Karen A. Glatt
- Molecular Biology
- Genetics top 5%
- Oncology
- Pulmonary and Respiratory Medicine
- Pediatrics, Perinatology and Child Health top 10%
- Co-authors
- M. LalandeJoan H.M. KnollDaniel SinnettMatthew MeyersonJohn M. GrahamRobert D. NichollsMarc LalandeJohn Wagstaff
- Topics
- Genetic Syndromes and Imprinting (8 papers)Genomic variations and chromosomal abnormalities (4 papers)Genomics and Chromatin Dynamics (4 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Karen A. Glatt
16 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 65
- Molecular Biology 664
- Genetics 498
- Oncology 206
- Pulmonary and Respiratory Medicine 184
- Pediatrics, Perinatology and Child Health 178
Countries citing papers authored by Karen A. Glatt
This map shows the geographic impact of Karen A. Glatt'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 Karen A. Glatt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karen A. Glatt more than expected).
Fields of papers citing papers by Karen A. Glatt
This network shows the impact of papers produced by Karen A. Glatt. 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 Karen A. Glatt. The network helps show where Karen A. Glatt may publish in the future.
Co-authorship network of co-authors of Karen A. Glatt
This figure shows the co-authorship network connecting the top 25 collaborators of Karen A. Glatt. A scholar is included among the top collaborators of Karen A. Glatt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karen A. Glatt. Karen A. Glatt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 103 | |
| 2 | 88 | |
| 3 | 65 | |
| 4 | 103 | |
| 5 | 62 | |
| 6 | 43 | |
| 7 | 13 | |
| 8 | 57 | |
| 9 | 33 | |
| 10 | 73 | |
| 11 | High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients. | 45 |
| 12 | 28 | |
| 13 | 80 | |
| 14 | Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers. | 114 |
| 15 | 127 | |
| 16 | Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP. | 24 |
About Karen A. Glatt
Karen A. Glatt is a scholar working on Genetics, Molecular Biology and Oncology, having authored 16 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Chromatin Dynamics (4 papers). The work is most often cited by research in Genetics (498 citations), Molecular Biology (664 citations) and Pediatrics, Perinatology and Child Health (178 citations). Karen A. Glatt has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include M. Lalande, Joan H.M. Knoll, Daniel Sinnett, Matthew Meyerson, John M. Graham, Robert D. Nicholls, Marc Lalande, John Wagstaff, Kwok‐Kin Wong and Geoffrey I. Shapiro. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Cancer 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.