Stephanie E. Vallee

585 total citations
3 papers, 43 citations indexed

About

Stephanie E. Vallee is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Stephanie E. Vallee has authored 3 papers receiving a total of 43 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Stephanie E. Vallee's work include Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). Stephanie E. Vallee is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). Stephanie E. Vallee collaborates with scholars based in United States. Stephanie E. Vallee's co-authors include Mary Beth Dinulos, Dustin L. Gable, Ashley L. Siniard, Isabelle Schrauwen, Jing You, Mary Armanios, Newell Belnap, Dorothy K. Grange, Szabolcs Szelinger and Ryan Richholt and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Human Genetics and Clinics in Laboratory Medicine.

In The Last Decade

Stephanie E. Vallee

3 papers receiving 42 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stephanie E. Vallee United States 3 28 24 7 7 4 3 43
Anna Lehman Canada 4 30 1.1× 32 1.3× 6 0.9× 10 1.4× 5 1.3× 8 66
Andrea Seeley United States 5 31 1.1× 17 0.7× 13 1.9× 3 0.4× 2 0.5× 8 57
Hana Zouk United States 4 43 1.5× 19 0.8× 4 0.6× 12 1.7× 1 0.3× 7 72
Catherine L. Mercer United Kingdom 5 49 1.8× 41 1.7× 13 1.9× 7 1.0× 2 0.5× 6 72
Sara Osimani Italy 4 12 0.4× 24 1.0× 7 1.0× 3 0.4× 10 2.5× 5 35
Henriette Roed Nielsen Denmark 3 26 0.9× 12 0.5× 4 0.6× 3 0.4× 5 1.3× 6 29
Edward J. Higginbotham Canada 4 28 1.0× 19 0.8× 5 0.7× 3 0.4× 2 0.5× 6 44
Hui Kang China 3 15 0.5× 19 0.8× 4 0.6× 8 1.1× 8 2.0× 6 39
Lamu Gusang China 4 21 0.8× 11 0.5× 3 0.4× 4 0.6× 2 0.5× 4 35
Loren D.M. Peña United States 3 32 1.1× 11 0.5× 6 0.9× 2 0.3× 2 0.5× 9 41

Countries citing papers authored by Stephanie E. Vallee

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Stephanie E. Vallee

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie E. Vallee. A scholar is included among the top collaborators of Stephanie E. Vallee 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 Stephanie E. Vallee. Stephanie E. Vallee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

3 of 3 papers shown
1.
Dinulos, Mary Beth & Stephanie E. Vallee. (2020). The Impact of Direct-to-Consumer Genetic Testing on Patient and Provider. Clinics in Laboratory Medicine. 40(1). 61–67. 10 indexed citations
2.
Jung, Hou-Sung, Stephanie E. Vallee, Mary Beth Dinulos, Gregory J. Tsongalis, & Joel A. Lefferts. (2018). Maternally inherited 133kb deletion of 14q32 causing Kagami–Ogata syndrome. Journal of Human Genetics. 63(12). 1231–1239. 7 indexed citations
3.
You, Jing, Nara Sobreira, Dustin L. Gable, et al.. (2016). A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2 , a Gene Encoding a Component of the TTT Complex. The American Journal of Human Genetics. 98(5). 909–918. 26 indexed citations

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.

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2026