Heidi Thiese
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 4
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
- BRCA gene mutations in cancer 1
- Genetics and Neurodevelopmental Disorders 1
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- Congenital heart defects research 2
- Epigenetics and DNA Methylation 1
- Co-authors
- Kathleen A. Leppig (4 shared papers)Lisa G. Shaffer (2 shared papers)Blake C. Ballif (2 shared papers)Anne M. Bandholz (2 shared papers)Jill A. Rosenfeld (2 shared papers)Beth S. Torchia (2 shared papers)Sarah Dyack (2 shared papers)J. Edward Spence (1 shared paper)
- Journals
- Genetics in Medicine (1 paper)Clinical Genetics (1 paper)American Journal of Medical Genetics Part A (1 paper)Molecular Genetics & Genomic Medicine (1 paper)
- Partner nations
- United StatesCanada
In The Last Decade
Heidi Thiese
4 papers receiving 98 citations
Peers
Comparison fields: 5 of 32
- Genetics 92
- Developmental Neuroscience 7
- Molecular Biology 66
- Developmental Biology 2
- Urology 4
Countries citing papers authored by Heidi Thiese
This map shows the geographic impact of Heidi Thiese'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 Heidi Thiese with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heidi Thiese more than expected).
Fields of papers citing papers by Heidi Thiese
This network shows the impact of papers produced by Heidi Thiese. 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 Heidi Thiese. The network helps show where Heidi Thiese may publish in the future.
Co-authors
The 25 scholars most cited alongside Heidi Thiese, 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 | 2009 | 55 | |
| 2 | 2013 | 33 | |
| 3 | 2010 | 20 | |
| 4 | 2016 | 5 |
About Heidi Thiese
Heidi Thiese is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Developmental Neuroscience and Infectious Diseases, having authored 4 papers that have together received 113 indexed citations. Recurring topics across this work include Congenital heart defects research (2 papers), Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Williams Syndrome Research (1 paper), Epigenetics and DNA Methylation (1 paper), BRCA gene mutations in cancer (1 paper), Genetic factors in colorectal cancer (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (92 citations), Developmental Neuroscience (7 citations), Molecular Biology (66 citations), Developmental Biology (2 citations) and Urology (4 citations). Heidi Thiese has collaborated with scholars based in United States and Canada. Frequent co-authors include Kathleen A. Leppig, Lisa G. Shaffer, Blake C. Ballif, Anne M. Bandholz, Jill A. Rosenfeld, Beth S. Torchia, Sarah Dyack, J. Edward Spence, Bassem A. Bejjani and Urvashi Surti. Their work appears in journals such as Genetics in Medicine, Clinical Genetics, American Journal of Medical Genetics Part A and Molecular Genetics & Genomic Medicine.
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.