Stuart W. Tinker

1.1k total citations
15 papers, 776 citations indexed

About

Stuart W. Tinker is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Stuart W. Tinker has authored 15 papers receiving a total of 776 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in Stuart W. Tinker's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (7 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Stuart W. Tinker is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (7 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Stuart W. Tinker collaborates with scholars based in United States. Stuart W. Tinker's co-authors include Stephanie L. Sherman, Emily G. Allen, Claudine P. Torfs, Eleanor Feingold, Sallie B. Freeman, Charlotte M. Druschel, Marjorie H. Royle, Paul A. Romitti, Charlotte A. Hobbs and Tiffany Oliver and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and PLoS Genetics.

In The Last Decade

Stuart W. Tinker

15 papers receiving 729 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stuart W. Tinker United States 15 302 298 283 209 190 15 776
Clotilde Mircher France 12 124 0.4× 150 0.5× 146 0.5× 217 1.0× 69 0.4× 22 613
Inn Soo Kang South Korea 21 384 1.3× 291 1.0× 158 0.6× 369 1.8× 23 0.1× 90 1.1k
Mei Baker United States 20 202 0.7× 620 2.1× 418 1.5× 49 0.2× 154 0.8× 58 1.4k
Chiara Cacciatore Italy 12 110 0.4× 240 0.8× 269 1.0× 380 1.8× 43 0.2× 24 795
Philip M. Marden United States 8 196 0.6× 323 1.1× 214 0.8× 84 0.4× 48 0.3× 12 710
Makoto Anzo Japan 18 133 0.4× 147 0.5× 259 0.9× 118 0.6× 82 0.4× 35 794
Delphine Zénaty France 18 168 0.6× 522 1.8× 438 1.5× 92 0.4× 46 0.2× 34 1000
Sandra Darilek United States 13 516 1.7× 456 1.5× 198 0.7× 44 0.2× 23 0.1× 24 780
R. Penketh United Kingdom 19 485 1.6× 238 0.8× 375 1.3× 186 0.9× 27 0.1× 49 1.1k
Mette Viuff Denmark 16 114 0.4× 592 2.0× 428 1.5× 76 0.4× 32 0.2× 26 814

Countries citing papers authored by Stuart W. Tinker

Since Specialization
Citations

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

Fields of papers citing papers by Stuart W. Tinker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stuart W. Tinker. 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 Stuart W. Tinker. The network helps show where Stuart W. Tinker may publish in the future.

Co-authorship network of co-authors of Stuart W. Tinker

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

All Works

15 of 15 papers shown
1.
Oliver, Tiffany, Candace D. Middlebrooks, Stuart W. Tinker, et al.. (2014). An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction. PLoS ONE. 9(6). e99560–e99560. 14 indexed citations
2.
Hollis, NaTasha D., Emily G. Allen, Tiffany Oliver, et al.. (2013). Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: A report from the National Down Syndrome Project. American Journal of Medical Genetics Part A. 161(3). 438–444. 41 indexed citations
3.
Bean, Lora Jh, Stuart W. Tinker, Cristina da Silva, & Madhuri Hegde. (2013). Free the Data: One Laboratory's Approach to Knowledge-Based Genomic Variant Classification and Preparation for EMR Integration of Genomic Data. Human Mutation. 34(9). 1183–1188. 39 indexed citations
4.
Middlebrooks, Candace D., Nandita Mukhopadhyay, Stuart W. Tinker, et al.. (2013). Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. Human Molecular Genetics. 23(2). 408–417. 17 indexed citations
5.
Hunter, Jessica Ezzell, Michael P. Epstein, Stuart W. Tinker, Ann Abramowitz, & Stephanie L. Sherman. (2011). The FMR1 Premutation and Attention-Deficit Hyperactivity Disorder (ADHD): Evidence for a Complex Inheritance. Behavior Genetics. 42(3). 415–422. 35 indexed citations
6.
Bean, Lora Jh, Emily G. Allen, Stuart W. Tinker, et al.. (2011). Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: A report from the National Down Syndrome Project. Birth Defects Research Part A Clinical and Molecular Teratology. 91(10). 885–893. 46 indexed citations
7.
Oliver, Tiffany, Stuart W. Tinker, Emily G. Allen, et al.. (2011). Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. Human Genetics. 131(7). 1039–1046. 35 indexed citations
8.
Locke, Adam E., Kenneth J. Dooley, Stuart W. Tinker, et al.. (2010). Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genetic Epidemiology. 34(6). 613–623. 63 indexed citations
9.
Oliver, Tiffany, et al.. (2009). Investigation of factors associated with paternal nondisjunction of chromosome 21. American Journal of Medical Genetics Part A. 149A(8). 1685–1690. 23 indexed citations
10.
Freeman, Sallie B., Lora Bean, Emily G. Allen, et al.. (2008). Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project. Genetics in Medicine. 10(3). 173–180. 204 indexed citations
11.
Oliver, Tiffany, Eleanor Feingold, Kai Yu, et al.. (2008). New Insights into Human Nondisjunction of Chromosome 21 in Oocytes. PLoS Genetics. 4(3). e1000033–e1000033. 130 indexed citations
12.
Hunter, Jessica Ezzell, Michael P. Epstein, Stuart W. Tinker, Krista Charen, & Stephanie L. Sherman. (2008). Fragile X‐associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. Genetic Epidemiology. 32(6). 553–559. 28 indexed citations
13.
Allen, Emily G., Jorge L. Juncos, Richard Letz, et al.. (2008). Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test battery. Journal of Medical Genetics. 45(5). 290–297. 27 indexed citations
14.
Freeman, Sallie B., Emily G. Allen, Stuart W. Tinker, et al.. (2007). The National down Syndrome Project: Design and Implementation. Public Health Reports. 122(1). 62–72. 60 indexed citations
15.
Kerstann, Kimberly F., Eleanor Feingold, Sallie B. Freeman, et al.. (2004). Linkage disequilibrium mapping in trisomic populations: Analytical approaches and an application to congenital heart defects in Down syndrome. Genetic Epidemiology. 27(3). 240–251. 14 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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