Emanuel Bs
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- Carcinogens and Genotoxicity Assessment 1
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- DNA Repair Mechanisms 2
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- Acute Myeloid Leukemia Research 2
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- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
- Genetic Syndromes and Imprinting 1
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- Congenital gastrointestinal and neural anomalies 1
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- T-cell and Retrovirus Studies 1
- Co-authors
- PC NowellME ConleyN B SpinnerTakema KatoHidehito InagakiTamae OhyeHiroki KurahashiHiroshi Kogo
- Journals
- Blood (2 papers)Clinical Genetics (1 paper)PubMed (5 papers)
- Partner nations
- United StatesQatarItaly
In The Last Decade
Emanuel Bs
8 papers receiving 251 citations
Peers
Comparison fields: 5 of 39
- Cancer Research 66
- Pediatrics, Perinatology and Child Health 62
- Ophthalmology 25
- Oncology 74
- Molecular Biology 160
Countries citing papers authored by Emanuel Bs
This map shows the geographic impact of Emanuel Bs'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 Emanuel Bs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emanuel Bs more than expected).
Fields of papers citing papers by Emanuel Bs
This network shows the impact of papers produced by Emanuel Bs. 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 Emanuel Bs. The network helps show where Emanuel Bs may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Emanuel Bs, 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 | 2010 | 51 | |
| 2 | Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region. | 1993 | 6 |
| 3 | Molecular and phenotypic analysis of the chromosome 22 microdeletion syndromes. | 1993 | 10 |
| 4 | Pre- and postconception factors associated with sporadic heritable and nonheritable retinoblastoma. | 1989 | 87 |
| 5 | 1986 | 49 | |
| 6 | 3' c-myc rearrangement in a human leukemic T-cell line. | 1986 | 20 |
| 7 | 1986 | 40 | |
| 8 | Chromosome rearrangements in oncogenesis. | 1984 | 6 |
About Emanuel Bs
Emanuel Bs is a scholar working on Hematology, Ophthalmology and Genetics, having authored 8 papers that have together received 269 indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (2 papers), DNA Repair Mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Congenital gastrointestinal and neural anomalies (1 paper), T-cell and Retrovirus Studies (1 paper), Genetic Syndromes and Imprinting (1 paper) and Carcinogens and Genotoxicity Assessment (1 paper). The work is most often cited by research in Cancer Research (66 citations), Pediatrics, Perinatology and Child Health (62 citations) and Ophthalmology (25 citations). Emanuel Bs has collaborated with scholars based in United States, Qatar and Italy. Frequent co-authors include PC Nowell, ME Conley, N B Spinner, Takema Kato, Hidehito Inagaki, Tamae Ohye, Hiroki Kurahashi, Hiroshi Kogo, Mengmeng Tong and Paolo Lusso. Their work appears in journals such as Blood, Clinical Genetics and PubMed.
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.