Ichiro Murano

529 total citations
26 papers, 340 citations indexed

About

Ichiro Murano is a scholar working on Genetics, Molecular Biology and Virology. According to data from OpenAlex, Ichiro Murano has authored 26 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Virology. Recurrent topics in Ichiro Murano's work include Genomic variations and chromosomal abnormalities (6 papers), Bartonella species infections research (4 papers) and Rabies epidemiology and control (4 papers). Ichiro Murano is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Bartonella species infections research (4 papers) and Rabies epidemiology and control (4 papers). Ichiro Murano collaborates with scholars based in Japan and United States. Ichiro Murano's co-authors include Tadashi Kajii, Akira Kuwano, Masato Tsukahara, A. Kuwano, Shinya Matsuura, Hirofumi Ohashi, Tadashi Kaname, Takashi Muramatsu, Hidehiro Tsuneoka and Masashi Uchida and has published in prestigious journals such as Journal of Clinical Microbiology, Genomics and Human Genetics.

In The Last Decade

Ichiro Murano

24 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ichiro Murano Japan	10	172	167	56	42	42	26	340
Paula Embury United States	10	53 0.3×	106 0.6×	24 0.4×	24 0.6×	60 1.4×	20	369
Heidi Gildersleeve United States	7	176 1.0×	400 2.4×	20 0.4×	12 0.3×	27 0.6×	8	667
Frédéric Eberlé France	6	60 0.3×	136 0.8×	28 0.5×	11 0.3×	7 0.2×	9	363
Robin Mueller United States	10	159 0.9×	270 1.6×	22 0.4×	4 0.1×	30 0.7×	14	381
Selina Pasquero Italy	8	25 0.1×	98 0.6×	47 0.8×	14 0.3×	13 0.3×	14	290
Robert Radeke United States	6	188 1.1×	252 1.5×	32 0.6×	25 0.6×	3 0.1×	11	412
Elizabeth J. Lawrence United States	11	52 0.3×	224 1.3×	178 3.2×	12 0.3×	19 0.5×	18	429
Karen Russell United States	9	176 1.0×	172 1.0×	3 0.1×	15 0.4×	33 0.8×	14	389
Mona Abed Israel	11	63 0.4×	316 1.9×	35 0.6×	32 0.8×	6 0.1×	16	390
Débora M. Portilho France	13	32 0.2×	252 1.5×	71 1.3×	12 0.3×	6 0.1×	18	400

Countries citing papers authored by Ichiro Murano

Since Specialization

Citations

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

Fields of papers citing papers by Ichiro Murano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ichiro Murano

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

All Works

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20 of 20 papers shown

Murano, Ichiro. (2020). Oculocerebrofacial syndrome, Kaufman type. Definitions. 339–339.

Murano, Ichiro, et al.. (2001). Two Patients with Bartonella henselae Infection from a Dog. Kansenshogaku zasshi. 75(9). 808–811. 8 indexed citations

Murano, Ichiro, et al.. (2001). GIANT HEPATIC GRANULOMA CAUSED BY BARTONELLA HENSELAE. The Pediatric Infectious Disease Journal. 20(3). 319–320. 7 indexed citations

Tsukahara, Masato, et al.. (2000). Bartonella henselae Infection as a Cause of Fever of Unknown Origin. Journal of Clinical Microbiology. 38(5). 1990–1991. 33 indexed citations

Murano, Ichiro, et al.. (1999). Three Children with Systemic Cat Scratch Disease. Kansenshogaku zasshi. 73(3). 248–252.

Tsukahara, Masato, et al.. (1995). Interstitial deletion of 8p: report of two patients and review of the literature. Clinical Genetics. 48(1). 41–45. 8 indexed citations

Murano, Ichiro, Masato Tsukahara, Tadashi Kajii, & Akira Yoshida. (1994). Mapping of the Human Guanosine Monophosphate Reductase Gene (GMPR) to Chromosome 6p23 by Fluorescence in Situ Hybridization. Genomics. 19(1). 179–180. 6 indexed citations

Pinkel, Daniel, et al.. (1994). Detection of a human chromosomal translocation t(8;9) in a baby with multiple malformations using two‐color fluorescence in situ hybridization. Pathology International. 44(2). 145–150. 1 indexed citations

Kaname, Tadashi, et al.. (1993). Midkine Gene (MDK), a Gene for Prenatal Differentiation and Neuroregulation, Maps to Band 11p11.2 by Fluorescence in Situ Hybridization. Genomics. 17(2). 514–515. 44 indexed citations

10.

Ohashi, Hirofumi, Masato Tsukahara, Ichiro Murano, et al.. (1993). Premature aging and immunodeficiency: Mulvihill‐Smith syndrome?. American Journal of Medical Genetics. 45(5). 597–600. 20 indexed citations

11.

Ohashi, Hirofumi, Masato Tsukahara, Ichiro Murano, et al.. (1992). Pigmentary dysplasias and chromosomal mosaicism: Report of 9 cases. American Journal of Medical Genetics. 43(4). 716–721. 34 indexed citations

12.

Matsuda, Yukihisa, et al.. (1991). Cardio‐Facio‐cutaneous (CFC) syndrome: Report of two patients without hyperkeratotic skin lesions. American Journal of Medical Genetics. 39(2). 144–147. 16 indexed citations

13.

Kishi, Fumio, et al.. (1991). Prenatal diagnosis of infantile hypophosphatasia. Prenatal Diagnosis. 11(5). 305–309. 9 indexed citations

14.

Murano, Ichiro, et al.. (1991). Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two cases. Clinical Genetics. 39(1). 68–74. 6 indexed citations

15.

Kuwano, Akira, Ichiro Murano, & Tadashi Kajii. (1990). Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts. Human Genetics. 84(6). 527–31. 7 indexed citations

16.

Murakami, Toshio, et al.. (1990). Chronic Nephritis, Sensorineural Deafness, Growth and Developmental Retardation, Hyperkinesis, and Cleft Soft Palate in a 5-Year-Old Boy. The Nephron journals/Nephron journals. 56(2). 214–217. 2 indexed citations

17.

Murano, Ichiro, Akira Kuwano, & Tadashi Kajii. (1989). Cell type-dependent difference in the distribution and frequency of aphidicolin-induced fragile sites: T and B lymphocytes and bone marrow cells. Human Genetics. 84(1). 71–74. 27 indexed citations

18.

Murano, Ichiro, A. Kuwano, & Tadashi Kajii. (1989). Fibroblast-specific common fragile sites induced by aphidicolin. Human Genetics. 83(1). 45–48. 48 indexed citations

19.

Matsumoto, Tadashi, Tatsuro Kondoh, Kenji Fujieda, et al.. (1988). Complex glycerol kinase deficiency: Molecular‐genetic, cytogenetic, and clinical studies of five Japanese patients. American Journal of Medical Genetics. 31(3). 603–616. 17 indexed citations

20.

Kajii, Tadashi & Ichiro Murano. (1984). A 7q-son of an XYY father. The Japanese Journal of Human Genetics. 29(3). 387–389. 4 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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