Kexin Xu - State Key Lab Complex Severe & Rare Dis, Peking Union Med Coll Hosp

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论文共 15 篇作者统计合作学者相似作者

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Variants in the SOX9 Transactivation Middle Domain Induce Axial Skeleton Dysplasia and Scoliosis

Lianlei Wang,Zhaoyang Liu,Sen Zhao,Kexin Xu, Valeria Aceves,Cheng Qiu, Hong Colleen Feng,Fangzhou Bian, Jingyu He, Christina J Song,Benjamin Troutwine,Lian Liu, Samuel Ma,Yuchen Niu,Shengru Wang,Suomao Yuan,Xiaoxin Li,Lina Zhao,Xinyu Liu,Guixing Qiu,Zhihong Wu, Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study group,Terry Jianguo Zhang,Ryan S Gray,Nan Wu

Proceedings of the National Academy of Sciences of the United States of Americano. 4 (2025): e2313978121-e2313978121

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Impaired Central Pattern Generators Due to Abnormal EPHA4 Signaling Leads to Idiopathic Scoliosis

Lianlei Wang,Sen Zhao,Xinyu Yang,Pengfei Zheng, Wen,Kexin Xu,Xi Cheng,Qing Li,Anas M. Khanshour,Yoshinao Koike,Junjun Liu,Xin Fan,Nao Otomo,Zefu Chen,Yaqi Li,Lulu Li,Haibo Xie,Panpan Zhu,Xiaoxin Li,Yuchen Niu,Shengru Wang,Sen Liu,Suomao Yuan,Chikashi Terao,Ziquan Li,Shaoke Chen,Xiuli Zhao,Pengfei Liu,Jennifer E. Posey,Zhihong Wu,Guixing Qiu, DISCO study group (Deciphering Disorders Involving Scoliosis & COmorbidities),Shiro Ikegawa,James R. Lupski,Jonathan J. Rios,Carol A. Wise,Terry Jianguo Zhang,Chengtian Zhao,Nan Wu

biorxiv（2024）

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Ehlers-Danlos综合征的临床遗传学研究进展

徐可欣,李国壮, 李晴,尹相杰,方堃, 吴志宏,仉建国, DISCO(Deciphering Disorders Involving Scoliosis & COmorbidities)Study Group,吴南

Journal of Rare Diseasesno. 3 (2024)

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Deep Learning in Cobb Angle Automated Measurement on X-rays: a Systematic Review and Meta-Analysis

Yuanpeng Zhu,Xiangjie Yin,Zefu Chen, Haoran Zhang,Kexin Xu,Jianguo Zhang,Nan Wu

Spine Deformitypp.1-9, (2024)

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First Copy Number Variant in Trans with Single Nucleotide Variant in CCN6 Causing Progressive Pseudorheumatoid Dysplasia Revealed by Genome Sequencing and Deep Phenotyping in Monozygotic Twins

Kexin Xu,Guozhuang Li,Yuchen Niu,Zhihong Wu,Terry Jianguo Zhang,Shuyang Zhang,Nan Wu

American Journal of Medical Genetics Part A（2024）

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SIGMA Leverages Protein Structural Information to Predict the Pathogenicity of Missense Variants

Hengqiang Zhao,Huakang Du,Sen Zhao,Zefu Chen,Yaqi Li,Kexin Xu,Bowen Liu,Xi Cheng, Wen,Guozhuang Li,Guilin Chen,Zhengye Zhao,Guixing Qiu,Pengfei Liu,Terry Jianguo Zhang,Zhihong Wu,Nan Wu

CELL REPORTS METHODSno. 1 (2024)

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Integrating Deep Phenotyping with Genetic Analysis: a Comprehensive Workflow for Diagnosis and Management of Rare Bone Diseases

Guozhuang Li,Kexin Xu,Xiangjie Yin, Jianle Yang, Jihao Cai, Xinyu Yang, Qing Li, Jie Wang,Zhengye Zhao, Aoran Mahesahti, Ning Zhang,Terry Jianguo Zhang,Nan Wu

ORPHANET JOURNAL OF RARE DISEASESno. 1 (2024)

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Diagnosis and Treatment of the Ehlers-Danlos Syndromes in China: Synopsis of the First Guidelines

Kexin Xu,Guozhuang Li,Zhihong Wu,Terry Jianguo Zhang,Nan Wu

Orphanet Journal of Rare Diseasesno. 1 (2024)

引用1浏览0WOS引用

P234: CCN6 Copy Number Variant and Null Variant in Monozygous Twins with Progressive Pseudorheumatoid Dysplasia Revealed by WGS and Deep Phenotyping

Kexin Xu,Guozhuang Li,Jianguo Zhang,Nan Wu

Genetics in Medicine Open (2024): 101130

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