Works by Liu, Hongqian

Results: 36

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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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