Works matching AU Liu, Hongqian

Results: 42

Correction: Identification of a novel phenuivirus with an unusual ambisense genome from the ascomycete fungus Fusarium fujikuroi.

Published in:

2025

By:

Xin, Tongle;
Liu, Bo;
Liu, Hongqian;
Wang, Ziqi;
Li, Junmin;
Chi, Shengqi;
Andika, Ida Bagus;
Cao, Xinran

Publication type:

Correction Notice

Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings.

Published in:

Human Genomics, 2020, v. 14, n. 1, p. 1, doi. 10.1186/s40246-020-00274-4

By:

Wang, Xiang;
Zhang, Zhu;
Zhang, Xueguang;
Shen, Ying;
Liu, Hongqian

Publication type:

Article

Impaired Function of a Rare Mutation in the MMUT Gene Causes Methylmalonic Acidemia in a Chinese Patient.

Published in:

Genetics Research, 2022, p. 1, doi. 10.1155/2022/5611697

By:

Dai, Siyu;
Yang, Yanting;
Li, Yaqian;
Liu, Hongqian

Publication type:

Article

1-calcium phosphate-uracil, a synthesized pyrimidine derivative agent, has anti-proliferative, pro-apoptotic and anti-invasion effects on multiple tumor cell lines.

Published in:

Molecular Medicine Reports, 2014, v. 10, n. 5, p. 2271, doi. 10.3892/mmr.2014.2489

By:

JING PENG;
XINLIAN CHEN;
QIAN HU;
MEI YANG;
HONGQIAN LIU;
WEI WEI;
SHANLING LIU;
HE WANG

Publication type:

Article

Maternal CHD7 gonosomal mosaicism in a fetus with CHARGE syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2024, v. 194, n. 4, p. 1, doi. 10.1002/ajmg.a.63491

By:

Bai, Ting;
Shen, Ying;
Yang, Yanting;
Dai, Siyu;
Liu, Hongqian

Publication type:

Article

A rare complex rearrangement in the β‐globin gene cluster causing a novel homozygous Gγ(Aγδβ)0‐thalassemia.

Published in:

American Journal of Hematology, 2021, v. 96, n. 6, p. E189, doi. 10.1002/ajh.26148

By:

Zhang, Xueguang;
Yang, Yihong;
Zhang, Haixia;
Du, Ze;
Liu, Hongqian;
Shen, Ying

Publication type:

Article

Transforming teaching: Global responses to teaching under the Covid-19 pandemic: L. Cooker, T. Cotton, and H. Toft, 2022, 187 pp., £120.00, Hardback, ISBN 9780367713843, £19.99, Paperback, ISBN 9780367713850; eBook, £16.99, ISBN 9781003150596

Published in:

2022

By:

Feng, Haoda;
Liu, Hongqian

Publication type:

Book Review

Clinical strategy study on prenatal screening and diagnostic model for Down syndrome.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-73183-4

By:

Luo, Wei;
Liu, Sha;
He, Bin;
Han, Daiwen;
Yuan, Lixing;
Zhao, Kai;
Tang, Jun;
Pang, Ling;
Zou, Fene;
Liu, Jianlong;
Liu, Hongqian;
Bai, Ting;
Jing, Xiaosha;
Xia, Tianyu;
Deng, Cechuan;
Liu, Yunyun;
Cheng, Jing;
Wei, Xiang;
Xing, Lingling;
Luo, Yuan

Publication type:

Article

CEP128 is involved in spermatogenesis in humans and mice.

Published in:

Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29109-7

By:

Zhang, Xueguang;
Wang, Lingbo;
Ma, Yongyi;
Wang, Yan;
Liu, Hongqian;
Liu, Mohan;
Qin, Lang;
Li, Jinghong;
Jiang, Chuan;
Zhang, Xiaojian;
Shan, Xudong;
Liu, Yuliang;
Li, Jinsong;
Li, Yaqian;
Zheng, Rui;
Sun, Yongkang;
Sun, Jianfeng;
Leng, Xiangyou;
Liang, Yan;
Zhang, Feng

Publication type:

Article

A novel mutation in CFAP47 causes male infertility due to multiple morphological abnormalities of the sperm flagella.

Published in:

Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1155639

By:

Mohan Liu;
Siyu Dai;
Jiying Zhang;
Yihong Yang;
Ying Shen;
Hongqian Liu;
Yanting Yang;
Chuan Jiang;
Erpo Tian

Publication type:

Article

Diagnostic Accuracy of Interleukin-27 in Bronchoalveolar Lavage Fluids for Pulmonary Tuberculosis.

