Pu Dai

4.2k citations

203 papers · 2.5k · h-index 28

Impact in

Sensory Systems top 0.1%
- Hearing, Cochlea, Tinnitus, Genetics
Otorhinolaryngology top 1%
- Ear Surgery and Otitis Media

Papers in

Sensory Systems 102
- Hearing, Cochlea, Tinnitus, Genetics 102
Molecular Biology 61
- Mitochondrial Function and Pathology 18
- RNA regulation and disease 13
- Connexins and lens biology 10
- RNA and protein synthesis mechanisms 9

Co-authors: Yongyi Yuan (69 shared papers)Dongyi Han (59 shared papers)Dongyang Kang (64 shared papers)Huijun Yuan (33 shared papers)Guojian Wang (41 shared papers)Deliang Huang (29 shared papers)Shasha Huang (45 shared papers)Xue Gao (40 shared papers)
Journals: Acta Oto-Laryngologica (16 papers)PLoS ONE (12 papers)Journal of Translational Medicine (9 papers)International Journal of Pediatric Otorhinolaryngology (7 papers)Human Genetics (5 papers)
Partner nations: China United States Philippines

In The Last Decade

Pu Dai

197 papers receiving 2.5k citations

Peers

Countries citing papers authored by Pu Dai

Since Specialization

Citations

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

Fields of papers citing papers by Pu Dai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Pu Dai, 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 Pu Dai Line = papers co-authored together Pu Dai links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 203 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China Journal of Translational Medicine ·Yongyi Yuan, Yiwen You, Deliang Huang, Jinghong Cui, Yong Wang, Qiang Wang, Fei Yu, Dongyang Kang, Huijun Yuan, Dongyi Han, Pu Dai	2009	131
2	Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31 Human Genetics ·Xue-Zhong Liu, Yongyi Yuan, Denise Yan, Emilie Hong Ding, Xiao Mei Ouyang, Fei Yu, Wenxue Tang, Huijun Yuan, Qing Chang, Li Du, Xin Zhang, Guojian Wang, Shoeb Ahmad, Dong Yang Kang, Xi Lin, Pu Dai	2008	90
3	Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes Human Gene Therapy ·Yilai Shu, Tao Yong, Zhengmin Wang, Yong Tang, Huawei Li, Pu Dai, Guangping Gao, Zheng‐Yi Chen	2016	84
4	The prevalence of the 235delC GJB2 mutation in a Chinese deaf population Genetics in Medicine ·Pu Dai, Fei Yu, Bing Han, Yongyi Yuan, Qi Li, Guojian Wang, Xin Liu, Jia He, Deliang Huang, Dongyang Kang, Xin Zhang, Huijun Yuan, Eric Schmitt, Dongyi Han, Lee‐Jun C. Wong	2007	65
5	Molecular Epidemiology and Functional Assessment of Novel Allelic Variants of SLC26A4 in Non-Syndromic Hearing Loss Patients with Enlarged Vestibular Aqueduct in China PLoS ONE ·Yongyi Yuan, Weiwei Guo, Jie Tang, Guozheng Zhang, Guojian Wang, Mingyu Han, Xun Zhang, Shiming Yang, David Z. Z. He, Pu Dai	2012	64
6	Variants in mitochondrial tRNA^Glu, tRNA^Arg, and tRNA^Thr may influence the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss American Journal of Medical Genetics Part A ·Wie‐Yen Young, Lidong Zhao, Yaping Qian, Ronghua Li, Jing Chen, Huijun Yuan, Pu Dai, Suoqiang Zhai, Dongyi Han, Min‐Xin Guan	2006	60
7	A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family Clinical Genetics ·Jing Cheng, DY Han, Pu Dai, HJ Sun, Ran Tao, Qing Sun, Dongmei Yan, Wei Qin, Huan‐Yu Wang, XM Ouyang, SZ Yang, JY Cao, GY Feng, LL Du, Yao-Zhong Zhang, SQ Zhai, WY Yang, Liu Xz, Lin He, HJ Yuan	2007	52
8	SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss Genetics in Medicine ·Pu Dai, Qi Li, Deliang Huang, Yongyi Yuan, Dongyang Kang, David T. Miller, Hong Shao, Qingwen Zhu, Jia He, Fei Yu, Xin Liu, Bing Han, Huijun Yuan, Orah S. Platt, Dongyi Han, Bai-Lin Wu	2008	51
9	Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening Human Mutation ·Caixia Li, Qian Pan, Yonggang Guo, Yan Li, Huafang Gao, Di Zhang, Hao Hu, Wanli Xing, Keith Mitchelson, Kun Xia, Pu Dai, Jing Cheng	2007	48
10	The genetic bases for non-syndromic hearing loss among Chinese Journal of Human Genetics ·Xiao Mei Ouyang, Denise Yan, Hui Jun Yuan, Pu Dai, Li Du, Don Yi Han, Xue Zhong Liu	2009	47
