Xiuli Zhao - Concepedia

Author

Xiuli Zhao

Chinese Academy of Medical Sciences & Peking Union Medical College ORCID

Also Known As

Jiulong Zhang, X L Zhao, X Zhao, X. Zhao, X.Z. Zhao, Xiu-li Zhao, Xiuli Zhao, Zhao, X., Zhao, Xiuli

Publications

933

Citations

H-Index

Concepts

All Affiliations

Chinese Academy of Medical Sciences & Peking Union Medical College Johns Hopkins University Shandong University Shandong Provincial Hospital Johns Hopkins Medicine

About

Xiuli Zhao is an author at Chinese Academy of Medical Sciences & Peking Union Medical College specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	451
2	Engineering	3	3	84
3	Natural Sciences	2	2	60
4	Biochemistry	2	2	48
5	Health Sciences	1	1	27

Xiuli Zhao

Publications

743

Citations

H-Index

Page 1

	Year	Citations
Mutations in HOXD13 Underlie Syndactyly Type V and a Novel Brachydactyly-Syndactyly Syndrome Xiuli Zhao, Miao Sun, Jin Zhao, The American Journal of Human Genetics Novel Brachydactyly-syndactyly SyndromeGenetic DisorderGeneticsMolecular BiologyMolecular Genetics	2007	105
Mutations of the<i>EPHA2</i>receptor tyrosine kinase gene cause autosomal dominant congenital cataract Tianxiao Zhang, Rui Hua, Wei Xiao, Human Mutation Human CcsDevelopmental BiologyOcular DiseaseOphthalmologyGenetic Disorder	2009	101
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
Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta Lulu Li, Bin Mao, Shan Li, Human Mutation	2019	43
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta Shan Li, Yixuan Cao, Han Wang, Frontiers in Genetics	2020	40
Novel Mutations of the RNA-Specific Adenosine Deaminase Gene (DSRAD) in Chinese Families with Dyschromatosis Symmetrica Hereditaria Qing Liu, Wenli Liu, Li Jiang, Journal of Investigative Dermatology Genetic DisorderMedicineGeneticsChinese FamiliesNovel Mutations	2004	39
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
Visible-light-induced α-oxyamination of 1,3-dicarbonyls with TEMPO <i>via</i> a photo(electro)catalytic process applying a DSSC anode or in a DSSC system Ming Gong, Jung Keun Kim, Xiuli Zhao, Green Chemistry Chemical EngineeringEngineeringPhotoredox ProcessPhotochemistrySynthetic Photochemistry	2019	36
A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression Miao Jiang, Xiuli Zhao, Weitian Han, Human Genetics Novel DeletionAutoimmune DiseaseDistal ArthrogryposisGeneticsGenetic Epidemiology	2006	29
Regioselective phosphinylation of coumarins under green LED irradiation and its mechanism Qingrui Li, Xiuli Zhao, Yabo Li, Organic & Biomolecular Chemistry 3-Phosphinylated CoumarinsEngineeringGreen ChemistrySynthetic PhotochemistryOrganic Chemistry	2017	27

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