Ji‐Qing Wei

1.5k total citations
18 papers, 1.1k citations indexed

About

Ji‐Qing Wei is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Urology. According to data from OpenAlex, Ji‐Qing Wei has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Endocrinology, Diabetes and Metabolism and 4 papers in Urology. Recurrent topics in Ji‐Qing Wei's work include Sexual Differentiation and Disorders (10 papers), Hormonal Regulation and Hypertension (5 papers) and Hormonal and reproductive studies (4 papers). Ji‐Qing Wei is often cited by papers focused on Sexual Differentiation and Disorders (10 papers), Hormonal Regulation and Hypertension (5 papers) and Hormonal and reproductive studies (4 papers). Ji‐Qing Wei collaborates with scholars based in United States, China and Croatia. Ji‐Qing Wei's co-authors include Maria I. New, Robert C. Wilson, Arlene Mercado, Madeleine D. Harbison, John W. Funder, Zygmunt S. Krozowski, Robert C. Wilson, C.H.L. Shackleton, Varuni Obeyesekere and Richard E. Neiberger and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Clinical Endocrinology & Metabolism and Journal of Chromatography A.

In The Last Decade

Ji‐Qing Wei

18 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ji‐Qing Wei United States 13 779 715 230 185 167 18 1.1k
Yue-Hua Huang China 6 181 0.2× 125 0.2× 74 0.3× 32 0.2× 18 0.1× 12 531
Inger Holmberg Sweden 19 302 0.4× 152 0.2× 80 0.3× 75 0.4× 42 0.3× 27 808
Ludwig Kornel United States 17 627 0.8× 217 0.3× 60 0.3× 115 0.6× 5 0.0× 57 866
J. K. McKenzie Canada 12 147 0.2× 173 0.2× 55 0.2× 23 0.1× 10 0.1× 24 586
Gail Galasko United States 11 139 0.2× 342 0.5× 27 0.1× 22 0.1× 34 0.2× 21 772
Asami Mori Japan 11 133 0.2× 256 0.4× 239 1.0× 43 0.2× 32 0.2× 17 549
Gregg D. Simonson United States 12 204 0.3× 151 0.2× 66 0.3× 94 0.5× 62 0.4× 32 556
Z. Zaman Belgium 13 22 0.0× 239 0.3× 107 0.5× 16 0.1× 43 0.3× 22 588
G. R. Cannell Australia 15 262 0.3× 73 0.1× 180 0.8× 39 0.2× 12 0.1× 28 619
Alfred Lohninger Austria 11 63 0.1× 219 0.3× 43 0.2× 32 0.2× 168 1.0× 30 568

Countries citing papers authored by Ji‐Qing Wei

Since Specialization
Citations

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

Fields of papers citing papers by Ji‐Qing Wei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ji‐Qing Wei. 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 Ji‐Qing Wei. The network helps show where Ji‐Qing Wei may publish in the future.

Co-authorship network of co-authors of Ji‐Qing Wei

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

All Works

18 of 18 papers shown
1.
Wei, Ji‐Qing, Zongyou Chen, Zheng‐Feng Wang, et al.. (2010). Isolation and characterization of polymorphic microsatellite loci in Camellia nitidissima Chi (Theaceae). American Journal of Botany. 97(10). e89–90. 9 indexed citations
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Chemaitilly, Wassim, Brian P. Betensky, I. Howard Marshall, et al.. (2005). The Natural History and Genotype-Phenotype Nonconcordance of HLA Identical Siblings with the Same Mutations of the 21-Hydroxylase Gene. Journal of Pediatric Endocrinology and Metabolism. 18(2). 143–53. 10 indexed citations
4.
Tükel, Turgut, Zehra Oya Uyguner, Ji‐Qing Wei, et al.. (2003). A Novel Semiquantitative Polymerase Chain Reaction/Enzyme Digestion-Based Method for Detection of Large Scale Deletions/Conversions of the CYP21 Gene and Mutation Screening in Turkish Families with 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 88(12). 5893–5897. 37 indexed citations
5.
New, Maria I., Ann D. Carlson, Jihad S. Obeid, et al.. (2003). Update: Prenatal Diagnosis for Congenital Adrenal Hyperplasia in 595 Pregnancies. The Endocrinologist. 13(3). 233–239. 18 indexed citations
6.
New, Maria I., Ann D. Carlson, Jihad S. Obeid, et al.. (2001). EXTENSIVE PERSONAL EXPERIENCE: Prenatal Diagnosis for Congenital Adrenal Hyperplasia in 532 Pregnancies. The Journal of Clinical Endocrinology & Metabolism. 86(12). 5651–5657. 147 indexed citations
7.
Nimkarn, Saroj, Barbara Cerame, Ji‐Qing Wei, et al.. (1999). Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) Without Demonstrable Genetic Mutations. The Journal of Clinical Endocrinology & Metabolism. 84(1). 378–381. 27 indexed citations
8.
Wilson, Robert, Madeleine D. Harbison, Ron S. Newfield, et al.. (1998). Examination of Genotype and Phenotype Relationships in 14 Patients with Apparent Mineralocorticoid Excess1. The Journal of Clinical Endocrinology & Metabolism. 83(7). 2244–2254. 138 indexed citations
9.
Wilson, Robert, Ji‐Qing Wei, Varuni Obeyesekere, et al.. (1998). A genetic defect resulting in mild low-renin hypertension. Proceedings of the National Academy of Sciences. 95(17). 10200–10205. 113 indexed citations
10.
Wilson, Robert C., Zygmunt S. Krozowski, Varuni Obeyesekere, et al.. (1995). A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess.. The Journal of Clinical Endocrinology & Metabolism. 80(7). 2263–2266. 162 indexed citations
11.
Wilson, Robert C., et al.. (1995). Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene.. The Journal of Clinical Endocrinology & Metabolism. 80(5). 1635–1640. 112 indexed citations
12.
Mercado, Arlene, et al.. (1995). Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency.. The Journal of Clinical Endocrinology & Metabolism. 80(7). 2014–2020. 138 indexed citations
13.
Wilson, Robert C., Madeleine D. Harbison, Z. Krozowski, et al.. (1995). Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess.. The Journal of Clinical Endocrinology & Metabolism. 80(11). 3145–3150. 119 indexed citations
14.
Wei, Ji‐Qing, et al.. (1992). Improved HPLC Determination of Plasma and Urine Oxalate in the Clinical Diagnostic Laboratory. Journal of Liquid Chromatography. 15(3). 501–511. 13 indexed citations
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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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