Rong Mao

13.9k total citations · 2 hit papers
135 papers, 4.8k citations indexed

About

Rong Mao is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Rong Mao has authored 135 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 41 papers in Genetics and 25 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Rong Mao's work include Genomics and Rare Diseases (25 papers), Genomic variations and chromosomal abnormalities (17 papers) and Metabolism and Genetic Disorders (15 papers). Rong Mao is often cited by papers focused on Genomics and Rare Diseases (25 papers), Genomic variations and chromosomal abnormalities (17 papers) and Metabolism and Genetic Disorders (15 papers). Rong Mao collaborates with scholars based in United States, Canada and Qatar. Rong Mao's co-authors include William H. Robinson, Christin M. Lepus, Harini Raghu, Tamsin M. Lindström, Jeremy Sokolove, Qian Wang, Jamie McDonald, Melinda Procter, Pinar Bayrak‐Toydemir and Jonathan Pevsner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Rong Mao

127 papers receiving 4.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Low-grade inflammation as a key mediator of the pathogenesis of osteoarthritis

2016 1.1k citations William H. Robinson, Rong Mao et al. profile →
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia

2015 216 citations Rong Mao, Melinda Procter et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rong Mao United States	35	1.8k	1.0k	1.0k	785	666	135	4.8k
Yasuteru Muragaki Japan	43	3.4k 1.9×	677 0.7×	1.1k 1.1×	646 0.8×	251 0.4×	145	7.0k
Martin K. Selig United States	32	2.6k 1.5×	883 0.9×	491 0.5×	541 0.7×	590 0.9×	79	5.5k
Gaetano Magro Italy	39	1.5k 0.8×	1.9k 1.9×	407 0.4×	1.0k 1.3×	310 0.5×	300	5.7k
Nicolas Cagnard France	35	2.3k 1.3×	498 0.5×	791 0.8×	300 0.4×	409 0.6×	83	7.2k
Stanislawa Weremowicz United States	43	2.8k 1.6×	509 0.5×	860 0.8×	803 1.0×	237 0.4×	81	5.6k
Kenjiro Kosaki Japan	35	2.7k 1.5×	388 0.4×	1.8k 1.8×	565 0.7×	464 0.7×	363	5.2k
Baruch Frenkel United States	41	3.1k 1.7×	371 0.4×	851 0.8×	482 0.6×	380 0.6×	89	4.9k
Yoko Aoki Japan	36	2.9k 1.7×	762 0.7×	777 0.8×	310 0.4×	255 0.4×	170	4.8k
Lidia Larizza Italy	43	3.7k 2.1×	413 0.4×	2.3k 2.3×	496 0.6×	413 0.6×	271	6.3k
Hans Scheffer Netherlands	47	3.7k 2.1×	411 0.4×	2.7k 2.6×	567 0.7×	1.1k 1.7×	191	7.9k

Countries citing papers authored by Rong Mao

Since Specialization

Citations

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

Fields of papers citing papers by Rong Mao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rong Mao

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Goldstein, Jennifer, Emily Groopman, Shruthi Mohan, et al.. (2024). Developing a scoring system for gene curation prioritization in lysosomal diseases. Molecular Genetics and Metabolism. 143(1-2). 108572–108572.

Dickson, Alexa, Marcus J. Miller, Elaine Spector, et al.. (2023). Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation. Molecular Genetics and Metabolism. 140(3). 107668–107668. 1 indexed citations

Mohan, Shruthi, Meredith Weaver, Irene De Biase, et al.. (2023). Evaluating the strength of evidence for genes implicated in peroxisomal disorders using the ClinGen clinical validity framework and providing updates to the peroxisomal disease nomenclature. Molecular Genetics and Metabolism. 139(3). 107604–107604.

Botas, Pablo, Christine E. Miller, Jian Zhao, et al.. (2023). Open-Source Artificial Intelligence System Supports Diagnosis of Mendelian Diseases in Acutely Ill Infants. Children. 10(6). 991–991. 2 indexed citations

Carey, John C., Lorenzo D. Botto, Matt Velinder, et al.. (2023). SON -Related Zhu-Tokita-Takenouchi-Kim Syndrome With Recurrent Hemiplegic Migraine. Neurology Genetics. 9(3). e200062–e200062.

