Arthur Robinson
Impact in
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 62
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 37
- Genomic variations and chromosomal abnormalities 22
- Genetics and Neurodevelopmental Disorders 15
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- Sexual Differentiation and Disorders 34
- Co-authors
- Bruce G. Bender (32 shared papers)Theodore T. Puck (11 shared papers)Mary G. Linden (19 shared papers)Mary Puck (24 shared papers)James A. Salbenblatt (17 shared papers)David Peakman (19 shared papers)Bruce F. Pennington (5 shared papers)J. H. Tjio (4 shared papers)
- Journals
- PEDIATRICS (13 papers)The Lancet (10 papers)Human Genetics (7 papers)Clinical Genetics (7 papers)Pediatric Research (6 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Arthur Robinson
130 papers receiving 4.0k citations
Arthur Robinson's Hit Papers
Peers
Comparison fields: 5 of 150
- Genetics 2.4k
- Pediatrics, Perinatology and Child Health 851
- Reproductive Medicine 311
- Molecular Biology 1.7k
- Hematology 226
Countries citing papers authored by Arthur Robinson
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
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-authors
The 25 scholars most cited alongside Arthur Robinson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 134 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | GENETICS OF SOMATIC MAMMALIAN CELLS Hit paper breakdown → | 1958 | 813 |
| 2 | 1960 | 178 | |
| 3 | 1995 | 167 | |
| 4 | 1993 | 133 | |
| 5 | 1985 | 109 | |
| 6 | 1982 | 91 | |
| 7 | 1982 | 90 | |
| 8 | 2002 | 75 | |
| 9 | 1988 | 74 | |
| 10 | Sex chromosome aneuploidy: the Denver Prospective Study. | 1990 | 66 |
| 11 | 1995 | 64 | |
| 12 | The parental origin of the extra X chromosome in 47,XXX females. | 1990 | 64 |
| 13 | Studies on chromosomal nondisjunction in man. 3. | 1967 | 63 |
| 14 | 1989 | 60 | |
| 15 | 1983 | 59 | |
| 16 | 1960 | 58 | |
| 17 | 1992 | 58 | |
| 18 | 1986 | 56 | |
| 19 | 1984 | 55 | |
| 20 | 1959 | 52 |
About Arthur Robinson
Arthur Robinson is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Hematology, having authored 134 papers that have together received 4.5k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (37 papers), Sexual Differentiation and Disorders (34 papers), Prenatal Screening and Diagnostics (27 papers), Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (15 papers), Acute Myeloid Leukemia Research (12 papers), Chronic Myeloid Leukemia Treatments (10 papers) and Acute Lymphoblastic Leukemia research (10 papers). The work is most often cited by research in Genetics (2.4k citations), Pediatrics, Perinatology and Child Health (851 citations), Reproductive Medicine (311 citations), Molecular Biology (1.7k citations) and Hematology (226 citations). Arthur Robinson has collaborated with scholars based in United States, Canada and United Kingdom. Frequent 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. Their work appears in journals such as PEDIATRICS, The Lancet, Human Genetics, Clinical Genetics and Pediatric Research.
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.