Fuxin Zhao

1.9k citations

52 papers · 1.2k indexed · h-index 22

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders 22
Ophthalmology top 2%
- Glaucoma and retinal disorders 4
- Retinal Diseases and Treatments 3
Molecular Biology top 10%
- Mitochondrial Function and Pathology 31
- ATP Synthase and ATPases Research 23
- Retinal Development and Disorders 5
Radiology, Nuclear Medicine and Imaging top 10%
- Corneal surgery and disorders 5
Sensory Systems top 10%
Epidemiology
- Ophthalmology and Visual Impairment Studies 10

Co-authors: Xiangtian Zhou Min‐Xin Guan Jia Qu Yi Tong Juanjuan Zhang Li Yang Yanhong Sun Yanchun Ji
Cited by: Clinical Biochemistry Ophthalmology Molecular Biology
Journals: Journal of Clinical Investigation (1 paper)PLoS ONE (1 paper)Biochemical and Biophysical Research Communications (5 papers)
Partner nations: China United States Hong Kong

In The Last Decade

Fuxin Zhao

51 papers receiving 1.2k citations

Peers

Countries citing papers authored by Fuxin Zhao

Since Specialization

Citations

This map shows the geographic impact of Fuxin Zhao'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 Fuxin Zhao with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fuxin Zhao more than expected).

