Lulu Meng

Beijing Center for Disease Prevention and Control — China

Medicine · Health Sciences

10h-index294citations29works1.42yr avg
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Research Topics

Prenatal Screening and Diagnostics(11), Genomic variations and chromosomal abnormalities(10), Reproductive System and Pregnancy(3), Genomics and Rare Diseases(3), Genetics and Neurodevelopmental Disorders(3)

Publications29 total

Sugar content and health risk assessment in freshly made sugary commercial beverages: A cross-sectional study
African Journal of Reproductive Health·2025Open Access
Underwater Image Quality Evaluation Via Multidimensional Perceptual Characterization
SSRN Electronic Journal·2025Open Access
Creatine Kinase-MM/Proto-oncogene Tyrosine-Protein Kinase Receptor as a Sensitive Indicator for Duchenne Muscular Dystrophy Carriers
Molecular Neurobiology·2024
A new strategy for prenatal genetic screening of copy number variations in the <i>DMD</i> gene: A large cohort study based on NIPT analysis
Clinical and Translational Medicine·2024· 2 citedOpen Access
Optical Genome Mapping for Chromosomal Aberrations Detection—False-Negative Results and Contributing Factors
Diagnostics·2024· 5 citedOpen Access
Residual risk of clinically significant copy number variations in fetuses with nasal bone absence or hypoplasia after excluding non-invasive prenatal screening-detectable findings
Clinica Chimica Acta·2023· 2 cited
Systematic analysis of copy number variants of uncertain significance partially overlapping with the haploinsufficient or triplosensitive genes in clinical testing
Annals of Medicine·2023· 2 citedOpen Access
Reproductive outcomes in couples with recurrent pregnancy loss after embryonic chromosomal microarray analysis
Journal of Assisted Reproduction and Genetics·2023· 1 citedOpen Access
Reproductive outcomes in couples with sporadic miscarriage after embryonic chromosomal microarray analysis
Annals of Medicine·2023· 4 citedOpen Access
Systematic analysis of copy number variants of uncertain significance partially overlapping with the haploinsufficient or triplosensitive genes in clinical testing
Figshare·2023Open Access
Reproductive outcomes in couples with sporadic miscarriage after embryonic chromosomal microarray analysis
Figshare·2023Open Access
Whole-transcriptome sequencing identifies key mRNAs, miRNAs, lncRNAs, and circRNAs associated with unexplained recurrent pregnancy loss
Cell and Tissue Research·2022· 15 cited
Analysis of Biomarkers for Congenital Heart Disease Based on Maternal Amniotic Fluid Metabolomics
Frontiers in Cardiovascular Medicine·2021· 37 citedOpen Access
Identification of Chromosomal Abnormalities in Early Pregnancy Loss Using a High-Throughput Ligation-Dependent Probe Amplification–Based Assay
Journal of Molecular Diagnostics·2020· 14 citedOpen Access
Chromosomal Abnormality in Fetuses with Isolated Antenatal Hydronephrosis: Update for Prenatal Diagnosis and Genetic Counseling
Research Square (Research Square)·2020Open Access
A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report
Frontiers in Genetics·2019· 14 citedOpen Access
Apert Syndrome With FGFR2 758 C &gt; G Mutation: A Chinese Case Report
Frontiers in Genetics·2018· 5 citedOpen Access
[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].
PubMed·2017
Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study
American Journal of Obstetrics and Gynecology·2017· 100 cited
Noninvasive prenatal diagnosis for X-linked disease by maternal plasma sequencing in a family of Hemophilia B
Taiwanese Journal of Obstetrics and Gynecology·2017· 4 citedOpen Access
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Frequent Co-authors

Zhengfeng Xu(19), Ping Hu(16), Ran Zhou(12), Fengchang Qiao(9), Dingyuan Ma(9), Yan Wang(7), Jianxin Tan(7), Yan Wang(6), Mingtao Huang(5), Zhengyi Xia(5), Yiming Li(5), Tao Jiang(4), XU Yi-yun(4), Xiuqing Ji(3), Chunyu Luo(3), Long Yi(3), Li Cao(2), Liang Dong(2), Yun Wu(2), Yahong Li(2)