Published in:

Infection & Drug Resistance, 2019, v. 12, p. 3755, doi. 10.2147/IDR.S231215

By:

Lin, Shan;
Wang, Yan;
Li, Yuhong;
Xiao, Di;
Guo, Jin;
Ma, Weixiu;
An, Wenjing;
Liu, Hongqian;
Shi, Yingqing;
Zhang, Lei;
Cui, Jingxia;
Guan, Wei

Publication type:

Article

Identification of POLR3B biallelic mutations‐associated hypomyelinating leukodystrophy‐8 in two siblings.

Published in:

Clinical Genetics, 2023, v. 103, n. 5, p. 596, doi. 10.1111/cge.14300

By:

Yang, Fan;
Sun, Huaqin;
Yang, Yanting;
Wang, Yanan;
Dai, Siyu;
Lin, Ziyuan;
Shen, Ying;
Liu, Hongqian

Publication type:

Article

Loss‐of‐function mutation in DNAH8 induces asthenoteratospermia associated with multiple morphological abnormalities of the sperm flagella.

Published in:

Clinical Genetics, 2020, v. 98, n. 4, p. 396, doi. 10.1111/cge.13815

By:

Yang, Yihong;
Jiang, Chuan;
Zhang, Xueguang;
Liu, Xue;
Li, Jinghong;
Qiao, Xiaoyong;
Liu, Hongqian;
Shen, Ying

Publication type:

Article

Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal age.

Published in:

Orphanet Journal of Rare Diseases, 2024, p. 1, doi. 10.1186/s13023-024-03066-4

By:

Liu, Yunyun;
Liu, Sha;
Liu, Jianlong;
Bai, Ting;
Jing, Xiaosha;
Deng, Cechuan;
Xia, Tianyu;
Cheng, Jing;
Xing, Lingling;
Wei, Xiang;
Luo, Yuan;
Zhou, Quanfang;
Xie, Dan;
Xiong, Yueyue;
Liu, Ling;
Zhu, Qian;
Liu, Hongqian

Publication type:

Article

USP9X expression correlates with tumor progression and poor prognosis in esophageal squamous cell carcinoma.

Published in:

Diagnostic Pathology, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1746-1596-8-177

By:

Jing Peng;
Qian Hu;
Weiping Liu;
Xiaoli He;
Ling Cui;
Xinlian Chen;
Mei Yang;
Hongqian Liu;
Wei Wei;
Shanling Liu;
He Wang

Publication type:

Article

Genomic amplification of the human telomerase gene (hTERC) associated with human papillomavirus is related to the progression of uterine cervical dysplasia to invasive cancer.

Published in:

Diagnostic Pathology, 2012, v. 7, n. 1, p. 147, doi. 10.1186/1746-1596-7-147

By:

Hongqian Liu;
Shanling Liu;
He Wang;
Xiaoyan Xie;
Xinlian Chen;
Xuemei Zhang;
Youcheng Zhang

Publication type:

Article

Crystal structure of 5-(2,2-difluoropropyl)-5-methyl-6-oxo-5,6-dihydrobenzo[4,5]imidazo[2,1-a]isoquinoline-3-carbonitrile, C20H15F2N3O.

Published in:

Zeitschrift für Kristallographie / New Crystal Structures, 2025, v. 240, n. 3, p. 545, doi. 10.1515/ncrs-2025-0128

By:

Liu, Hongqian;
Liu, Hongmei;
Fu, Shaoyan;
Tang, Wenqiang

Publication type:

Article

Crystal structure of 2-chloro-11-(((fluoromethyl)sulfonyl)methyl)-6-methyl-6,11-dihydrodibenzo[c,f][1,2]thiazepine 5,5-dioxide, C16H13ClFNO4S2.

Published in:

Zeitschrift für Kristallographie / New Crystal Structures, 2025, v. 240, n. 3, p. 543, doi. 10.1515/ncrs-2025-0126

By:

Fu, Shaoyan;
Liu, Hongqian;
Gao, Yanrong;
Wang, Ji;
Tang, Wenqiang

Publication type:

Article

Noninvasive prenatal screening for fetal sex chromosome aneuploidies.

Published in:

Expert Review of Molecular Diagnostics, 2021, v. 21, n. 4, p. 405, doi. 10.1080/14737159.2021.1911651

By:

Deng, Cechuan;
Cheung, Sau Wai;
Liu, Hongqian

Publication type:

Article

Identification of a novel phenuivirus with an unusual ambisense genome from the ascomycete fungus Fusarium fujikuroi.

Published in:

Archives of Virology, 2025, v. 170, n. 7, p. 1, doi. 10.1007/s00705-025-06311-8

By:

Xin, Tongle;
Liu, Bo;
Liu, Hongqian;
Wang, Ziqi;
Li, Junmin;
Chi, Shengqi;
Andika, Ida Bagus;
Cao, Xinran

Publication type:

Article

Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans.

