James Tepperberg
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 16
- Genomics and Rare Diseases 4
- Genetic Syndromes and Imprinting 3
-
- Prenatal Screening and Diagnostics 8
- Co-authors
- Peter Papenhausen (10 shared papers)Stuart Schwartz (8 shared papers)Rachel D. Burnside (6 shared papers)Inder Gadi (6 shared papers)Romela Pasion (4 shared papers)Vikram Jaswaney (3 shared papers)Hiba Risheg (2 shared papers)Kenneth J. Friedman (1 shared paper)
- Journals
- Genetics in Medicine (5 papers)Cytogenetic and Genome Research (2 papers)Human Genetics (2 papers)Prenatal Diagnosis (2 papers)SpringerPlus (1 paper)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
James Tepperberg
27 papers receiving 884 citations
Peers
Comparison fields: 5 of 64
- Genetics 484
- Pediatrics, Perinatology and Child Health 254
- Hematology 84
- Genetics 66
- Cancer Research 72
Countries citing papers authored by James Tepperberg
This map shows the geographic impact of James Tepperberg'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 James Tepperberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James Tepperberg more than expected).
Fields of papers citing papers by James Tepperberg
This network shows the impact of papers produced by James Tepperberg. 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 James Tepperberg. The network helps show where James Tepperberg may publish in the future.
Co-authors
The 25 scholars most cited alongside James Tepperberg, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 190 | |
| 2 | 2011 | 134 | |
| 3 | 2001 | 97 | |
| 4 | Molecular characterization and sensitivity of STI-571 (imatinib mesylate, Gleevec)-resistant, Bcr-Abl-positive, human acute leukemia cells to SRC kinase inhibitor PD180970 and 17-allylamino-17-demethoxygeldanamycin. | 2002 | 95 |
| 5 | 2011 | 62 | |
| 6 | 2003 | 43 | |
| 7 | 2009 | 42 | |
| 8 | 1997 | 41 | |
| 9 | 2011 | 41 | |
| 10 | 2017 | 29 | |
| 11 | 2000 | 25 | |
| 12 | 2011 | 19 | |
| 13 | 2008 | 18 | |
| 14 | 2013 | 18 | |
| 15 | 2005 | 17 | |
| 16 | 2006 | 14 | |
| 17 | 2011 | 13 | |
| 18 | 2007 | 10 | |
| 19 | 2018 | 10 | |
| 20 | 2012 | 8 |
About James Tepperberg
James Tepperberg is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Genetics, having authored 28 papers that have together received 946 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (8 papers), Genomics and Rare Diseases (4 papers), Chromosomal and Genetic Variations (4 papers), Congenital heart defects research (3 papers), Genetic Syndromes and Imprinting (3 papers), Chronic Myeloid Leukemia Treatments (2 papers) and Lymphoma Diagnosis and Treatment (2 papers). The work is most often cited by research in Genetics (484 citations), Pediatrics, Perinatology and Child Health (254 citations), Hematology (84 citations), Genetics (66 citations) and Cancer Research (72 citations). James Tepperberg has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Peter Papenhausen, Stuart Schwartz, Rachel D. Burnside, Inder Gadi, Romela Pasion, Vikram Jaswaney, Hiba Risheg, Kenneth J. Friedman, Elisabeth A. Keitges and John Pappas. Their work appears in journals such as Genetics in Medicine, Cytogenetic and Genome Research, Human Genetics, Prenatal Diagnosis and SpringerPlus.
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.