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Fu, Qihua
300  results:
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1

Association between CYP2C9 and VKORC1 genetic polymorphisms..:

Zhang, Suli ; Zhao, Mingzhe ; Zhong, Shilong...
Pharmacogenetics and Genomics.  34 (2024)  4 - p. 105-116 , 2024
Link: https://doi.org/10.1097/..
 
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2

The clinical application and laboratory management of molec..:

Bao, Wenjie ; Fu, Qihua ; Zhang, Xiaoqing..
Clinical and Translational Discovery.  4 (2024)  3 - p. , 2024
Link: https://doi.org/10.1002/..
 
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3

Bi-allelic variants in CEP295 cause Seckel-like syndrome pr..:

Li, Niu ; Xu, Yufei ; Chen, Hongzhu...
eBioMedicine.  99 (2024)  - p. 104940 , 2024
Link: https://doi.org/10.1016/..
 
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4

Copy number variation-associated lncRNAs may contribute to ..:

Lu, Yibo ; Fang, Qing ; Qi, Ming...
Communications Biology.  6 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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5

Rare loss-of-function variants reveal threshold and multifa..:

Chen, Zhongzhong ; Gao, Yunqian ; Lu, Lei...
Science Bulletin.  68 (2023)  18 - p. 1993-1998 , 2023
Link: https://doi.org/10.1016/..
 
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6

Analysis of pathogenic variants in 605 Chinese children wit..:

Ye, JiaJun ; Niu, Yiwei ; Peng, Yongxuan...
Genomics.  115 (2023)  5 - p. 110676 , 2023
Link: https://doi.org/10.1016/..
 
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7

Integrated analysis of copy number variation-associated lnc..:

Lu, Yibo ; Zhou, Yiyang ; Guo, Jing...
Communications Biology.  6 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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8

Cardiac Computed Tomography-Derived Left Atrial Strain and ..:

Xie, Wei-Hui ; Chen, Li-Jun ; Hu, Li-Wei...
Frontiers in Cardiovascular Medicine.  9 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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9

NEIL3 contributes to the Fanconi anemia/BRCA pathway by pro..:

Li, Niu ; Xu, Yufei ; Chen, Hongzhu...
Cell Reports.  41 (2022)  6 - p. 111600 , 2022
Link: https://doi.org/10.1016/..
 
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10

Corrigendum to "Generation of a homozygous CRISPR/Cas9-medi..:

Zu, Bailing ; Zhang, Xiaoqing ; You, Guoling.
Stem Cell Research.  62 (2022)  - p. 102817 , 2022
Link: https://doi.org/10.1016/..
 
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11

Predisposition to atrioventricular septal defects may be ca..:

Li, Baolei ; Li, Zhuoyan ; Yang, Jianping...
Molecular Genetics and Genomics.  297 (2022)  3 - p. 671-687 , 2022
Link: https://doi.org/10.1007/..
 
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12

De novo disruptive heterozygous MMP21 variants are potentia..:

Qin, Xi-ji ; Xu, Meng-meng ; Ye, Jia-jun...
Human Genomics.  16 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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13

Variants in a cis-regulatory element of TBX1 in conotruncal..:

Jiang, Xuechao ; Li, Tingting ; Liu, Sijie...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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14

Copy number variation analysis in Chinese children with com..:

Zhang, Xingyu ; Wang, Bo ; You, Guoling...
BMC Medical Genomics.  14 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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15

Clinical features, laboratory findings and persistence of v..:

Jiang, Hong ; Cheng, Hongbin ; Cao, Qing...
Biomedical Journal.  44 (2021)  1 - p. 94-100 , 2021
Link: https://doi.org/10.1016/..
 
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