Heju Zhang

588 total citations
7 papers, 471 citations indexed

About

Heju Zhang is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Heju Zhang has authored 7 papers receiving a total of 471 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in Heju Zhang's work include Hereditary Neurological Disorders (3 papers), Bone health and treatments (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Heju Zhang is often cited by papers focused on Hereditary Neurological Disorders (3 papers), Bone health and treatments (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Heju Zhang collaborates with scholars based in United States and Japan. Heju Zhang's co-authors include Pentao Liu, Pragna I. Patel, Allan Bradley, Carol A. Wise, James R. Lupski, Alejandro Abuin, Andrew McLellan, Hannes Vogel, Frank Greenberg and Jolene J. Windle and has published in prestigious journals such as Molecular and Cellular Biology, Genetics and Human Molecular Genetics.

In The Last Decade

Heju Zhang

7 papers receiving 465 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Heju Zhang	238	163	143	83	77	7	471
Jacek Pilch	275 1.2×	117 0.7×	117 0.8×	43 0.5×	39 0.5×	24	469
Israel Ben‐Dor	304 1.3×	69 0.4×	49 0.3×	59 0.7×	88 1.1×	9	472
Lucia Pedace	200 0.8×	77 0.5×	66 0.5×	59 0.7×	58 0.8×	27	391
Sabrina A. Volpi	389 1.6×	167 1.0×	48 0.3×	42 0.5×	29 0.4×	9	667
Lynn Greenhalgh	226 0.9×	87 0.5×	181 1.3×	22 0.3×	29 0.4×	11	507
Simon Duley	239 1.0×	177 1.1×	69 0.5×	73 0.9×	38 0.5×	5	607
Elizabeth Nacheva	161 0.7×	39 0.2×	99 0.7×	37 0.4×	130 1.7×	16	410
Christoffer Jonsrud	246 1.0×	99 0.6×	94 0.7×	47 0.6×	27 0.4×	19	409
Julie Wallis	478 2.0×	316 1.9×	97 0.7×	133 1.6×	71 0.9×	14	671
Jason Dapper	267 1.1×	45 0.3×	131 0.9×	29 0.3×	38 0.5×	12	421

Countries citing papers authored by Heju Zhang

Since Specialization

Citations

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

Fields of papers citing papers by Heju Zhang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heju Zhang

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

All Works

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7 of 7 papers shown

Lu, Ganwei, Mark A. Subler, Heju Zhang, et al.. (2010). ADAM8 enhances osteoclast precursor fusion and osteoclast formation in vitro and in vivo. Journal of Bone and Mineral Research. 26(1). 169–181. 33 indexed citations

Hiruma, Yuko, Noriyoshi Kurihara, Mark A. Subler, et al.. (2008). A SQSTM1/p62 mutation linked to Paget’s disease increases the osteoclastogenic potential of the bone microenvironment. Human Molecular Genetics. 17(23). 3708–3719. 67 indexed citations

Abuin, Alejandro, Heju Zhang, & Allan Bradley. (2000). Genetic Analysis of Mouse Embryonic Stem Cells Bearing Msh3 and Msh2 Single and Compound Mutations. Molecular and Cellular Biology. 20(1). 149–157. 42 indexed citations

Liu, Pentao, Heju Zhang, Andrew McLellan, Hannes Vogel, & Allan Bradley. (1998). Embryonic Lethality and Tumorigenesis Caused by Segmental Aneuploidy on Mouse Chromosome 11. Genetics. 150(3). 1155–1168. 69 indexed citations

Zori, Roberto T., James R. Lupski, Heju Zhang, et al.. (1993). Clinical, cytogenetic, and molecular evidence for an infant with Smith–Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion. American Journal of Medical Genetics. 47(4). 504–511. 65 indexed citations

Wise, Carol A., et al.. (1993). Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication.. PubMed. 53(4). 853–63. 158 indexed citations

Guzzetta, Vito, Brunella Franco, B. J. Trask, et al.. (1992). Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p. Genomics. 13(3). 551–559. 37 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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