B. Biederman
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Mapping and Diversity in Plants and Animals
- Animal Genetics and Reproduction
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 10
- Animal Genetics and Reproduction 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetic Mapping and Diversity in Plants and Animals 2
- Genetics and Neurodevelopmental Disorders 1
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- Chromosomal and Genetic Variations 8
- Co-authors
- Phyllis E. Bowen (7 shared papers)Peter Bowen (2 shared papers)Cheng‐Chieh Lin (3 shared papers)Robert B. Church (1 shared paper)John M. Opitz (1 shared paper)A. B. Hawthorne (1 shared paper)Ching‐Shwun Lin (3 shared papers)R. J. M. Gardner (1 shared paper)
- Journals
- Human Genetics (5 papers)Journal of Heredity (1 paper)Journal of Intellectual Disability Research (1 paper)Cancer (1 paper)American Journal of Medical Genetics (2 papers)
- Partner nations
- CanadaUnited StatesNew Zealand
In The Last Decade
B. Biederman
17 papers receiving 252 citations
Peers
Comparison fields: 5 of 43
- Genetics 251
- Pediatrics, Perinatology and Child Health 62
- Plant Science 128
- Developmental Biology 5
- Molecular Biology 130
Countries citing papers authored by B. Biederman
This map shows the geographic impact of B. Biederman'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 B. Biederman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B. Biederman more than expected).
Fields of papers citing papers by B. Biederman
This network shows the impact of papers produced by B. Biederman. 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 B. Biederman. The network helps show where B. Biederman may publish in the future.
Co-authors
The 22 scholars most cited alongside B. Biederman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1980 | 56 | |
| 2 | 1978 | 42 | |
| 3 | 1983 | 41 | |
| 4 | 1977 | 29 | |
| 5 | The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12. | 1985 | 27 |
| 6 | 1976 | 24 | |
| 7 | 1978 | 19 | |
| 8 | 1980 | 14 | |
| 9 | 1982 | 10 | |
| 10 | Balanced translocations involving chromosome 12: report of a case and possible evidence for position effect. | 1976 | 10 |
| 11 | 1982 | 8 | |
| 12 | 1978 | 6 | |
| 13 | 2008 | 3 | |
| 14 | 1979 | 3 | |
| 15 | 1977 | 3 | |
| 16 | 1981 | 3 | |
| 17 | 1979 | 2 | |
| 18 | 2008 | 0 |
About B. Biederman
B. Biederman is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 18 papers that have together received 300 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (8 papers), Prenatal Screening and Diagnostics (5 papers), Animal Genetics and Reproduction (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genetics and Neurodevelopmental Disorders (1 paper) and Acute Myeloid Leukemia Research (1 paper). The work is most often cited by research in Genetics (251 citations), Pediatrics, Perinatology and Child Health (62 citations), Plant Science (128 citations), Developmental Biology (5 citations) and Molecular Biology (130 citations). B. Biederman has collaborated with scholars based in Canada, United States and New Zealand. Frequent co-authors include Phyllis E. Bowen, Peter Bowen, Cheng‐Chieh Lin, Robert B. Church, John M. Opitz, A. B. Hawthorne, Ching‐Shwun Lin, R. J. M. Gardner, P. H. Fitzgerald and A. M. O. Veale. Their work appears in journals such as Human Genetics, Journal of Heredity, Journal of Intellectual Disability Research, Cancer and American Journal of Medical Genetics.
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.