B S Emanuel
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Glioma Diagnosis and Treatment
- Molecular Biology top 5%
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
- Genetics 22
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 5
- Chronic Lymphocytic Leukemia Research 4
- Virus-based gene therapy research 3
- Co-authors
- Marcia L. BudarfTamim H. ShaikhD.A. DriscollJaclyn A. BiegelRoger J. PackerElaine H. ZackaiLucy B. RorkeAnita L. Hawkins
- Journals
- Proceedings of the National Academy of Sciences (6 papers)Genes Chromosomes and Cancer (3 papers)Journal of Clinical Investigation (3 papers)Genomics (3 papers)The Journal of Pediatrics (2 papers)
- Partner nations
- United StatesItalyNetherlands
In The Last Decade
B S Emanuel
44 papers receiving 2.8k citations
Peers
Comparison fields: 5 of 98
- Genetics 459
- Genetics 1.1k
- Molecular Biology 1.8k
- Hematology 232
- Neurology 290
Countries citing papers authored by B S Emanuel
This map shows the geographic impact of B S Emanuel'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 S Emanuel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B S Emanuel more than expected).
Fields of papers citing papers by B S Emanuel
This network shows the impact of papers produced by B S Emanuel. 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 S Emanuel. The network helps show where B S Emanuel may publish in the future.
Co-authors
The 25 scholars most cited alongside B S Emanuel, 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 | 2017 | 56 | |
| 2 | 2007 | 77 | |
| 3 | 2003 | 1 | |
| 4 | 2001 | 215 | |
| 5 | The 22q11.2 deletion syndrome. | 2001 | 86 |
| 6 | 2000 | 85 | |
| 7 | 1998 | 10 | |
| 8 | 1994 | 116 | |
| 9 | 1993 | 20 | |
| 10 | 1993 | 48 | |
| 11 | 1992 | 60 | |
| 12 | 1990 | 44 | |
| 13 | 1990 | 2 | |
| 14 | 1990 | 24 | |
| 15 | 1990 | 17 | |
| 16 | 1989 | 56 | |
| 17 | 1989 | 73 | |
| 18 | 1988 | 68 | |
| 19 | 1988 | 17 | |
| 20 | 1986 | 67 |
About B S Emanuel
B S Emanuel is a scholar working on Genetics, Genetics, Hematology, Molecular Biology and Neurology, having authored 44 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (10 papers), Sarcoma Diagnosis and Treatment (6 papers), Neuroblastoma Research and Treatments (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Chronic Lymphocytic Leukemia Research (4 papers), Genomics and Chromatin Dynamics (4 papers) and Virus-based gene therapy research (3 papers). The work is most often cited by research in Genetics (459 citations), Genetics (1.1k citations), Molecular Biology (1.8k citations), Hematology (232 citations) and Neurology (290 citations). B S Emanuel has collaborated with scholars based in United States, Italy and Netherlands. Frequent co-authors include Marcia L. Budarf, Tamim H. Shaikh, D.A. Driscoll, Jaclyn A. Biegel, Roger J. Packer, Elaine H. Zackai, Lucy B. Rorke, Anita L. Hawkins, Donna M. McDonald‐McGinn and Chandi Griffin. Their work appears in journals such as Proceedings of the National Academy of Sciences, Genes Chromosomes and Cancer, Journal of Clinical Investigation, Genomics and The Journal of Pediatrics.
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.