Stephanie E. Vallee
Impact in
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- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 3
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 1
- BRCA gene mutations in cancer 1
- Genetic Syndromes and Imprinting 1
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- Ion channel regulation and function 1
- Co-authors
- Mary Beth Dinulos (5 shared papers)Dustin L. Gable (1 shared paper)Julie Hoover‐Fong (1 shared paper)David Valle (1 shared paper)Szabolcs Szelinger (1 shared paper)Jing You (1 shared paper)Mary Armanios (1 shared paper)Isabelle Schrauwen (1 shared paper)
- Journals
- Frontiers in Pharmacology (1 paper)The American Journal of Human Genetics (1 paper)Journal of Human Genetics (1 paper)Clinics in Laboratory Medicine (1 paper)
- Partner nations
- United StatesCzechiaFrance
In The Last Decade
Stephanie E. Vallee
3 papers receiving 44 citations
Peers
Comparison fields: 5 of 25
- Genetics 27
- Aging 1
- Transplantation 1
- Pediatrics, Perinatology and Child Health 6
- Molecular Biology 19
Countries citing papers authored by Stephanie E. Vallee
This map shows the geographic impact of Stephanie E. Vallee'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 Stephanie E. Vallee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie E. Vallee more than expected).
Fields of papers citing papers by Stephanie E. Vallee
This network shows the impact of papers produced by Stephanie E. Vallee. 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 Stephanie E. Vallee. The network helps show where Stephanie E. Vallee may publish in the future.
Co-authors
The 25 scholars most cited alongside Stephanie E. Vallee, 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 | 2016 | 27 | |
| 2 | 2020 | 11 | |
| 3 | 2018 | 7 | |
| 4 | 2025 | 0 | |
| 5 | 2015 | 0 |
About Stephanie E. Vallee
Stephanie E. Vallee is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine, having authored 5 papers that have together received 45 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Folate and B Vitamins Research (1 paper), Cardiac electrophysiology and arrhythmias (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Ion channel regulation and function (1 paper), BRCA gene mutations in cancer (1 paper), Genetic Syndromes and Imprinting (1 paper) and Tumors and Oncological Cases (1 paper). The work is most often cited by research in Genetics (27 citations), Aging (1 citation), Transplantation (1 citation), Pediatrics, Perinatology and Child Health (6 citations) and Molecular Biology (19 citations). Stephanie E. Vallee has collaborated with scholars based in United States, Czechia and France. Frequent co-authors include Mary Beth Dinulos, Dustin L. Gable, Julie Hoover‐Fong, David Valle, Szabolcs Szelinger, Jing You, Mary Armanios, Isabelle Schrauwen, Newell Belnap and Nara Sobreira. Their work appears in journals such as Frontiers in Pharmacology, The American Journal of Human Genetics, Journal of Human Genetics and Clinics in Laboratory 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.