Works by Jiwu, Lou

Results: 11

Retrospective Analysis of the Effects of Maternal Thyroid Dysfunction on Obstetrical Complications and Outcomes in a Cohort of 17,219 Pregnant Women.

Published in:

Clinical & Experimental Obstetrics & Gynecology, 2025, v. 52, n. 4, p. 1, doi. 10.31083/CEOG27087

By:

Manna Sun;
Haiwen Zhuo;
Yunyong Fang;
Jiezhen Liang;
Jiwu Lou;
Bingmei Dai;
Xinghe Wang;
Jingsi Chen

Publication type:

Article

Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1.

Published in:

BMC Medical Genomics, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s12920-020-0728-8

By:

Wang, Qingming;
Chen, Pengliang;
Liu, Jianxin;
Lou, Jiwu;
Liu, Yanhui;
Yuan, Haiming

Publication type:

Article

Rapid and simultaneous detection of common aneuploidies by quadruplex real-time polymerase chain reaction combined with melting curve analysis.

Published in:

PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171886

By:

Lou, Jiwu;
Sun, Manna;
Zhao, Ying;
Ji, Zhisong;
Liu, Fenghua;
Li, Dongzhi;
Xu, Wanfang;
Lin, Yangyang;
Liu, Yanhui

Publication type:

Article

Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2022, v. 35, n. 16, p. 3064, doi. 10.1080/14767058.2020.1808612

By:

Lou, Jiwu;
Sun, Manna;
Zhao, Ying;
Fu, Youqing;
Yuan, Haiming;
Dai, Yunshi;
Liang, Fuxiao;
He, Yi;
Liu, Yanhui

Publication type:

Article

Hb H disease associated with compound heterozygosity for --SEA deletion and a novel alpha globin chain variant (HBA2:c.175C>A) on the distal histidine in a Chinese family.

Published in:

Hematology, 2024, v. 29, n. 1, p. 1, doi. 10.1080/16078454.2024.2339559

By:

Sun, Manna;
Lou, Jiwu;
Xinghe, Wang;
Zhao, Ying;
Dai, Yunshi;
Liu, Shuangai;
Yan, Tizhen

Publication type:

Article

Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families.

Published in:

Hemoglobin, 2019, v. 43, n. 2, p. 101, doi. 10.1080/03630269.2019.1607372

By:

Sun, Manna;
Lou, Jiwu;
Zhag, Ying;
Fu, Youqing;
Dai, Yunshi;
Liu, Yanhui

Publication type:

Article

Hb H Disease Results from Compound Heterozygosity of – –SEA and –αMAL3.5 in a Chinese Family.

Published in:

Hemoglobin, 2019, v. 43, n. 1, p. 69, doi. 10.1080/03630269.2019.1575849

By:

Zhao, Ying;
Lou, Jiwu;
Sun, Manna;
Fu, Youqing;
Ye, Wanling;
Li, Yanjin;
Dai, Yunshi;
Liu, Yanhui

Publication type:

Article

Molecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals.

Published in:

Hemoglobin, 2018, v. 42, n. 2, p. 132, doi. 10.1080/03630269.2018.1458628

By:

Sun, Manna;
Lou, Jiwu;
Zhao, Ying;
Liu, Yanhui

Publication type:

Article

A stepwise haematological screening and whole‐exome sequencing reveal multiple mutations from SUPT5H causing an elevation of Hb A2 from a cohort of 47336 individuals.

Published in:

International Journal of Laboratory Hematology, 2023, v. 45, n. 1, p. 90, doi. 10.1111/ijlh.13959

By:

Lou, Jiwu;
Ye, Yuhua;
Sun, Manna;
Zhao, Ying;
Fu, Youqing;
Liu, Yanhui

Publication type:

Article

Novel SLC16A2 Frameshift Mutation as a Cause of Allan-Herndon-Dudley Syndrome and its Implications for Carrier Screening.

Published in:

Pharmacogenomics & Personalized Medicine, 2025, v. 18, p. 85, doi. 10.2147/PGPM.S492647

By:

Lin, Peng;
Liu, Huituan;
Lou, Jiwu;
Lyu, Guizhen;
Li, Yanwei;
He, Peiqing;
Fu, Youqing;
Zhang, Ronghua;
Zhang, Yuqiong;
Yan, Tizhen

Publication type:

Article

Hyperhaemolysis in a pregnant woman with a homozygous β0‐thalassemia mutation and two genetic modifiers.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 7, p. 1, doi. 10.1002/mgg3.1696

By:

Jiwu, Lou;
Manna, Sun;
Lai, Meixiang;
Ying, Zhao;
Yanhui, Liu

Publication type:

Article

Works by Jiwu, Lou

Retrospective Analysis of the Effects of Maternal Thyroid Dysfunction on Obstetrical Complications and Outcomes in a Cohort of 17,219 Pregnant Women.

Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1.

Rapid and simultaneous detection of common aneuploidies by quadruplex real-time polymerase chain reaction combined with melting curve analysis.

Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis.

Hb H disease associated with compound heterozygosity for --<sup>SEA</sup> deletion and a novel alpha globin chain variant (HBA2:c.175C>A) on the distal histidine in a Chinese family.

Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families.

Hb H Disease Results from Compound Heterozygosity of – –<sup>SEA</sup> and –α<sup>MAL3.5</sup> in a Chinese Family.

Molecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals.

A stepwise haematological screening and whole‐exome sequencing reveal multiple mutations from SUPT5H causing an elevation of Hb A<sub>2</sub> from a cohort of 47336 individuals.

Novel SLC16A2 Frameshift Mutation as a Cause of Allan-Herndon-Dudley Syndrome and its Implications for Carrier Screening.

Hyperhaemolysis in a pregnant woman with a homozygous β<sup>0</sup>‐thalassemia mutation and two genetic modifiers.