Wie‐Yen Young

773 citations

19 papers · 624 indexed · h-index 16

Co-authors: Min‐Xin Guan Yaping Qian Dongyi Han Lidong Zhao Qiuju Wang Huijun Yuan Suoqiang Zhai Pu Dai
Topics: Mitochondrial Function and Pathology (11 papers)Hearing, Cochlea, Tinnitus, Genetics (10 papers)RNA and protein synthesis mechanisms (7 papers)
Cited by: Sensory Systems Clinical Biochemistry Neurology
Journals: PLoS ONE Biochemical and Biophysical Research Communications Developmental Dynamics
Partner nations: China United States Hong Kong

In The Last Decade

Wie‐Yen Young

19 papers receiving 620 citations

Peers

Countries citing papers authored by Wie‐Yen Young

Since Specialization

Citations

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

Fields of papers citing papers by Wie‐Yen Young

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wie‐Yen Young. 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 Wie‐Yen Young. The network helps show where Wie‐Yen Young may publish in the future.

Co-authorship network of co-authors of Wie‐Yen Young

This figure shows the co-authorship network connecting the top 25 collaborators of Wie‐Yen Young. A scholar is included among the top collaborators of Wie‐Yen Young 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 Wie‐Yen Young. Wie‐Yen Young is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Effects of DAPT and Atoh1 Overexpression on Hair Cell Production and Hair Bundle Orientation in Cultured Organ of Corti from Neonatal Rats 2011 ·PLoS ONE ·Lidong Zhao,Weiwei Guo,(unknown),(unknown),(unknown),(unknown),Lili Ren,Xinxin Li,Huizhan Liu,Wie‐Yen Young,Wei‐Qiang Gao,Shiming Yang	28
2	Surgical treatment of endolymphatic sac tumor 2011 ·Acta Oto-Laryngologica ·(unknown),Deliang Huang,Dongyi Han,Pu Dai,Wie‐Yen Young,Shiming Yang	18
3	Math1 Gene Transfer Based on the Delivery System of Quaternized Chitosan/Na-Carboxymethyl-<I>β</I>-Cyclodextrin Nanoparticles 2010 ·Journal of Nanoscience and Nanotechnology ·Lili Ren,(unknown),Dong‐Wook Han,Lidong Zhao,(unknown),Weiwei Guo,Jianhe Sun,Nan Wu,Xingqi Li,(unknown),(unknown),Wie‐Yen Young,Shiming Yang	15
4	The role of Smad4 in vestibular development in mice 2010 ·International Journal of Developmental Neuroscience ·Shiming Yang,Anchun Deng,(unknown),Jianhe Sun,Guan Yang,(unknown),Zhaohui Hou,Weiwei Guo,(unknown),David Z. Z. He,Dongyi Han,Wie‐Yen Young,Xiao Yang	2
5	Chondrocyte‐specific Smad4 gene conditional knockout results in hearing loss and inner ear malformation in mice 2009 ·Developmental Dynamics ·Shiming Yang,Zhaohui Hou,Guan Yang,Jishuai Zhang,(unknown),Jianhe Sun,(unknown),David Z. Z. He,Dongyi Han,Wie‐Yen Young,Xiao Yang	19
6	Mutations at position 7445 in the precursor of mitochondrial tRNASer(UCN) gene in three maternal Chinese pedigrees with sensorineural hearing loss 2008 ·Mitochondrion ·Jing Chen,Huijun Yuan,Jianxin Lü,Xin Liu,Guojian Wang,Yi Zhu,Jing Cheng,Xinjian Wang,Bing Han,Li Yang,(unknown),Aifeng Yang,Qing Sun,Dongyang Kang,Xin Zhang,Pu Dai,Suoqiang Zhai,Dongyi Han,Wie‐Yen Young,Min‐Xin Guan	19
7	Smad5 haploinsufficiency leads to hair cell and hearing loss 2008 ·Developmental Neurobiology ·Shiming Yang,(unknown),(unknown),(unknown),Zhaohui Hou,Jianhe Sun,Xiang Wang,David Z. Z. He,(unknown),Wie‐Yen Young,Dongyi Han,Xiao Yang	8
8	The mitochondrial tRNAAla T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss 2007 ·Biochemical and Biophysical Research Communications ·Dongyi Han,Pu Dai,(unknown),Xin Liu,Deliang Huang,Yongyi Yuan,Huijun Yuan,Xinjian Wang,Yaping Qian,Wie‐Yen Young,Min‐Xin Guan	32
