N. Fang

2.4k total citations
6 papers, 150 citations indexed

About

N. Fang is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, N. Fang has authored 6 papers receiving a total of 150 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pathology and Forensic Medicine. Recurrent topics in N. Fang's work include Genetic Associations and Epidemiology (2 papers), Advanced Numerical Analysis Techniques (1 paper) and Genomics and Rare Diseases (1 paper). N. Fang is often cited by papers focused on Genetic Associations and Epidemiology (2 papers), Advanced Numerical Analysis Techniques (1 paper) and Genomics and Rare Diseases (1 paper). N. Fang collaborates with scholars based in United States. N. Fang's co-authors include R Mayer, Joseph G. Hacia, Francis S. Collins, Dennis D. Weisenburger, Jamés O. Armitage, Julie M. Vose, Wing C. Chan, Lynette M. Smith, Donald W. Hadley and M. Hoff and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biological Psychiatry and Human Molecular Genetics.

In The Last Decade

N. Fang

6 papers receiving 147 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
N. Fang United States	5	74	54	41	40	16	6	150
M. Elizabeth McCready Canada	10	80 1.1×	120 2.2×	17 0.4×	22 0.6×	10 0.6×	25	254
Laurence Faivre France	6	117 1.6×	188 3.5×	15 0.4×	14 0.3×	6 0.4×	7	252
Stefano Petrocchi Italy	8	84 1.1×	129 2.4×	12 0.3×	16 0.4×	5 0.3×	15	236
Jianhong Hu United States	10	136 1.8×	80 1.5×	12 0.3×	12 0.3×	4 0.3×	17	206
Simone Heidemann Germany	7	66 0.9×	96 1.8×	16 0.4×	25 0.6×	6 0.4×	14	140
Donald J. McGuire United States	8	54 0.7×	13 0.2×	41 1.0×	15 0.4×	10 0.6×	16	195
Katalin Szakszon Hungary	10	178 2.4×	103 1.9×	14 0.3×	17 0.4×	10 0.6×	29	276
P. Ceverha	2	51 0.7×	42 0.8×	14 0.3×	17 0.4×	4 0.3×	6	96
Sylvia Redon France	8	139 1.9×	158 2.9×	23 0.6×	16 0.4×	3 0.2×	12	227
Joshua L. Deignan United States	7	79 1.1×	155 2.9×	12 0.3×	27 0.7×	9 0.6×	8	249

Countries citing papers authored by N. Fang

Since Specialization

Citations

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

Fields of papers citing papers by N. Fang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Fang

This figure shows the co-authorship network connecting the top 25 collaborators of N. Fang. A scholar is included among the top collaborators of N. Fang 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 N. Fang. N. Fang 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:

6 of 6 papers shown

1.

Fang, N., Timothy C. Greiner, Dennis D. Weisenburger, et al.. (2003). Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma. Proceedings of the National Academy of Sciences. 100(9). 5372–5377. 76 indexed citations

2.

Hacia, Joseph G., et al.. (2000). Oligonucleotide microarray based detection of repetitive sequence changes. Human Mutation. 16(4). 354–363. 19 indexed citations

3.

Coon, Hilary, M. Hoff, John Holik, et al.. (1996). Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression. Biological Psychiatry. 39(8). 689–696. 42 indexed citations

4.

Fang, N., Hilary Coon, M. Hoff, et al.. (1995). Search for a schizophrenia susceptibility gene on chromosome 18. Psychiatric Genetics. 5(1). 31–36. 6 indexed citations

5.

Gregor, Paul, M. Hoff, John Holik, et al.. (1994). Dinucleotide repeat polymorphism in the human taurine transporter gene (TAUT). Human Molecular Genetics. 3(12). 2263–2263. 6 indexed citations

6.

Tai, C. T. & N. Fang. (1991). A systematic treatment of vector analysis. IEEE Transactions on Education. 34(2). 167–174. 1 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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