11	Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis Journal of Translational Medicine ·Pu Dai, Yongyi Yuan, Deliang Huang, Xiuhui Zhu, Fei Yu, Dongyang Kang, Huijun Yuan, Bai-Lin Wu, Dongyi Han, Lee‐Jun C. Wong	2008	44
12	Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness Biochemical and Biophysical Research Communications ·Pu Dai, Xin Liu, Dongyi Han, Yaping Qian, Deliang Huang, Huijun Yuan, Weiming Li, Fei Yu, Ruining Zhang, Hongyan Lin, Yong He, Youjun Yu, Quanzhu Sun, Huaiyi Qin, Ronghua Li, Xin Zhang, Dongyang Kang, Juyang Cao, Wie‐Yen Young, Min‐Xin Guan	2005	43
13	Correlation of Cochlear Blood Supply with Mitochondrial DNA Common Deletion in Presbyacusis Acta Oto-Laryngologica ·Pu Dai, Yang Wei–yan, Sichang Jiang, Rui Gu, Huijun Yuan, Dongyi Han, Weiwei Guo, Juyang Cao	2004	43
14	Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China Journal of Translational Medicine ·Feng Xin, Yongyi Yuan, Xiaoming Deng, Mingyu Han, Guojian Wang, Jiandong Zhao, Xue Gao, Jun Liu, Fei Yu, Dongyi Han, Pu Dai	2013	42
15	Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness Genetics in Medicine ·Meng Meng, Xuchao Li, Huijuan Ge, Fang Chen, Mingyu Han, Yanyan Zhang, Dongyang Kang, Weiwei Xie, Zhiying Gao, Xiaoyu Pan, Pu Dai, Fanglu Chi, Sheng‐Pei Chen, Ping Liu, Chunlei Zhang, Jianjun Cao, Hui Jiang, Xun Xu, Wei Wang, Tao Duan	2014	38
16	Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct Journal of Translational Medicine ·Shasha Huang, Dongyi Han, Yongyi Yuan, Guojian Wang, Dongyang Kang, Xin Zhang, Xiaofei Yan, Xiaoxiao Meng, Min Dong, Pu Dai	2011	38
17	Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNASer(UCN) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss Biochemical and Biophysical Research Communications ·Huijun Yuan, Jing Chen, Xin Liu, Jing Cheng, Xinjian Wang, Li Yang, Shuzhi Yang, Juyang Cao, Dongyang Kang, Pu Dai, Suoqiang Zhai, Dongyi Han, Wie‐Yen Young, Min‐Xin Guan	2007	35
18	Whole-Exome Sequencing Identifies a Variant inTMEM132ECausing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99 Human Mutation ·Jiangxia Li, Xiaohan Zhao, Qian Xin, Shan Shan, Baichun Jiang, Yecheng Jin, Huijun Yuan, Pu Dai, Ruo Xiao, Qingyan Zhang, Jingjing Xiao, Changshun Shao, Yaoqin Gong, Qiji Liu	2014	34
19	Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls European Journal of Human Genetics ·Yongyi Yuan, Qi Li, Yu Su, Qiongfen Lin, Xue Gao, Hankui Liu, Shasha Huang, Dongyang Kang, N. Wendell Todd, Douglas E. Mattox, Jianguo Zhang, Xi Lin, Pu Dai	2019	32
20	Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation Mitochondrion ·Yuhua Zhu, Qi Li, Zheng‐Yi Chen, (unknown), Lijia Liu, Xin Liu, Huijun Yuan, Suoqiang Zhai, Dongyi Han, Pu Dai	2009	32

About Pu Dai

Pu Dai is a scholar working on Sensory Systems, Molecular Biology, Neurology, Otorhinolaryngology and Genetics, having authored 203 papers that have together received 2.5k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (102 papers), Vestibular and auditory disorders (25 papers), Ear Surgery and Otitis Media (21 papers), Mitochondrial Function and Pathology (18 papers), RNA regulation and disease (13 papers), Connexins and lens biology (10 papers), RNA and protein synthesis mechanisms (9 papers) and Hearing Loss and Rehabilitation (8 papers). The work is most often cited by research in Sensory Systems (1.5k citations), Otorhinolaryngology (312 citations), Neurology (438 citations), Endocrine and Autonomic Systems (98 citations) and Molecular Biology (1.0k citations). Pu Dai has collaborated with scholars based in China, United States and Philippines. Frequent co-authors include Yongyi Yuan, Dongyi Han, Dongyang Kang, Huijun Yuan, Guojian Wang, Deliang Huang, Shasha Huang, Xue Gao, Mingyu Han and Fei Yu. Their work appears in journals such as Acta Oto-Laryngologica, PLoS ONE, Journal of Translational Medicine, International Journal of Pediatric Otorhinolaryngology and Human Genetics.

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