang Y, Jia W, Li Z, He M, Sun L, Song P, Sun X, Zhao X, Yang S, Liang C, Wan S, Zhou F, Chen C, Zhu J, Li X, Jian M, Zhou L, Ye R, Huang P, Chen J, Jiang T, Liu X, Wang Y, Zou J, Jiang Z, Wu R, Wu S, Fan F, Zhang Z, Liu L, Yang R, Liu X, Wu H, Yin W, Zhao X, Liu Y, Peng H, Jiang B, Feng Q, Li C, Xie J, Lu J, Kristiansen K, Li Y, Zhang X, Li S, Wang J, Yang H, Cai Z, Wang J. Guo G, et al. Among authors: peng h. Nat Genet. 2011 Dec 4;44(1):17-9. doi: 10.1038/ng.1014. Nat Genet. 2011. PMID: 22138691
Noninvasive preeclampsia prediction using plasma cell-free RNA signatures.
Zhou S, Li J, Yang W, Xue P, Yin Y, Wang Y, Tian P, Peng H, Jiang H, Xu W, Huang S, Zhang R, Wei F, Sun HX, Zhang J, Zhao L. Zhou S, et al. Among authors: peng h. Am J Obstet Gynecol. 2023 Nov;229(5):553.e1-553.e16. doi: 10.1016/j.ajog.2023.05.015. Epub 2023 May 19. Am J Obstet Gynecol. 2023. PMID: 37211139 Free article.
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