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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 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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

Found: 33

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

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

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

A rare complex rearrangement in the β‐globin gene cluster causing a novel homozygous <sup>G</sup>γ(<sup>A</sup>γδβ)<sup>0</sup>‐thalassemia.

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

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

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

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

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

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

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

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

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

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

CEP128 is involved in spermatogenesis in humans and mice.

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

Novel biallelic mutations in TTC29 cause asthenoteratospermia and male infertility.

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

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

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

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

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

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

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

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

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

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

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

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

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

Maternal CHD7 gonosomal mosaicism in a fetus with CHARGE syndrome.

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

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