Karin Weiss
- Co-authors
- Kenneth K. KíddI. BalazsJ.R. KiddFrancis L. BlackMaximilian MuenkeEllen SidranskyGrisel LopezCatherine Groden
- Topics
- Genomics and Rare Diseases (8 papers)Genomic variations and chromosomal abnormalities (8 papers)Genetics and Neurodevelopmental Disorders (7 papers)
- Journals
- Journal of Clinical InvestigationThe American Journal of Human GeneticsJournal of Hepatology
- Partner nations
- IsraelUnited StatesAustralia
In The Last Decade
Karin Weiss
29 papers receiving 415 citations
Peers
Comparison fields: 5 of 75
- Genetics 190
- Molecular Biology 188
- Physiology 86
- Cell Biology 65
- Epidemiology 50
Countries citing papers authored by Karin Weiss
This map shows the geographic impact of Karin Weiss'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 Karin Weiss with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Weiss more than expected).
Fields of papers citing papers by Karin Weiss
This network shows the impact of papers produced by Karin Weiss. 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 Karin Weiss. The network helps show where Karin Weiss may publish in the future.
Co-authorship network of co-authors of Karin Weiss
This figure shows the co-authorship network connecting the top 25 collaborators of Karin Weiss. A scholar is included among the top collaborators of Karin Weiss 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 Karin Weiss. Karin Weiss is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 0 | |
| 3 | 0 | |
| 4 | 1 | |
| 5 | 1 | |
| 6 | 6 | |
| 7 | 0 | |
| 8 | 1 | |
| 9 | 2 | |
| 10 | 16 | |
| 11 | 2 | |
| 12 | 25 | |
| 13 | 6 | |
| 14 | 15 | |
| 15 | 4 | |
| 16 | 25 | |
| 17 | 10 | |
| 18 | 10 | |
| 19 | How to evaluate the child presenting with an apparent life-threatening event? | 12 |
| 20 | Studies of three Amerindian populations using nuclear DNA polymorphisms. | 86 |
About Karin Weiss
Karin Weiss is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 36 papers that have together received 433 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). The work is most often cited by research in Genetics (190 citations), Cell Biology (65 citations) and Medical Terminology (1 citation). Karin Weiss has collaborated with scholars based in Israel, United States and Australia. Frequent co-authors include Kenneth K. Kídd, I. Balazs, J.R. Kidd, Francis L. Black, Maximilian Muenke, Ellen Sidransky, Grisel Lopez, Catherine Groden, Ashley N. Gonzalez and Paul Kruszka. Their work appears in journals such as Journal of Clinical Investigation, The American Journal of Human Genetics and Journal of Hepatology.
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.