Wen, Ting, Andrew Farrell, Rong Mao, et al.. (2022). Rapid genome sequencing identifies a novel de novoSNAP25variant for neonatal congenital myasthenic syndrome. Molecular Case Studies. 8(7). a006242–a006242. 5 indexed citations

Kongpachith, Sarah, Nithya Lingampalli, Chia‐Hsin Ju, et al.. (2019). Affinity Maturation of the Anti–Citrullinated Protein Antibody Paratope Drives Epitope Spreading and Polyreactivity in Rheumatoid Arthritis. Arthritis & Rheumatology. 71(4). 507–517. 44 indexed citations

Elliott, Serra E., Sarah Kongpachith, Nithya Lingampalli, et al.. (2018). Affinity Maturation Drives Epitope Spreading and Generation of Proinflammatory Anti–Citrullinated Protein Antibodies in Rheumatoid Arthritis. Arthritis & Rheumatology. 70(12). 1946–1958. 56 indexed citations

Cheung, Peggie, Francesco Vallania, Mai Dvorak, et al.. (2018). Single-cell epigenetics – Chromatin modification atlas unveiled by mass cytometry. Clinical Immunology. 196. 40–48. 24 indexed citations

10.

Bayrak‐Toydemir, Pınar, Lora Jh Bean, Alicia Braxton, et al.. (2018). Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization. Genetics in Medicine. 21(4). 861–866. 14 indexed citations

11.

Christensen, Robert D., et al.. (2018). Non-Immune Hydrops, Hypotonia, Encephalopathy, and Liver Failure with Novel Compound Heterozygous <b><i>AHCY</i></b> Mutations. Neonatology. 114(4). 337–340. 5 indexed citations

12.

Yuzyuk, Tatiana, Bijina Balakrishnan, Irene De Biase, et al.. (2018). Effect of genotype on galactose-1-phosphate in classic galactosemia patients. Molecular Genetics and Metabolism. 125(3). 258–265. 4 indexed citations

13.

Zárate, Yuri A., Hazel Perry, Tawfeg Ben‐Omran, et al.. (2015). Further supporting evidence for the SATB2‐associated syndrome found through whole exome sequencing. American Journal of Medical Genetics Part A. 167(5). 1026–1032. 37 indexed citations

14.

Hegde, Madhuri, Sherri J. Bale, Pınar Bayrak‐Toydemir, et al.. (2015). Reporting Incidental Findings in Genomic Scale Clinical Sequencing—A Clinical Laboratory Perspective. Journal of Molecular Diagnostics. 17(2). 107–117. 44 indexed citations

15.

Dames, Shale, Karen Eilbeck, & Rong Mao. (2015). A High-Throughput Next-Generation Sequencing Assay for the Mitochondrial Genome. Methods in molecular biology. 1264. 77–88. 14 indexed citations

16.

Sumner, Kelli, Jeffrey Swensen, Melinda Procter, et al.. (2014). Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing. Journal of Molecular Diagnostics. 16(5). 477–480. 3 indexed citations

17.

Svensson, Annika, Lan‐Szu Chou, Cindy Meadows, et al.. (2011). Implementation of a Cost-Effective Unlabeled Probe High-Resolution Melt Assay for Genotyping of Factor V Leiden. Genetic Testing and Molecular Biomarkers. 15(4). 207–213. 2 indexed citations

18.

Svensson, Annika, Lan-Szu Chou, Christine E. Miller, et al.. (2010). Detection of Large Rearrangements in the Cystic Fibrosis Transmembrane Conductance Regulator Gene by Multiplex Ligation-Dependent Probe Amplification Assay When Sequencing Fails to Detect Two Disease-Causing Mutations. Genetic Testing and Molecular Biomarkers. 14(2). 171–174. 11 indexed citations

19.

Jama, Mohamed, Lesa Nelson, Rong Mao, & Elaine Lyon. (2007). Simultaneous Amplification, Detection, and Analysis of Common Mutations in the Galactose-1-Phosphate Uridyl Transferase Gene. Journal of Molecular Diagnostics. 9(5). 618–623. 11 indexed citations

20.

Mao, Rong, et al.. (2005). The Implication of De Novo 21-Hydroxylase Mutation in Clinical and Prenatal Molecular Diagnoses. Genetic Testing. 9(2). 121–125. 7 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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