Baoheng Gui

1.1k total citations
26 papers, 607 citations indexed

About

Baoheng Gui is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Baoheng Gui has authored 26 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Baoheng Gui's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Connective tissue disorders research (5 papers). Baoheng Gui is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Connective tissue disorders research (5 papers). Baoheng Gui collaborates with scholars based in China, United States and Hong Kong. Baoheng Gui's co-authors include Jesse Slone, Taosheng Huang, Shiyu Luo, Ni‐Chung Lee, Lee-Jun Wong, C. Alexander Valencia, Paldeep S. Atwal, Jinglan Zhang, Xinjian Wang and Zhuo Li and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Scientific Reports and Gene.

In The Last Decade

Baoheng Gui

23 papers receiving 598 citations

Peers

Countries citing papers authored by Baoheng Gui

Since Specialization

Citations

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

Fields of papers citing papers by Baoheng Gui

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Baoheng Gui

This figure shows the co-authorship network connecting the top 25 collaborators of Baoheng Gui. A scholar is included among the top collaborators of Baoheng Gui 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 Baoheng Gui. Baoheng Gui 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	Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohort 2025 ·Scientific Reports ·Yiyun Huang, Chunyi Peng, Chuan Li, Bobo Xie, (unknown), Baoheng Gui, Juan Meng, Shaoke Chen, Xinxiang Fan	1
2	The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping 2024 ·Human Genomics ·(unknown), (unknown), (unknown), (unknown), (unknown), Bobo Xie, (unknown), Xiaoyun Lei, (unknown), (unknown), (unknown), Shaoke Chen, Jiefeng Luo, Yan Huang, Baoheng Gui	1
3	Complex genotype–phenotype correlation of MYH11: new insights from monozygotic twins with highly variable expressivity and outcomes 2024 ·BMC Medical Genomics ·(unknown), (unknown), Bobo Xie, (unknown), (unknown), (unknown), Yan Huang, Xin Fan, (unknown), Qingmei Huang, Li Deng, Chengqi Zhang, (unknown), Baoheng Gui, Yujun Chen	0
4	Third generation sequencing transforms the way of the screening and diagnosis of thalassemia: a mini-review 2023 ·Frontiers in Pediatrics ·(unknown), (unknown), Wei Wei, (unknown), Baoheng Gui	2
5	Importance of comprehensive genetic testing for patients with suspected vascular Ehlers–Danlos syndrome: a family case report and literature review 2023 ·Frontiers in Genetics ·(unknown), Xu Zhou, Bobo Xie, (unknown), (unknown), Бо Лю, Caiyan Li, Chengqi Zhang, Jiefeng Luo, (unknown), Baoheng Gui	0
6	Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2: Clinical and genetic evaluation of eight patients from a five‐generation family 2022 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), Baoheng Gui, Bobo Xie, Shaoke Chen, Xin Fan, (unknown)	3
7	Long-Molecule Sequencing 2020 ·Journal of Molecular Diagnostics ·Liangpu Xu, Aiping Mao, Hui Liu, Baoheng Gui, Kwong Wai Choy, Hailong Huang, Qian Yu, Xiaojie Zhang, Meihuan Chen, Na Lin, Lingji Chen, Jin‐Yeong Han, Yan Wang, Min Zhang, Xiaoyu Li, (unknown), Yuan Lin, Jianguang Zhang, David S. Cram, Hua Cao	64
