Mingchu Xu

1.7k total citations
28 papers, 760 citations indexed

About

Mingchu Xu is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Mingchu Xu has authored 28 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 10 papers in Ophthalmology and 7 papers in Genetics. Recurrent topics in Mingchu Xu's work include Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (10 papers) and Genomics and Rare Diseases (4 papers). Mingchu Xu is often cited by papers focused on Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (10 papers) and Genomics and Rare Diseases (4 papers). Mingchu Xu collaborates with scholars based in United States, China and Canada. Mingchu Xu's co-authors include Rui Chen, Yumei Li, Keqing Wang, Feng Wang, Li Zhao, Ruifang Sui, Aiden Eblimit, Hui Wang, Zhongqi Ge and Huajin Li and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Cancer Research.

In The Last Decade

Mingchu Xu

28 papers receiving 752 citations

Peers

Countries citing papers authored by Mingchu Xu

Since Specialization

Citations

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

Fields of papers citing papers by Mingchu Xu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mingchu Xu

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

#	Work	Indexed citations
1	Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily 2022 ·Genetics in Medicine ·(unknown), (unknown), Alexey Obolensky, (unknown), Mingchu Xu, Yumei Li, (unknown), Prakadeeswari Gopalakrishnan, Menachem Gross, Boris Rosin, Mor Hanany, Andrew R. Webster, (unknown), Robert K. Koenekoop, Rui Chen, Gavin Arno, Ora Schueler‐Furman, Susanne Roosing, Eyal Banin, Dror Sharon	7
2	Spatially resolved transcriptomics of high-grade serous ovarian carcinoma 2022 ·iScience ·Elaine Stur, Sara Corvigno, Mingchu Xu, Ken Chen, (unknown), Sanghoon Lee, Jinsong Liu, (unknown), Daniel C. Kraushaar, Patricia Castro, Jianhua Zhang, Anil K. Sood	42
3	Single-cell evaluation reveals shifts in the tumor-immune niches that shape and maintain aggressive lesions in the breast 2021 ·Nature Communications ·(unknown), Amanda L. Rinkenbaugh, Mingchu Xu, Xinhui Zhou, Xiaomei Zhang, Sabrina L. Jeter-Jones, Jiansu Shao, Yuan Qi, John A. Zebala, Dean Y. Maeda, Florencia McAllister, Helen Piwnica‐Worms	13
4	GRIPT: a novel case-control analysis method for Mendelian disease gene discovery 2018 ·Genome biology ·Jun Wang, Li Zhao, Xia Wang, Yong Chen, Mingchu Xu, Zachry T. Soens, Zhongqi Ge, (unknown), Fei Wang, Rui Chen	3
5	The source code and scripts of GRIPT package: a novel case-control analysis method for Mendelian disease gene discovery 2018 ·Zenodo (CERN European Organization for Nuclear Research) ·Jun Wang, (unknown), Xia Wang, Yong Chen, Mingchu Xu, Zachry T. Soens, Zhongqi Ge, (unknown), Fei Wang, Rui Chen	1
6	A Novel Dominant Mutation in SAG , the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States 2017 ·Investigative Ophthalmology & Visual Science ·Lori S. Sullivan, Sara J. Bowne, Daniel C. Koboldt, (unknown), John R. Heckenlively, Kari Branham, Dianna H. Wheaton, Kaylie Webb-Jones, Robert R. German, Mark E. Pennesi, Paul Yang, David Davis-Boozer, Hope Northrup, (unknown), Rui Chen, Mingchu Xu, Yumei Li, David G. Birch, Stephen P. Daiger	26
7	Leveraging splice‐affecting variant predictors and a minigene validation system to identify Mendelian disease‐causing variants among exon‐captured variants of uncertain significance 2017 ·Human Mutation ·Zachry T. Soens, (unknown), Shijing Wu, (unknown), Yumei Li, Hui Li, (unknown), Mingchu Xu, (unknown), Fabiana Louise Motta, Renata Toscano Simões, (unknown), Radwan Ajlan, David G. Birch, Peiquan Zhao, Fernanda Belga Ottoni Porto, Juliana Maria Ferraz Sallum, (unknown), Ruifang Sui, Rui Chen	19
