Ying‐Xia Cui

810 total citations
68 papers, 533 citations indexed

About

Ying‐Xia Cui is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Ying‐Xia Cui has authored 68 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 36 papers in Molecular Biology and 20 papers in Reproductive Medicine. Recurrent topics in Ying‐Xia Cui's work include Sperm and Testicular Function (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers) and Sexual Differentiation and Disorders (16 papers). Ying‐Xia Cui is often cited by papers focused on Sperm and Testicular Function (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers) and Sexual Differentiation and Disorders (16 papers). Ying‐Xia Cui collaborates with scholars based in China, United States and Czechia. Ying‐Xia Cui's co-authors include Xinyi Xia, Qiuyue Wu, Lian‐Jun Pan, Yu‐Feng Huang, Tianfu Li, Cui Zhang, Yichao Shi, Chunxia Jiang, Xiaojun Li and Na Li and has published in prestigious journals such as PLoS ONE, Biochemical and Biophysical Research Communications and Life Sciences.

In The Last Decade

Ying‐Xia Cui

64 papers receiving 513 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ying‐Xia Cui China	15	264	256	141	56	51	68	533
Rebecca P. Green United States	9	424 1.6×	619 2.4×	167 1.2×	39 0.7×	78 1.5×	9	919
Jadranka Popović United States	10	144 0.5×	245 1.0×	128 0.9×	201 3.6×	47 0.9×	12	522
Maria Garofalo Italy	16	119 0.5×	285 1.1×	129 0.9×	215 3.8×	70 1.4×	32	799
Hongguo Zhang China	14	294 1.1×	268 1.0×	227 1.6×	16 0.3×	135 2.6×	101	672
Omar Abidi Morocco	14	137 0.5×	215 0.8×	72 0.5×	28 0.5×	19 0.4×	36	473
Aki Murashima Japan	11	123 0.5×	293 1.1×	73 0.5×	49 0.9×	94 1.8×	19	490
Nancy Vinson United States	8	74 0.3×	164 0.6×	154 1.1×	203 3.6×	67 1.3×	10	534
Gudrun Engels Germany	8	88 0.3×	294 1.1×	53 0.4×	12 0.2×	66 1.3×	10	617
Andrea Kwan United States	14	260 1.0×	209 0.8×	32 0.2×	46 0.8×	53 1.0×	19	553
Cornelia Schulze Germany	12	100 0.4×	217 0.8×	360 2.6×	53 0.9×	123 2.4×	24	624

Countries citing papers authored by Ying‐Xia Cui

Since Specialization

Citations

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

Fields of papers citing papers by Ying‐Xia Cui

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ying‐Xia Cui. 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 Ying‐Xia Cui. The network helps show where Ying‐Xia Cui may publish in the future.

Co-authorship network of co-authors of Ying‐Xia Cui

This figure shows the co-authorship network connecting the top 25 collaborators of Ying‐Xia Cui. A scholar is included among the top collaborators of Ying‐Xia Cui 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 Ying‐Xia Cui. Ying‐Xia Cui 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

Wu, Weiqing, Ying‐Xia Cui, Mingchao Zhang, et al.. (2023). A mouse model for X-linked Alport syndrome induced by Del-ATGG in the Col4a5 gene. Frontiers in Medicine. 10. 1086756–1086756. 1 indexed citations

Lv, Xing, Weiqing Wu, Jiaxun Zhang, et al.. (2020). Comparative Functional Analysis in vitro of 2 <b><i>COL4A5</i></b> Splicing Mutations at the Same Site in 2 Unrelated Alport Syndrome Chinese Families. Cytogenetic and Genome Research. 160(5). 238–244.

