Erika Carter

612 total citations
15 papers, 338 citations indexed

About

Erika Carter is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Erika Carter has authored 15 papers receiving a total of 338 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Erika Carter's work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital heart defects research (4 papers). Erika Carter is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital heart defects research (4 papers). Erika Carter collaborates with scholars based in United States and Kosovo. Erika Carter's co-authors include Patricia Heard, Daniel E. Hale, Jannine D. Cody, Bridgette Soileau, Courtney Sebold, Louise O’Donnell, Brian P. Perry, Jack L. Lancaster, Annice Hill and Jon Gelfond and has published in prestigious journals such as International Journal of Environmental Research and Public Health, Human Genetics and Otology & Neurotology.

In The Last Decade

Erika Carter

15 papers receiving 268 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erika Carter United States	10	268	118	82	54	26	15	338
Bridgette Soileau United States	11	345 1.3×	165 1.4×	102 1.2×	71 1.3×	27 1.0×	16	408
Annice Hill United States	7	212 0.8×	108 0.9×	69 0.8×	49 0.9×	16 0.6×	10	253
Nathalie Marle France	11	237 0.9×	170 1.4×	56 0.7×	42 0.8×	29 1.1×	23	373
Patricia Heard United States	13	391 1.5×	210 1.8×	111 1.4×	98 1.8×	30 1.2×	22	499
Magdalena Bartnik Poland	10	168 0.6×	140 1.2×	56 0.7×	37 0.7×	8 0.3×	23	266
Alison Yeung Australia	11	283 1.1×	130 1.1×	69 0.8×	16 0.3×	37 1.4×	19	385
Fernando Santos Spain	9	228 0.9×	193 1.6×	84 1.0×	21 0.4×	23 0.9×	13	325
Mariana Moysés‐Oliveira Brazil	11	206 0.8×	130 1.1×	53 0.6×	35 0.6×	16 0.6×	45	300
Antoinet C.J. Gijsbers Netherlands	12	356 1.3×	212 1.8×	94 1.1×	67 1.2×	19 0.7×	15	426
Patricia D. Ghidoni United States	7	257 1.0×	181 1.5×	99 1.2×	71 1.3×	21 0.8×	8	329

Countries citing papers authored by Erika Carter

Since Specialization

Citations

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

Fields of papers citing papers by Erika Carter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erika Carter

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

All Works

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15 of 15 papers shown

Tosi, Laura L., et al.. (2023). “Osteogenesis Imperfecta Patients Wish Orthopedic Surgeons Had Better Strategies to Help with…”—Results of a Patient and Parent-Oriented Survey. Children. 10(8). 1345–1345. 1 indexed citations

Romero, Devan R., et al.. (2021). Naturalistic Topography Assessment in a Randomized Clinical Trial of Smoking Unfiltered Cigarettes: Challenges, Opportunities, and Recommendations. International Journal of Environmental Research and Public Health. 18(22). 11857–11857. 3 indexed citations

Oren, Eyal, Kim Pulvers, Devan R. Romero, et al.. (2020). Effects of Unfiltered Cigarettes on Smoking Behavior and Toxicant Exposure: Protocol for a Randomized Crossover Clinical Trial. JMIR Research Protocols. 9(12). e19603–e19603. 5 indexed citations

Khalil, Lafi S., et al.. (2020). Extensor Mechanism Ruptures and Reruptures: Perioperative Opioid Management. The Journal of Knee Surgery. 35(2). 167–175. 2 indexed citations

Sebold, Courtney, Patricia Heard, Erika Carter, et al.. (2015). A review of 18p deletions. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(3). 251–264. 57 indexed citations

Cody, Jannine D., Courtney Sebold, Patricia Heard, et al.. (2015). Consequences of chromsome18q deletions. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(3). 265–280. 46 indexed citations

Sebold, Courtney, Bridgette Soileau, Patricia Heard, et al.. (2015). Whole arm deletions of 18p: Medical and developmental effects. American Journal of Medical Genetics Part A. 167(2). 313–323. 32 indexed citations

Perry, Brian P., Courtney Sebold, Patricia Heard, et al.. (2014). Sensorineural Hearing Loss in People With Deletions of 18q. Otology & Neurotology. 35(5). 782–786. 7 indexed citations

Carter, Erika, Patricia Heard, Bridgette Soileau, et al.. (2014). Ring 18 molecular assessment and clinical consequences. American Journal of Medical Genetics Part A. 167(1). 54–63. 28 indexed citations

10.

Cody, Jannine D., Bridgette Soileau, Patricia Heard, et al.. (2013). Establishing a reference group for distal 18q-: clinical description and molecular basis. Human Genetics. 133(2). 199–209. 39 indexed citations

11.

Daviss, W. Burleson, Louise O’Donnell, Bridgette Soileau, et al.. (2013). Mood disorders in individuals with distal 18q deletions. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(8). 879–888. 10 indexed citations

12.

Sebold, Courtney, Elizabeth Roeder, Bridgette Soileau, et al.. (2010). Tetrasomy 18p: Report of the molecular and clinical findings of 43 individuals. American Journal of Medical Genetics Part A. 152A(9). 2164–2172. 50 indexed citations

13.

O’Donnell, Louise, Bridgette Soileau, Patricia Heard, et al.. (2010). Genetic determinants of autism in individuals with deletions of 18q. Human Genetics. 128(2). 155–164. 17 indexed citations

14.

Medina, Rolando, Patricia Heard, Erika Carter, et al.. (2009). Psychiatric syndromes in individuals with chromosome 18 abnormalities. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(3). 837–845. 10 indexed citations

15.

Cody, Jannine D., Courtney Sebold, Patricia Heard, et al.. (2007). Recurrent interstitial deletions of proximal 18q: A new syndrome involving expressive speech delay. American Journal of Medical Genetics Part A. 143A(11). 1181–1190. 31 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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