9	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 2007 ·Biochemical and Biophysical Research Communications ·Huijun Yuan,Jing Chen,Xin Liu,Jing Cheng,Xinjian Wang,Li Yang,(unknown),(unknown),Dongyang Kang,Pu Dai,Suoqiang Zhai,Dongyi Han,Wie‐Yen Young,Min‐Xin Guan	35
10	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 2006 ·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	60
11	Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families 2006 ·Biochemical and Biophysical Research Communications ·Pu Dai,Yongyi Yuan,Deliang Huang,Yaping Qian,Xin Liu,Dongyi Han,Huijun Yuan,Xinjiang Wang,Wie‐Yen Young,Min‐Xin Guan	14
12	Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation 2005 ·Biochemical and Biophysical Research Communications ·Qiuju Wang,Qingzhong Li,Dongyi Han,Yali Zhao,Lidong Zhao,Yaping Qian,Yuan Hu,Ronghua Li,Suoqiang Zhai,Wie‐Yen Young,Min‐Xin Guan	44
13	Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside‐induced and nonsyndromic hearing loss 2005 ·American Journal of Medical Genetics Part A ·Huijun Yuan,Yaping Qian,(unknown),(unknown),(unknown),Weidong Shen,Fei Ji,Xin Zhang,Dongyang Kang,Jun Qin Mo,John H. Greinwald,Dongyi Han,Suoqiang Zhai,Wie‐Yen Young,Min‐Xin Guan	72
14	Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation 2005 ·American Journal of Medical Genetics Part A ·Qiuju Wang,(unknown),Hui Zhao,Jennifer L. Peters,Qiong Liu,Li Yang,Dongyi Han,John H. Greinwald,Wie‐Yen Young,Min‐Xin Guan	49
15	Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation 2005 ·Biochemical and Biophysical Research Communications ·Wie‐Yen Young,Lidong Zhao,Yaping Qian,Qiuju Wang,Ning Li,John H. Greinwald,Min‐Xin Guan	59
16	Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness 2005 ·Biochemical and Biophysical Research Communications ·Pu Dai,Xin Liu,Dongyi Han,Yaping Qian,Deliang Huang,Huijun Yuan,Weiming Li,Fei Yu,Ruining Zhang,(unknown),Yong He,Youjun Yu,(unknown),(unknown),Ronghua Li,Xin Zhang,Dongyang Kang,(unknown),Wie‐Yen Young,Min‐Xin Guan	43
17	Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss 2005 ·Biochemical and Biophysical Research Communications ·Lidong Zhao,Qiuju Wang,Yaping Qian,Ronghua Li,(unknown),Laura C. Hart,Suoqiang Zhai,Dongyi Han,Wie‐Yen Young,Min‐Xin Guan	27
18	Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation 2004 ·Biochemical and Biophysical Research Communications ·Lidong Zhao,Wie‐Yen Young,(unknown),Qiuju Wang,Yaping Qian,Min‐Xin Guan	51
19	Influence of digits, ectoderm, and retinoic acid on chondrogenesis by mouse interdigital mesoderm in culture 1994 ·Developmental Dynamics ·KK Lee,Felix C.H. Li,Wie‐Yen Young,(unknown),(unknown),Kathryn S.E. Cheah	29

About Wie‐Yen Young

Wie‐Yen Young is a scholar working on Sensory Systems, Otorhinolaryngology and Neurology, having authored 19 papers that have together received 624 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (11 papers), Hearing, Cochlea, Tinnitus, Genetics (10 papers) and RNA and protein synthesis mechanisms (7 papers). The work is most often cited by research in Sensory Systems (272 citations), Clinical Biochemistry (77 citations) and Neurology (82 citations). Wie‐Yen Young has collaborated with scholars based in China, United States and Hong Kong. Frequent co-authors include Min‐Xin Guan, Yaping Qian, Dongyi Han, Lidong Zhao, Qiuju Wang, Huijun Yuan, Suoqiang Zhai, Pu Dai, John H. Greinwald and Ronghua Li. Their work appears in journals such as PLoS ONE, Biochemical and Biophysical Research Communications and Developmental Dynamics.

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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