Shozo Ohdo

729 total citations
30 papers, 224 citations indexed

About

Shozo Ohdo is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shozo Ohdo has authored 30 papers receiving a total of 224 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shozo Ohdo's work include Congenital heart defects research (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (4 papers). Shozo Ohdo is often cited by papers focused on Congenital heart defects research (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (4 papers). Shozo Ohdo collaborates with scholars based in Japan. Shozo Ohdo's co-authors include Tohru Sonoda, Ken‐ichi Ohba, Kenji Kawaguchi, Hiroko Tsukamoto, Keisuke Hamada, Yutaka Hase, Tomoko Hasegawa, Shintaro Okada, Seiichi Sugama and Kenji Naritomi and has published in prestigious journals such as Clinical Genetics, Brain and Development and Analytical Letters.

In The Last Decade

Shozo Ohdo

28 papers receiving 218 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shozo Ohdo Japan 9 117 107 52 36 26 30 224
Patrick L. Wilmot United States 10 148 1.3× 95 0.9× 49 0.9× 18 0.5× 21 0.8× 26 238
Jean‐Pierre Fryns Belgium 9 113 1.0× 160 1.5× 57 1.1× 27 0.8× 64 2.5× 15 270
Koen Devriendt Belgium 9 137 1.2× 205 1.9× 61 1.2× 19 0.5× 17 0.7× 13 290
Sophie Julia France 12 241 2.1× 163 1.5× 42 0.8× 42 1.2× 26 1.0× 27 372
J. M. Cant� Mexico 11 220 1.9× 189 1.8× 81 1.6× 8 0.2× 37 1.4× 17 378
Fernando Santos Spain 9 228 1.9× 193 1.8× 84 1.6× 30 0.8× 23 0.9× 13 325
Marie‐Louise Bondeson Sweden 10 108 0.9× 202 1.9× 39 0.8× 15 0.4× 13 0.5× 13 305
Lailá Bastaki Kuwait 11 104 0.9× 142 1.3× 83 1.6× 28 0.8× 49 1.9× 35 308
Kevin D. Josephson United States 10 119 1.0× 135 1.3× 30 0.6× 30 0.8× 59 2.3× 14 256
Jack H. Jung Canada 13 208 1.8× 218 2.0× 83 1.6× 9 0.3× 30 1.2× 19 411

Countries citing papers authored by Shozo Ohdo

Since Specialization
Citations

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

Fields of papers citing papers by Shozo Ohdo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shozo Ohdo

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

All Works

20 of 20 papers shown
1.
Ono, Jiro, Tomoko Hasegawa, Seiichi Sugama, et al.. (1996). Partial deletion of the long arm of chromosome 11: ten Japanese children. Clinical Genetics. 50(6). 474–478. 31 indexed citations
3.
Matsuoka, Yuji, et al.. (1992). Cardiovascular anomalies in chick embryos produced by bis‐diamine in dimethylsulfoxide. Teratology. 45(2). 155–162. 8 indexed citations
4.
Ohdo, Shozo, et al.. (1992). Etiologic and Pathogenetic Study of Mental Retardation with Multiple Congenital Anomalies. Pediatrics International. 34(2). 144–150. 7 indexed citations
5.
Sonoda, Tohru, et al.. (1991). 9p Deletion and distal 9q duplication due to a paternal pericentric inversion 9(p22q32). The Japanese Journal of Human Genetics. 36(1). 111–116. 5 indexed citations
6.
Sonoda, Tohru, et al.. (1990). Teratogenic Effects of Sodium Valproate in the Jcl: ICR Mouse Fetus. Pediatrics International. 32(5). 502–507. 11 indexed citations
7.
Ohdo, Shozo, et al.. (1990). Association of cephalic neural crest cells with cardiovascular development, particularly that of the semilunar valves. Anatomy and Embryology. 182(3). 263–72. 32 indexed citations
8.
Ohba, Ken‐ichi, et al.. (1989). Acromesomelic Dysplasia in a Father and Son: Autosomal Dominant Inheritance. Pediatrics International. 31(5). 595–599. 1 indexed citations
9.
Ohdo, Shozo, et al.. (1989). Infantile Autism and the Fragile X Syndrome in Japanese Children. Pediatrics International. 31(2). 163–165. 4 indexed citations
10.
Sonoda, Tohru, et al.. (1989). Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion 5(p15.1q35.1). The Japanese Journal of Human Genetics. 34(2). 129–134. 9 indexed citations
11.
Naritomi, Kenji, et al.. (1988). Proximal 3p Deletion: Case Report and Review of the Literature. Pediatrics International. 30(1). 78–83. 11 indexed citations
12.
Sonoda, Tohru, et al.. (1987). Clinical and Postmortem Findings of Two Cases With Karyotype: 48, XXX, +18. Pediatrics International. 29(1). 173–177. 4 indexed citations
13.
Ohdo, Shozo, et al.. (1987). Association of Severe Microcephaly, Short Palpebral Fissures, Micrognathia, Growth Retardation and Early Death: A New Syndrome. Pediatrics International. 29(1). 186–188. 1 indexed citations
14.
Ohdo, Shozo, et al.. (1986). Incidence and Etiology of Mental Retardation in Patients with Congenital Heart Disease. Pediatrics International. 28(1). 31–37.
15.
Ohdo, Shozo, et al.. (1986). Pathogenesis of Persistent Truncus Arteriosus Produced by Bis‐Diamine in Rats. Pediatrics International. 28(3). 403–418. 4 indexed citations
16.
Ohdo, Shozo, et al.. (1985). Pathogenesis of a Bisdiamine‐Induced Malformation Complex in Rat Resembling DiGeorge Syndrome. Congenital Anomalies. 25(1). 29–44. 11 indexed citations
17.
Ohdo, Shozo, et al.. (1984). Association of Hirschsprung Disease and Bilateral Preaxial Polydactyly. Pediatrics International. 26(2). 255–261. 1 indexed citations
18.
Ohdo, Shozo, et al.. (1984). Congenital Heart Disease in a Case with Fetal Alcohol Syndrome: Clinical And Postmortem Findings. Pediatrics International. 26(2). 241–247. 2 indexed citations
19.
Ohdo, Shozo, et al.. (1983). Association ofectodermal dysplasia, ectrodactyly, andmacular dystrophy: theEEM syndrome. 1 indexed citations
20.
Hamada, Keisuke, et al.. (1979). Incontinentia pigmenti achromians as part of a neurocutaneous syndrome: A case report. Brain and Development. 1(4). 313–317. 11 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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