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Jiwu Lou

Observed names: J Lou, J. LOU, Ji-Wu Lou, Ji-wu Lou, Ji‐Wu Lou, Lou Jiwu
ORCID: 0000-0001-8250-1498
Observed ORCID: 0000-0001-8250-1498
OpenAlex ID: A5033893376
Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China
2010 · F Xiong, M Sun, et al. · Clinical Genetics · 248
Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals
2014 · Ji-Wu Lou, Dong-Zhi Li, et al. · Blood Cells Molecules and Diseases · 25
Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring ( HBA2 : c.427T > C)
2016 · Yi He, Ying Zhao, et al. · Hemoglobin · 17
Screening and Diagnosis of Hb Quong Sze [HBA2: c.377T > C (orHBA1)] in a Prenatal Control Program for Thalassemia
2014 · Yu Yang, Ji-Wu Lou, et al. · Hemoglobin · 17
Molecular spectrum and prevalence of thalassemia investigated by third-generation sequencing in the Dongguan region of Guangdong Province, Southern China
2023 · Jiwu Lou, Manna Sun, et al. · Clinica Chimica Acta · 15
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
2022 · Jiwu Lou, Yuhua Ye, et al. · International Journal of Laboratory Hematology · 12
Prevalence and Molecular Characterization of Structural Hemoglobin Variants in the Dongguan Region of Guangdong Province, Southern China
2014 · Ji-Wu Lou, Ting Wang, et al. · Hemoglobin · 11
Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene
2019 · Manna Sun, Jiwu Lou, et al. · Taiwanese Journal of Obstetrics and Gynecology · 10
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Identification of the Linkage of a 1.357 KB β-Globin Gene Deletion and A γ-Globin Gene Triplication in a Chinese Family
2010 · Ji-wu Lou, Qian Li, et al. · Hemoglobin · 9
Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1
2020 · Qingming Wang, Pengliang Chen, et al. · BMC Medical Genomics · 8
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Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATCorHBA2: c.3G>C)
2019 · Ya-Li Lei, Hong Sui, et al. · Hemoglobin · 6
Rapid and simultaneous detection of common aneuploidies by quadruplex real-time polymerase chain reaction combined with melting curve analysis
2017 · Jiwu Lou, Manna Sun, et al. · PLoS ONE · 6
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[Analysis of hematological characteristics on the 79 co-inheritance of α-thalassemia and β-thalassemia carriers in Guangxi].
2012 · Fu Xiong, Ji-wu Lou, et al. · PubMed · 6
Detection of Hb Anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese Individuals
2014 · Ji-Wu Lou, Yi He, et al. · Hemoglobin · 5
Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis
2020 · Jiwu Lou, Manna Sun, et al. · The Journal of Maternal-Fetal & Neonatal Medicine · 4
Rapid detection of α-thalassaemia alleles of -- SEA /, -α 3.7 / and -α 4.2 / using a dual labelling, self-quenching hybridization probe/melting curve analysis
2015 · Lan Gao, Yanhui Liu, et al. · Molecular and Cellular Probes · 4
Quantification of human embryonic ζ-globin chains in Southeast Asian deletion (-- SEA ) carriers
2022 · Yuhua Ye, Guoying Sun, et al. · Journal of Clinical Pathology · 3
Hyperhaemolysis in a pregnant woman with a homozygous β0‐thalassemia mutation and two genetic modifiers
2021 · Lou Jiwu, Sun Manna, et al. · Molecular Genetics & Genomic Medicine · 3
Tetrasomy 18p Case Report
2020 · Yi He, Juan-Juan Liao, et al. · Clinical Laboratory · 3
Can cell-free DNA testing be used in pregnancies with isolated fetal omphalocele? Preliminary evidence from cytogenetic results of prenatal cases
2019 · Li-Li Xu, Li Zhen, et al. · The Journal of Maternal-Fetal & Neonatal Medicine · 3
Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families
2019 · Manna Sun, Jiwu Lou, et al. · Hemoglobin · 3
Compound heterozygosity for a rare small deletion and a common point mutation in the beta‐globin gene: report of two Chinese families
2010 · X. SHANG, Z. RAO, et al. · International Journal of Laboratory Hematology · 3
Recurrent Wilms tumor in a Chinese family caused by a novel WT1 variant inherited from a mosaic parent
2020 · Yi He, Ji-Wu Lou, et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 2
Hb H Disease Results from Compound Heterozygosity of – –SEA and –αMAL3.5 in a Chinese Family
2019 · Ying Zhao, Jiwu Lou, et al. · Hemoglobin · 2
Molecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals
2018 · Manna Sun, Jiwu Lou, et al. · Hemoglobin · 2
Works count: 48
Citation count: 437
H-index: 9
I10-index: 8
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