Tracie C. Rosser

715 total citations
13 papers, 444 citations indexed

About

Tracie C. Rosser is a scholar working on Public Health, Environmental and Occupational Health, Molecular Biology and Epidemiology. According to data from OpenAlex, Tracie C. Rosser has authored 13 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Public Health, Environmental and Occupational Health, 5 papers in Molecular Biology and 4 papers in Epidemiology. Recurrent topics in Tracie C. Rosser's work include Down syndrome and intellectual disability research (9 papers), Congenital heart defects research (4 papers) and Congenital Heart Disease Studies (3 papers). Tracie C. Rosser is often cited by papers focused on Down syndrome and intellectual disability research (9 papers), Congenital heart defects research (4 papers) and Congenital Heart Disease Studies (3 papers). Tracie C. Rosser collaborates with scholars based in United States and United Kingdom. Tracie C. Rosser's co-authors include Yunlong Qin, Yue Feng, Abrar Qurashi, Donghua Tian, Peng Jin, Huijie Liu, Ranhui Duan, Stephen T. Warren, Stephanie L. Sherman and George T. Capone and has published in prestigious journals such as Neuron, Scientific Reports and Journal of Autism and Developmental Disorders.

In The Last Decade

Tracie C. Rosser

13 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tracie C. Rosser United States	10	260	205	121	91	86	13	444
Heidi Cope United States	15	148 0.6×	291 1.4×	134 1.1×	86 0.9×	141 1.6×	37	615
Laëtitia Lambert France	11	235 0.9×	351 1.7×	49 0.4×	41 0.5×	77 0.9×	32	509
Eulália Calado Portugal	14	176 0.7×	217 1.1×	54 0.4×	121 1.3×	150 1.7×	21	615
Matthieu Raveau Japan	10	232 0.9×	229 1.1×	212 1.8×	93 1.0×	99 1.2×	13	535
A. C. Warren United States	9	286 1.1×	222 1.1×	201 1.7×	25 0.3×	43 0.5×	15	611
Jes Fagerness United States	7	206 0.8×	143 0.7×	32 0.3×	38 0.4×	78 0.9×	7	685
Elisabeth Gabau Spain	16	336 1.3×	463 2.3×	45 0.4×	39 0.4×	103 1.2×	36	675
Carmela Lopes France	12	243 0.9×	223 1.1×	219 1.8×	43 0.5×	31 0.4×	21	482
Heidi Mateus Colombia	11	165 0.6×	119 0.6×	91 0.8×	45 0.5×	33 0.4×	32	362

Countries citing papers authored by Tracie C. Rosser

Since Specialization

Citations

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

Fields of papers citing papers by Tracie C. Rosser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tracie C. Rosser. 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 Tracie C. Rosser. The network helps show where Tracie C. Rosser may publish in the future.

Co-authorship network of co-authors of Tracie C. Rosser

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

All Works

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13 of 13 papers shown

Feldman, E., Yunqi Li, David J. Cutler, et al.. (2025). Genome‐Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS. Genetic Epidemiology. 49(4). e70010–e70010. 1 indexed citations

Fidler, Deborah J., Nathaniel R. Riggs, Anna J. Esbensen, et al.. (2022). Outreach and engagement efforts in research on Down syndrome: An NIH INCLUDE Working Group consensus statement. PubMed. 63. 247–267. 3 indexed citations

Soriano, Laura del Hoyo, et al.. (2021). Relationship between Apgar scores and long-term cognitive outcomes in individuals with Down syndrome. Scientific Reports. 11(1). 12707–12707. 3 indexed citations

Channell, Marie Moore, George T. Capone, E. Mark Mahone, et al.. (2021). Capturing cognitive and behavioral variability among individuals with Down syndrome: a latent profile analysis. Journal of Neurodevelopmental Disorders. 13(1). 16–16. 20 indexed citations

Soriano, Laura del Hoyo, et al.. (2020). Gestational age is related to symptoms of attention-deficit/hyperactivity disorder in late-preterm to full-term children and adolescents with down syndrome. Scientific Reports. 10(1). 20345–20345. 9 indexed citations

Channell, Marie Moore, Laura J. Hahn, Tracie C. Rosser, et al.. (2019). Characteristics Associated with Autism Spectrum Disorder Risk in Individuals with Down Syndrome. Journal of Autism and Developmental Disorders. 49(9). 3543–3556. 27 indexed citations

Rosser, Tracie C., Jamie O. Edgin, George T. Capone, et al.. (2018). Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project. American Journal on Intellectual and Developmental Disabilities. 123(6). 514–528. 23 indexed citations

Rambo‐Martin, Benjamin L., David J. Cutler, Lora Jh Bean, et al.. (2017). Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 Genes Genomes Genetics. 8(1). 105–111. 11 indexed citations

Edgin, Jamie O., Payal Anand, Tracie C. Rosser, et al.. (2017). The Arizona Cognitive Test Battery for Down Syndrome: Test-Retest Reliability and Practice Effects. American Journal on Intellectual and Developmental Disabilities. 122(3). 215–234. 33 indexed citations

10.

Charen, Krista, et al.. (2017). Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome. Journal of Genetic Counseling. 26(6). 1333–1340. 12 indexed citations

11.

Zeng, Zhen, Adam E. Locke, Lora Jh Bean, et al.. (2015). Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. G3 Genes Genomes Genetics. 5(10). 1961–1971. 27 indexed citations

12.

Locke, Adam E., Lora Jh Bean, Tracie C. Rosser, et al.. (2014). Contribution of copy-number variation to Down syndrome–associated atrioventricular septal defects. Genetics in Medicine. 17(7). 554–560. 20 indexed citations

13.

Jin, Peng, Ranhui Duan, Abrar Qurashi, et al.. (2007). Pur α Binds to rCGG Repeats and Modulates Repeat-Mediated Neurodegeneration in a Drosophila Model of Fragile X Tremor/Ataxia Syndrome. Neuron. 55(4). 556–564. 255 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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