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ZHU Dan, WEI Xing, ZHOU Xin-yao, DENG Lin-bei, XIONG Shi-yi, CHEN Jian-ping, CHEN Guang-quan, ZOU Gang, SUN Lu-ming. Chromosomal abnormalities in recurrent pregnancy loss and its association with clinical characteristics. Journal of Assisted Reproduction and Genetics, accepted
Jiang H, Li L, Zhu D, Zhou X, Yu Y, Zhou Q, Sun L. A Review of Nanotechnology for Treating Dysfunctional Placenta. Front Bioeng Biotechnol. 2022 Mar 24;10:845779. doi: 10.3389/fbioe.2022.845779. PMID: 35402416; PMCID: PMC8987505.
Wei X, Yang Y, Zhou J, Zhou X, Xiong S, Chen J, Zhou F, Zou G, Sun L. An Investigation of the Etiologies of Non-Immune Hydrops Fetalis in the Era of Next-Generation Sequence-A Single Center Experience. Genes (Basel). 2022 Nov 28;13(12):2231. doi: 10.3390/genes13122231. PMID: 36553497; PMCID: PMC9778190.
Hu X, Xiong S, Zhou X, Sun L. Generation of a human induced pluripotent stem cell line FMUPDCi001-A from a patient with mental retardation, autosomal recessive 36 (MRT36) carrying the variants c.219dupA and c.587C > T in ADAT3. Stem Cell Res. 2022 May;61:102777. doi: 10.1016/j.scr.2022.102777. Epub 2022 Apr 4. PMID: 35405382.
Kong L, Li S, Zhao Z, Feng J, Liu L, Tang W, Zhang H, Wu D, Sun L*, Kong X*. Noninvasive prenatal testing of Duchenne muscular dystrophy in a twin gestation. Prenat Diagn. 2022 Apr;42(4):518-523. doi: 10.1002/pd.6124. Epub 2022 Mar 7.PMID: 35220584
Chen G, Xiong S, Jing Q, van Gestel CAM, van Straalen NM, Roelofs D, Sun L*, Qiu H*. Maternal exposure to polystyrene nanoparticles retarded fetal growth and triggered metabolic disorders of placenta and fetus in mice. Sci Total Environ. 2022 Sep 13;854:158666. doi: 10.1016/j.scitotenv.2022.158666. Epub ahead of print. PMID: 36108837.
Sun K, Yao Y, Yun L, Zhang C, Xie J, Qian X, Tang Q, Sun L*. Application of machine learning for ancestry inference using multi-InDel markers. Forensic Sci Int Genet. 2022 Jul;59:102702. doi: 10.1016/j.fsigen.2022.102702. Epub 2022 Mar 30. PMID: 35378426.
Xing Y, Zhang Y, Chen J, Wu F, Yuan M, Zou G, Yang Y, Zhou F, Zhou J, Sun L*. Prenatal diagnosis for fetuses with isolated and non-isolated congenital heart defects using chromosomal microarray and exome sequencing. Prenat Diagn. 2022 Jun;42(7):873-880. doi: 10.1002/pd.6168. Epub 2022 May 24. PMID: 35584285.
Deng L, Liu Y, Yuan M, Meng M, Yang Y, Sun L*. Prenatal diagnosis and outcome of fetal hyperechogenic kidneys in the era of antenatal next-generation sequencing. Clin Chim Acta. 2022 Mar 1;528:16-28. doi: 10.1016/j.cca.2022.01.012. Epub 2022 Jan 20. PMID: 35065907.
Wei X, Zhou X, Zhou J, Zou G, Yang Y, Zhou F, Xiong S, Chen J, Sun L*. The value of exome sequencing in thoracoamniotic shunt for severe pleural effusion with fetal hydrops: a retrospective clinical study. Fetal Diagn Ther. 2022 Feb 9. doi: 10.1159/000521212. Epub ahead of print. PMID: 35139508.
Cai L, Yang Y, Zou G, Zhang Y, Wu F, Yuan M, Zhou Y, Chen J, Sun L*. Pregnancy Loss After Amniocentesis with Double-Needle Insertions in Twin Pregnancies. Twin Res Hum Genet. 2022 Mar 7:1-6. doi: 10.1017/thg.2022.1. Epub ahead of print. PMID: 35249587.
