Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
Etude au microscope électronique de plasmas contenant de l’acide désoxyribonucléique
This map shows the geographic impact of A Ryter'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 Ryter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Ryter more than expected).
This network shows the impact of papers produced by A Ryter. 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 Ryter. The network helps show where A Ryter may publish in the future.
Co-authorship network of co-authors of A Ryter
This figure shows the co-authorship network connecting the top 25 collaborators of A Ryter.
A scholar is included among the top collaborators of A Ryter 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 Ryter. A Ryter is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Benoliel, A M, Christian Capo, Pierre Bongrand, A Ryter, & R Depieds. (1980). Non-specific binding by macrophages: existence of different adhesive mechanisms and modulation by metabolic inhibitors.. PubMed. 41(3). 547–60.32 indexed citations
12.
Ryter, A. (1974). [Comparison between mode of incorporation of DAP into murein and insertion of lambda phage receptor into the external membrane of E. coli].. PubMed. 125 B(2). 167–80.1 indexed citations
13.
Ryter, A. (1973). [Autoradiographic study of the replication state in the sporangium and spore nucleus of Bacillus subtilis].. PubMed. 124(1). 1–19.2 indexed citations
14.
Millet, J & A Ryter. (1972). [Mutants of Bacillus subtilis Marburg with late blockage in their sporulation].. PubMed. 122(3). 395–406.5 indexed citations
15.
Giroud, P, et al.. (1971). [Positive sero-reactions with the neorickettsial group (Bedsonia, Cytoecetes phagocytaphilia) observed in animals parasitized with Anaplasma, Babesia, Theileria, in different countries: Oriental and Central Africa, Madagascar, Iran, Sardinia, France].. PubMed. 63(6). 630–5.1 indexed citations
Ryter, A, et al.. (1967). Ségrégation des noyaux pendant la croissance et la germination de B. subtilis.. Comptes rendus hebdomadaires des séances de l Académie des sciences. 264(18).4 indexed citations
Ryter, A, et al.. (1966). [Intracellular localization ribonucleic acids synthesized during sporulation in Bacillus subtilis].. PubMed. 262(11). 1305–7.3 indexed citations
20.
Pillot, Jean‐Paul, P. Dupouey, & A Ryter. (1964). [THE SIGNIFICANCE OF ATYPICAL FORMS AND THE NOTION OF EVOLUTIVE CYCLE IN THE SPIROCHETES].. PubMed. 107. 663–77.7 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.