Yuchen Niu - Concepedia

Author

Yuchen Niu

Peking Union Medical College Hospital ORCID

Also Known As

Fei Liu, Hengqiang Zhao, Lianlei Wang, Niu, Yuchen, Qiankun Zhu, Shengru Wang, Stavros Glentis, Y Niu, Yuchen Niu, Zefu Chen

Publications

Citations

H-Index

Concepts

All Affiliations

Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Baylor College of Medicine Baylor Genetics Capital Medical University

About

Yuchen Niu is an author at Peking Union Medical College Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	370
2	Public Health	3	3	63
3	Engineering	1	1	12
4	Natural Sciences	1	1	16
5	Biomedical Engineering	1	1	12

Yuchen Niu

Publications

701

Citations

H-Index

Page 1

	Year	Citations
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model Jiaqi Liu, Nan Wu, Nan Yang, Genetics in Medicine Compound InheritanceSpinal Cord InjuryCongenital ScoliosisSpine DeformityThoracic Spine	2019	89
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome Na Chen, Sen Zhao, Angad Jolly, The American Journal of Human Genetics Wölffian Duct DevelopmentDevelopmental BiologyMendelian DisorderGenetic DisorderDevelopmental Genetics	2021	89
Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM) Kun Wang, Sen Zhao, Bowen Liu, Journal of Medical Genetics	2018	69
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS) Sen Zhao, Yuanqiang Zhang, Wei‐Sheng Chen, Journal of Medical Genetics	2020	63
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature Xin Fan, Sen Zhao, Chenxi Yu, Journal of genetics and genomics/Journal of Genetics and Genomics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsMolecular Genetics	2021	37
Genetic polymorphisms of <i><scp>GPR</scp>126</i> are functionally associated with <scp>PUMC</scp> classifications of adolescent idiopathic scoliosis in a Northern Han population Gang Liu, Sen Liu, Mao Lin, Journal of Cellular and Molecular Medicine	2018	28
Identification of novel FBN1 variations implicated in congenital scoliosis Mao Lin, Sen Zhao, Gang Liu, Journal of Human Genetics Congenital ScoliosisGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2019	28
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral–basilar artery dissection (IVAD) Kun Wang, Sen Zhao, Qianqian Zhang, Journal of Human Genetics	2018	25
Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis Gang Liu, Lianlei Wang, Xinyu Wang, Frontiers in Bioengineering and Biotechnology	2019	24
Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders Sen Zhao, Yuanqiang Zhang, Sigrún Hallgrímsdóttir, npj Genomic Medicine Short StatureGeneticsGenetic EpidemiologyPathologyDisease Gene Identification	2022	24

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