Arthur Robinson

6.5k total citations · 1 hit paper
134 papers, 4.5k citations indexed

About

Arthur Robinson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Arthur Robinson has authored 134 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Genetics, 51 papers in Molecular Biology and 34 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Arthur Robinson's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (36 papers), Sexual Differentiation and Disorders (35 papers) and Prenatal Screening and Diagnostics (27 papers). Arthur Robinson is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (36 papers), Sexual Differentiation and Disorders (35 papers) and Prenatal Screening and Diagnostics (27 papers). Arthur Robinson collaborates with scholars based in United States, Canada and United Kingdom. Arthur Robinson's co-authors include Bruce G. Bender, Theodore T. Puck, Mary G. Linden, Mary Puck, James A. Salbenblatt, David Peakman, Bruce F. Pennington, J. H. Tjio, Helvise G. Morse and Robert J. Harmon and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Arthur Robinson

130 papers receiving 4.0k citations

Hit Papers

GENETICS OF SOMATIC MAMMALIAN CELLS 1958 2026 1980 2003 1958 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arthur Robinson United States 37 2.5k 1.9k 944 431 403 134 4.5k
Barbara R. Migeon United States 46 3.2k 1.2× 4.2k 2.2× 737 0.8× 880 2.0× 128 0.3× 136 6.3k
Yutaka Nakahori Japan 31 2.2k 0.9× 2.6k 1.4× 308 0.3× 407 0.9× 573 1.4× 140 4.3k
Stanley M. Gartler United States 42 3.3k 1.3× 4.7k 2.5× 504 0.5× 751 1.7× 218 0.5× 133 6.8k
P. E. Polani United Kingdom 35 1.7k 0.7× 1.5k 0.8× 1.0k 1.1× 586 1.4× 202 0.5× 130 4.1k
Larry J. Shapiro United States 42 2.8k 1.1× 3.5k 1.8× 298 0.3× 565 1.3× 364 0.9× 105 5.6k
Nabeel A. Affara United Kingdom 49 3.2k 1.3× 4.2k 2.2× 800 0.8× 863 2.0× 944 2.3× 167 7.1k
Daniela Toniolo Italy 47 2.4k 0.9× 5.6k 2.9× 744 0.8× 271 0.6× 391 1.0× 139 8.6k
Karl Sperling Germany 44 1.9k 0.7× 4.7k 2.5× 804 0.9× 1.0k 2.4× 243 0.6× 174 6.6k
J.L. Hamerton Canada 33 2.8k 1.1× 2.0k 1.0× 1.0k 1.1× 1.3k 3.0× 229 0.6× 134 5.3k
J Lejeune France 30 2.3k 0.9× 1.7k 0.9× 938 1.0× 984 2.3× 78 0.2× 165 4.1k

Countries citing papers authored by Arthur Robinson

Since Specialization
Citations

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

Fields of papers citing papers by Arthur Robinson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arthur Robinson

This figure shows the co-authorship network connecting the top 25 collaborators of Arthur Robinson. A scholar is included among the top collaborators of Arthur Robinson 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 Arthur Robinson. Arthur Robinson 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.
Bender, Bruce G., Robert J. Harmon, Mary G. Linden, Becki Bucher‐Bartelson, & Arthur Robinson. (1999). Psychosocial competence of unselected young adults with sex chromosome abnormalities. American Journal of Medical Genetics. 88(2). 200–206. 33 indexed citations
2.
Harmon, Robert J., Bruce G. Bender, Mary G. Linden, & Arthur Robinson. (1998). Transition From Adolescence to Early Adulthood: Adaptation and Psychiatric Status of Women With 47,XXX. Journal of the American Academy of Child & Adolescent Psychiatry. 37(3). 286–291. 33 indexed citations
3.
Robinson, Arthur. (1994). Genetic diagnosis: present and prospects.. PubMed. 150(1). 49–52. 1 indexed citations
4.
Bender, Bruce G., Mary G. Linden, & Arthur Robinson. (1993). Neuropsychological impairment in 42 adolescents with sex chromosome abnormalities. American Journal of Medical Genetics. 48(3). 169–173. 133 indexed citations
5.
Sujansky, Eva, et al.. (1993). Natural history of the recombinant (8) syndrome. American Journal of Medical Genetics. 47(4). 512–525. 28 indexed citations
6.
Evans, Jane, J.L. Hamerton, & Arthur Robinson. (1991). Children and young adults with sex chromosome aneuploidy : follow-up, clinical, and molecular studies : proceedings of the 5th International Workshop on Sex Chromosome Anomalies held at Minaki, Ontario, Canada, June 7-10, 1989. 4 indexed citations
7.
Jacobs, P. A., et al.. (1990). The parental origin of the extra X chromosome in 47,XXX females.. PubMed Central. 46(4). 754–61. 64 indexed citations
8.
Robinson, Arthur. (1990). Living history: An autobiography of Arthur Robinson. American Journal of Medical Genetics. 35(4). 475–480. 2 indexed citations
9.
Robinson, Arthur, Bruce G. Bender, & Mary G. Linden. (1989). Decisions following the intrauterine diagnosis of sex chromosome aneuploidy. American Journal of Medical Genetics. 34(4). 552–554. 60 indexed citations
10.
Ward, Brian E., et al.. (1988). Isochromosome 12p mosaicism (Pallister‐Killian syndrome): Newborn diagnosis by direct bone marrow analysis. American Journal of Medical Genetics. 31(4). 835–839. 47 indexed citations
11.
Steenbrugge, G.J. van, et al.. (1981). Neutrons and X-rays, comparative studies with Drosophila melanogaster. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 84(1). 101–105. 4 indexed citations
12.
Peakman, David, et al.. (1979). Chromosomal mosaicism in amniotic fluid cell cultures.. Europe PMC (PubMed Central). 31(2). 149–55. 48 indexed citations
13.
Robinson, Arthur, Herbert A. Lubs, & Daniel Bergsma. (1979). Sex chromosome aneuploidy : prospective studies on children. 20 indexed citations
14.
Hecht, Frederick, B. Kaiser McCaw, David Peakman, & Arthur Robinson. (1979). New translocations in human lymphocytes: a mutagen monitoring system.. Environmental Health Perspectives. 31. 19–22. 2 indexed citations
15.
Robinson, Arthur. (1977). Population cytogenetics: Studies in humans.. The American Journal of Human Genetics. 29(5). 548–549. 1 indexed citations
16.
Peakman, David, et al.. (1971). Screening of newborn infants for abnormalities of the Y chromosome. The Journal of Pediatrics. 79(2). 305–306. 8 indexed citations
17.
Chemke, Juan & Arthur Robinson. (1969). The third fontanelle. The Journal of Pediatrics. 75(4). 617–622. 8 indexed citations
18.
Githens, John H., et al.. (1969). Thymic alymphoplasia with XX/XY lymphoid chimerism secondary to probable maternal-fetal transfusion. The Journal of Pediatrics. 75(1). 87–94. 25 indexed citations
19.
Robinson, Arthur. (1963). THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. The Journal of Experimental Medicine. 118(3). 359–370. 32 indexed citations
20.
Puck, Theodore T., et al.. (1958). GENETICS OF SOMATIC MAMMALIAN CELLS. The Journal of Experimental Medicine. 108(6). 945–956. 811 indexed citations breakdown →

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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