Dihong Zhou

544 total citations
6 papers, 14 citations indexed

About

Dihong Zhou is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Dihong Zhou has authored 6 papers receiving a total of 14 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Dihong Zhou's work include Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Craniofacial Disorders and Treatments (2 papers). Dihong Zhou is often cited by papers focused on Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Craniofacial Disorders and Treatments (2 papers). Dihong Zhou collaborates with scholars based in United States and Japan. Dihong Zhou's co-authors include Joseph T. Alaimo, Susan Hughes, Jennifer Hanson, Michael D. Fountain, Sarah H. Elsea, Shivarajan Amudhavalli, Emily Fleming, Penelope E. Bonnen, Ana S.A. Cohen and Kendra Engleman and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Autism and Developmental Disorders and Clinical Genetics.

In The Last Decade

Dihong Zhou

4 papers receiving 14 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dihong Zhou United States	3	8	8	3	2	2	6	14
Kimberley Gamet New Zealand	2	7 0.9×	8 1.0×	3 1.0×			5	14
Jackie Tahiliani United States	2	7 0.9×	7 0.9×	3 1.0×	1 0.5×	1 0.5×	2	24
Tian Wu Hong Kong	3	6 0.8×	13 1.6×	2 0.7×	1 0.5×	2 1.0×	4	20
Elvira Mingazheva Russia	3	5 0.6×	4 0.5×	2 0.7×		2 1.0×	5	10
Danielle Pasternack Canada	2	13 1.6×	4 0.5×	3 1.0×	3 1.5×	2 1.0×	2	20
Yvonne Moyer United States	2	9 1.1×	4 0.5×	4 1.3×		2 1.0×	2	12
Guoyun Yu United States	3	11 1.4×	6 0.8×	4 1.3×	1 0.5×	3 1.5×	7	18
Shawn Leonard United States	3	4 0.5×	6 0.8×	3 1.0×	1 0.5×	2 1.0×	3	17
Yanjuan Ma China	3	13 1.6×	5 0.6×	3 1.0×	3 1.5×	1 0.5×	3	18
Wenwen Li Denmark	2	6 0.8×	5 0.6×	3 1.0×			3	11

Countries citing papers authored by Dihong Zhou

Since Specialization

Citations

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

Fields of papers citing papers by Dihong Zhou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dihong Zhou

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

All Works

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6 of 6 papers shown

1.

Viso, Florencia Del, et al.. (2024). SF3B2 Haploinsufficiency Associated With Hirschprung Disease and Complex Cardiac Defect Without Craniofacial Microsomia. American Journal of Medical Genetics Part A. 197(2). e63886–e63886.

2.

Viso, Florencia Del, et al.. (2023). P448: SF3B2-Related cardiac defects and Hirschsprung disease without craniofacial microsomia. SHILAP Revista de lepidopterología. 1(1). 100495–100495.

3.

Cadieux‐Dion, Maxime, Emily Farrow, Isabelle Thiffault, et al.. (2022). Phenotypic expansion and variable expressivity in individuals with JARID2 ‐related intellectual disability: A case series. Clinical Genetics. 102(2). 136–141. 2 indexed citations

4.

Viso, Florencia Del, Dihong Zhou, Isabelle Thiffault, et al.. (2022). Recurrent FOXP4 nonsense variant in two unrelated patients: Association with neurodevelopmental disease and congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 191(1). 259–264. 1 indexed citations

5.

Hanson, Jennifer, Susan Hughes, Shivarajan Amudhavalli, et al.. (2021). TAB2 variants cause cardiovascular heart disease, connective tissue disorder, and developmental delay. Clinical Genetics. 101(2). 214–220. 7 indexed citations

6.

Zhou, Dihong, et al.. (2020). Composite Sleep Problems Observed Across Smith–Magenis Syndrome, MBD5-Associated Neurodevelopmental Disorder, Pitt–Hopkins Syndrome, and ASD. Journal of Autism and Developmental Disorders. 51(6). 1852–1865. 4 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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