Zhengfeng Xu - Concepedia

Author

Zhengfeng Xu

Nanjing Medical University ORCID

Also Known As

Jia-Wei Cheng, Jianxin Tan, Wen-Hai Xie, Xu Zhengfeng, Xu, Zhengfeng, Xuemei Jia, Y L He, Yan Wang, Z Xu, Z. Xu

187

Publications

3.2K

Citations

H-Index

125

Concepts

All Affiliations

Nanjing Medical University Nanjing Maternity and Child Health Care Hospital Nanjing University BGI Group (China)University of Copenhagen

About

Zhengfeng Xu is an author at Nanjing Medical University specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	20	890
2	Public Health	7	7	383
3	Engineering	3	3	163
4	Health Sciences	1	1	11
5	Natural Sciences	1	1	12

Zhengfeng Xu

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Clinical application of massively parallel sequencing‐based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors Dan Shan, Wei Wang, Jinghui Ren, Prenatal Diagnosis	2012	235
Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach Zirui Dong, Jun Zhang, Ping Hu, Genetics in Medicine	2016	223
Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population Jing Xu, Zhibin Hu, Zhengfeng Xu, Human Mutation Hox Gene ClustersGeneticsGenetic EpidemiologyCongenital Heart AnomalyFunctional Variant	2009	132
A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing Sheng‐Pei Chen, Tze Kin Lau, Chunlei Zhang, Prenatal Diagnosis	2013	130
Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study Yan Wang, Li Cao, Liang Dong, American Journal of Obstetrics and Gynecology MedicineGeneticsGenetic EpidemiologyPediatricsMaternal Health	2017	100
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations Zhibin Hu, Yongyong Shi, Xuming Mo, Nature Genetics Genome-wide Association StudyEpidemiologyGeneticsRisk LociGenetic Epidemiology	2013	99
Transcriptomic Profiling of Human Placenta in Gestational Diabetes Mellitus at the Single-Cell Level Yuqi Yang, Fang Guo, Yue Peng, Frontiers in Endocrinology Transcriptomic ProfilingGeneticsGdm TreatmentTranscriptomics TechnologyEpigenetics	2021	87
Systematic analysis of copy‐number variations associated with early pregnancy loss Yishuang Wang, Y. Li, Yiyao Chen, Ultrasound in Obstetrics and Gynecology	2019	81
The Cation Channel TMEM63B Is an Osmosensor Required for Hearing Han Du, Chang Ye, Dan Wu, Cell Reports	2020	79
A Single Cell Level Based Method for Copy Number Variation Analysis by Low Coverage Massively Parallel Sequencing Chun-Lei Zhang, Chunsheng Zhang, Sheng‐Pei Chen, PLoS ONE Cnvs DetectionGeneticsGenomicsHigh Throughput SequencingMolecular Ecology	2013	71

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