Zailong Qin
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Explore the profile of Zailong Qin including associated specialties, affiliations and a list of published articles.
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Articles
79
Citations
767
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Recent Articles
1.
Su J, Zhang S, Li W, Wei Y, Lin F, Zhou C, et al.
Mol Genet Genomic Med
. 2025 Feb;
13(2):e70082.
PMID: 39976347
Background: The 10q26 microdeletion syndrome (OMIM #609625) is a distinct genomic disorder characterized by a spectrum of clinical features including craniofacial anomalies, developmental delay (DD)/intellectual disability (ID), hypotonia, cardiovascular, and...
2.
Yang Q, Zhang Q, Zhou X, Feng J, Zhang S, Lin L, et al.
Front Genet
. 2024 Dec;
15:1503048.
PMID: 39720179
UBAP2L-deficiency syndrome, also known as neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies (NEDLBF, OMIM 620494), is an extremely rare autosomal dominant disorder. This condition is caused by...
3.
Liu Z, Lv S, Qin Z, Shu J, Zhu F, Luo Y, et al.
Mol Biol Rep
. 2024 Nov;
51(1):1152.
PMID: 39541046
Background: Testicular germ cell tumor (TGCT) is a common malignant tumor in adolescents. Now, many long non-coding RNAs (LncRNAs) have been found to have an important function in TGCT. LINC00470...
4.
Cao J, Du L, Zhao X, Liu Z, Yuan J, Luo Y, et al.
Genes Immun
. 2024 Oct;
25(6):552.
PMID: 39472734
No abstract available.
5.
Gong M, Li J, Qin Z, Machado Bressan Wilke M, Liu Y, Li Q, et al.
Am J Hum Genet
. 2024 Oct;
111(11):2392-2410.
PMID: 39419027
Microtubule affinity-regulating kinase 2 (MARK2) contributes to establishing neuronal polarity and developing dendritic spines. Although large-scale sequencing studies have associated MARK2 variants with autism spectrum disorder (ASD), the clinical features...
6.
Zhang S, Qin H, Wang Q, Wang Y, Liu Y, Yang Q, et al.
Orphanet J Rare Dis
. 2024 Oct;
19(1):376.
PMID: 39394138
Biallelic pathogenic variants in TARS2 lead to combined oxidative phosphorylation deficiency, subtype 21 (COXPD21, MIM #615918), which is a rare mitochondrial encephalomyopathy (ME) characterized by early-onset severe axial hypotonia, limb...
7.
Yang Q, Zhou X, Yi S, Li X, Zhang Q, Zhang S, et al.
Front Pediatr
. 2024 Oct;
12:1429586.
PMID: 39363971
Introduction: Mutations in the protein WD repeat structural domain 26 (, MIM 617424) have been identified as the cause of autosomal dominant Skraban-Deardorff syndrome, a rare genetic disorder characterized by...
8.
Cao J, Du L, Zhao X, Liu Z, Yuan J, Luo Y, et al.
Genes Immun
. 2024 Sep;
25(6):447-458.
PMID: 39242755
Penile squamous cell carcinoma (PSCC) is becoming increasingly common and posing a severe threat to men's health, particularly in developing countries. The function of long non-coding RNAs (lncRNAs) in PSCC...
9.
Zhang M, Ju Y, Xue L, Zhao X, Xu X, Wu G, et al.
J Cancer
. 2024 Jun;
15(12):3890-3902.
PMID: 38911384
Skin cutaneous melanoma (SKCM) is a highly malignant tumor that is prone to immune escape and distant metastasis. Immunotherapy is considered to be the best treatment for patients with SKCM....
10.
Yang Q, Zhang Q, Qin Z, Yi S, Luo J
BMC Med Genomics
. 2024 Apr;
17(1):95.
PMID: 38643142
NSUN2-intellectual disability syndrome, also known as intellectual disability type 5 (MRT5), is an autosomal recessive disorder that is characterized by intellectual disability (ID), postnatal growth retardation, dysmorphic facies, microcephaly, short...