Fang Shen

No. 86 Ziyuan Road
Changsha, 410007, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Frequent FBN2 variants in pectus excavatum highlight underlying phenotypic variability.

Frequent FBN2 variants in pectus excavatum highlight underlying phenotypic variability.

Journal: Journal of medical genetics

Published: March 12, 2026

AUTS2 disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: evidence from four unrelated cases.

AUTS2 disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: evidence from four unrelated cases.

Journal: Journal of medical genetics

Published: April 29, 2025

Heterozygous loss of OSR2 can cause radioulnar synostosis with ancillary skeletal manifestations.

Heterozygous loss of OSR2 can cause radioulnar synostosis with ancillary skeletal manifestations.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 14, 2025

Research on similarity test design and characteristic verification for tank fires under environmental wind conditions.

Research on similarity test design and characteristic verification for tank fires under environmental wind conditions.

Journal: PloS one

Published: March 06, 2025

From victims to aggressors: the link between childhood family abuse and adolescent peer bullying.

From victims to aggressors: the link between childhood family abuse and adolescent peer bullying.

Journal: BMC psychology

Published: March 02, 2025

Synostosis of joints caused by mutant FBN2 is linked to the abnormalities and misdifferentiation of articular surface cells.

Synostosis of joints caused by mutant FBN2 is linked to the abnormalities and misdifferentiation of articular surface cells.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 19, 2024

Advances in genetic research on Non-syndromic congenital joint synostosis

Advances in genetic research on Non-syndromic congenital joint synostosis

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 03, 2024

Familial pancreatitis associated with a splice-site variant in CPA1.

Familial pancreatitis associated with a splice-site variant in CPA1.

Journal: Gut

Published: May 10, 2024

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192.

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192.

Journal: HGG advances

Published: August 03, 2023

Lysine demethylase KDM3A alleviates hyperoxia-induced bronchopulmonary dysplasia in mice by promoting ETS1 expression.

Lysine demethylase KDM3A alleviates hyperoxia-induced bronchopulmonary dysplasia in mice by promoting ETS1 expression.

Journal: Experimental cell research

Published: July 26, 2023

Comprehensive exosomal microRNA profile and construction of competing endogenous RNA network in autism spectrum disorder: A pilot study.

Comprehensive exosomal microRNA profile and construction of competing endogenous RNA network in autism spectrum disorder: A pilot study.

Journal: Biomolecules & biomedicine

Published: July 21, 2023

ETS1 Ameliorates Hyperoxia-Induced Bronchopulmonary Dysplasia in Mice by Activating Nrf2/HO-1 Mediated Ferroptosis.

ETS1 Ameliorates Hyperoxia-Induced Bronchopulmonary Dysplasia in Mice by Activating Nrf2/HO-1 Mediated Ferroptosis.

Journal: Lung

Published: June 08, 2023

Showing 1-12 of 23

Last Updated: 09/26/2026