Yaping Qian

3.7k total citations
50 papers, 1.7k citations indexed

About

Yaping Qian is a scholar working on Molecular Biology, Sensory Systems and Clinical Biochemistry. According to data from OpenAlex, Yaping Qian has authored 50 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 12 papers in Sensory Systems and 9 papers in Clinical Biochemistry. Recurrent topics in Yaping Qian's work include Mitochondrial Function and Pathology (26 papers), Hearing, Cochlea, Tinnitus, Genetics (12 papers) and RNA and protein synthesis mechanisms (11 papers). Yaping Qian is often cited by papers focused on Mitochondrial Function and Pathology (26 papers), Hearing, Cochlea, Tinnitus, Genetics (12 papers) and RNA and protein synthesis mechanisms (11 papers). Yaping Qian collaborates with scholars based in United States, China and France. Yaping Qian's co-authors include Min‐Xin Guan, Ronghua Li, Xiangtian Zhou, Jia Qu, Wie‐Yen Young, Yi Tong, Jun Qin Mo, Li Yang, Lidong Zhao and Yi Zhu and has published in prestigious journals such as PLoS ONE, Circulation Research and Genetics.

In The Last Decade

Yaping Qian

50 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Yaping Qian United States	28	1.3k	384	369	157	139	50	1.7k
Valentina Labay Israel	10	767 0.6×	328 0.9×	372 1.0×	96 0.6×	14 0.1×	11	1.3k
Pu Dai China	28	1.3k 1.0×	1.6k 4.1×	95 0.3×	189 1.2×	61 0.4×	202	2.5k
Bahareh Rabbani Iran	14	548 0.4×	185 0.5×	32 0.1×	337 2.1×	48 0.3×	48	1.1k
Suoqiang Zhai China	17	411 0.3×	441 1.1×	52 0.1×	30 0.2×	34 0.2×	42	781
Dongyi Han China	22	1.1k 0.8×	1.1k 3.0×	104 0.3×	82 0.5×	52 0.4×	130	1.8k
Jun Shen United States	20	807 0.6×	555 1.4×	19 0.1×	307 2.0×	71 0.5×	44	1.6k
Lei Song China	21	452 0.3×	745 1.9×	32 0.1×	108 0.7×	45 0.3×	71	1.3k
Jerzy Bal Poland	19	486 0.4×	85 0.2×	60 0.2×	244 1.6×	111 0.8×	113	1.1k
Brice Marcet France	16	653 0.5×	67 0.2×	58 0.2×	213 1.4×	131 0.9×	24	1.2k
Abdelaziz Tlili United Arab Emirates	17	496 0.4×	371 1.0×	46 0.1×	72 0.5×	9 0.1×	61	801

Countries citing papers authored by Yaping Qian

Since Specialization

Citations

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

Fields of papers citing papers by Yaping Qian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yaping Qian

This figure shows the co-authorship network connecting the top 25 collaborators of Yaping Qian. A scholar is included among the top collaborators of Yaping Qian 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 Yaping Qian. Yaping Qian 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

Li, Dong, et al.. (2023). Development of a machine learning-based signature utilizing inflammatory response genes for predicting prognosis and immune microenvironment in ovarian cancer. Open Medicine. 18(1). 20230734–20230734. 1 indexed citations

Qian, Yaping, Debora Mancini‐DiNardo, Thaddeus Judkins, et al.. (2017). Identification of pathogenic retrotransposon insertions in cancer predisposition genes. Cancer Genetics. 216-217. 159–169. 29 indexed citations

Lindsley, Andrew, Yaping Qian, C. Alexander Valencia, et al.. (2014). Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation. Journal of Clinical Immunology. 34(8). 910–915. 42 indexed citations

Sun, Hao, Wataru Satake, Chang-Jun Zhang, et al.. (2011). Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family. Journal of Human Genetics. 56(4). 330–334. 10 indexed citations

Lü, Jianxin, Yaping Qian, Zhiyuan Li, et al.. (2009). Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation. Mitochondrion. 10(1). 69–81. 91 indexed citations

Bockstaele, Elisabeth J. Van, Yaping Qian, Robert C. Sterling, & Michelle E. Page. (2008). Low dose naltrexone administration in morphine dependent rats attenuates withdrawal-induced norepinephrine efflux in forebrain. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 32(4). 1048–1056. 20 indexed citations

Tang, Xiaowen, Li Yang, Yi Zhu, et al.. (2007). Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation. Gene. 393(1-2). 11–19. 44 indexed citations

Qu, Jia, Ronghua Li, Xiangtian Zhou, et al.. (2006). Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family. Mitochondrion. 7(1-2). 140–146. 44 indexed citations

Young, Wie‐Yen, Lidong Zhao, Yaping Qian, et al.. (2006). 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. 140A(20). 2188–2197. 60 indexed citations

10.

Sun, Yanhong, Qi-Ping Wei, Xiangtian Zhou, et al.. (2006). Leber’s hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families. Biochemical and Biophysical Research Communications. 347(1). 221–225. 13 indexed citations

11.

Zhou, Xiangtian, Qi-Ping Wei, Li Yang, et al.. (2005). Leber’s hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families. Biochemical and Biophysical Research Communications. 340(1). 69–75. 47 indexed citations

12.

Li, Zhiyuan, Ronghua Li, Jian‐Fu Chen, et al.. (2005). Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss. Human Genetics. 117(1). 9–15. 143 indexed citations

13.

Wang, Qiuju, Qingzhong Li, Dongyi Han, et al.. (2005). 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. Biochemical and Biophysical Research Communications. 340(2). 583–588. 44 indexed citations

14.

Yuan, Huijun, Yaping Qian, Weidong Shen, et al.. (2005). 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. American Journal of Medical Genetics Part A. 138A(2). 133–140. 72 indexed citations

15.

Young, Wie‐Yen, Lidong Zhao, Yaping Qian, et al.. (2005). Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation. Biochemical and Biophysical Research Communications. 328(4). 1244–1251. 59 indexed citations

16.

Dai, Pu, Xin Liu, Dongyi Han, et al.. (2005). 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. 340(1). 194–199. 43 indexed citations

17.

Xu, Huailiang, Yaping Qian, Wenhui Nie, et al.. (2004). Construction, characterization and chromosomal mapping of bacterial artificial chromosome (BAC) library of Yunnan snub-nosed monkey (Rhinopithecus bieti. Chromosome Research. 12(3). 251–262. 8 indexed citations

18.

Zhao, Lidong, et al.. (2004). Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. Biochemical and Biophysical Research Communications. 325(4). 1503–1508. 51 indexed citations

19.

Li, Yi, Yaping Qian, Xiao‐Jing Yu, et al.. (2004). Recent Origin of a Hominoid-Specific Splice Form of Neuropsin, a Gene Involved in Learning and Memory. Molecular Biology and Evolution. 21(11). 2111–2115. 15 indexed citations

20.

Qian, Yaping, Bin‐Zhi Qian, Bing Su, et al.. (2000). Multiple origins of Tibetan Y chromosomes. Human Genetics. 106(4). 453–454. 48 indexed citations

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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