Wentao Yuan - Concepedia

Author

Wentao Yuan

Chinese National Human Genome Center at Shanghai ORCID

Also Known As

J. Huang, Kaiyue Zhang, W Yuan, W. T. Yuan, W. Yuan, W.-T. Yuan, W.T. Yuan, Wen-Tao Yuan, Wen-tao Yuan, Wentao Yuan

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

Chinese National Human Genome Center at Shanghai Chinese National Human Genome Center Fudan University Ruijin Hospital Huazhong University of Science and Technology

About

Wentao Yuan is an author at Chinese National Human Genome Center at Shanghai specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	17	1.6K
2	Engineering	5	5	250
3	Public Health	2	2	63
4	Natural Sciences	1	1	723
5	Biostatistics	1	1	35

Wentao Yuan

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Mapping Human Genetic Diversity in Asia Mahmood Ameen Abdulla, Ikhlak Ahmed, Anunchai Assawamakin, Science Haplotype DeterminationGenotype-phenotype AssociationMolecular EcologyHuman VariationHaplotype Diversity	2009	723
A genome-wide search for Type II diabetes susceptibility genes in Chinese Hans Tianhong Luo, Yajie Zhao, G. Li, Diabetologia Genome-wide Association StudyGenetic DeterminantGeneticsChinese HansGenetic Epidemiology	2001	116
Identification of a Locus for Dyschromatosis Symmetrica Hereditaria at Chromosome 1q11–1q21 Xuejun Zhang, Min Gao, Ming Li, Journal of Investigative Dermatology CytogeneticsMedicineGeneticsGenetic DisorderPathology	2003	112
High strain rate superplasticity in friction stir processed ultrafine grained Mg–Al–Zn alloys A. Mohan, Wentao Yuan, Rajiv S. Mishra Materials Science and Engineering A Materials ScienceMaterials EngineeringEngineeringSevere Plastic DeformationMechanical Engineering	2012	94
The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives A‐Yong Cao, Juan Huang, Zhen Hu, Breast Cancer Research and Treatment Breast OncologyOncologyCancer EpidemiologyPalb2 Germline MutationsSomatic Variant	2008	90
Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene Xiaolin Wu, Ming-min Gu, Lei Huang, The American Journal of Human Genetics Mendelian DisorderMultiple Synostoses SyndromeFgf9 GeneConnective Tissue DiseaseGenetic Disorder	2009	85
A Nonsense Mutation in DHTKD1 Causes Charcot-Marie-Tooth Disease Type 2 in a Large Chinese Pedigree Wangyang Xu, Ming-min Gu, Lianhua Sun, The American Journal of Human Genetics Mendelian DisorderLarge Chinese PedigreeGenetic DisorderGeneticsHuman Polymorphism	2012	82
A Novel Linkage to Generalized Vitiligo on 4q13-q21 Identified in a Genomewide Linkage Analysis of Chinese Families Jianjun Chen, Wei Huang, Jin-Ping Gui, The American Journal of Human Genetics Next-generation SequencingGeneticsNovel LinkageGenetic EpidemiologyChinese Families	2005	74
Magnetic properties of iron-based soft magnetic composites prepared via phytic acid surface treatment Guodong Zhang, Guangyue Shi, Wentao Yuan, Ceramics International Materials ScienceMagnetismFerromagnetismMagnetic PropertiesEngineering	2020	70
A mutation in SART3 gene in a Chinese pedigree with disseminated superficial actinic porokeratosis Zhengyu Zhang, Zhenmin Niu, Wentao Yuan, British Journal of Dermatology	2005	51

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