Kun Ma

1.1k total citations
9 papers, 798 citations indexed

About

Kun Ma is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Kun Ma has authored 9 papers receiving a total of 798 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Reproductive Medicine. Recurrent topics in Kun Ma's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Sperm and Testicular Function (6 papers) and Chromosomal and Genetic Variations (4 papers). Kun Ma is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Sperm and Testicular Function (6 papers) and Chromosomal and Genetic Variations (4 papers). Kun Ma collaborates with scholars based in United Kingdom, United States and Australia. Kun Ma's co-authors include Ann C. Chandley, Jonathan Wolfe, Kay Taylor, Howard J. Cooke, R.M. Speed, T. B. Hargreave, Andrew Sharkey, Wendy A. Bickmore, Robert E. Hill and E.J. Thomson and has published in prestigious journals such as Cell, Nature Genetics and Fertility and Sterility.

In The Last Decade

Kun Ma

9 papers receiving 749 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kun Ma United Kingdom	8	671	543	433	176	67	9	798
Guy Longepied France	14	606 0.9×	525 1.0×	387 0.9×	99 0.6×	123 1.8×	17	807
Áine Rattigan United Kingdom	10	394 0.6×	274 0.5×	167 0.4×	91 0.5×	65 1.0×	10	483
Barbara Arredi Italy	9	633 0.9×	356 0.7×	373 0.9×	55 0.3×	136 2.0×	11	840
C. Boucekkine France	10	592 0.9×	580 1.1×	313 0.7×	62 0.4×	37 0.6×	18	758
Danièle Carré‐Eusèbe France	9	494 0.7×	414 0.8×	300 0.7×	37 0.2×	177 2.6×	11	683
Anthony D. Krentz United States	10	390 0.6×	397 0.7×	135 0.3×	161 0.9×	84 1.3×	14	677
Paulo Navarro‐Costa Portugal	9	281 0.4×	302 0.6×	269 0.6×	51 0.3×	136 2.0×	13	466
M Hartung France	16	260 0.4×	465 0.9×	63 0.1×	245 1.4×	70 1.0×	36	640
A.C. Chandley United Kingdom	8	324 0.5×	217 0.4×	71 0.2×	199 1.1×	19 0.3×	8	435

Countries citing papers authored by Kun Ma

Since Specialization

Citations

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

Fields of papers citing papers by Kun Ma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kun Ma

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

All Works

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9 of 9 papers shown

1.

Speed, R.M., et al.. (2003). Meiotic Chromosome Preparation. Humana Press eBooks. 29. 27–40. 3 indexed citations

2.

Bhasin, Shalender, Con Mallidis, & Kun Ma. (2000). The genetic basis of infertility in men. Best Practice & Research Clinical Endocrinology & Metabolism. 14(3). 363–388. 21 indexed citations

3.

Cram, David S., Kun Ma, Shalender Bhasin, et al.. (2000). Y chromosome analysis of infertile men and their sons conceived through intracytoplasmic sperm injection: vertical transmission of deletions and rarity of de novo deletions. Fertility and Sterility. 74(5). 909–915. 106 indexed citations

4.

Bhasin, Shalender, et al.. (1998). THE GENETIC BASIS OF MALE INFERTILITY. Endocrinology and Metabolism Clinics of North America. 27(4). 783–805. 45 indexed citations

5.

Delbridge, Margaret L., Kun Ma, Makam N. Subbarao, et al.. (1998). Evolution of mammalian HNRPG and its relationship with the putative azoospermia factor RBM. Mammalian Genome. 9(2). 168–170. 14 indexed citations

6.

Delbridge, Margaret L., Jenny L. Harry, Roland Toder, et al.. (1997). A human candidate spermatogenesis gene, RBM1, is conserved and amplified on the marsupial Y chromosome. Nature Genetics. 15(2). 131–136. 87 indexed citations

7.

Schempp, W., Joachim Arnemann, Kun Ma, et al.. (1995). Comparative mapping ofYRRM- andTSPY-related cosmids in man and hominoid apes. Chromosome Research. 3(4). 227–234. 81 indexed citations

8.

Ma, Kun, John D. Inglis, Andrew Sharkey, et al.. (1993). A Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesis. Cell. 75(7). 1287–1295. 421 indexed citations

9.

Shi, Liming, et al.. (1988). Synaptonemal complex formation among supernumerary B chromosomes: an electron microscopic study on spermatocytes of Chinese raccoon dogs. Chromosoma. 97(2). 178–183. 20 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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