Fenghua Lan

903 total citations
62 papers, 712 citations indexed

About

Fenghua Lan is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Fenghua Lan has authored 62 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 14 papers in Pulmonary and Respiratory Medicine and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Fenghua Lan's work include RNA modifications and cancer (9 papers), Peroxisome Proliferator-Activated Receptors (8 papers) and Neonatal Health and Biochemistry (7 papers). Fenghua Lan is often cited by papers focused on RNA modifications and cancer (9 papers), Peroxisome Proliferator-Activated Receptors (8 papers) and Neonatal Health and Biochemistry (7 papers). Fenghua Lan collaborates with scholars based in China, Germany and Canada. Fenghua Lan's co-authors include Qiaojia Huang, Lihong Dong, Junyong Han, Yinghao Yu, Xuenong Ouyang, Feng Zheng, Youdong Lin, Ming Jen Tan, Xiaoting Wang and Zhiyong Zheng and has published in prestigious journals such as Journal of Biological Chemistry, Blood and PLoS ONE.

In The Last Decade

Fenghua Lan

60 papers receiving 702 citations

Peers

Countries citing papers authored by Fenghua Lan

Since Specialization

Citations

This map shows the geographic impact of Fenghua Lan's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fenghua Lan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fenghua Lan more than expected).

Fields of papers citing papers by Fenghua Lan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fenghua Lan. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fenghua Lan. The network helps show where Fenghua Lan may publish in the future.

Co-authorship network of co-authors of Fenghua Lan

This figure shows the co-authorship network connecting the top 25 collaborators of Fenghua Lan. A scholar is included among the top collaborators of Fenghua Lan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Fenghua Lan. Fenghua Lan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Biallelic mutations in DCDC2 cause neonatal sclerosing cholangitis in a Chinese family 2020 ·Clinics and Research in Hepatology and Gastroenterology ·Yuxiang Lin, Jianxing Zhang, Xiaoli Li, (unknown), (unknown), Yichu Liu, Fenghua Lan, (unknown)	6
2	The clinical application of preimplantation genetic diagnosis for X-linked retinitis pigmentosa 2019 ·Journal of Assisted Reproduction and Genetics ·(unknown), Yun Liu, (unknown), Qiuxiang Huang, (unknown), Jian Zeng, Fenghua Lan, (unknown)	6
3	Hybrid minigene splicing assay verified the pathogenicity of a novel splice site variant in the dystrophin gene of a Chinese patient with typical Duchenne muscular dystrophy phenotype 2016 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·Zhihong Wang, (unknown), Liping Qiu, (unknown), (unknown), Jian Zeng, Fenghua Lan	6
4	Bioinformatics analysis of gene expression profiles of dermatomyositis 2016 ·Molecular Medicine Reports ·(unknown), Zhaolei Cui, (unknown), (unknown), (unknown), Fenghua Lan	4
5	The advances of familial adenomatous polyposis 2014 ·Min Zhang, Fenghua Lan	1
6	BAX and CDKN1A polymorphisms correlated with clinical outcomes of gastric cancer patients treated with postoperative chemotherapy 2014 ·Medical Oncology ·Xiaoting Wang, Youdong Lin, Fenghua Lan, Yinghao Yu, Xuenong Ouyang, Wei Liu, (unknown), (unknown), Qiaojia Huang	15
7	Prognostic value of differential CCND1 expression in patients with resected gastric adenocarcinoma 2014 ·Medical Oncology ·(unknown), Xiaoting Wang, Fenghua Lan, Yinghao Yu, Xuenong Ouyang, Wei Liu, (unknown), Qiaojia Huang	15
8	Additive effects of EGF and IL-1β regulate tumor cell migration and invasion in gastric adenocarcinoma via activation of ERK1/2 2014 ·International Journal of Oncology ·Junyong Han, (unknown), Fenghua Lan, Yinghao Yu, Wei Liu, Jinhua Chen, Feng Zheng, Xuenong Ouyang, (unknown), Yanhong Lin, Qiaojia Huang, Lie Wang, Ming Jen Tan	15
9	Familial Skewed X Chromosome Inactivation in Adrenoleukodystrophy Manifesting Heterozygotes from a Chinese Pedigree 2013 ·PLoS ONE ·Zhihong Wang, (unknown), Yuxiang Lin, Haihua Xie, (unknown), Fenghua Lan	20
10	Immunoassay for LMP1 in nasopharyngeal tissue based on surface-enhanced Raman scattering 2011 ·International Journal of Nanomedicine ·Yanping Chen, Zheng, (unknown), He He, Zhu Zhu, Feng, (unknown), Fenghua Lan, Haishan Zeng	38
11	Molecular diagnosis of X-linked adrenoleukodystrophy: Experience from a clinical genetic laboratory in mainland China with report of 13 novel mutations 2011 ·Clinica Chimica Acta ·Fenghua Lan, (unknown), Haihua Xie, Lianghu Huang, (unknown), (unknown), (unknown)	4
12	A rapid and sensitive protocol for prenatal molecular diagnosis of X-linked adrenoleukodystrophy 2010 ·Clinica Chimica Acta ·Fenghua Lan, (unknown), (unknown), Haihua Xie, Lianghu Huang, Huijuan Huang, (unknown), (unknown), Jian Zeng, Huizhong Li, Na Xin, (unknown)	6
13	A new method avoids interference of ABCD1 pseudogenes in molecular diagnosis of X-linked adrenoleukodystrophy 2009 ·Academic Journal of Second Military Medical University ·Fenghua Lan, (unknown)	1
14	Pre-symptomatic molecular diagnosis of X-linked adrenoleukodystrophy in Chinese families 2009 ·Neurological Research ·Zhihong Wang, (unknown), Haihua Xie, (unknown), Lianghu Huang, Fenghua Lan	1
15	Evaluation of an in-house protocol for prenatal molecular diagnosis of SMA in Chinese 2008 ·Clinica Chimica Acta ·Jian Zeng, Fenghua Lan, Xiaojun Deng, (unknown), (unknown), Lianghu Huang, (unknown), (unknown)	7
16	Construction of sperm-specific lactate dehydrogenase DNA vaccine and experimental study of its immunocontraceptive effect on mice 2008 ·Science in China Series C Life Sciences ·Yong Chen, Duo Zhang, Na Xin, (unknown), Ping Chen, Bo Li, (unknown), Fenghua Lan	13
17	Characterization of a Cys329Gly Mutation Causing Hereditary Factor VII Deficiency 2006 ·Acta Haematologica ·(unknown), (unknown), (unknown), Feng Chen, Fenghua Lan, (unknown)	6
18	Molecular Diagnostics in China 2001 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·Fenghua Lan	1
19	Determination of Concentration of Cytosolic NADH-Cytochrome b5 Reductase in Erythrocytes from Normal Chinese Adults, Neonates and Patients with Hereditary Methemoglobinemia by Double-Antibody Sandwich ELISA 1998 ·Acta Haematologica ·Fenghua Lan, (unknown), (unknown), (unknown)	5
20	Establishment of Monoclonal Antibodies against Human Erythrocyte NADH-Cytochrome b ₅ Reductase 1996 ·Hybridoma ·Fenghua Lan, (unknown), (unknown), (unknown)	5

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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