Tiffany Vu

2.4k total citations
9 papers, 691 citations indexed

About

Tiffany Vu is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tiffany Vu has authored 9 papers receiving a total of 691 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tiffany Vu's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (3 papers) and Genomics and Rare Diseases (2 papers). Tiffany Vu is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (3 papers) and Genomics and Rare Diseases (2 papers). Tiffany Vu collaborates with scholars based in United States and Italy. Tiffany Vu's co-authors include Evan E. Eichler, Santhosh Girirajan, Wendy H. Raskind, Bradley P. Coe, Raphael Bernier, Carl Baker, Zoran Brkanac, Maika Malig, Laura Vives and Mark Matsushita and has published in prestigious journals such as The American Journal of Human Genetics, PLoS Genetics and Journal of the Neurological Sciences.

In The Last Decade

Tiffany Vu

8 papers receiving 683 citations

Peers

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-authorship network of co-authors of Tiffany Vu

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	An examination of predisposing and enabling factors that predict dental utilization among individuals with serious mental illness in Detroit, Michigan 2022 ·Community Dentistry And Oral Epidemiology ·Kristen M. Abraham, Tiffany Vu, (unknown), (unknown), (unknown)	0
2	Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder 2013 ·The American Journal of Human Genetics ·Santhosh Girirajan, Megan Y. Dennis, Carl Baker, Maika Malig, Bradley P. Coe, Colin Campbell, Kenneth M. K. Mark, Tiffany Vu, Can Alkan, Ze Cheng, Leslie G. Biesecker, Raphael Bernier, Evan E. Eichler	211
3	Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects 2012 ·American Journal of Medical Genetics Part A ·James R. Priest, Santhosh Girirajan, Tiffany Vu, Aaron Olson, Evan E. Eichler, Michael A. Portman	29
4	Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms 2011 ·The American Journal of Human Genetics ·Catarina D. Campbell, Nick Sampas, Anya Tsalenko, Peter H. Sudmant, Jeffrey M. Kidd, Maika Malig, Tiffany Vu, Laura Vives, Peter Tsang, Laurakay Bruhn, Evan E. Eichler	64
5	Genomic architecture of aggression: Rare copy number variants in intermittent explosive disorder 2011 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Tiffany Vu, Emil F. Coccaro, Evan E. Eichler, Santhosh Girirajan	11
6	Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes 2011 ·PLoS Genetics ·Santhosh Girirajan, Zoran Brkanac, Bradley P. Coe, Carl Baker, Laura Vives, Tiffany Vu, (unknown), Raphael Bernier, Giovanni Battista Ferrero, Margherita Silengo, Stephen T. Warren, Carlos S. Moreno, Marco Fichera, Corrado Romano, Wendy H. Raskind, Evan E. Eichler	221
7	A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations 2010 ·Journal of the Neurological Sciences ·Dong-Hui Chen, Wendy H. Raskind, William W. Parson, Joshua A. Sonnen, Tiffany Vu, (unknown), Mark Matsushita, John Wolff, Hillary Lipe, Thomas D. Bird	32
8	Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample 2010 ·Journal of Neurodevelopmental Disorders ·Beate Peter, Wendy H. Raskind, Mark Matsushita, (unknown), Tiffany Vu, Virginia W. Berninger, Ellen M. Wijsman, Zoran Brkanac	88
9	IFRD1 Is a Candidate Gene for SMNA on Chromosome 7q22-q23 2009 ·The American Journal of Human Genetics ·Zoran Brkanac, David H. Spencer, Jay Shendure, Peggy D. Robertson, Mark Matsushita, Tiffany Vu, Thomas D. Bird, Maynard V. Olson, Wendy H. Raskind	35

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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