Heidi A. Heilstedt
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
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- Epigenetics and DNA Methylation 2
- Glycosylation and Glycoproteins Research 1
- RNA modifications and cancer 1
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- Congenital limb and hand anomalies 1
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- Prenatal Screening and Diagnostics 2
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- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
- Co-authors
- Lisa G. ShafferCarlos A. BacinoCatherine D. KashorkBlake C. BallifStuart K. ShapiraRichard A. LewisSamuel StalStuart Schwartz
- Journals
- The Lancet (1 paper)Nature Genetics (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
Heidi A. Heilstedt
9 papers receiving 542 citations
Peers
Comparison fields: 5 of 55
- Genetics 415
- Molecular Biology 307
- Developmental Biology 9
- Pediatrics, Perinatology and Child Health 70
- Genetics 37
Countries citing papers authored by Heidi A. Heilstedt
This map shows the geographic impact of Heidi A. Heilstedt'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 A. Heilstedt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heidi A. Heilstedt more than expected).
Fields of papers citing papers by Heidi A. Heilstedt
This network shows the impact of papers produced by Heidi A. Heilstedt. 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 A. Heilstedt. The network helps show where Heidi A. Heilstedt may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Heidi A. Heilstedt, 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 | 2004 | 68 | |
| 2 | 2004 | 23 | |
| 3 | 2003 | 181 | |
| 4 | 2003 | 37 | |
| 5 | 2002 | 40 | |
| 6 | 2001 | 65 | |
| 7 | 2001 | 102 | |
| 8 | 2001 | 31 | |
| 9 | 2000 | 21 |
About Heidi A. Heilstedt
Heidi A. Heilstedt is a scholar working on Developmental Biology, Genetics and Dermatology, having authored 9 papers that have together received 568 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Epigenetics and DNA Methylation (2 papers), Prenatal Screening and Diagnostics (2 papers), Glycosylation and Glycoproteins Research (1 paper), Congenital limb and hand anomalies (1 paper), Genomics and Rare Diseases (1 paper), RNA modifications and cancer (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (415 citations), Molecular Biology (307 citations) and Developmental Biology (9 citations). Heidi A. Heilstedt has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Lisa G. Shaffer, Carlos A. Bacino, Catherine D. Kashork, Blake C. Ballif, Stuart K. Shapira, Richard A. Lewis, Samuel Stal, Stuart Schwartz, Clemencia Colmenares and Ed Stavnezer. Their work appears in journals such as The Lancet, Nature Genetics and The American Journal of Human Genetics.
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.