Published in:

BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05921-x

By:

Chen, Lin;
Wang, Li;
Zeng, Yang;
Yin, Daishu;
Tang, Feng;
Xie, Dan;
Zhu, Hongmei;
Liu, Hongqian;
Wang, Jing

Publication type:

Article

Rapid Detection of Aneuploidy and Unbalanced Chromosomal Rearrangements by Subtelomeric Multiplex Ligation-Dependent Probe Amplification in Fetuses with Congenital Heart Disease.

Published in:

Fetal Diagnosis & Therapy, 2013, v. 34, n. 2, p. 110, doi. 10.1159/000350272

By:

Wang, Jing;
Liu, Zhen;
Liu, Hongqian;
Li, Nana;
Li, Shengli;
Chen, Xinlin;
Lin, Yuan;
Wang, He;
Zhu, Jun;
Liu, Shanling

Publication type:

Article

Identification of a Novel Missense Mutation of the PHEX Gene in a Large Chinese Family with X-Linked Hypophosphataemia.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.792183

By:

Yang, Yanting;
Wang, Yuanda;
Shen, Ying;
Liu, Mohan;
Dai, Siyu;
Wang, Xiaodong;
Liu, Hongqian

Publication type:

Article

Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2021.811414

By:

Jing, Xiaosha;
Liu, Hongqian;
Zhu, Qian;
Liu, Sha;
Liu, Jianlong;
Bai, Ting;
Deng, Cechuan;
Xia, Tianyu;
Liu, Yunyun;
Cheng, Jing;
Wei, Xiang;
Xing, Lingling;
Luo, Yuan;
Zhou, Quanfang;
Chen, Lin;
Li, Lingping;
Wang, Jiamin

Publication type:

Article

Noninvasive Prenatal Screening Based on Second-Trimester Ultrasonographic Soft Markers in Low-Risk Pregnant Women.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.793894

By:

Liu, Yunyun;
Jing, Xiaosha;
Xing, Lingling;
Liu, Sha;
Liu, Jianlong;
Cheng, Jing;
Deng, Cechuan;
Bai, Ting;
Xia, Tianyu;
Wei, Xiang;
Luo, Yuan;
Zhou, Quanfang;
Zhu, Qian;
Liu, Hongqian

Publication type:

Article

Follow-up in Patients With Non-invasive Prenatal Screening Failures: A Reflection on the Choice of Further Prenatal Diagnosis.

Published in:

Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.666648

By:

Liu, Sha;
Liu, Hongqian;
Liu, Jianlong;
Bai, Ting;
Jing, Xiaosha;
Xia, Tianyu;
Deng, Cechuan;
Liu, Yunyun;
Cheng, Jing;
Wei, Xiang;
Xing, Lingling;
Luo, Yuan;
Zhou, Quanfang;
Zhu, Qian

Publication type:

Article

Performance of noninvasive prenatal screening in twin pregnancies: a retrospective study of 5469 twin pregnancies.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2022, v. 35, n. 25, p. 5999, doi. 10.1080/14767058.2021.1903860

By:

Bai, Ting;
Liu, Sha;
Liu, Jianlong;
Jing, Xiaosha;
Deng, Cechuan;
Xia, Tianyu;
Liu, Yunyun;
Cheng, Jing;
Li, Zhunduo;
Wei, Xiang;
Xing, Lingling;
Luo, Yuan;
Zhou, Quanfang;
Luo, Wei;
He, Bin;
Han, Daiwen;
Zhu, Qian;
Liu, Hongqian

Publication type:

Article

Genetic etiology of agenesis of the corpus callosum: a retrospective single-center cohort analysis of 114 fetuses.

Published in:

Archives of Gynecology & Obstetrics, 2024, v. 310, n. 1, p. 181, doi. 10.1007/s00404-024-07544-9

By:

Yu, Hui;
Li, Juan;
Yang, Qian;
Yang, Bo;
Li, Yali;
Ren, Yameng;
Han, Xiao;
Wang, Mengru;
Liu, Hongqian;
Wang, Kaijuan;
Liu, Ling

Publication type:

Article

The study of laparoscopic electrosurgical instruments on thermal effect of uterine tissues.

Published in:

Archives of Gynecology & Obstetrics, 2012, v. 285, n. 6, p. 1637, doi. 10.1007/s00404-011-2207-0

By:

Zhu, Qian;
Ruan, Jiaying;
Zhang, Li;
Jiang, Wei;
Liu, Hongqian;
Shi, Gang

Publication type:

Article

Ovarian masses in children and adolescents in China: analysis of 203 cases.

Published in:

Journal of Ovarian Research, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1757-2215-6-47

By:

Hongqian Liu;
Xiangao Wang;
Donghao Lu;
Zhihong Liu;
Gang Shi

Publication type:

Article

Establishment of a new representative model of human ovarian cancer in mice.

