Lisa Belter

485 total citations
31 papers, 300 citations indexed

About

Lisa Belter is a scholar working on Genetics, Surgery and Clinical Psychology. According to data from OpenAlex, Lisa Belter has authored 31 papers receiving a total of 300 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 13 papers in Surgery and 6 papers in Clinical Psychology. Recurrent topics in Lisa Belter's work include Neurogenetic and Muscular Disorders Research (27 papers), Congenital Anomalies and Fetal Surgery (8 papers) and Family and Disability Support Research (6 papers). Lisa Belter is often cited by papers focused on Neurogenetic and Muscular Disorders Research (27 papers), Congenital Anomalies and Fetal Surgery (8 papers) and Family and Disability Support Research (6 papers). Lisa Belter collaborates with scholars based in United States, United Kingdom and Switzerland. Lisa Belter's co-authors include Jill Jarecki, Rosángel Cruz, Michael S. Wolf, Stacy Cooper Bailey, Anjali U. Pandit, Delesha M. Carpenter, Mary Schroth, Mary Ann Curry, Cynthia C. Jones and Kenneth Hobby and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Medical Care.

In The Last Decade

Lisa Belter

28 papers receiving 280 citations

Peers

Lisa Belter
Daniel Birchmore United States
Andréa Rodrigues da Costa Brazil
Jeanette Blacklock United Kingdom
Jingfang Hong China
Nani Draman Malaysia
Elaine Y. L. Tsui Canada
Pınar Ergenekon Türkiye
Carla W. Roberts United States
Alyssa M. Schlenz United States
Julie Coffey United States
Daniel Birchmore United States
Lisa Belter
Citations per year, relative to Lisa Belter Lisa Belter (= 1×) peers Daniel Birchmore

Countries citing papers authored by Lisa Belter

Since Specialization
Citations

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

Fields of papers citing papers by Lisa Belter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa Belter

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa Belter. A scholar is included among the top collaborators of Lisa Belter 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 Lisa Belter. Lisa Belter 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.
Lavelle, Tara A., Stacey Kowal, Sheila Shapouri, et al.. (2025). Mental Health, Quality of Life, and Work Functioning of Parents of Children Who Have Died of Spinal Muscular Atrophy. Value in Health. 29(2). 257–266. 1 indexed citations
2.
Lerner, Debra, Michael Song, Lisa Belter, et al.. (2025). Bereavement Experiences Among Parents of Children With Spinal Muscular Atrophy Type 1. Journal of Pain and Symptom Management. 71(1). 89–98.e3.
3.
Lefton‐Greif, Maureen A., Lisa Belter, Jill Jarecki, et al.. (2025). Patient-reported assessment of bulbar function in spinal muscular atrophy (SMA): Validation of a self-report scale. Journal of Neuromuscular Diseases. 12(3). 394–407.
4.
Belter, Lisa, et al.. (2024). Newborn Screening and Birth Prevalence for Spinal Muscular Atrophy in the US. JAMA Pediatrics. 178(9). 946–946. 3 indexed citations
5.
Curry, Mary Ann, Rosángel Cruz, Lisa Belter, Mary Schroth, & Jill Jarecki. (2024). Assessment of Barriers to Referral and Appointment Wait Times for the Evaluation of Spinal Muscular Atrophy (SMA): Findings from a Web-Based Physician Survey. Neurology and Therapy. 13(3). 583–598. 1 indexed citations
6.
Belter, Lisa, et al.. (2023). Telemedicine Use, Comfort, and Perceived Effectiveness in the Spinal Muscular Atrophy Community. Telemedicine Journal and e-Health. 30(2). 536–544. 4 indexed citations
7.
Staunton, Hannah, Sophie Cleanthous, Stefan Cano, et al.. (2023). A Mixed-method Approach to Develop an Ambulatory Module of the SMA Independence Scale. Journal of Neuromuscular Diseases. 10(6). 1093–1109. 2 indexed citations
8.
Belter, Lisa, et al.. (2023). Evaluating Perceived Fatigue within an Adult Spinal Muscular Atrophy Population. Neurology and Therapy. 12(6). 2161–2175. 3 indexed citations
9.
Lerner, Debra, Lisa Belter, Stacey Kowal, et al.. (2023). Assessing the impact of grief on quality of life, work productivity, and health outcomes for parents bereaved from SMA: A study protocol. Cost Effectiveness and Resource Allocation. 21(1). 55–55. 2 indexed citations
10.
Curry, Mary Ann, et al.. (2023). Effects of the COVID-19 Pandemic on SMA Screening and Care: Physician and Community Insights. Neurology and Therapy. 12(5). 1631–1647. 1 indexed citations
11.
12.
Belter, Lisa, Rosángel Cruz, & Jill Jarecki. (2020). Health Utility Index Scores in treated and untreated patients with Spinal Muscular Atrophy: Findings from the 2019 Cure SMA Community Update Survey (4564). Neurology. 94(15_supplement). 1 indexed citations
13.
Belter, Lisa, et al.. (2020). Economic burden of spinal muscular atrophy: an analysis of claims data. SHILAP Revista de lepidopterología. 8(1). 1843277–1843277. 17 indexed citations
14.
Belter, Lisa, Rosángel Cruz, & Jill Jarecki. (2020). Quality of life data for individuals affected by spinal muscular atrophy: a baseline dataset from the Cure SMA Community Update Survey. Orphanet Journal of Rare Diseases. 15(1). 217–217. 39 indexed citations
15.
16.
Cruz, Rosángel, et al.. (2019). Evaluating Benefit-risk Decision-making in Spinal Muscular Atrophy: A First-ever Study to Assess Risk Tolerance in the SMA Patient Community. Clinical Therapeutics. 41(5). 943–960.e4. 19 indexed citations
17.
Belter, Lisa, Rosángel Cruz, & Jill Jarecki. (2019). Work Productivity Activity Impairment Results from the Cure SMA 2018 Community Update Survey (P1.9-070). Neurology. 92(15_supplement).
18.
Jones, Cynthia C., Suzanne F. Cook, Jill Jarecki, et al.. (2019). Spinal Muscular Atrophy (SMA) Subtype Concordance in Siblings: Findings From the Cure SMA Cohort. Journal of Neuromuscular Diseases. 7(1). 33–40. 15 indexed citations
19.
Wolf, Michael S., Stacy Cooper Bailey, Marina Serper, et al.. (2014). Comparative Effectiveness of Patient-centered Strategies to Improve FDA Medication Guides. Medical Care. 52(9). 781–789. 33 indexed citations
20.
Bailey, Stacy Cooper, et al.. (2013). The availability, functionality, and quality of mobile applications supporting medication self-management. Journal of the American Medical Informatics Association. 21(3). 542–546. 52 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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