Zhishuo Ou

2.9k total citations
26 papers, 1.1k citations indexed

About

Zhishuo Ou is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Zhishuo Ou has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 12 papers in Molecular Biology and 12 papers in Plant Science. Recurrent topics in Zhishuo Ou's work include Genomic variations and chromosomal abnormalities (20 papers), Chromosomal and Genetic Variations (12 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Zhishuo Ou is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Chromosomal and Genetic Variations (12 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Zhishuo Ou collaborates with scholars based in United States, Canada and China. Zhishuo Ou's co-authors include Sau Wai Cheung, A. Craig Chinault, Ankita Patel, James R. Lupski, Chad A. Shaw, M. Lance Cooper, Paweł Stankiewicz, Arthur L. Beaudet, V. Reid Sutton and John W. Belmont and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Neurobiology of Disease.

In The Last Decade

Zhishuo Ou

26 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Zhishuo Ou United States	14	862	602	230	214	95	26	1.1k
Roberto Ciccone Italy	23	956 1.1×	681 1.1×	283 1.2×	270 1.3×	63 0.7×	51	1.4k
Sung‐Hae Kang United States	20	925 1.1×	737 1.2×	348 1.5×	180 0.8×	88 0.9×	30	1.4k
Jannine D. Cody United States	25	971 1.1×	729 1.2×	275 1.2×	312 1.5×	35 0.4×	63	1.5k
Ewa Obersztyn Poland	19	711 0.8×	692 1.1×	130 0.6×	170 0.8×	32 0.3×	78	1.2k
Leslie Domenici Kulikowski Brazil	15	487 0.6×	337 0.6×	174 0.8×	188 0.9×	52 0.5×	87	799
Susan Gribble United Kingdom	18	765 0.9×	579 1.0×	179 0.8×	349 1.6×	29 0.3×	29	1.2k
Marijke Bauters Belgium	17	911 1.1×	809 1.3×	90 0.4×	138 0.6×	44 0.5×	25	1.3k
N R Dennis United Kingdom	20	793 0.9×	628 1.0×	98 0.4×	157 0.7×	113 1.2×	32	1.3k
Brigitte Benzacken France	20	737 0.9×	462 0.8×	426 1.9×	156 0.7×	25 0.3×	61	1.3k
Fabiola Quintero‐Rivera United States	16	907 1.1×	634 1.1×	357 1.6×	57 0.3×	42 0.4×	54	1.4k

Countries citing papers authored by Zhishuo Ou

Since Specialization

Citations

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

Fields of papers citing papers by Zhishuo Ou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhishuo Ou

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

Lu, Xingyu, Ying Shi, Xueqiang Hu, et al.. (2025). The projection from the rostral anterior cingulate cortex to the ventral tegmental area regulates 5-HT-induced itch aversion and scratching in rats. Neurobiology of Disease. 207. 106844–106844. 3 indexed citations

Wang, Yating, Juan Yao, Xuan Li, et al.. (2025). The parietal association cortex and its projections to the dorsal striatum are involved in histaminergic and nonhistaminergic itch processing. Brain Research Bulletin. 226. 111352–111352. 2 indexed citations

Zou, Kang, et al.. (2025). Single-cell analysis identifies MKI67+ microglia as drivers of neovascularization in proliferative diabetic retinopathy. Journal of Translational Medicine. 23(1). 310–310. 2 indexed citations

Gu, Jun, Sandesh C. Sreenath Nagamani, Vicki L. Hopwood, et al.. (2011). Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic craniofacial features, and developmental delay. American Journal of Medical Genetics Part A. 155(10). 2589–2592. 1 indexed citations

Celestino-Soper, Patrícia B. S., Chad A. Shaw, Stephan Sanders, et al.. (2011). Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Human Molecular Genetics. 20(22). 4360–4370. 85 indexed citations

Kang, Sung‐Hae, Chad A. Shaw, Zhishuo Ou, et al.. (2010). Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results. American Journal of Medical Genetics Part A. 152A(5). 1111–1126. 79 indexed citations

Yatsenko, Svetlana A., Chad A. Shaw, Zhishuo Ou, et al.. (2009). Microarray-Based Comparative Genomic Hybridization Using Sex-Matched Reference DNA Provides Greater Sensitivity for Detection of Sex Chromosome Imbalances than Array-Comparative Genomic Hybridization with Sex-Mismatched Reference DNA. Journal of Molecular Diagnostics. 11(3). 226–237. 10 indexed citations

El‐Hattab, Ayman W., Teresa A. Smolarek, Elizabeth K. Schorry, et al.. (2009). Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping. Human Genetics. 126(4). 589–602. 56 indexed citations

Nagamani, Sandesh C. Sreenath, Ayelet Erez, Christine M. Eng, et al.. (2008). Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss. European Journal of Human Genetics. 17(5). 573–581. 39 indexed citations

10.

Ou, Zhishuo, Donna M. Martin, Jirair K. Bedoyan, et al.. (2008). Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication ofSIX1,SIX6, andOTX2resulting from a complex chromosomal rearrangement. American Journal of Medical Genetics Part A. 146A(19). 2480–2489. 45 indexed citations

11.

Ben‐Shachar, Shay, Zhishuo Ou, Chad A. Shaw, et al.. (2008). 22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome. The American Journal of Human Genetics. 82(1). 214–221. 142 indexed citations

12.

Ou, Zhishuo, Sung‐Hae Kang, Chad A. Shaw, et al.. (2008). Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses. Genetics in Medicine. 10(4). 278–289. 64 indexed citations

13.

Shchelochkov, Oleg A., M. Lance Cooper, Zhishuo Ou, et al.. (2008). Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement. Molecular Cytogenetics. 1(1). 16–16. 11 indexed citations

14.

Brunetti‐Pierri, Nicola, et al.. (2007). Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization. Clinical Genetics. 72(5). 411–419. 10 indexed citations

15.

Ou, Zhishuo, Jessica Shu Nan Li, Fernando Scaglia, et al.. (2007). Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome. Clinical Genetics. 72(4). 329–338. 40 indexed citations

16.

Nowakowska, Beata, Anna Kutkowska‐Kaźmierczak, Paweł Stankiewicz, et al.. (2007). A girl with deletion 9q22.1–q22.32 including thePTCHandROR2genes identified by genome‐wide array‐CGH. American Journal of Medical Genetics Part A. 143A(16). 1885–1889. 17 indexed citations

17.

Ou, Zhishuo, Małgorzata Jarmuż‐Szymczak, Steven Sparagana, et al.. (2006). Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocations. Human Genetics. 120(2). 227–237. 7 indexed citations

18.

Lennon, Patrick A., M. Lance Cooper, Cynthia Lim, et al.. (2006). Array‐based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation. American Journal of Medical Genetics Part A. 140A(11). 1156–1163. 3 indexed citations

19.

Cheung, Sau Wai, Chad A. Shaw, Wei Yu, et al.. (2005). Development and validation of a CGH microarray for clinical cytogenetic diagnosis. Genetics in Medicine. 7(6). 422–432. 185 indexed citations

20.

Pearson, Margaret A., Paweł Stankiewicz, Patrick A. Lennon, et al.. (2005). Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array‐based comparative genomic hybridization in a patient with mental retardation and dysmorphic features. American Journal of Medical Genetics Part A. 137A(1). 88–93. 7 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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