Erin M. Carter

534 total citations
20 papers, 310 citations indexed

About

Erin M. Carter is a scholar working on Genetics, Rheumatology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Erin M. Carter has authored 20 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 6 papers in Rheumatology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Erin M. Carter's work include Connective tissue disorders research (18 papers), Bone and Dental Protein Studies (3 papers) and Aortic Disease and Treatment Approaches (2 papers). Erin M. Carter is often cited by papers focused on Connective tissue disorders research (18 papers), Bone and Dental Protein Studies (3 papers) and Aortic Disease and Treatment Approaches (2 papers). Erin M. Carter collaborates with scholars based in United States, United Kingdom and Norway. Erin M. Carter's co-authors include Cathleen Raggio, Wayne A. Cabral, Aileen M. Barnes, Weizhong Chang, MaryAnn Weis, David R. Eyre, Elena Makareeva, Sergey Leikin, Joan C. Marini and Charles N. Rotimi and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Erin M. Carter

15 papers receiving 304 citations

Peers

Erin M. Carter
Ok-Hwa Kim South Korea
A Nicholls United Kingdom
Patrick L. Wilson United States
Ok-Hwa Kim South Korea
Erin M. Carter
Citations per year, relative to Erin M. Carter Erin M. Carter (= 1×) peers Ok-Hwa Kim

Countries citing papers authored by Erin M. Carter

Since Specialization
Citations

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

Fields of papers citing papers by Erin M. Carter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erin M. Carter

This figure shows the co-authorship network connecting the top 25 collaborators of Erin M. Carter. A scholar is included among the top collaborators of Erin M. 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 Erin M. Carter. Erin M. Carter 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
2.
Carter, Erin M., et al.. (2025). Health-related quality of life in individuals with osteogenesis imperfecta in the United States: a cross-sectional study. Orphanet Journal of Rare Diseases. 20(1). 537–537.
3.
Htwe, Su, Sandra McDonald, Marta Bértoli, et al.. (2025). Mental health conditions, physical functioning, and health-related quality of life in adults with a skeletal dysplasia: a cross-sectional multinational study. Orphanet Journal of Rare Diseases. 20(1). 116–116. 1 indexed citations
4.
Carter, Erin M., Julian Vallejo, Michael Wacker, et al.. (2025). Cardiac health, type I collagen, and aging in the oim/oim mouse model of osteogenesis imperfecta and a cohort of adults with OI. American Journal of Physiology-Heart and Circulatory Physiology. 328(3). H565–H580. 1 indexed citations
5.
Folkestad, Lars, Siddharth K. Prakash, Sandesh C.S. Nagamani, et al.. (2024). Cardiovascular disease in adults with osteogenesis imperfecta: clinical characteristics, care recommendations, and research priorities identified using a modified Delphi technique. Journal of Bone and Mineral Research. 40(2). 211–221.
6.
Morales, Julia, Andrew D. Wiese, Kristin M. Kostick, et al.. (2024). Qualitative investigation of school experiences in children with osteogenesis imperfecta. Children s Health Care. 1–28.
7.
Ashton, Katie A., K.T. Lee, Omkar L. Patkar, et al.. (2024). Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia. SHILAP Revista de lepidopterología. 3. 101958–101958.
8.
Carter, Erin M., et al.. (2022). Patient‐reported prevalence of gastrointestinal issues in the adult skeletal dysplasia population with a concentration on osteogenesis imperfecta. American Journal of Medical Genetics Part A. 188(5). 1435–1442. 8 indexed citations
9.
Carter, Erin M., et al.. (2021). Orthopedic considerations and surgical outcomes in Ehlers–Danlos syndromes. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 187(4). 458–465. 15 indexed citations
10.
Raggio, Cathleen, et al.. (2020). Joint Replacements in Individuals With Skeletal Dysplasias: One Institution’s Experience and Response to Operative Complications. The Journal of Arthroplasty. 35(8). 1993–2001. 7 indexed citations
11.
Carter, Erin M., et al.. (2020). Cardiopulmonary Status in Adults with Osteogenesis Imperfecta: Intrinsic Lung Disease May Contribute More Than Scoliosis. Clinical Orthopaedics and Related Research. 478(12). 2833–2843. 21 indexed citations
12.
Carter, Erin M., et al.. (2020). Respiratory impairment impacts QOL in osteogenesis imperfecta independent of skeletal abnormalities. Archives of Osteoporosis. 15(1). 153–153. 13 indexed citations
13.
Carter, Erin M., et al.. (2020). Quality of life in adults with achondroplasia in the United States. American Journal of Medical Genetics Part A. 185(3). 695–701. 21 indexed citations
14.
Carter, Erin M., et al.. (2017). Bone robusticity in two distinct skeletal dysplasias diverges from established patterns. Journal of Orthopaedic Research®. 35(11). 2392–2396. 5 indexed citations
15.
Ashinsky, Beth G., Kenneth W. Fishbein, Erin M. Carter, et al.. (2016). Multiparametric Classification of Skin from Osteogenesis Imperfecta Patients and Controls by Quantitative Magnetic Resonance Microimaging. PLoS ONE. 11(7). e0157891–e0157891. 3 indexed citations
16.
Boskey, Adele L., Lyudmila Spevak, Nancy Pleshko, et al.. (2015). Are Changes in Composition in Response to Treatment of a Mouse Model of Osteogenesis Imperfecta Sex-dependent?. Clinical Orthopaedics and Related Research. 473(8). 2587–2598. 17 indexed citations
17.
Barnes, Aileen M., Erin M. Carter, Wayne A. Cabral, et al.. (2010). Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding. New England Journal of Medicine. 362(6). 521–528. 121 indexed citations
18.
Carter, Erin M. & Cathleen Raggio. (2009). Genetic and orthopedic aspects of collagen disorders. Current Opinion in Pediatrics. 21(1). 46–54. 42 indexed citations
19.
Carter, Erin M., et al.. (2008). The Kathryn O. and Alan C. Greenberg Center for Skeletal Dysplasias: An Interdisciplinary Approach. HSS Journal® The Musculoskeletal Journal of Hospital for Special Surgery. 4(2). 112–116. 3 indexed citations
20.
Carter, Erin M., Jessica G. Davis, & Cathleen Raggio. (2007). Advances in understanding etiology of achondroplasia and review of management. Current Opinion in Pediatrics. 19(1). 32–37. 32 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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