Tiffany Oliver

451 total citations
9 papers, 302 citations indexed

About

Tiffany Oliver is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Tiffany Oliver has authored 9 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Tiffany Oliver's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Chromosomal and Genetic Variations (3 papers). Tiffany Oliver is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Chromosomal and Genetic Variations (3 papers). Tiffany Oliver collaborates with scholars based in United States. Tiffany Oliver's co-authors include Stephanie L. Sherman, Stuart W. Tinker, Eleanor Feingold, Vivian G. Cheung, Emily G. Allen, Kai Yu, Emmanuel Peprah, Weiya He, NaTasha D. Hollis and Reshmi Chowdhury and has published in prestigious journals such as PLoS ONE, PLoS Genetics and Human Genetics.

In The Last Decade

Tiffany Oliver

7 papers receiving 276 citations

Peers

Countries citing papers authored by Tiffany Oliver

Since Specialization

Citations

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

Fields of papers citing papers by Tiffany Oliver

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tiffany Oliver

This figure shows the co-authorship network connecting the top 25 collaborators of Tiffany Oliver. A scholar is included among the top collaborators of Tiffany Oliver 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 Oliver. Tiffany Oliver 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	Building the Corps: an HBCU+PWI Partnership to Broaden Participation in Data Science (Experience) 2024 ·Papers on Engineering Education Repository (American Society for Engineering Education) ·(unknown), Dirk Colbry, (unknown), (unknown), Tiffany Oliver	0
2	Increasing the Persistence of Black Women in STEM (WiSTEM) by Implementing and Sustaining a Successful Cohort Model for First-Year Undergraduate Women at an HBCU 2024 ·Papers on Engineering Education Repository (American Society for Engineering Education) ·(unknown), Tiffany Oliver, (unknown)	0
3	Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin 2016 ·PubMed ·Tiffany Oliver, Candace D. Middlebrooks, (unknown)	7
4	An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction 2014 ·PLoS ONE ·Tiffany Oliver, Candace D. Middlebrooks, Stuart W. Tinker, Emily G. Allen, Lora Jh Bean, Ferdouse Begum, Eleanor Feingold, Reshmi Chowdhury, Vivian G. Cheung, Stephanie L. Sherman	14
5	Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: A report from the National Down Syndrome Project 2013 ·American Journal of Medical Genetics Part A ·NaTasha D. Hollis, Emily G. Allen, Tiffany Oliver, Stuart W. Tinker, Charlotte M. Druschel, Charlotte A. Hobbs, Leslie A. O’Leary, Paul A. Romitti, Marjorie H. Royle, Claudine P. Torfs, (unknown), (unknown), Lora Bean	41
6	Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21 2011 ·Human Genetics ·Tiffany Oliver, Stuart W. Tinker, Emily G. Allen, NaTasha D. Hollis, Adam E. Locke, Lora Jh Bean, Reshmi Chowdhury, Ferdouse Begum, Mary L. Marazita, Vivian G. Cheung, Eleanor Feingold, Stephanie L. Sherman	35
7	Examination of FMR1 transcript and protein levels among 74 premutation carriers 2009 ·Journal of Human Genetics ·Emmanuel Peprah, Weiya He, Emily G. Allen, Tiffany Oliver, (unknown), Stephanie L. Sherman	52
8	Investigation of factors associated with paternal nondisjunction of chromosome 21 2009 ·American Journal of Medical Genetics Part A ·Tiffany Oliver, (unknown), Eleanor Feingold, Stuart W. Tinker, (unknown), Stephanie L. Sherman	23
9	New Insights into Human Nondisjunction of Chromosome 21 in Oocytes 2008 ·PLoS Genetics ·Tiffany Oliver, Eleanor Feingold, Kai Yu, Vivian G. Cheung, Stuart W. Tinker, (unknown), (unknown), Stephanie L. Sherman	130

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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