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Huakang Du
Observed name:
Du, Huakang
Institutions:
Chinese Academy of Medical Sciences & Peking Union Medical College,
Peking Union Medical College Hospital
Observed institutions:
Chinese Academy of Medical Sciences & Peking Union Medical College,
Peking Union Medical College Hospital
OpenAlex ID:
A5000704664
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome
2021
·
Na Chen
, Sen Zhao
, et al.
·
The American Journal of Human Genetics
·
82
PDF
The Progress of CRISPR/Cas9-Mediated Gene Editing in Generating Mouse/Zebrafish Models of Human Skeletal Diseases
2019
·
Nan Wu
, Bowen Liu
, et al.
·
Computational and Structural Biotechnology Journal
·
26
SIGMA leverages protein structural information to predict the pathogenicity of missense variants
2024
·
Hengqiang Zhao
, Huakang Du
, et al.
·
Cell Reports Methods
·
23
A Recurrent Rare SOX9 Variant (M469V) is Associated with Congenital Vertebral Malformations
2019
·
Nan Wu
, Lianlei Wang
, et al.
·
Current Gene Therapy
·
17
Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosis
2021
·
Bowen Liu
, Sen Zhao
, et al.
·
Gene
·
12
Delineation of dual molecular diagnosis in patients with skeletal deformity
2022
·
Lian Liu
, Liying Sun
, et al.
·
Orphanet Journal of Rare Diseases
·
8
PDF
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
2020
·
Zefu Chen
, Zihui Yan
, et al.
·
Orphanet Journal of Rare Diseases
·
6
Global competence of medical students: An assessment scale and preliminary investigation in China
2023
·
Yue Shi
, Huakang Du
, et al.
·
PLoS ONE
·
5
PDF
Rare variant association analyses reveal the significant contribution of carbohydrate metabolic disturbance in severe adolescent idiopathic scoliosis
2024
·
Wen Wen
, Zhengye Zhao
, et al.
·
Journal of Medical Genetics
·
3
Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patients
2022
·
Defu Lin
, Huakang Du
, et al.
·
Orphanet Journal of Rare Diseases
·
3
PDF
Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformation
2022
·
Zhenlei Liu
, Huakang Du
, et al.
·
Human Genetics
·
2
Global Competence of Medical Students: An Assessment Scale and Preliminary Investigation in China
2019
·
Yue Shi
, Huakang Du
, et al.
·
1
PDF
Epidemiology and Phenotypic Characteristics of Dual Molecular Diagnosis Cases in Skeletal Abnormality
2021
·
Lian Liu
, Liying Sun
, et al.
·
Research Square
PDF
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Works count:
16
Citation count:
191
H-index:
6
I10-index:
5
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