Tasha Cate‐Carter

685 total citations
12 papers, 546 citations indexed

About

Tasha Cate‐Carter is a scholar working on Developmental and Educational Psychology, Molecular Biology and Genetics. According to data from OpenAlex, Tasha Cate‐Carter has authored 12 papers receiving a total of 546 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Developmental and Educational Psychology, 4 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Tasha Cate‐Carter's work include Reading and Literacy Development (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Tasha Cate‐Carter is often cited by papers focused on Reading and Literacy Development (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Tasha Cate‐Carter collaborates with scholars based in Canada, Italy and United States. Tasha Cate‐Carter's co-authors include James L. Kennedy, Erin Dalton, Emanuela Mundo, Sagar V. Parikh, Maureen W. Lovett, Cathy L. Barr, Rosemary Tannock, Tom Humphries, Jillian M. Couto and Barbara Anderson and has published in prestigious journals such as Molecular Psychiatry, Schizophrenia Research and Bipolar Disorders.

In The Last Decade

Tasha Cate‐Carter

12 papers receiving 529 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tasha Cate‐Carter Canada 10 224 217 189 138 76 12 546
Laura Vanzin Italy 10 78 0.3× 157 0.7× 103 0.5× 171 1.2× 33 0.4× 14 397
Kimberly E. Bodner United States 13 182 0.8× 133 0.6× 74 0.4× 70 0.5× 60 0.8× 19 484
Helen Pay United Kingdom 7 280 1.3× 48 0.2× 59 0.3× 53 0.4× 35 0.5× 8 404
Valentina Riva Italy 14 57 0.3× 289 1.3× 108 0.6× 81 0.6× 137 1.8× 47 631
Jacquelyn J. Gillis United States 8 204 0.9× 201 0.9× 63 0.3× 77 0.6× 10 0.1× 10 382
Audrey S. Bahrick United States 7 99 0.4× 124 0.6× 22 0.1× 116 0.8× 16 0.2× 8 465
Glenn Richmond United States 8 194 0.9× 104 0.5× 16 0.1× 66 0.5× 16 0.2× 17 361
Jane L. Ebejer Australia 6 168 0.8× 40 0.2× 21 0.1× 75 0.5× 25 0.3× 8 329
Hannah Kirk Australia 12 122 0.5× 114 0.5× 45 0.2× 61 0.4× 22 0.3× 26 397
Holly Garwood United Kingdom 7 94 0.4× 254 1.2× 91 0.5× 103 0.7× 19 0.3× 9 572

Countries citing papers authored by Tasha Cate‐Carter

Since Specialization
Citations

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

Fields of papers citing papers by Tasha Cate‐Carter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tasha Cate‐Carter. 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 Tasha Cate‐Carter. The network helps show where Tasha Cate‐Carter may publish in the future.

Co-authorship network of co-authors of Tasha Cate‐Carter

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

All Works

12 of 12 papers shown
1.
Tran, Christopher, K. Wigg, Tasha Cate‐Carter, et al.. (2014). Association of the ROBO1 gene with reading disabilities in a family‐based analysis. Genes Brain & Behavior. 13(4). 430–438. 25 indexed citations
2.
Tran, Christopher, France Gagnon, K. Wigg, et al.. (2013). A family‐based association analysis and meta‐analysis of the reading disabilities candidate gene DYX1C1. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(2). 146–156. 16 indexed citations
3.
Lovett, Maureen W., et al.. (2011). Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia. Behavior Genetics. 41(1). 77–89. 28 indexed citations
4.
Couto, Jillian M., Katherine Huang, Zhaodong Xu, et al.. (2009). Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(2). 447–462. 46 indexed citations
5.
Couto, Jillian M., Lissette Gomez, Karen Wigg, et al.. (2008). The KIAA0319-Like(KIAA0319L)Gene on Chromosome 1p34 as a Candidate for Reading Disabilities. Journal of Neurogenetics. 22(4). 295–313. 43 indexed citations
6.
Barr, Cathy L., K. Wigg, Nancy Laurin, et al.. (2008). Attention deficit/hyperactivity disorder and dyslexia: evidence for shared genetic susceptibility. European Psychiatry. 23. S25–S26. 1 indexed citations
7.
Luca, Pietro De, Nancy Laurin, Virginia L. Misener, et al.. (2007). Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems. Molecular Psychiatry. 12(8). 776–785. 27 indexed citations
8.
Wigg, Karen, Jillian M. Couto, Yu Feng, et al.. (2005). Investigation of the Relationship of Attention Deficit Hyperactivity Disorder to the EKN1 Gene on Chromosome 15q21. Scientific Studies of Reading. 9(3). 261–283. 11 indexed citations
9.
Wigg, K., Jillian M. Couto, Yu Feng, et al.. (2004). Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Molecular Psychiatry. 9(12). 1111–1121. 100 indexed citations
10.
Wong, Albert H.C., Joseph Trakalo, Tasha Cate‐Carter, et al.. (2003). N‐methyl‐d‐aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia: TDT and case‐control analyses. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 119B(1). 24–27. 24 indexed citations
11.
Dalton, Erin, Tasha Cate‐Carter, Emanuela Mundo, Sagar V. Parikh, & James L. Kennedy. (2003). Suicide risk in bipolar patients: the role of co‐morbid substance use disorders. Bipolar Disorders. 5(1). 58–61. 224 indexed citations
12.
Trakalo, Joseph, Tasha Cate‐Carter, F. Ajmar, et al.. (2003). Glutamate receptor gene (GRIN1, GRIN2B) in schizophrenia: TDT and case-controls analyses. Schizophrenia Research. 60(1). 85–85. 1 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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