8	A prospective study of non-invasive preimplantation genetic testing for aneuploidies (NiPGT-A) using next-generation sequencing (NGS) on spent culture media (SCM) 2019 ·Journal of Assisted Reproduction and Genetics ·(unknown), (unknown), Jacqueline Pui Wah Chung, Wai Ting Lui, Yvonne K. Kwok, Baoheng Gui, Grace Kong, Ye Cao, Tin Chiu Li, Kwong Wai Choy	70
9	Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis 2019 ·Genetics in Medicine ·Huilin Wang, Zirui Dong, Rui Zhang, Matthew Hoi Kin Chau, Zhenjun Yang, (unknown), Hoi Kin Wong, Baoheng Gui, Zhuo‐Xian Meng, (unknown), Xiaofan Zhu, Yanfang Wang, Shaoyun Chen, (unknown), Sau Wai Cheung, Yvonne K. Kwok, Cynthia C. Morton, Yuanfang Zhu, Kwong Wai Choy	78
10	Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy 2019 ·Journal of Visualized Experiments ·Baoheng Gui, Yingxin Zhang, Bo Liang, (unknown), Wai Ting Lui, (unknown), (unknown), Liming Xuan, Jacqueline Pui Wah Chung, Kwong Wai Choy	2
11	The current landscape for the treatment of mitochondrial disorders 2018 ·Journal of genetics and genomics ·Jesse Slone, Baoheng Gui, Taosheng Huang	8
12	Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome 2018 ·Gene ·Baoheng Gui, Yanning Song, Xuyun Hu, (unknown), Zailong Qin, Jiasun Su, Chuan Li, Xin Fan, Mengting Li, Jingsi Luo, Ying Feng, Liping Song, Shaoke Chen, Chunxiu Gong, Yiping Shen	5
13	Biparental Inheritance of Mitochondrial DNA in Humans 2018 ·Proceedings of the National Academy of Sciences ·Shiyu Luo, C. Alexander Valencia, Jinglan Zhang, Ni‐Chung Lee, Jesse Slone, Baoheng Gui, Xinjian Wang, Zhuo Li, (unknown), (unknown), (unknown), Yin‐Hsiu Chien, Wuh‐Liang Hwu, Pi‐Chuan Fan, Lee-Jun Wong, Paldeep S. Atwal, Taosheng Huang	253
14	Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants 2017 ·Clinica Chimica Acta ·Xuyun Hu, (unknown), Baoheng Gui, Yufei Xu, Jin Wang, Niu Li, Jiasun Su, Shujie Zhang, Yanning Song, Yi Wang, Jingsi Luo, Xin Fan, Jian Wang, Shaoke Chen, Chunxiu Gong, Yiping Shen	11
15	Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients 2016 ·Clinica Chimica Acta ·Chunyun Fu, Jin Wang, Shiyu Luo, Qi Yang, Qifei Li, (unknown), Xuyun Hu, Jiasun Su, Shujie Zhang, Rongyu Chen, Jingsi Luo, Yue Zhang, Yiping Shen, (unknown), (unknown), Baoheng Gui, (unknown), Xin Fan, Shaoke Chen	25
16	Chromosomal analysis of blastocysts from balanced chromosomal rearrangement carriers 2016 ·Reproduction ·Baoheng Gui, Zhongyuan Yao, Yanping Li, (unknown), Nenghui Liu, Yan Xia, Yanru Huang, (unknown), (unknown), Sijia Lü, Desheng Liang, Lingqian Wu	6
17	Novel de novo nonsense mutation of the PHEX gene (p.Lys50Ter) in a Chinese patient with hypophosphatemic rickets 2015 ·Gene ·Yanru Huang, (unknown), Qian Pan, Hu Tan, Yi Quan, Baoheng Gui, (unknown), (unknown), Ying Peng, Pu Yang, Desheng Liang, Lingqian Wu	4
18	Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome 2015 ·Molecular Cytogenetics ·(unknown), Ying Peng, (unknown), Yan Xia, (unknown), (unknown), Ruolan Guo, Baoheng Gui, Yanru Huang, Chen Chen, Desheng Liang, Lingqian Wu	6
19	[Etiology and diagnosis of intellectual disability]. 2015 ·PubMed ·Pu Yang, Baoheng Gui, (unknown)	2
20	A novel deletion mutation in RS1 gene caused X-linked juvenile retinoschisis in a Chinese family 2014 ·Eye ·Yuzhou Huang, Lingyun Mei, Baoheng Gui, Wan‐Fu Su, Desheng Liang, Lingqian Wu, Qian Pan	5

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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