Hao Hu

8.4k total citations
128 papers, 3.6k citations indexed

About

Hao Hu is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Hao Hu has authored 128 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 56 papers in Genetics and 13 papers in Cancer Research. Recurrent topics in Hao Hu's work include Genetics and Neurodevelopmental Disorders (27 papers), Genomics and Rare Diseases (25 papers) and RNA modifications and cancer (15 papers). Hao Hu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (27 papers), Genomics and Rare Diseases (25 papers) and RNA modifications and cancer (15 papers). Hao Hu collaborates with scholars based in China, Germany and United States. Hao Hu's co-authors include Mark Yandell, Wei Chen, Philipp Khaitovich, Baldomero M. Olivera, Pradip K. Bandyopadhyay, Vera M. Kalscheuer, Barry Moore, Corinna Menzel, Martin G. Reese and Hans‐Hilger Ropers and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and SHILAP Revista de lepidopterología.

In The Last Decade

Hao Hu

121 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hao Hu China 33 2.5k 1.1k 665 287 231 128 3.6k
Sheng Zhong United States 34 3.4k 1.4× 601 0.5× 602 0.9× 266 0.9× 206 0.9× 98 4.3k
Marcelo A. Nóbrega United States 35 4.7k 1.9× 1.4k 1.3× 616 0.9× 574 2.0× 167 0.7× 69 5.8k
Mei Zhong China 32 3.3k 1.3× 491 0.4× 561 0.8× 439 1.5× 134 0.6× 89 4.4k
Edward J. Kulbokas United States 8 2.7k 1.1× 975 0.9× 768 1.2× 329 1.1× 150 0.6× 9 3.7k
Alexej Abyzov United States 30 3.2k 1.3× 1.9k 1.7× 820 1.2× 595 2.1× 124 0.5× 68 4.4k
Gert Jan C. Veenstra Netherlands 32 4.7k 1.9× 1.5k 1.3× 364 0.5× 375 1.3× 181 0.8× 70 5.4k
Lennart Opitz Switzerland 28 2.1k 0.8× 606 0.5× 484 0.7× 148 0.5× 158 0.7× 79 3.4k
Aaron M. Wenger United States 21 4.2k 1.7× 1.7k 1.5× 818 1.2× 488 1.7× 177 0.8× 33 5.7k
Concepción Rodrı́guez Esteban United States 34 4.0k 1.6× 749 0.7× 355 0.5× 114 0.4× 361 1.6× 48 4.9k

Countries citing papers authored by Hao Hu

Since Specialization
Citations

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

Fields of papers citing papers by Hao Hu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hao Hu

This figure shows the co-authorship network connecting the top 25 collaborators of Hao Hu. A scholar is included among the top collaborators of Hao Hu 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 Hao Hu. Hao Hu 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.
Huang, Gang, et al.. (2025). New perspectives on DNA methylation modifications in ocular diseases. International Journal of Ophthalmology. 18(2). 340–350. 2 indexed citations
2.
Hu, Hao, et al.. (2025). Research hotspots and trends of robotic rectal cancer surgery: a bibliometric analysis (2006-2025). Journal of Robotic Surgery. 20(1). 38–38.
3.
Zhou, Pei, et al.. (2024). Wybutosine hypomodification of tRNAphe activates HERVK and impairs neuronal differentiation. iScience. 27(5). 109748–109748. 5 indexed citations
4.
5.
Hu, Hao, et al.. (2023). Exercise, Spinal Microglia and Neuropathic Pain: Potential Molecular Mechanisms. Neurochemical Research. 49(1). 29–37. 12 indexed citations
6.
Yao, Huan, et al.. (2023). Selective adsorption of trace morpholine impurities overN-ethyl morpholine by tetralactam solids. Chemical Communications. 59(47). 7204–7207. 11 indexed citations
7.
Ou, Yang, Shanyong Chen, Xiaoqiang Fan, et al.. (2023). Design and simulation of a conformal optical window pair by the quasi-quantitative Schlieren measurement in a cylindrical isolator. Optical Engineering. 62(3). 1 indexed citations
8.
Li, Huang, Xiaoqiang Peng, Chaoliang Guan, & Hao Hu. (2022). Ultra-Precision Cutting and Characterization of Reflective Convex Spherical Blazed Grating Elements. Micromachines. 13(7). 1115–1115. 8 indexed citations
9.
Arashiki, Nobuto, Lena‐Luise Becker, Jonathan Lévy, et al.. (2022). Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife. 11. 5 indexed citations
10.
Ali, Ghazanfar, Nadine Kraemer, Sami Zaqout, et al.. (2021). Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability. Journal of Medical Genetics. 59(5). 453–461. 6 indexed citations
11.
Gamallat, Yaser, Zhiheng Chen, Pei Zhou, et al.. (2021). Hypomorphic and hypermorphic mouse models of Fsip2 indicate its dosage-dependent roles in sperm tail and acrosome formation. Development. 148(11). 21 indexed citations
12.
Li, Na, Pei Zhou, Miaomiao Yang, et al.. (2021). Zebrafish modeling mimics developmental phenotype of patients with RAPGEF1 mutation. Clinical Genetics. 100(2). 144–155. 3 indexed citations
13.
Beheshtian, Maryam, Tara Akhtarkhavari, Marzieh Mohseni, et al.. (2020). Comprehensive genotype‐phenotype correlation in AP ‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients. Clinical Genetics. 99(1). 187–192. 2 indexed citations
14.
Lin, Yunting, Chunhua Zeng, Xiaodan Chen, et al.. (2020). Chinese family with Blau syndrome: Mutated NOD2 allele transmitted from the father with de novo somatic and germ line mosaicism. The Journal of Dermatology. 47(11). e395–e395. 3 indexed citations
15.
Yan, Zhenwei, et al.. (2019). Study on mechanism and genetic analysis of lipid metabolism disorder in pregnant rats. SHILAP Revista de lepidopterología. 1 indexed citations
16.
Wai, Timothy, Hao Hu, Thomas MacVicar, et al.. (2016). Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. eLife. 5. 96 indexed citations
17.
18.
Masurel‐Paulet, Alice, Vera M. Kalscheuer, Nicolas Lebrun, et al.. (2013). Expanding the clinical phenotype of patients with a ZDHHC9 mutation. American Journal of Medical Genetics Part A. 164(3). 789–795. 28 indexed citations
19.
Lesca, Gaëtan, Marie‐Pierre Moizard, Gérald Bussy, et al.. (2013). Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. American Journal of Medical Genetics Part A. 161(12). 3063–3071. 30 indexed citations
20.
Bainbridge, Matthew N., Hao Hu, Donna M. Muzny, et al.. (2013). De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. Genome Medicine. 5(2). 11–11. 102 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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