Published in:

Journal of Ovarian Research, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1757-2215-6-9

By:

Jianjun Zhang;
Xinlian Chen;
Gang Shi;
Xiaoyan Xie;
Hongqian Liu;
Xuemei Zhang;
Yi Lai;
Yan Zuo;
Zhong Chen;
Shanling Liu;
He Wang

Publication type:

Article

Upregulated miR-221/222 promotes cell proliferation and invasion and is associated with invasive features in retinoblastoma.

Published in:

Cancer Biomarkers, 2018, v. 22, n. 4, p. 621, doi. 10.3233/CBM-170721

By:

Liu, Hongqian;
Cao, Bofeng;
Zhao, Yuanyuan;
Liang, Haijing;
Liu, Xinfeng

Publication type:

Article

Copy number variation of GATA4 and NKX2-5 in Chinese fetuses with congenital heart disease.

Published in:

Pediatrics International, 2015, v. 57, n. 2, p. 234, doi. 10.1111/ped.12489

By:

Liu, Zhen;
Wang, Jing;
Liu, Shanling;
Deng, Ying;
Liu, Hongqian;
Li, Nana;
Li, Shengli;
Chen, Xinlin;
Lin, Yuan;
Wang, He;
Zhu, Jun

Publication type:

Article

Segmental aneuploidies in fetuses with isolated echogenic intracardiac focus among women younger than 35 years.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-67501-9

By:

Wang, Jing;
Chen, Lin;
Wang, Li;
Yin, Daishu;
Zeng, Yang;
Tang, Feng;
Tian, Yu;
Liu, Hongqian

Publication type:

Article

A Retrospective Analysis Of Different Contingent Screening Models For Fetal Down Syndrome In Southwestern China.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66320-2

By:

Luo, Wei;
He, Bin;
Han, Daiwen;
Yuan, Lixing;
Chen, Xinlian;
Pang, Ling;
Tang, Jun;
Zou, Fene;
Zhao, Kai;
Du, Yepei;
Liu, Hongqian

Publication type:

Article

Identification of a novel ST3GAL5 variant in a Chinese boy with GM3 synthase deficiency and literature review of variants in the ST3GAL5 gene.

Published in:

Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03369-6

By:

Mu, Dan;
Yang, Yanting;
Liu, Yao;
Shen, Ying;
Liu, Hongqian;
Wang, Jing

Publication type:

Article

Customizing carrier screening in the Chinese population: Insights from a 334‐gene panel.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 11, p. 1335, doi. 10.1002/pd.6635

By:

Liu, Sha;
Huang, Shuang;
Zhang, Victor Wei;
Cao, Liyuan;
Liu, Haipeng;
Wei, Xiang;
Luo, Yuan;
Li, Yue;
Zhou, Lin;
Li, Fuping;
Zhu, Qian;
Liu, Hongqian

Publication type:

Article

Multifunctional N,S co-doped carbon dots for sensitive probing of temperature, ferric ion, and methotrexate.

Published in:

Analytical & Bioanalytical Chemistry, 2019, v. 411, n. 8, p. 1647, doi. 10.1007/s00216-019-01617-4

By:

Zuo, Pengli;
Liu, Jianhua;
Guo, Hongna;
Wang, Chenghong;
Liu, Hongqian;
Zhang, Zhigang;
Liu, Qingyou

Publication type:

Article

Novel biallelic mutations in TTC29 cause asthenoteratospermia and male infertility.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 12, p. 1, doi. 10.1002/mgg3.2078

By:

Dai, Siyu;
Liang, Yan;
Liu, Mohan;
Yang, Yanting;
Liu, Hongqian;
Shen, Ying

Publication type:

Article

Long‐read Oxford nanopore sequencing reveals a de novo case of complex chromosomal rearrangement involving chromosomes 2, 7, and 13.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 9, p. 1, doi. 10.1002/mgg3.2011

By:

Xing, Lingling;
Shen, Ying;
Wei, Xiang;
Luo, Yuan;
Yang, Yan;
Liu, Haipeng;
Liu, Hongqian

Publication type:

Article

REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 11, p. 1, doi. 10.1002/mgg3.1488

By:

Liu, Mengmeng;
Zhong, Yunshan;
Liu, Hongqian;
Liang, Desheng;
Liu, Erhong;
Zhang, Yu;
Tian, Feng;
Liang, Qiaowei;
Cram, David S.;
Wang, Hua;
Wu, Lingqian;
Yu, Fuli

Publication type:

Article

A 17q24.3 duplication identified in a large Chinese family with brachydactyly‐anonychia.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1392

By:

Liu, Mohan;
Zhang, Xueguang;
Liu, Hongqian;
Shen, Ying

Publication type:

Article