Li, Weiwei, Cui Zhang, Qiuyue Wu, et al.. (2016). The P20R mutation of αB-crystallin diminishes its anti-apoptotic activity in human lens epithelial cells. Biochemical and Biophysical Research Communications. 483(1). 463–467. 3 indexed citations

Xia, Xinyi, Cui Zhang, Qiuyue Wu, et al.. (2015). A duplication upstream of SOX9 was not positively correlated with the SRY-negative 46,XX testicular disorder of sex development: A case report and literature review. Molecular Medicine Reports. 12(4). 5659–5664. 9 indexed citations

Zhou, Yuchun, Cui Zhang, Qiuyue Wu, et al.. (2015). A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): A case report. Molecular Medicine Reports. 12(1). 155–158. 2 indexed citations

Wu, Qiuyue, Na Li, Weiwei Li, et al.. (2014). Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive. BMC Urology. 14(1). 70–70. 41 indexed citations

Jiang, Han-Wei, et al.. (2014). Meiotic Chromosome Behavior in a Human Male t(8;15) Carrier. Journal of genetics and genomics. 41(3). 177–185. 23 indexed citations

Li, Tianfu, Qiuyue Wu, Cui Zhang, et al.. (2014). Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis. Reproductive Biology and Endocrinology. 12(1). 79–79. 10 indexed citations

Xia, Xinyi, Weiping Wang, Tianfu Li, et al.. (2014). A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex development. Molecular Cytogenetics. 7(1). 16–16. 8 indexed citations

10.

Zhou, Yang, Qi Yao, Ying‐Xia Cui, et al.. (2013). Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement. American Journal of Medical Genetics Part A. 161(4). 897–900. 2 indexed citations

11.

Cui, Ying‐Xia, Xinyi Xia, Yang Zhou, et al.. (2013). Novel Mutations of ABCB6 Associated with Autosomal Dominant Dyschromatosis Universalis Hereditaria. PLoS ONE. 8(11). e79808–e79808. 21 indexed citations

12.

Yao, Bing, Haiyan Liu, Yuchun Gu, et al.. (2011). Gonadotropin-releasing hormone positively regulates steroidogenesis via extracellular signal-regulated kinase in rat Leydig cells. Asian Journal of Andrology. 13(3). 438–445. 17 indexed citations

13.

Xia, Xinyi, Ying‐Xia Cui, Yuchun Zhou, et al.. (2009). A novel insertion mutation in the SEDL gene results in X-linked spondyloepiphyseal dysplasia tarda in a large Chinese pedigree. Clinica Chimica Acta. 410(1-2). 39–42. 7 indexed citations

14.

Cui, Ying‐Xia, Xinyi Xia, Guohua Zhou, et al.. (2008). Rapid Molecular Prenatal Diagnosis of Spondyloepiphyseal Dysplasia Congenita by PCR-SSP Assay. Genetic Testing. 12(4). 533–536. 2 indexed citations

15.

Xia, Xinyi, Ying‐Xia Cui, Yu‐Feng Huang, et al.. (2008). A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family. Clinica Chimica Acta. 398(1-2). 148–151. 11 indexed citations

16.

Cui, Ying‐Xia, Yu‐Feng Huang, Yichao Shi, et al.. (2008). A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 662(1-2). 22–27. 15 indexed citations

17.

Pan, Lian‐Jun, et al.. (2007). Exposure of Juvenile Rats to the Phytoestrogen Daidzein Impairs Erectile Function in a Dose‐Related Manner in Adulthood. Journal of Andrology. 29(1). 55–62. 39 indexed citations

18.

Xia, Xinyi, Ying‐Xia Cui, Yufeng Huang, et al.. (2007). Molecular prenatal diagnosis in 2 pregnancies at risk for spondyloepiphyseal dysplasia congenita. Clinica Chimica Acta. 387(1-2). 153–157. 7 indexed citations

19.

Cui, Ying‐Xia, Xinyi Xia, Lian‐Jun Pan, et al.. (2007). An infertile male with apparent 45,X turned out to have 45,X,der(Y)t(Y;13)(q11.2;q12),-13: clinicopathologic and cytogenomic studies. Fertility and Sterility. 88(6). 1676.e7–1676.e11. 4 indexed citations

20.

Cui, Ying‐Xia, Xinyi Xia, Lian‐Jun Pan, et al.. (2007). Gonosomal Mosaicism From Deleted Y Chromosomal Nondisjunction. Journal of Andrology. 28(3). 377–380. 17 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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