Author

Dairong Feng

Observed names: D. Feng, Dai-Rong Feng

Institutions: Qingdao University, Shandong Maternal and Child Health Hospital

Observed institutions: Qingdao University, Weifang Medical University, Chinese Academy of Medical Sciences & Peking Union Medical College, Shandong Maternal and Child Health Hospital, Institute of Basic Medical Sciences of the Chinese Academy of Medical Sciences, University of Manitoba

ORCID: 0000-0002-6162-0727

Observed ORCID: 0000-0002-6162-0727

OpenAlex ID: A5076596305

Control of alternative splicing by forskolin through hnRNP K during neuronal differentiation

2012 · Wenguang Cao, Aleh Razanau, et al. · Nucleic Acids Research · 61

Aberrant splicing in neurological diseases

2013 · Dairong Feng, Jiuyong Xie · Wiley Interdisciplinary Reviews - RNA · 44

Effects of bisphenol A exposure on DNA integrity and protamination of mouse spermatozoa

2019 · D. Pan, D. Feng, et al. · Andrology · 29

Increase of a group of PTC+ transcripts by curcumin through inhibition of the NMD pathway

2015 · Dairong Feng, Ruey-Chyi Su, et al. · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · 15

[Two novel EIF2AK3 mutations in a Chinese boy with Wolcott-Rallison syndrome].

2011 · Dai-Rong Feng, Yan Meng, et al. · PubMed · 7

Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcript

2015 · Dairong Feng, Yi Cheng, et al. · Genes & Nutrition · 5

[Analysis of ITD characteristics in acute myeloid leukemia patients with FLT3-ITD positive].

2011 · Liang Ma, Dai-Rong Feng, et al. · PubMed · 3

Whole‐exome sequencing identified a novel pathogenic mutation of the CYP4F22 gene in a Chinese patient with autosomal recessive congenital ichthyosis and in vitro study of the mutant CYP4F22 protein

2022 · Lina Zhao, Caixia Wang, et al. · The Journal of Dermatology · 2

Application of trio-based whole-exome sequencing in fetal ultrasound anomalies: a single-center retrospective study of 454 cases

2025 · Dongyi Yu, Dairong Feng, et al. · Frontiers in Genetics · 1

[Analysis of COL1A1 and COL1A2 gene variants in two fetuses with osteogenesis imperfecta].

2023 · Yaning Zhang, Xinyue Wu, et al. · PubMed · 1

Detection of NPM1 gene mutation in acute myeloid leukemia

2012 · Liang Ma, Minghua Zhong, et al. · Zhonghua jianyan yixue zazhi

[FMS-like tyrosine kinase 3 gene mutation in acute myeloid leukemia detected by denaturing PAGE and its clinical significance].

2010 · Liang Ma, Ming-Hua Zhong, et al. · PubMed

Works count: 12

Citation count: 168

H-index: 5

I10-index: 4