Fengxia Xiao

540 total citations
24 papers, 394 citations indexed

About

Fengxia Xiao is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Fengxia Xiao has authored 24 papers receiving a total of 394 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Fengxia Xiao's work include BRCA gene mutations in cancer (6 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic factors in colorectal cancer (5 papers). Fengxia Xiao is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic factors in colorectal cancer (5 papers). Fengxia Xiao collaborates with scholars based in United States, China and Macao. Fengxia Xiao's co-authors include Xueliang Wang, Tao Wang, Hongying Li, San Ming Wang, Dennis E. Bulman, Lemuel Racacho, Yeong C. Kim, Michel Panisset, David A. Grimes and Fabin Han and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Cancer.

In The Last Decade

Fengxia Xiao

24 papers receiving 385 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fengxia Xiao United States	11	178	131	68	62	56	24	394
Dekang Liu China	10	200 1.1×	29 0.2×	19 0.3×	54 0.9×	57 1.0×	43	425
Jiaqi Yao China	13	520 2.9×	35 0.3×	141 2.1×	31 0.5×	9 0.2×	29	731
Laura M. Williamson Canada	9	414 2.3×	44 0.3×	17 0.3×	34 0.5×	6 0.1×	15	548
Yihao Wang China	9	99 0.6×	10 0.1×	11 0.2×	63 1.0×	35 0.6×	24	263
Alessia Nasca Italy	15	535 3.0×	68 0.5×	55 0.8×	10 0.2×	4 0.1×	27	605
Markus Fußer Norway	12	416 2.3×	23 0.2×	94 1.4×	8 0.1×	8 0.1×	15	506
Imen Dorboz France	14	492 2.8×	94 0.7×	59 0.9×	23 0.4×	2 0.0×	30	650
Nadimpalli Ravi S. Varma United States	10	219 1.2×	29 0.2×	20 0.3×	7 0.1×	6 0.1×	13	514
Mingyang Cai China	11	163 0.9×	36 0.3×	10 0.1×	14 0.2×	8 0.1×	29	264
Satadru K. Lahiri United States	14	420 2.4×	79 0.6×	29 0.4×	3 0.0×	7 0.1×	29	580

Countries citing papers authored by Fengxia Xiao

Since Specialization

Citations

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

Fields of papers citing papers by Fengxia Xiao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fengxia Xiao

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Li, Jiaheng, Siddharth Sinha, Fengxia Xiao, et al.. (2024). Pathogenic variants in human DNA damage repair genes mostly arose in recent human history. BMC Cancer. 24(1). 415–415. 3 indexed citations

Li, Jiaheng, et al.. (2024). Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes. Human Genomics. 18(1). 5–5. 2 indexed citations

Xiao, Fengxia, et al.. (2023). Evolutionary Origin of MUTYH Germline Pathogenic Variations in Modern Humans. Biomolecules. 13(3). 429–429. 3 indexed citations

Li, Jiaheng, et al.. (2023). TP53 germline pathogenic variants in modern humans were likely originated during recent human history. NAR Cancer. 5(3). zcad025–zcad025. 5 indexed citations

Xiao, Fengxia, et al.. (2022). Elevated β-catenin and C-myc promote malignancy, relapse, and indicate poor prognosis in patients with relapsed glioma. Journal of Cancer Research and Therapeutics. 18(2). 553–559. 3 indexed citations

Li, Hongying, Xueliang Wang, Tao Wang, & Fengxia Xiao. (2020). A facile, green and time-saving method to prepare partially crystalline NiFe layered double hydroxide nanosheets on nickel foam for superior OER catalysis. Journal of Alloys and Compounds. 844. 156224–156224. 68 indexed citations

Wang, Qiang, et al.. (2019). Risk Factors for Cognitive Impairment in High-Grade Glioma Patients Treated with Postoperative Radiochemotherapy. Cancer Research and Treatment. 52(2). 586–593. 15 indexed citations

Kim, Yeong C., Jian Cui, Jiangtao Luo, et al.. (2016). Exome-based Variant Detection in Core Promoters. Scientific Reports. 6(1). 30716–30716. 4 indexed citations

Downs, Bradley M., Yeong C. Kim, Fengxia Xiao, et al.. (2015). Two PALB2 germline mutations found in both BRCA1+ and BRCAx familial breast cancer. Breast Cancer Research and Treatment. 151(1). 219–224. 1 indexed citations

10.

Xiao, Fengxia, Yeong C. Kim, Carrie Snyder, et al.. (2014). Genome instability in blood cells of a BRCA1 + breast cancer family. BMC Cancer. 14(1). 342–342. 7 indexed citations

11.

Wen, Hongxiu, Yeong C. Kim, Carrie Snyder, et al.. (2014). Family-specific, novel, deleterious germline variants provide a rich resource to identify genetic predispositions for BRCAx familial breast cancer. BMC Cancer. 14(1). 470–470. 15 indexed citations

12.

Xiao, Fengxia, et al.. (2014). Asymmetric dimethyl-arginine metabolism in a murine model of cigarette smoke-mediated lung inflammation. Journal of Immunotoxicology. 12(3). 273–282. 14 indexed citations

13.

Xiao, Fengxia, Yeong C. Kim, Hongxiu Wen, et al.. (2013). The Genome of Polymorphonuclear Neutrophils Maintains Normal Coding Sequences. PLoS ONE. 8(11). e78685–e78685. 1 indexed citations

14.

Wen, Hongxiu, Yongjin Li, Sami N. Malek, et al.. (2012). New Fusion Transcripts Identified in Normal Karyotype Acute Myeloid Leukemia. PLoS ONE. 7(12). e51203–e51203. 25 indexed citations

15.

Racacho, Lemuel, Sarah M. Nikkel, Fengxia Xiao, et al.. (2010). Mutations in GDF5 presenting as semidominant brachydactyly A1. Human Mutation. 31(10). 1155–1162. 21 indexed citations

16.

Yotova, Vania, et al.. (2004). Polymorphisms within a polymorphism: SNPs in and around a polymorphic Alu insertion in intron 44 of the human dystrophin gene. Journal of Human Genetics. 49(5). 269–272. 3 indexed citations

17.

Xiao, Fengxia, Vania Yotova, Ewa Ziętkiewicz, et al.. (2003). Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contacts. European Journal of Human Genetics. 12(4). 301–311. 17 indexed citations

18.

Xiao, Fengxia, Junfang Yang, Jean‐Jacques Cassiman, & Ronny Decorte. (2002). Diversity at Eight Polymorphic Alu Insertion Loci in Chinese Populations Shows Evidence for European Admixture in an Ethnic Minority Population from Northwest China. Human Biology. 74(4). 555–568. 23 indexed citations

19.

Xiao, Fengxia, et al.. (1998). Genetic data obtained for two Chinese Han populations with a quadruplex fluorescent STR typing system (HUMVWA, HUMTH01, D21S11 and HPRT). International Journal of Legal Medicine. 111(6). 343–345. 4 indexed citations

20.

Xiao, Fengxia, Anja Gilissen, J.J. Cassiman, & Ronny Decorte. (1998). Quadruplex fluorescent STR typing system (HUMVWA, HUMTH01, D21S11 and HPRT) with sequence-defined allelic ladders. Forensic Science International. 94(1-2). 39–46. 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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