Renkui Bai

4.1k total citations
38 papers, 1.8k citations indexed

About

Renkui Bai is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Renkui Bai has authored 38 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Renkui Bai's work include Mitochondrial Function and Pathology (28 papers), Metabolism and Genetic Disorders (16 papers) and ATP Synthase and ATPases Research (10 papers). Renkui Bai is often cited by papers focused on Mitochondrial Function and Pathology (28 papers), Metabolism and Genetic Disorders (16 papers) and ATP Synthase and ATPases Research (10 papers). Renkui Bai collaborates with scholars based in United States, Canada and Taiwan. Renkui Bai's co-authors include Lee‐Jun C. Wong, Duan‐Jun Tan, Suzanne M. Leal, Aiyi Liu, Chang-Hung Hsu, Cherng‐Lih Perng, Haeyoung Kwon, Robert I. Glazer, Yuzhi Yin and Yewei Ma and has published in prestigious journals such as PLoS ONE, Neurology and Cancer Research.

In The Last Decade

Renkui Bai

38 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Renkui Bai United States 24 1.5k 543 396 218 125 38 1.8k
Jason C. Poole United States 15 1.1k 0.8× 278 0.5× 237 0.6× 183 0.8× 337 2.7× 32 1.6k
Maya R. Vilà Spain 19 911 0.6× 223 0.4× 173 0.4× 167 0.8× 223 1.8× 31 1.3k
Nitin Udar United States 25 1.1k 0.8× 129 0.2× 261 0.7× 235 1.1× 194 1.6× 58 1.8k
Marilyn Chwa United States 28 906 0.6× 181 0.3× 244 0.6× 91 0.4× 38 0.3× 81 2.4k
Susan Chung United States 16 1.4k 1.0× 166 0.3× 213 0.5× 116 0.5× 391 3.1× 21 2.0k
Joanna D. Stewart Germany 18 770 0.5× 333 0.6× 100 0.3× 62 0.3× 128 1.0× 27 1.1k
Eva Richard Spain 23 820 0.6× 609 1.1× 85 0.2× 104 0.5× 80 0.6× 61 1.2k
Nancy G. Kennaway United States 22 1.5k 1.0× 906 1.7× 68 0.2× 120 0.6× 66 0.5× 37 2.0k
C R Scriver Canada 18 485 0.3× 362 0.7× 92 0.2× 161 0.7× 132 1.1× 37 1.1k
Sandesh C.S. Nagamani United States 17 544 0.4× 106 0.2× 245 0.6× 548 2.5× 113 0.9× 43 1.2k

Countries citing papers authored by Renkui Bai

Since Specialization
Citations

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

Fields of papers citing papers by Renkui Bai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renkui Bai

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

All Works

20 of 20 papers shown
1.
2.
Rakić, Bojana, Catherine Brunel‐Guitton, Glenda Hendson, et al.. (2019). Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency. Molecular Genetics and Metabolism Reports. 18. 32–38. 7 indexed citations
3.
Beck, David B., Megan T. Cho, Francisca Millan, et al.. (2016). A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 17(3). 173–178. 25 indexed citations
4.
5.
Tanaka, Akemi, Renkui Bai, Megan T. Cho, et al.. (2015). De novo mutations in PURA are associated with hypotonia and developmental delay. Molecular Case Studies. 1(1). a000356–a000356. 49 indexed citations
6.
Huang, Jee‐Fu, Yi‐Chu Liao, Renkui Bai, et al.. (2011). Mitochondrial polymorphism 12361A>G is associated with nonalcoholic fatty liver disease. Translational research. 159(1). 58–59. 11 indexed citations
7.
Juo, Suh‐Hang Hank, et al.. (2010). A common mitochondrial polymorphism 10398A>G is associated metabolic syndrome in a Chinese population. Mitochondrion. 10(3). 294–299. 23 indexed citations
8.
Ma, Yewei, et al.. (2009). Mitochondrial dysfunction in human breast cancer cells and their transmitochondrial cybrids. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797(1). 29–37. 73 indexed citations
9.
Bai, Renkui, et al.. (2008). Mitochondrial DNA variant interactions modify breast cancer risk. Journal of Human Genetics. 53(10). 924–928. 46 indexed citations
10.
Dimmock, David, Bruno Maranda, Carlo Dionisi‐Vici, et al.. (2008). Citrin deficiency, a perplexing global disorder. Molecular Genetics and Metabolism. 96(1). 44–49. 77 indexed citations
11.
Bai, Renkui, et al.. (2007). Mitochondrial Genetic Background Modifies Breast Cancer Risk. Cancer Research. 67(10). 4687–4694. 200 indexed citations
12.
Gambello, Michael J., Renkui Bai, Tianjian Chen, Mazen M. Dimachkie, & Lee‐Jun C. Wong. (2006). Exercise intolerance associated with a novel 8300t>C mutation in mitochondrial transfer RNAlys. Muscle & Nerve. 34(4). 437–443. 8 indexed citations
13.
Wong, Lee‐Jun C. & Renkui Bai. (2006). Real-Time Quantitative Polymerase Chain Reaction Analysis of Mitochondrial DNA Point Mutation. Humana Press eBooks. 335. 187–200. 12 indexed citations
14.
Xie, Zhihui, Hongyan Yuan, Yuzhi Yin, et al.. (2006). 3-Phosphoinositide-dependent Protein Kinase-1 (PDK1) promotes invasion and activation of matrix metalloproteinases. BMC Cancer. 6(1). 77–77. 49 indexed citations
15.
Tan, Duan‐Jun, Julia Chang, Lingling Liu, et al.. (2006). Significance of somatic mutations and content alteration of mitochondrial DNA in esophageal cancer. BMC Cancer. 6(1). 93–93. 61 indexed citations
16.
Scaglia, Fernando, Chang-Hung Hsu, Haeyoung Kwon, et al.. (2006). Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy. Genetics in Medicine. 8(10). 641–652. 9 indexed citations
17.
Enns, Gregory M., Renkui Bai, Anita E. Beck, & Lee‐Jun C. Wong. (2006). Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load. Molecular Genetics and Metabolism. 88(4). 364–371. 32 indexed citations
18.
Hsu, Chang-Hung, Haeyoung Kwon, Cherng‐Lih Perng, et al.. (2005). Hearing Loss in Mitochondrial Disorders. Annals of the New York Academy of Sciences. 1042(1). 36–47. 16 indexed citations
19.
Bai, Renkui & Lee‐Jun C. Wong. (2005). Simultaneous Detection and Quantification of Mitochondrial DNA Deletion(s), Depletion, and Over-Replication in Patients with Mitochondrial Disease. Journal of Molecular Diagnostics. 7(5). 613–622. 133 indexed citations
20.
Wong, Lee‐Jun C., et al.. (2002). A cystic fibrosis patient with two novel mutations in mitochondrial DNA: Mild disease led to delayed diagnosis of both disorders. American Journal of Medical Genetics. 113(1). 59–64. 26 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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