Fields of papers citing papers by Fuxin Zhao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fuxin Zhao. 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 Fuxin Zhao. The network helps show where Fuxin Zhao may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Fuxin Zhao, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Fuxin Zhao Line = papers co-authored together Fuxin Zhao links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Causality between autoimmune diseases and breast cancer: a two-sample Mendelian randomization study in a European population Discover Oncology ·Hengheng Zhang,Guoshuang Shen,Ping Yang,Meijie Wu,Jinming Li,Zitao Li,Fuxin Zhao,Hongxia Liang,Mengting Da,Ronghua Wang,Cheng-Rong Zhang,Jiuda Zhao,Yi Zhao	2024	1
2	Form-deprivation myopia downregulates calcium levels in retinal horizontal cells in mice Experimental Eye Research ·Qihang Li,He Zhu,Miaomiao Fan,Jing Sun,Peter S. Reinach,Yuhan Wang,Jia Qu,Xiangtian Zhou,Fuxin Zhao	2022	8
3	Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber’s hereditary optic neuropathy Human Molecular Genetics ·Zhipeng Nie,Chenghui Wang,Jia‐Rong Chen,Yanchun Ji,Hong‐Xing Zhang,Fuxin Zhao,Xiangtian Zhou,Min‐Xin Guan	2022	13
4	Declines in PDE4B activity promote myopia progression through downregulation of scleral collagen expression Experimental Eye Research ·Fuxin Zhao,Hui Zhou,Wei Chen,Chenchen Zhao,Yangyang Zheng,Yijin Tao,Miaozhen Pan,Peter S. Reinach,Jiadi Zhu,Jianhong An,Runxia Lu,Jiang‐Fan Chen,Huifang Tang,Changqing Zeng,Jia Qu,Xiangtian Zhou	2021	19
5	Dysfunction of VIPR2 leads to myopia in humans and mice Journal of Medical Genetics ·Fuxin Zhao,Qihang Li,Wei Chen,He Zhu,Dengke Zhou,Peter S. Reinach,Zhenglin Yang,Mingguang He,Anquan Xue,Deng Wu,Tianzi Liu,Qian Fu,Changqing Zeng,Jia Qu,Xiangtian Zhou	2020	17
6	The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea Frontiers in Microbiology ·Kang Zhang,Xuemei Yuan,Jinping Zang,Min Wang,Fuxin Zhao,Peifen Li,Hongzhe Cao,Jianmin Han,Jihong Xing,Jingao Dong	2018	15
7	Study on mRNA expression and DNA methylation of Pax6 in form-deprived myopia in C57BL/6 mice Chinese Journal of Optometry & Ophthalmology ·Xiaojing Wang,Ayin Chen,Mao Liu,Fuxin Zhao,Furong Huang	2015	1
8	Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families Journal of Human Genetics ·Yanchun Ji,Min Liang,Juanjuan Zhang,Minglian Zhang,Jinping Zhu,Xiangjuan Meng,Sai Zhang,Min Gao,Fuxin Zhao,Qi-Ping Wei,Pingping Jiang,Yi Tong,Xiaoling Liu,Jun Qin Mo,Min‐Xin Guan	2014	17
9	cAMP Level Modulates Scleral Collagen Remodeling, a Critical Step in the Development of Myopia PLoS ONE ·Yijin Tao,Miaozhen Pan,Shufeng Liu,Fang Fang,Runxia Lu,Chanyi Lu,Min Zheng,Jianhong An,Hongjia Xu,Fuxin Zhao,Jiang‐Fan Chen,Jia Qu,Xiangtian Zhou	2013	46
10	Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families Mitochondrion ·Juanjuan Zhang,Fuxin Zhao,Qun Fu,Min Liang,Yi Tong,Xiaoling Liu,Bei Lin,Hui Mi,Minglian Zhang,Qi-Ping Wei,Ling Xue,Pingping Jiang,Xiangtian Zhou,Jun Qin Mo,Taosheng Huang,Jia Qu,Min‐Xin Guan	2013	21
11	The mitochondrial <I>ND5</I> T12338C mutation may be associ-ated with Leber’s hereditary optic neuropathy in two Chinese fami-lies Hereditas (Beijing) ·Yanchun Ji,Xiaoling Liu,Fuxin Zhao,Juanjuan Zhang,Yu Zhang,Xiangtian Zhou,Jia Qu,Min‐Xin Guan	2011	2
12	Leber's hereditary optic neuropathy may be associated with the mitochondrial tRNA<SUP>Glu</SUP> A14693G mutation in three Chinese families Hereditas (Beijing) ·Yongmei Zhang,Yanchun Ji,Xiaoling Liu,Xiangtian Zhou,Fuxin Zhao,Yanhong Sun,Qi-Ping Wei,Juanjuan Zhang,Yan Liu,Jia Qu,Min‐Xin Guan	2010	2
13	Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial <I>ND1</I> T3866C mutation Hereditas (Beijing) ·Yan Liu,Shu-Liu ZHUANG,Yi Tong,Jia Qu,Xiangtian Zhou,Fuxin Zhao,Juanjuan Zhang,Yongmei Zhang,Yu Zhang,Min‐Xin Guan	2010	1
14	Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation Biochemical and Biophysical Research Communications ·Fuxin Zhao,Minqiang Guan,Minqiang Guan,Xiangtian Zhou,Meixia Yuan,Ming Liang,Qi Liu,Yan Liu,Yongmei Zhang,Li Yang,Yi Tong,Qi-Ping Wei,Yanhong Sun,Jia Qu,(unknown),(unknown)	2009	29
15	Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation Biochimica et Biophysica Acta (BBA) - General Subjects ·Jia Qu,Xiangtian Zhou,Fuxin Zhao,Xiaoling Liu,Minglian Zhang,Yanhong Sun,Min Liang,Meixia Yuan,Qi Liu,Yi Tong,Qi-Ping Wei,Li Yang,Min‐Xin Guan	2009	15
16	Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation Mitochondrion ·Jianxin Lü,Yaping Qian,Zhiyuan Li,Aifen Yang,Yi Zhu,Ronghua Li,Li Yang,Xiaowen Tang,Bobei Chen,Yu Ding,Yongyan Li,Junyan You,Jing Zheng,Zhihua Tao,Fuxin Zhao,Jindan Wang,Dongmei Sun,Jianyue Zhao,Yanzi Meng,Min‐Xin Guan	2009	91
17	Very low penetrance of Leber’s hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation Molecular Genetics and Metabolism ·Yi Tong,Yanhong Sun,Xiangtian Zhou,Fuxin Zhao,Yijian Mao,Qi-Ping Wei,Li Yang,Jia Qu,Min‐Xin Guan	2009	12
18	Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation Biochemical and Biophysical Research Communications ·Min Liang,Minqiang Guan,Fuxin Zhao,Xiangtian Zhou,Meixia Yuan,Yi Tong,Li Yang,Qi-Ping Wei,Yanhong Sun,Fan Lü,Jia Qu,Min‐Xin Guan	2009	60
19	The mitochondrial tRNAGlu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber’s hereditary optic neuropathy Biochemical and Biophysical Research Communications ·Yi Tong,Yijian Mao,Xiangtian Zhou,Li Yang,Juanjuan Zhang,Wanshi Cai,Fuxin Zhao,Xinjian Wang,Fan Lü,Jia Qu,Min‐Xin Guan	2007	28
20	Leber’s hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families Biochemical and Biophysical Research Communications ·Xiangtian Zhou,Qi-Ping Wei,Li Yang,Yi Tong,Fuxin Zhao,Chunjie Lu,Yaping Qian,Yanghong Sun,Fan Lü,Jia Qu,Min‐Xin Guan	2005	47

About Fuxin Zhao

Fuxin Zhao is a scholar working on Clinical Biochemistry, Ophthalmology and Molecular Biology, having authored 52 papers that have together received 1.2k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (31 papers), ATP Synthase and ATPases Research (23 papers), Metabolism and Genetic Disorders (22 papers), Ophthalmology and Visual Impairment Studies (10 papers), Retinal Development and Disorders (5 papers), Corneal surgery and disorders (5 papers), Glaucoma and retinal disorders (4 papers) and Retinal Diseases and Treatments (3 papers). The work is most often cited by research in Clinical Biochemistry (362 citations), Ophthalmology (262 citations) and Molecular Biology (889 citations). Fuxin Zhao has collaborated with scholars based in China, United States and Hong Kong. Frequent co-authors include Xiangtian Zhou, Min‐Xin Guan, Jia Qu, Yi Tong, Juanjuan Zhang, Li Yang, Yanhong Sun, Yanchun Ji, Min Liang and Qi-Ping Wei. Their work appears in journals such as Journal of Clinical Investigation, PLoS ONE and Biochemical and Biophysical Research Communications.

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