P.S.N. Menon

991 total citations
9 papers, 337 citations indexed

About

P.S.N. Menon is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, P.S.N. Menon has authored 9 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Sensory Systems and 3 papers in Genetics. Recurrent topics in P.S.N. Menon's work include Hearing, Cochlea, Tinnitus, Genetics (3 papers), RNA regulation and disease (2 papers) and Insect and Arachnid Ecology and Behavior (2 papers). P.S.N. Menon is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (3 papers), RNA regulation and disease (2 papers) and Insect and Arachnid Ecology and Behavior (2 papers). P.S.N. Menon collaborates with scholars based in India, Pakistan and United States. P.S.N. Menon's co-authors include Manju Ghosh, Madhulika Kabra, Shivaram Shastri, Saima Riazuddin, Sheikh Riazuddin, Thomas B. Friedman, Zubair M. Ahmed, Edward R. Wilcox, Tenesha N. Smith and Tomoko Makishima and has published in prestigious journals such as Cellular and Molecular Life Sciences, Hydrobiologia and Human Genetics.

In The Last Decade

P.S.N. Menon

9 papers receiving 326 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P.S.N. Menon India	6	198	197	66	58	42	9	337
W. J. Kimberling United States	8	126 0.6×	167 0.8×	80 1.2×	94 1.6×	27 0.6×	19	374
Leenamaija Pakarinen Finland	7	334 1.7×	299 1.5×	72 1.1×	43 0.7×	25 0.6×	9	463
Barbara Günther Austria	7	277 1.4×	180 0.9×	58 0.9×	51 0.9×	16 0.4×	9	343
Nathalie Pallarès-Ruiz France	8	279 1.4×	262 1.3×	81 1.2×	41 0.7×	92 2.2×	13	440
Christy B. Erbe United States	11	126 0.6×	108 0.5×	56 0.8×	13 0.2×	24 0.6×	24	317
Valérie Faugère France	14	438 2.2×	277 1.4×	83 1.3×	85 1.5×	11 0.3×	21	550
Marzieh Mohseni Iran	13	259 1.3×	223 1.1×	125 1.9×	120 2.1×	8 0.2×	37	470
Mariem Ben Saïd Tunisia	11	174 0.9×	214 1.1×	101 1.5×	95 1.6×	11 0.3×	26	369
Shaked Shivatzki Israel	10	249 1.3×	162 0.8×	46 0.7×	25 0.4×	26 0.6×	16	462
Xue Gao China	13	223 1.1×	301 1.5×	133 2.0×	44 0.8×	18 0.4×	50	428

Countries citing papers authored by P.S.N. Menon

Since Specialization

Citations

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

Fields of papers citing papers by P.S.N. Menon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P.S.N. Menon

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

9 of 9 papers shown

1.

Shastri, Shivaram, Madhulika Kabra, Sushil Kumar Kabra, Ravindra Mohan Pandey, & P.S.N. Menon. (2007). Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India. Journal of Cystic Fibrosis. 7(2). 110–115. 39 indexed citations

2.

Maheshwari, M., et al.. (2003). Screening of families with autosomal recessive non‐syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario. American Journal of Medical Genetics Part A. 120A(2). 180–184. 55 indexed citations

3.

Ahmed, Zubair M., Tenesha N. Smith, Saima Riazuddin, et al.. (2002). Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC. Human Genetics. 110(6). 527–531. 125 indexed citations

4.

Mathur, Roli, Geeta Singh, Deepika Deka, et al.. (2002). Rapid prenatal karyotyping using foetal blood obtained by cordocentesis.. PubMed. 15(2). 75–7. 7 indexed citations

5.

Ghosh, Manju, Saima Riazuddin, Sadaf Naz, et al.. (2001). Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome. Human Genetics. 109(5). 535–541. 94 indexed citations

6.

Menon, P.S.N.. (1969). Population ecology of Gammarus lacustris sars in Big Island Lake. I Habitat preference and relative abundance. Hydrobiologia. 33(1). 14–32. 10 indexed citations

7.

Menon, P.S.N.. (1959). On the chromosome behaviour in a membracid,Leptocentrus substitutus Walk.. Genetica. 29(1). 312–318. 2 indexed citations

8.

Menon, P.S.N.. (1958). Studies on the Chromosome Behaviour in Three Species of Indian Homoptera. Caryologia. 11(1). 57–67. 4 indexed citations

9.

Menon, P.S.N.. (1955). On the multiple sex chromosome mechanism in a lygaeid,Oxycarenus hyalinipennis (Costa). Cellular and Molecular Life Sciences. 11(12). 483–485. 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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