Chen G, Xiong S, Zou G, Wu F, Qu X, Alawbathani S, Sun L. A 6.3 Mb maternally derived microduplication of 20p13p12.2 in a fetus with Brachydactyly type D and related literature review. Mol Cytogenet. 2022 Feb 28;15(1):6. doi: 10.1186/s13039-022-00584-3. PMID: 35227291; PMCID: PMC8887085.
Jia Zhou#, Ziying Yang#, Jun Sun#, Lipei Liu, Xinyao Zhou, Fengxia Liu, Ya Xing, Shuge Cui, ShiyiXiong, Xiaoyu Liu, Yingjun Yang, Xiuxiu Wei, Gang Zou, Zhonghua Wang, Xing Wei, Yaoshen Wang, Yun Zhang, Saiying Yan, Fengyu Wu1, Fanwei Zeng, Jian Wang, Tao Duan, ZhiyuPeng* and Luming Sun*(通讯). Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing. Genes (Basel). 2021 Mar 6;12(3):376. doi: 10.3390/genes12030376. PMID: 33800913; PMCID: PMC7999180.
Jianping Chen, Jun Zhang, Yang Liu, Xing Wei, Yingjun Yang, Gang Zou, Yun Zhang, Tao Duan, Luming Sun*(通讯). Fetal growth standards for Chinese twin pregnancies.BMC Pregnancy Childbirth.2021 Jun 22;21(1):436.
Xinyao Zhou, Jia Zhou, Xing Wei, Ruen Yao, Yingjun Yang, Linbei Deng, Gang Zou, Xietong Wang, YAPING YANG, Tao Duan, Jian Wang, Luming Sun*(通讯). Value of exome sequencing in diagnosis and management of recurrent nonimmune hydrops fetalis: A retrospective analysis. Frontiers in Genetics, 2021 Apr 9;12:616392.
Jianping Chen, Depeng Zhao, Yang Liu , Jia Zhou , Gang Zou, Yun Zhang , Ming Guo , Tao Duan , Tim Van Mieghem , Luming Sun*(通讯). Screening for Preeclampsia in Low-Risk Twin Pregnancies at Early Gestation. Acta Obstet Gynecol Scand. 2020 Apr 30. doi: 10.1111/aogs.13890. Online ahead of print.
Meizhen Yuan#, Linbei Deng#, Yingjun Yang, Luming Sun*(通讯).Intrauterine phenotype features of fetuses withWilliams–Beuren syndrome and literature review. Ann Hum Genet. 2019;1–8. Accepted: 23 September 2019 DOI: 10.1111/ahg.12360 IF= 1.319
Sun L*, Zou G, Yang Y, Zhou F, Tao D*. Risk factors for fetal death after radiofrequency ablation for complicated monochorionic twin pregnancies. Prenat Diagn. 2018 Jun;38(7):499-503.
Deng L, Cheung SW, Schmitt ES, Xiong S, Yuan M, Chen Z, Chen L, Sun L*(通讯). Targeted gene panel sequencing prenatally detects two novel mutations of DYNC2H1 in a fetus with increased biparietal diameter and polyhydramnios. Birth Defects Res. 2018 Mar 1;110(4):364-371.
Zhou X, Chandler N, Deng L, Zhou J, Yuan M, Sun L*(通讯). Prenatal diagnosis of skeletal dysplasias using a targeted skeletal gene panel. Prenat Diagn. 2018 Aug;38(9):692-699.
Xing Y, Holder JL Jr, Liu Y, Yuan M, Sun Q, Qu X, Deng L, Zhou J, Yang Y, Guo M, Cheung SW, Sun L*(通讯). Prenatal diagnosis of Wolf-Hirschhorn syndrome: from ultrasound findings, diagnostic technology to genetic counseling. Arch Gynecol Obstet. 2018 Aug;298(2):289-295.
Sun L*, Zou G, Zhou F, Yang Y, Oepkes D, Duan T. Outcome of dichorionic triamniotic triplet: the experience from an emerging fetal therapy center. J Matern Fetal Neonatal Med. 2018 Dec;31(23):3075-3079.
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