Fei‐Yu Han

828 total citations
11 papers, 654 citations indexed

About

Fei‐Yu Han is a scholar working on Neurology, Molecular Biology and Epidemiology. According to data from OpenAlex, Fei‐Yu Han has authored 11 papers receiving a total of 654 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Neurology, 5 papers in Molecular Biology and 3 papers in Epidemiology. Recurrent topics in Fei‐Yu Han's work include Neurofibromatosis and Schwannoma Cases (4 papers), Glycosylation and Glycoproteins Research (2 papers) and Neuroblastoma Research and Treatments (2 papers). Fei‐Yu Han is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (4 papers), Glycosylation and Glycoproteins Research (2 papers) and Neuroblastoma Research and Treatments (2 papers). Fei‐Yu Han collaborates with scholars based in Sweden, Canada and Belgium. Fei‐Yu Han's co-authors include Martin Ruttledge, Jan P. Dumanski, Ya‐Gang Xie, Myriam Peyrard, Ingegerd Fransson, Ian Dunham, Karen Rooke, Magnus Nordenskjöld, Denise A. Figlewicz and Guy A. Rouleau and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Human Molecular Genetics.

In The Last Decade

Fei‐Yu Han

11 papers receiving 641 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fei‐Yu Han Sweden	8	362	263	241	120	73	11	654
Tanya Basu United Kingdom	7	380 1.0×	191 0.7×	159 0.7×	113 0.9×	70 1.0×	18	686
Peter Dirks Canada	15	424 1.2×	295 1.1×	118 0.5×	84 0.7×	57 0.8×	31	935
Raimund Fahsold Germany	14	397 1.1×	344 1.3×	90 0.4×	128 1.1×	50 0.7×	27	777
Heli Ylä‐Outinen Finland	13	372 1.0×	121 0.5×	87 0.4×	137 1.1×	87 1.2×	22	660
Mary Jo Wenning United States	8	390 1.1×	182 0.7×	82 0.3×	79 0.7×	50 0.7×	9	581
Patricia Thompson United States	12	405 1.1×	571 2.2×	81 0.3×	69 0.6×	66 0.9×	22	1.1k
Donna C. Rich United States	7	241 0.7×	260 1.0×	89 0.4×	75 0.6×	24 0.3×	8	580
Silke Frahm Germany	8	431 1.2×	128 0.5×	82 0.3×	98 0.8×	24 0.3×	8	534
Mateusz Kolanczyk Germany	15	197 0.5×	315 1.2×	56 0.2×	114 0.9×	82 1.1×	23	680
Smita M. Purandare United States	11	207 0.6×	323 1.2×	59 0.2×	84 0.7×	35 0.5×	15	598

Countries citing papers authored by Fei‐Yu Han

Since Specialization

Citations

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

Fields of papers citing papers by Fei‐Yu Han

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fei‐Yu Han. 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 Fei‐Yu Han. The network helps show where Fei‐Yu Han may publish in the future.

Co-authorship network of co-authors of Fei‐Yu Han

This figure shows the co-authorship network connecting the top 25 collaborators of Fei‐Yu Han. A scholar is included among the top collaborators of Fei‐Yu Han 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 Fei‐Yu Han. Fei‐Yu Han 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:

11 of 11 papers shown

Aloyz, Raquel, Zhiyuan Xu, Josée Bergeron, et al.. (2002). Regulation of cisplatin resistance and homologous recombinational repair by the TFIIH subunit XPD.. PubMed. 62(19). 5457–62. 72 indexed citations

Peyrard, Myriam, Eyal Seroussi, Ann-Christin Sandberg-Nordqvist, et al.. (1999). The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family. Proceedings of the National Academy of Sciences. 96(2). 598–603. 97 indexed citations

Xie, Ya‐Gang, Daniel Rochefort, Bernard Brais, et al.. (1998). Restriction Map of a YAC and Cosmid Contig Encompassing the Oculopharyngeal Muscular Dystrophy Candidate Region on Chromosome 14q11.2–q13. Genomics. 52(2). 201–204. 7 indexed citations

Lafrenière, Ronald G., Zoha Kibar, Daniel Rochefort, et al.. (1997). Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3. Gene. 198(1-2). 313–321. 5 indexed citations

Rooke, Karen, Denise A. Figlewicz, Fei‐Yu Han, & Guy A. Rouleau. (1996). Analysis of the KSP repeat of the neurofilament heavy subunit in familial amyotrophic lateral sclerosis. Neurology. 46(3). 789–790. 55 indexed citations

Ruttledge, Martin, Anne Andermann, Catherine M. Phelan, et al.. (1996). Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.. PubMed. 59(2). 331–42. 196 indexed citations

Peyrard, Myriam, Ingegerd Fransson, Ya‐Gang Xie, et al.. (1994). Characterization of a new member of the human /-adaptin gene family from chromosome 22q12, a candidate meningioma gene. Human Molecular Genetics. 3(8). 1393–1399. 81 indexed citations

Ruttledge, Martin, Ya‐Gang Xie, Fei‐Yu Han, et al.. (1994). Physical Mapping of the NF2/Meningioma Region on Human Chromosome 22q12. Genomics. 19(1). 52–59. 11 indexed citations

Han, Fei‐Yu, et al.. (1994). Direct and inverted reciprocal chromosome insertions between chromosomes 7 and 14 in a woman with recurrent miscarriages. American Journal of Medical Genetics. 52(3). 349–351. 7 indexed citations

10.

Ruttledge, Martin, Ya‐Gang Xie, Fei‐Yu Han, et al.. (1994). Deletions on chromosome 22 in sporadic meningioma. Genes Chromosomes and Cancer. 10(2). 122–130. 101 indexed citations

11.

Han, Fei‐Yu, Martin Ruttledge, Ingegerd Fransson, et al.. (1993). Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12. Human Molecular Genetics. 2(9). 1361–1368. 22 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.

Explore authors with similar magnitude of impact