8	Folic acid exerts antidepressant effects by upregulating brain-derived neurotrophic factor and glutamate receptor 1 expression in brain 2017 ·Neuroreport ·Liangcai Gao, Xinnan Liu, Yu Li, Junlin Wu, Mingchu Xu, (unknown)	26
9	REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking 2017 ·Human Molecular Genetics ·Smriti A. Agrawal, Thomas Burgoyne, Aiden Eblimit, James Bellingham, David A. Parfitt, Amelia Lane, (unknown), (unknown), Matthew A. Hayes, Peter Munro, Mingchu Xu, Keqing Wang, Clare E. Futter, Yumei Li, Rui Chen, Michael E. Cheetham	37
10	SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data 2017 ·BMC Bioinformatics ·Yong Chen, Li Zhao, Yi Wang, Ming Cao, Violet Gelowani, Mingchu Xu, Smriti A. Agrawal, Yumei Li, Stephen P. Daiger, Richard A. Gibbs, Fei Wang, Rui Chen	48
11	The phenotypic variability of HK1-associated retinal dystrophy 2017 ·Scientific Reports ·(unknown), Baiyu Li, Mingchu Xu, Emmanuel Chang, Huajin Li, Lizhu Yang, Shijing Wu, Zachry T. Soens, Yumei Li, Lee‐Jun C. Wong, Richard A. Lewis, Ruifang Sui, Rui Chen	17
12	Diagnosis of a mild peroxisomal phenotype with next-generation sequencing 2016 ·Molecular Genetics and Metabolism Reports ·(unknown), Dianna K. Wheaton, Mingchu Xu, David G. Birch, Sara J. Bowne, Lori S. Sullivan, Stephen P. Daiger, (unknown), Richard O. Jones, Ann B. Moser, Rui Chen, Michael F. Wangler	27
13	Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genes 2016 ·Genome Research ·Li Zhao, Yiyun Chen, (unknown), Aiden Eblimit, Mingchu Xu, Zachry T. Soens, Feng Wang, Zhongqi Ge, Sung Yun Jung, Feng He, Yumei Li, Theodore G. Wensel, Jun Qin, Rui Chen	13
14	Improved Diagnosis of Inherited Retinal Dystrophies by High-Fidelity PCR of ORF15 followed by Next-Generation Sequencing 2016 ·Journal of Molecular Diagnostics ·Jianli Li, Jia Tang, Yanming Feng, Mingchu Xu, Rui Chen, Xuan Zou, Ruifang Sui, Emmanuel Chang, Richard A. Lewis, Victor Wei Zhang, Jing Wang, Lee‐Jun C. Wong	19
15	Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity 2016 ·Scientific Reports ·(unknown), Mingchu Xu, Qing Fu, (unknown), (unknown), Yumei Li, Aiden Eblimit, Ruifang Sui, Rui Chen, Haji Akber Aisa	16
16	Mutations inPOMGNT1cause non-syndromic retinitis pigmentosa 2016 ·Human Molecular Genetics ·Mingchu Xu, (unknown), Zixi Sun, Aiden Eblimit, Irma López, Feng Wang, Hiroshi Manya, (unknown), Li Zhao, Yumei Li, (unknown), Dror Sharon, Ruifang Sui, Tamao Endo, Robert K. Koenekoop, Rui Chen	29
17	Next-generation sequencing-based molecular diagnosis of 35 Hispanic retinitis pigmentosa probands 2016 ·Scientific Reports ·Qi Zhang, Mingchu Xu, Jennifer Verriotto, Yumei Li, Hui Wang, Lin Gan, Byron L. Lam, Rui Chen	41
18	Mutations in human IFT140 cause non-syndromic retinal degeneration 2015 ·Human Genetics ·Mingchu Xu, Lizhu Yang, Feng Wang, Huajin Li, Xia Wang, Weichen Wang, Zhongqi Ge, Keqing Wang, Li Zhao, Hui Li, Yumei Li, Ruifang Sui, Rui Chen	55
19	ATF6Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement 2015 ·Investigative Ophthalmology & Visual Science ·Mingchu Xu, Violet Gelowani, Aiden Eblimit, Feng Wang, (unknown), (unknown), Li Zhao, Glen Jenkins, Donnell J. Creel, Keqing Wang, Zhongqi Ge, Hui Wang, Yumei Li, M. Elizabeth Hartnett, Rui Chen	45
20	ADIPOR1Is Mutated in Syndromic Retinitis Pigmentosa 2015 ·Human Mutation ·Mingchu Xu, Aiden Eblimit, Jing Wang, Jianli Li, Feng Wang, Li Zhao, Xia Wang, (unknown), Yumei Li, Lee‐Jun C. Wong, Richard A. Lewis, Rui Chen	37

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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