This map shows the geographic impact of A Amemiya'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 A Amemiya with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Amemiya more than expected).
This network shows the impact of papers produced by A Amemiya. 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 A Amemiya. The network helps show where A Amemiya may publish in the future.
Co-authorship network of co-authors of A Amemiya
This figure shows the co-authorship network connecting the top 25 collaborators of A Amemiya.
A scholar is included among the top collaborators of A Amemiya 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 A Amemiya. A Amemiya is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Progressive Myoclonus Epilepsy, Lafora Type -- GeneReviews®.
9.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). 15q24 Microdeletion Syndrome -- GeneReviews(®).1 indexed citations
10.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Hypertrophic Cardiomyopathy Overview -- GeneReviews®.1 indexed citations
11.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Mitochondrial DNA-Associated Leigh Syndrome and NARP -- GeneReviews®.3 indexed citations
12.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Alpha-Thalassemia -- GeneReviews(®).
13.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Gaucher Disease -- GeneReviews(®).4 indexed citations
14.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Autosomal Dominant Nocturnal Frontal Lobe Epilepsy -- GeneReviews(®).2 indexed citations
15.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Rothmund-Thomson Syndrome -- GeneReviews®.1 indexed citations
16.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). MED12-Related Disorders -- GeneReviews®.
17.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Polymicrogyria Overview -- GeneReviews®.1 indexed citations
18.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Spinal Muscular Atrophy, X-Linked Infantile -- GeneReviews(®).1 indexed citations
19.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Primary Ciliary Dyskinesia -- GeneReviews(®).
20.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Hemophagocytic Lymphohistiocytosis, Familial -- GeneReviews(®).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.