Qihua Fu
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Explore the profile of Qihua Fu including associated specialties, affiliations and a list of published articles.
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Articles
97
Citations
585
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Recent Articles
1.
Zhao Y, Ding C, Su H, Wang A, Tang A, Zhao H, et al.
Adv Sci (Weinh)
. 2025 Mar;
:e2416454.
PMID: 40047331
Pulmonary hypertension (PH) often leads to poor survival outcomes and encompasses diverse subtypes with distinct underlying causes. Specifically, PH resulting from fibrosing mediastinitis (FM-PH) presents significant diagnostic challenges due to...
2.
Fang Q, Xu Y, Feng J, Zhang X, Wang B, Fu Q, et al.
Pediatr Res
. 2024 Aug;
96(7):1626-1635.
PMID: 39217261
Background: CREBBP has been extensively studied in syndromic diseases associated with skeletal dysplasia. However, there is limited research on the molecular mechanisms through which CREBBP may impact bone development. We...
3.
Zhang S, Zhao M, Zhong S, Niu J, Zhou L, Zhu B, et al.
Pharmacogenet Genomics
. 2024 Mar;
34(4):105-116.
PMID: 38470454
Objectives: Genetic variation has been a major contributor to interindividual variability of warfarin dosage requirement. The specific genetic factors contributing to warfarin bleeding complications are largely unknown, particularly in Chinese...
4.
Li N, Xu Y, Chen H, Lin J, AlAbdi L, Bekheirnia M, et al.
EBioMedicine
. 2023 Dec;
99:104940.
PMID: 38154379
Background: Pathogenic variants in the centrosome protein (CEP) family have been implicated in primary microcephaly, Seckel syndrome, and classical ciliopathies. However, most CEP genes remain unlinked to specific Mendelian genetic...
5.
Li L, Shi G, Zhang X, Wang T, Wang B, Gao Y, et al.
Transl Pediatr
. 2023 Sep;
12(8):1476-1489.
PMID: 37692537
Background: Primary ciliary dyskinesia (PCD) is a clinically heterogeneous group of autosomal or, less frequently, X-chromosomal recessive inheritance syndrome of motile cilia dysfunction characterized by neonatal respiratory distress, oto-sino-pulmonary disease,...
6.
Chen Z, Gao Y, Lu L, Li N, Liu P, Peng R, et al.
Sci Bull (Beijing)
. 2023 Aug;
68(18):1993-1998.
PMID: 37573248
No abstract available.
7.
Lu Y, Zhou Y, Guo J, Qi M, Lin Y, Zhang X, et al.
Commun Biol
. 2023 Jul;
6(1):735.
PMID: 37460814
Congenital anomalies of the kidney and urinary tract (CAKUT) are disorders resulting from defects in the development of the kidneys and their outflow tract. Copy number variations (CNVs) have been...
8.
Ye J, Niu Y, Peng Y, Huang J, Wang H, Fu Q, et al.
Genomics
. 2023 Jul;
115(5):110676.
PMID: 37406974
Objective: Deleterious genetic variants comprise one cause of cardiac conotruncal defects (CTDs). Genes associated with CTDs are gradually being identified. In the present study, we aimed to explore the profile...
9.
Lu Y, Fang Q, Qi M, Li X, Zhang X, Lin Y, et al.
Commun Biol
. 2023 Feb;
6(1):189.
PMID: 36806749
Copy number variations (CNVs) have long been recognized as pathogenic factors for congenital heart disease (CHD). Few CHD associated CNVs could be interpreted as dosage effect due to disruption of...
10.
Li N, Xu Y, Chen H, Chen L, Zhang Y, Yu T, et al.
Cell Rep
. 2022 Nov;
41(6):111600.
PMID: 36351389
Interstrand crosslinks (ICLs) repair by the canonical Fanconi anemia (FA) pathway generates double-strand breaks (DSBs), which are subsequently repaired by the homologous recombination (HR) pathway. Recent studies show that the...