Jiadi Wen

413 total citations
22 papers, 264 citations indexed

About

Jiadi Wen is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Jiadi Wen has authored 22 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 7 papers in Molecular Biology. Recurrent topics in Jiadi Wen's work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genetic Syndromes and Imprinting (4 papers). Jiadi Wen is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genetic Syndromes and Imprinting (4 papers). Jiadi Wen collaborates with scholars based in United States, Canada and China. Jiadi Wen's co-authors include Peter C. K. Leung, Evica Rajcan‐Separovic, Sally Martell, Mary D. Stephenson, Ying Qiao, Peining Li, Hongyan Chai, Hua Zhu, M. E. Suzanne Lewis and Qinghua Zhou and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Biology of Reproduction.

In The Last Decade

Jiadi Wen

22 papers receiving 259 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jiadi Wen United States	9	125	124	84	57	42	22	264
Masood Bazrgar Iran	9	103 0.8×	67 0.5×	89 1.1×	28 0.5×	112 2.7×	26	293
Denise Molina‐Gomes France	12	130 1.0×	162 1.3×	101 1.2×	57 1.0×	133 3.2×	32	406
Laura Kasak Estonia	8	91 0.7×	159 1.3×	135 1.6×	28 0.5×	81 1.9×	12	293
Judy F.C. Chow Hong Kong	11	157 1.3×	119 1.0×	146 1.7×	38 0.7×	131 3.1×	22	338
Feodora Stipoljev Croatia	10	126 1.0×	104 0.8×	50 0.6×	14 0.2×	54 1.3×	33	244
Katherine L. Palmerola United States	8	125 1.0×	75 0.6×	225 2.7×	15 0.3×	102 2.4×	22	401
Fiona Norris Australia	8	76 0.6×	63 0.5×	153 1.8×	61 1.1×	27 0.6×	11	282
C. Méndez Mexico	10	99 0.8×	77 0.6×	75 0.9×	12 0.2×	75 1.8×	27	284
Maribel Forero‐Castro Colombia	8	41 0.3×	43 0.3×	87 1.0×	50 0.9×	90 2.1×	29	269
Huai-Liang Feng United States	11	108 0.9×	65 0.5×	130 1.5×	54 0.9×	286 6.8×	20	445

Countries citing papers authored by Jiadi Wen

Since Specialization

Citations

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

Fields of papers citing papers by Jiadi Wen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiadi Wen

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

Chai, Hongyan, Mei Ling Chong, Guilin Wang, et al.. (2024). Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages. SHILAP Revista de lepidopterología. 11(1). 123–131. 1 indexed citations

Peng, Gang, Qinghua Zhou, Hongyan Chai, et al.. (2023). Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses. Molecular Genetics & Genomic Medicine. 11(8). e2181–e2181. 7 indexed citations

Chai, Hongyan, et al.. (2022). Genotype–Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature. SHILAP Revista de lepidopterología. 9(2). 166–174. 5 indexed citations

Wen, Jiadi, Hongyan Chai, Daniel Dykas, et al.. (2022). Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients. American Journal of Medical Genetics Part A. 188(6). 1728–1738. 1 indexed citations

Wen, Jiadi, Hongyan Chai, Sok Meng Evelyn Ng, et al.. (2021). Detection of cytogenomic abnormalities by OncoScan microarray assay for products of conception from formalin-fixed paraffin-embedded and fresh fetal tissues. Molecular Cytogenetics. 14(1). 21–21. 2 indexed citations

Zhao, Chen, Hongyan Chai, Qinghua Zhou, et al.. (2020). Exome sequencing analysis on products of conception: a cohort study to evaluate clinical utility and genetic etiology for pregnancy loss. Genetics in Medicine. 23(3). 435–442. 33 indexed citations

Chai, Hongyan, Weizhen Ji, Jiadi Wen, et al.. (2020). Ring chromosome formation by intra‐strand repairing of subtelomeric double stand breaks and clinico‐cytogenomic correlations for ring chromosome 9. American Journal of Medical Genetics Part A. 182(12). 3023–3028. 7 indexed citations

Li, Fuguang, et al.. (2020). Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence. Molecular Genetics & Genomic Medicine. 8(7). e1297–e1297. 12 indexed citations

Chai, Hongyan, Fang Xu, Qinghua Zhou, et al.. (2019). A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings. Frontiers in Genetics. 10. 1162–1162. 12 indexed citations

10.

Wen, Jiadi, et al.. (2019). Analytical validation and chromosomal distribution of regions of homozygosity by oligonucleotide array comparative genomic hybridization from normal prenatal and postnatal case series. Molecular Cytogenetics. 12(1). 12–12. 7 indexed citations

11.

Chai, Hongyan, et al.. (2019). Inverted duplication, triplication and quintuplication through sequential breakage‐fusion‐bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion. Molecular Genetics & Genomic Medicine. 7(10). e00965–e00965. 3 indexed citations

12.

Koduru, Prasad, et al.. (2017). Cytogenetic and Cytogenomic Microarray Characterization of Chromothripsis in Chromosome 8 Affecting MOZ/NCOA2 (TIF2), FGFR1, RUNX1T1, and RUNX1 in a Pediatric Acute Myeloid Leukemia. Journal of Pediatric Hematology/Oncology. 39(4). e227–e232. 1 indexed citations

13.

Qiao, Ying, Jiadi Wen, Sally Martell, et al.. (2016). Whole exome sequencing in recurrent early pregnancy loss. Molecular Human Reproduction. 22(5). 364–372. 69 indexed citations

14.

Qiao, Ying, Rita Colnaghi, Diana Alcantara, et al.. (2016). Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis. JCI Insight. 1(3). e85461–e85461. 23 indexed citations

15.

Koduru, Prasad, et al.. (2016). A unique rearrangement of PDGFRα and ETV6 in a patient with acute myeloid leukemia with myelodysplasia-related changes progressed from chronic myelomonocytic leukemia. 4(1). 1–1. 1 indexed citations

16.

Wen, Jiadi, Courtney W. Hanna, Sally Martell, et al.. (2015). Functional consequences of copy number variants in miscarriage. Molecular Cytogenetics. 8(1). 6–6. 15 indexed citations

17.

Qiao, Ying, Kajari Mondal, Valentina Trapani, et al.. (2013). Variant ATRX Syndrome with Dysfunction ofATRXandMAGT1Genes. Human Mutation. 35(1). 58–62. 8 indexed citations

18.

Wen, Jiadi, Fátima Lopes, Gabriela Soares, et al.. (2013). Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2. Orphanet Journal of Rare Diseases. 8(1). 100–100. 21 indexed citations

19.

Wen, Jiadi, Hua Zhu, & Colin D. MacCalman. (2008). Complex Regulatory Effects of Gonadal Steroids on the Expression Levels of the Distinct Aggrecanases Present in Human Endometrial Stromal Cells In Vitro.. Biology of Reproduction. 78(Suppl_1). 173–173. 1 indexed citations

20.

Wen, Jiadi, Hua Zhu, Shuko Murakami, Peter C. K. Leung, & Colin D. MacCalman. (2006). Regulation of A Disintegrin And Metalloproteinase with ThromboSpondin Repeats-1 Expression in Human Endometrial Stromal Cells by Gonadal Steroids Involves Progestins, Androgens, and Estrogens. The Journal of Clinical Endocrinology & Metabolism. 91(12). 4825–4835. 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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