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Qiu, Xing-Biao
1792  results:
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1

Discovery of TBX20 as a Novel Gene Underlying Atrial Fibril..:

Li, Ning ; Li, Yan-Jie ; Guo, Xiao-Juan...
Biology.  12 (2023)  9 - p. 1186 , 2023
Link: https://doi.org/10.3390/..
 
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2

VEZF1 loss-of-function mutation underlying familial dilated..:

Shi, Hong-Yu ; Xie, Meng-Shi ; Guo, Yu-Han...
European Journal of Medical Genetics.  66 (2023)  3 - p. 104705 , 2023
Link: https://doi.org/10.1016/..
 
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3

Discovery of GJC1 (Cx45) as a New Gene Underlying Congenita..:

Li, Yan-Jie ; Wang, Juan ; Ye, Willy G....
Biology.  12 (2023)  3 - p. 346 , 2023
Link: https://doi.org/10.3390/..
 
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4

A novel PRRX1 loss-of-function variation contributing to fa..:

Ke, Zun-Ping ; Zhang, Gao-Feng ; Guo, Yu-Han...
Genetics and Molecular Biology.  45 (2022)  2 - p. , 2022
Link: https://doi.org/10.1590/..
 
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5

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillat..:

Li, Ning ; Xu, Ying-Jia ; Shi, Hong-Yu...
Genes.  12 (2021)  3 - p. 408 , 2021
Link: https://doi.org/10.3390/..
 
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6

SOX17 loss-of-function variation underlying familial congen..:

Zhao, Lan ; Jiang, Wei-Feng ; Yang, Chen-Xi...
European Journal of Medical Genetics.  64 (2021)  5 - p. 104211 , 2021
Link: https://doi.org/10.1016/..
 
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7

ISL1 loss-of-function variation causes familial atrial fibr..:

Wu, Shao-Hui ; Wang, Xin-Hua ; Xu, Ying-Jia...
European Journal of Medical Genetics.  63 (2020)  11 - p. 104029 , 2020
Link: https://doi.org/10.1016/..
 
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8

A novel TBX5 mutation predisposes to familial cardiac septa..:

Jiang, Wei-Feng ; Xu, Ying-Jia ; Zhao, Cui-Mei...
Genetics and Molecular Biology.  43 (2020)  4 - p. , 2020
Link: https://doi.org/10.1590/..
 
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9

HAND2 loss-of-function mutation causes familial dilated car..:

Liu, Hua ; Xu, Ying-Jia ; Li, Ruo-Gu...
European Journal of Medical Genetics.  62 (2019)  9 - p. 103540 , 2019
Link: https://doi.org/10.1016/..
 
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10

A New ISL1 Loss-of-Function Mutation Predisposes to Congeni..:

Wang, Zhi ; Song, Hao-Ming ; Wang, Fei...
International Heart Journal.  60 (2019)  5 - p. 1113-1122 , 2019
Link: https://doi.org/10.1536/..
 
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11

ISL1 loss-of-function mutation contributes to congenital he..:

Ma, Lan ; Wang, Juan ; Li, Li...
Heart and Vessels.  34 (2018)  4 - p. 658-668 , 2018
Link: https://doi.org/10.1007/..
 
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12

A SHOX2 loss-of-function mutation underlying familial atria..:

Li, Ning ; Wang, Zhang-Sheng ; Wang, Xin-Hua...
International Journal of Medical Sciences.  15 (2018)  13 - p. 1564-1572 , 2018
Link: https://doi.org/10.7150/..
 
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13

GATA4 Loss-of-Function Mutation and the Congenitally Bicusp..:

Li, Ruo-Gu ; Xu, Ying-Jia ; Wang, Juan...
The American Journal of Cardiology.  121 (2018)  4 - p. 469-474 , 2018
Link: https://doi.org/10.1016/..
 
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14

A novel NR2F2 loss-of-function mutation predisposes to cong..:

Qiao, Xiao-Hui ; Wang, Qian ; Wang, Juan...
European Journal of Medical Genetics.  61 (2018)  4 - p. 197-203 , 2018
Link: https://doi.org/10.1016/..
 
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15

ZBTB17 loss-of-function mutation contributes to familial di..:

Sun, Yu-Min ; Wang, Jun ; Xu, Ying-Jia...
Heart and Vessels.  33 (2018)  7 - p. 722-732 , 2018
Link: https://doi.org/10.1007/..
 
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