Tiffany Vu

2.4k citations
10 papers · 693 · h-index 8

Impact in

  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Autism Spectrum Disorder Research

Papers in

    • Genomic variations and chromosomal abnormalities 5
    • Genomics and Rare Diseases 2
    • Genetics and Neurodevelopmental Disorders 2
    • Neurogenetic and Muscular Disorders Research 1
    • Congenital heart defects research 2

Tiffany Vu

8 papers receiving 685 citations

Peers

Tiffany Vu
Comparison fields: 5 of 73
  • Genetics 419
  • Cognitive Neuroscience 171
  • Developmental and Educational Psychology 62
  • Molecular Biology 308
  • Developmental Biology 8
Replace Angelika Rieß with:
Angelika Rieß Germany
Alexis Rea United States
Susan Zeesman Canada
Terry Vrijenhoek Netherlands
R. Curtis Rogers United States
Matthew F. Hunter Australia
Kristin Herman United States
Liesbeth Rooms Belgium
Gordon C. Gowans United States
Kay MacDermot United Kingdom
Tiffany Vu relative to Angelika Rieß Germany Angelika Rieß's profile →
Citations per field
00.5×3.4×
Angelika Rieß · 1×
Citations per year

Countries citing papers authored by Tiffany Vu

Since Specialization
Citations

This map shows the geographic impact of Tiffany Vu'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 Tiffany Vu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tiffany Vu more than expected).

Fields of papers citing papers by Tiffany Vu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tiffany Vu. 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 Tiffany Vu. The network helps show where Tiffany Vu may publish in the future.

Co-authors

The 25 scholars most cited alongside Tiffany Vu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tiffany Vu Line = papers co-authored together Tiffany Vu links everyone, so they are left out of the graph.

All Works

10 of 10 papers shown
#Work
1 2011222
2 2013212
3 201088
4 201164
5 200935
6 201032
7 201229
8 201111
9 20220
10 20250

About Tiffany Vu

Tiffany Vu is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Cardiology and Cardiovascular Medicine, having authored 10 papers that have together received 693 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers), Autism Spectrum Disorder Research (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Genetics (419 citations), Cognitive Neuroscience (171 citations), Developmental and Educational Psychology (62 citations), Molecular Biology (308 citations) and Developmental Biology (8 citations). Tiffany Vu has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Evan E. Eichler, Santhosh Girirajan, Wendy H. Raskind, Raphael Bernier, Bradley P. Coe, Carl Baker, Zoran Brkanac, Maika Malig, Laura Vives and Mark Matsushita. Their work appears in journals such as The American Journal of Human Genetics, Journal of Neurodevelopmental Disorders, European Journal of Marketing, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Community Dentistry And Oral Epidemiology.

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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