Jiale Xiang

859 total citations
24 papers, 345 citations indexed

About

Jiale Xiang is a scholar working on Sensory Systems, Molecular Biology and Genetics. According to data from OpenAlex, Jiale Xiang has authored 24 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Sensory Systems, 9 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Jiale Xiang's work include Hearing, Cochlea, Tinnitus, Genetics (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Prenatal Screening and Diagnostics (5 papers). Jiale Xiang is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Prenatal Screening and Diagnostics (5 papers). Jiale Xiang collaborates with scholars based in China, United States and Denmark. Jiale Xiang's co-authors include Zhiyu Peng, Jiguang Peng, Xiang Fu, Samantha Baxter, Lisha Chen, Melis Kücükoglu, Weibing Yang, Ykä Helariutta, Jing Zhang and Gugan Eswaran and has published in prestigious journals such as Scientific Reports, Clinical Chemistry and BMC Genomics.

In The Last Decade

Jiale Xiang

23 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jiale Xiang China 9 172 88 85 82 43 24 345
Jennifer McCallum United States 5 280 1.6× 112 1.3× 41 0.5× 36 0.4× 11 0.3× 5 355
Michelle M. Simon United Kingdom 7 169 1.0× 46 0.5× 50 0.6× 18 0.2× 19 0.4× 15 253
Janice C. Palumbos United States 8 245 1.4× 161 1.8× 32 0.4× 28 0.3× 13 0.3× 13 391
R. Farcas Germany 6 210 1.2× 54 0.6× 35 0.4× 17 0.2× 64 1.5× 8 282
Prachi Kothiyal United States 7 171 1.0× 211 2.4× 28 0.3× 15 0.2× 64 1.5× 12 373
Stuart Townsend United Kingdom 7 287 1.7× 50 0.6× 109 1.3× 22 0.3× 56 1.3× 8 411
H Dahl Australia 9 300 1.7× 158 1.8× 69 0.8× 42 0.5× 9 0.2× 12 459
Teresa Palladino Italy 9 123 0.7× 141 1.6× 52 0.6× 25 0.3× 6 0.1× 15 246
Tihua Zheng China 10 173 1.0× 15 0.2× 170 2.0× 21 0.3× 40 0.9× 28 299
Sameera Sogaty Saudi Arabia 8 179 1.0× 105 1.2× 33 0.4× 7 0.1× 20 0.5× 8 255

Countries citing papers authored by Jiale Xiang

Since Specialization
Citations

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

Fields of papers citing papers by Jiale Xiang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiale Xiang

This figure shows the co-authorship network connecting the top 25 collaborators of Jiale Xiang. A scholar is included among the top collaborators of Jiale Xiang 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 Jiale Xiang. Jiale Xiang 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.
Xiang, Jiale, Jiguang Peng, Hongfu Zhang, et al.. (2025). Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndrome. Scientific Reports. 15(1). 24755–24755.
2.
Xiang, Jiale, Jing Yang, Hongfu Zhang, et al.. (2024). Genome Sequencing Unveils the Role of Copy Number Variants in Hearing Loss and Identifies Novel Deletions With Founder Effect in the DFNB1 Locus. Human Mutation. 2024(1). 9517114–9517114. 3 indexed citations
3.
Xiang, Jiale, Jiguang Peng, Dongdong Li, et al.. (2023). The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing Data. Clinical Chemistry. 69(7). 763–770. 3 indexed citations
4.
Xiang, Jiale, et al.. (2022). Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss. BMC Medical Genomics. 15(1). 142–142. 7 indexed citations
5.
6.
Yu, Dandan, et al.. (2022). The effect of hemolysis on quality control metrics for noninvasive prenatal testing. BMC Medical Genomics. 15(1). 125–125. 2 indexed citations
7.
Xiang, Jiale, et al.. (2022). Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns. Frontiers in Genetics. 13. 883617–883617. 5 indexed citations
8.
Xiang, Jiale & Zhiyu Peng. (2022). Applications of Noninvasive Prenatal Testing for Subchromosomal Copy Number Variations Using Cell-Free DNA. Clinics in Laboratory Medicine. 42(4). 613–625. 3 indexed citations
9.
10.
Peng, Jiguang, et al.. (2021). VIP‐HL: Semi‐automated ACMG/AMP variant interpretation platform for genetic hearing loss. Human Mutation. 42(12). 1567–1575. 11 indexed citations
11.
Wang, Jing, Jiale Xiang, Lisha Chen, et al.. (2021). Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach. Scientific Reports. 11(1). 4036–4036. 8 indexed citations
12.
Yang, Haiyan, et al.. (2021). A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns. BMC Medical Genomics. 14(1). 61–61. 6 indexed citations
13.
Xiang, Jiale, Jiguang Peng, Samantha Baxter, & Zhiyu Peng. (2020). AutoPVS1: An automatic classification tool for PVS1 interpretation of null variants. Human Mutation. 41(9). 1488–1498. 36 indexed citations
14.
Xiang, Jiale, Lisha Chen, Qiang Chen, et al.. (2020). Author Correction: Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades. Scientific Reports. 10(1). 11593–11593. 2 indexed citations
15.
Xiang, Jiale, Lisha Chen, Qiang Chen, et al.. (2020). Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades. Scientific Reports. 10(1). 331–331. 26 indexed citations
16.
Xiang, Jiale, Jingjing Yang, Haiyan Wu, et al.. (2020). Concurrent hearing and genetic screening in a general newborn population. Human Genetics. 139(4). 521–530. 32 indexed citations
17.
Sun, Yu, Jiale Xiang, Sen Chen, et al.. (2019). Increased diagnostic yield by reanalysis of data from a hearing loss gene panel. BMC Medical Genomics. 12(1). 76–76. 22 indexed citations
18.
Zhang, Jing, Gugan Eswaran, Juan Alonso‐Serra, et al.. (2019). Transcriptional regulatory framework for vascular cambium development in Arabidopsis roots. Nature Plants. 5(10). 1033–1042. 85 indexed citations
19.
Luo, Haining, Chao Chen, Yun Yang, et al.. (2019). Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysis. BMC Medical Genomics. 12(1). 157–157. 5 indexed citations
20.
Xiang, Jiale, et al.. (2017). Grhl2 reduces invasion and migration through inhibition of TGFβ-induced EMT in gastric cancer. Oncogenesis. 6(1). e284–e284. 61 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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