Curtis Rogers

495 total citations
22 papers, 249 citations indexed

About

Curtis Rogers is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Curtis Rogers has authored 22 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Curtis Rogers's work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Curtis Rogers is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Curtis Rogers collaborates with scholars based in United States, Italy and Australia. Curtis Rogers's co-authors include Perry V. Halushka, Julius Sagel, John A. Colwell, Katy Phelan, Sara M. Sarasua, Luigi Boccuto, Charles E. Schwartz, Duane Superneau, John M. Graham and Ken Corning and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Metabolism.

In The Last Decade

Curtis Rogers

20 papers receiving 234 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Curtis Rogers United States 10 101 96 31 26 21 22 249
Tanushree Haldar United States 8 114 1.1× 177 1.8× 18 0.6× 35 1.3× 44 2.1× 16 298
Muhammad Arshad Pakistan 8 145 1.4× 13 0.1× 11 0.4× 17 0.7× 19 0.9× 22 291
Annunziata Fragasso Germany 8 184 1.8× 82 0.9× 36 1.2× 13 0.5× 10 0.5× 16 353
Ioanna Tachmazidou United Kingdom 7 91 0.9× 165 1.7× 18 0.6× 15 0.6× 21 1.0× 11 284
Hugues Henry Switzerland 10 103 1.0× 58 0.6× 8 0.3× 89 3.4× 14 0.7× 12 362
Amy Shealy United States 5 87 0.9× 75 0.8× 18 0.6× 16 0.6× 24 1.1× 9 178
Ren‐Hua Chung Taiwan 12 166 1.6× 148 1.5× 7 0.2× 10 0.4× 16 0.8× 52 410
Hiroyuki Shigeta Japan 7 148 1.5× 179 1.9× 15 0.5× 18 0.7× 41 2.0× 31 357
Said Al‐Yahyaee Oman 11 84 0.8× 64 0.7× 31 1.0× 54 2.1× 56 2.7× 29 271
Sébastien Robiou-du-Pont Canada 8 112 1.1× 88 0.9× 7 0.2× 15 0.6× 35 1.7× 12 326

Countries citing papers authored by Curtis Rogers

Since Specialization
Citations

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

Fields of papers citing papers by Curtis Rogers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Curtis Rogers

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

All Works

20 of 20 papers shown
1.
Boccuto, Luigi, Giuseppe Guido Maria Scarlata, Sara M. Sarasua, et al.. (2025). Metabolic Dysfunction-Associated Steatotic Liver Disease in a Patient with Phelan–McDermid Syndrome. Life. 15(10). 1586–1586.
2.
Sarasua, Sara M., Jane M. DeLuca, Curtis Rogers, et al.. (2023). Head Size in Phelan–McDermid Syndrome: A Literature Review and Pooled Analysis of 198 Patients Identifies Candidate Genes on 22q13. Genes. 14(3). 540–540. 4 indexed citations
3.
Sarasua, Sara M., Linda Ward, William E. Bennett, et al.. (2023). Stratification of a Phelan–McDermid Syndrome Population Based on Their Response to Human Growth Hormone and Insulin-like Growth Factor. Genes. 14(2). 490–490. 3 indexed citations
4.
Sarasua, Sara M., et al.. (2023). Lymphedema is associated with CELSR1 in Phelan–McDermid syndrome. Clinical Genetics. 104(4). 472–478. 6 indexed citations
5.
Sohn, Young Bae, Curtis Rogers, Tim Wood, et al.. (2022). RNA analysis of the GALNS transcript reveals novel pathogenic mechanisms associated with Morquio syndrome A. Molecular Genetics and Metabolism Reports. 31. 100875–100875. 1 indexed citations
6.
Sarasua, Sara M., et al.. (2022). Sleep and Phelan–McDermid Syndrome: Lessons from the International Registry and the scientific literature. Molecular Genetics & Genomic Medicine. 10(10). e2035–e2035. 4 indexed citations
7.
Boccuto, Luigi, Andrew R. Mitz, Ludovico Abenavoli, et al.. (2022). Phenotypic Variability in Phelan–McDermid Syndrome and Its Putative Link to Environmental Factors. Genes. 13(3). 528–528. 6 indexed citations
8.
Oberman, Lindsay M., Melanie May, Sujata Srikanth, et al.. (2021). Genetic and metabolic profiling of individuals with Phelan‐McDermid syndrome presenting with seizures. Clinical Genetics. 101(1). 87–100. 13 indexed citations
9.
Srikanth, Sujata, Cinthya Zepeda‐Mendoza, Kelly L. Jones, et al.. (2021). Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome. PLoS ONE. 16(7). e0253859–e0253859. 6 indexed citations
10.
Sarasua, Sara M., et al.. (2021). Genetic Findings as the Potential Basis of Personalized Pharmacotherapy in Phelan-McDermid Syndrome. Genes. 12(8). 1192–1192. 10 indexed citations
11.
Li, Dong, Rebecca C. Ahrens‐Nicklas, Janice Baker, et al.. (2020). The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?. American Journal of Medical Genetics Part A. 182(9). 2058–2067. 14 indexed citations
12.
DuPont, Barbara R., Curtis Rogers, Sara M. Sarasua, et al.. (2020). Neurofibromatosis type 2 in Phelan-McDermid syndrome: Institutional experience and review of the literature. European Journal of Medical Genetics. 63(11). 104042–104042. 11 indexed citations
13.
Rogers, Curtis, et al.. (2017). Marfan Syndrome (MFS): Visual Diagnosis and Early Identification. Journal of Pediatric Health Care. 31(5). 609–617. 1 indexed citations
14.
Goff, Carine Le, Curtis Rogers, Wilfried Le Goff, et al.. (2016). Heterozygous Mutations in MAP3K7 , Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome. The American Journal of Human Genetics. 99(2). 407–413. 25 indexed citations
15.
Holaday, Bonnie, et al.. (2016). Breastfeeding and Growth of Children in the Peri/postnatal Epigenetic Twins Study (PETS). Journal of Human Lactation. 32(3). 481–488. 9 indexed citations
16.
Rogers, Curtis. (2009). Social Media, Libraries, and Web 2.0: How American Libraries are Using New Tools for Public Relations and to Attract New Users. The South Carolina State Library Digital Collections (South Carolina State Library). 19 indexed citations
17.
Graham, John M., et al.. (1998). FG syndrome: Report of three new families with linkage to xq12-q22.1. American Journal of Medical Genetics. 80(2). 145–156. 27 indexed citations
18.
Rogers, Curtis. (1998). A Theoretical Look at Electronic Community's Conversation and Curriculum.. 2 indexed citations
19.
Graham, John M., et al.. (1998). FG syndrome: Report of three new families with linkage to xq12‐q22.1. American Journal of Medical Genetics. 80(2). 145–156. 2 indexed citations
20.
Colwell, John A., et al.. (1979). Platelet adhesion and aggregation in diabetes mellitus. Metabolism. 28(4). 394–400. 70 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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