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Nan Yang
Nan Yang
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Cited by
Year
TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, ...
New England Journal of Medicine 372 (4), 341-350, 2015
2742015
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene …
J Liu, N Wu, ...
Genetics in Medicine 21 (7), 1548-1558, 2019
632019
TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice
N Yang, N Wu, L Zhang, Y Zhao, J Liu, X Liang, X Ren, W Li, W Chen, ...
Human molecular genetics 28 (4), 539-547, 2019
512019
Retinal pigment epithelium-specific CLIC4 mutant is a mouse model of dry age-related macular degeneration
JZ Chuang, N Yang, N Nakajima, W Otsu, C Fu, HH Yang, MP Lee, ...
Nature communications 13 (1), 374, 2022
202022
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11. 2 microdeletion syndrome
N Yang, N Wu, S Dong, L Zhang, Y Zhao, W Chen, R Du, C Song, X Ren, ...
Kidney international 98 (4), 1020-1030, 2020
202020
Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice
X Ren, N Yang, N Wu, X Xu, W Chen, L Zhang, Y Li, RQ Du, S Dong, ...
Journal of medical genetics 57 (6), 371-379, 2020
202020
Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies
L Wang, Y Zhang, X Fu, S Dong, S Tang, N Zhang, C Song, N Yang, ...
Cell Research 30 (1), 91-94, 2020
152020
Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract
S Dong, C Wang, X Li, Q Shen, X Fu, M Wu, C Song, N Yang, Y Wu, ...
Molecular genetics and genomics 294, 493-500, 2019
92019
A de novo mutation in DHD domain of SKI causing spina bifida with no craniofacial malformation or intellectual disability
L Zhang, X Xu, K Sun, J Sun, Y Wang, Y Liu, N Yang, C Tao, B Cai, G Shi, ...
American Journal of Medical Genetics Part A 179 (6), 936-939, 2019
52019
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