S. Nanko

509 total citations
11 papers, 285 citations indexed

About

S. Nanko is a scholar working on Genetics, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, S. Nanko has authored 11 papers receiving a total of 285 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Molecular Biology. Recurrent topics in S. Nanko's work include Genetics and Neurodevelopmental Disorders (3 papers), Genetic Associations and Epidemiology (2 papers) and Neurotransmitter Receptor Influence on Behavior (2 papers). S. Nanko is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genetic Associations and Epidemiology (2 papers) and Neurotransmitter Receptor Influence on Behavior (2 papers). S. Nanko collaborates with scholars based in Japan, United Kingdom and Ireland. S. Nanko's co-authors include Hiroshi Kunugi, Michael Gill, Peter McGuffin, David Collier, Robin Murray, M J Owen, Homero Vallada, Tao Li, Pak C. Sham and M J Arranz and has published in prestigious journals such as Molecular Psychiatry, Schizophrenia Research and American Journal of Medical Genetics.

In The Last Decade

S. Nanko

11 papers receiving 271 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Nanko Japan	6	157	97	94	78	53	11	285
Т. В. Лежейко Russia	10	96 0.6×	126 1.3×	68 0.7×	69 0.9×	49 0.9×	60	305
Johanna Daniels United Kingdom	7	176 1.1×	109 1.1×	41 0.4×	44 0.6×	38 0.7×	7	310
Margherita Comazzi Italy	9	215 1.4×	147 1.5×	211 2.2×	183 2.3×	49 0.9×	13	528
T Pathare Canada	7	76 0.5×	67 0.7×	138 1.5×	190 2.4×	107 2.0×	7	326
G. Shields United States	6	87 0.6×	52 0.5×	227 2.4×	106 1.4×	30 0.6×	14	341
Keith E. Dudleston United Kingdom	2	281 1.8×	99 1.0×	59 0.6×	99 1.3×	47 0.9×	5	424
Monica Conciatori Italy	6	176 1.1×	123 1.3×	235 2.5×	56 0.7×	136 2.6×	10	402
Ben Neale United Kingdom	5	102 0.6×	52 0.5×	157 1.7×	190 2.4×	22 0.4×	5	338
Tempei Ikegame Japan	7	104 0.7×	209 2.2×	68 0.7×	42 0.5×	42 0.8×	10	339
Gabrielle Allio France	6	52 0.3×	160 1.6×	155 1.6×	73 0.9×	78 1.5×	10	363

Countries citing papers authored by S. Nanko

Since Specialization

Citations

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

Fields of papers citing papers by S. Nanko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Nanko

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

All Works

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11 of 11 papers shown

Nanko, S.. (2001). [Molecular genetics of schizophrenia].. PubMed. 103(9). 698–701. 3 indexed citations

Kunugi, Hiroshi, et al.. (1999). Cytogenetic findings in 250 schizophrenics: evidence confirming an excess of the X chromosome aneuploidies and pericentric inversion of chromosome 9. Schizophrenia Research. 40(1). 43–47. 40 indexed citations

Rees, Mark I., Iain Fenton, Nigel Williams, et al.. (1999). Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry. 4(4). 353–359. 14 indexed citations

Laval, Steven H., Robert J. Butler, J. Loftus, et al.. (1998). Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome. American Journal of Medical Genetics. 81(5). 420–427. 80 indexed citations

Laval, Steven H., Robert J. Butler, J. Loftus, et al.. (1998). Evidence for linkage of psychosis and cerebral asymmetry to the centromeric region of the X chromosome. Schizophrenia Research. 29(1-2). 133–133. 1 indexed citations

Kunugi, Hiroshi, Homero Vallada, Pak C. Sham, et al.. (1997). Catechol-O-methyltransferase polymorphisms and schizophrenia. Psychiatric Genetics. 7(3). 97–102. 89 indexed citations

Walsh, Cathy, S. Nanko, Robin Murray, et al.. (1996). Linkage analysis of the fragile X gene FMR-1 and schizophrenia. Psychiatric Genetics. 6(2). 81–86. 9 indexed citations

Kunugi, Hiroshi, Homero Vallada, David Curtis, et al.. (1996). A transmission disequilibrium study on Catechol-O-Methyltransferase polymorphism in schizophrenia families. Schizophrenia Research. 18(2-3). 165–165. 1 indexed citations

Nanko, S. & Mineko Hattori. (1996). Association of neurotrophin-3 gene variant with severe forms of schizophrenia. European Neuropsychopharmacology. 6. 174–174. 2 indexed citations

10.

Shaikh, Saleem, Michael Gill, M J Owen, et al.. (1994). Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia. American Journal of Medical Genetics. 54(1). 8–11. 45 indexed citations

11.

Kunugi, Hiroshi, S. Nanko, N Takei, et al.. (1993). [Schizophrenia following prenatal exposure to influenza during second trimester].. PubMed. 95(6). 453–62. 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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