Zhanwen He
Overview
Explore the profile of Zhanwen He including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
172
Followers
0
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Recent Articles
1.
Wu R, Li X, Meng Z, Li P, He Z, Liang L
Orphanet J Rare Dis
. 2024 May;
19(1):205.
PMID: 38764027
Background: Trio-based whole-exome sequencing (trio-WES) enables identification of pathogenic variants, including copy-number variants (CNVs), in children with unexplained neurodevelopmental delay (NDD) and neurodevelopmental comorbidities (NDCs), including autism spectrum disorder (ASD),...
2.
Tang W, Shao Q, He Z, Zhang X, Li X, Wu R
BMC Cancer
. 2023 Apr;
23(1):303.
PMID: 37013511
Background: Nonerythrocytic spectrin beta 1 (SPTBN1) is an important cytoskeletal protein that involves in normal cell growth and development via regulating TGFβ/Smad signaling pathway, and is aberrantly expressed in various...
3.
Xia D, Deng S, Gao C, Li X, Zhang L, Xiao X, et al.
Am J Med Genet A
. 2023 Feb;
191(5):1240-1249.
PMID: 36756859
Coffin-Siris syndrome (CSS) 6 is caused by heterozygous pathogenic variants in the AT-rich interaction domain 2 (ARID2) gene on 12q12. Currently, only 26 cases with both detailed clinical and genetic...
4.
Feng S, He Z, Que L, Luo X, Liang L, Li D, et al.
Front Pediatr
. 2022 Sep;
10:796149.
PMID: 36052366
Background: Primary erythrocytic (PEM) is a rare autosomal dominant single gene disease. Most of the changes of gene loci can be found by whole exon gene sequencing, and the clinical...
5.
Wu R, Tang W, Qiu K, Li X, He Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2022 Jul;
39(7):727-730.
PMID: 35810430
Objective: To explore the genetic basis for a child with congenital disorder of glycosylation type 1y (CDG-1y) in conjunct with congenital dysplasia of external auditory canal. Methods: Trio-whole exome sequencing...
6.
Wu R, Tang W, Qiu K, Li P, Li Y, Li D, et al.
Int J Gen Med
. 2021 Oct;
14:6215-6232.
PMID: 34621130
Background: Although emerging animal- or cell-based evidence supports the relationship between casein kinase 2 alpha protein 1 (CSNK2A1) and cancers, no pan-cancer analysis is available. Thus, this report aimed to...
7.
Tang W, Wu R, Qiu K, Zhang X, He Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2021 Sep;
38(9):857-860.
PMID: 34487530
Objective: To report on a patient with congenital muscular dystrophy (CMD) due to a missense variant of LMNA gene and explore its pathogenicity. Methods: The 1-year-and-1-month-old boy has presented with...
8.
Wu R, Tang W, Qiu K, Li Y, He Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2021 Jun;
38(6):561-564.
PMID: 34096026
Objective: To explore the genetic basis for a child suspected for Say-Barber-Biesecker-Young-Simpson syndrome. Methods: Genomic DNA was extracted from peripheral blood samples of the child and her parents. Whole exome...
9.
He Z, Wu R, Bai P, Qiu K
Int J Clin Pharmacol Ther
. 2020 Sep;
58(12):740-748.
PMID: 32909538
Background: MOG-IgG-associated encephalomyelitis (MOG-EM), a of common type of autoimmune encephalomyelitis (AE), is an autoimmune disease (AID) of the central nervous system that predominantly affects the brain and spinal cord....
10.
Sun Y, Ma J, Li D, Li P, Zhou X, Li Y, et al.
J Neuroinflammation
. 2019 Mar;
16(1):66.
PMID: 30922332
Background: Microglia are important for secreting chemical mediators of inflammatory responses in the central nervous system. Interleukin (IL)-10 and IL-1β secreted by glial cells support neuronal functions, but the related...