Natalie Street

3.5k total citations · 3 hit papers
28 papers, 2.2k citations indexed

About

Natalie Street is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Natalie Street has authored 28 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Natalie Street's work include Muscle Physiology and Disorders (20 papers), Genetic Neurodegenerative Diseases (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Natalie Street is often cited by papers focused on Muscle Physiology and Disorders (20 papers), Genetic Neurodegenerative Diseases (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Natalie Street collaborates with scholars based in United States, Canada and United Kingdom. Natalie Street's co-authors include Carla Bann, Angela Glover Blackwell, David J. Birnkrant, Leanne M. Ward, David R. Weber, Susan Apkon, Shree Pandya, Stasia Hadjiyannakis, Laura E. Case and Jean Tomezsko and has published in prestigious journals such as Neurology, PEDIATRICS and Annals of Neurology.

In The Last Decade

Natalie Street

28 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management

2018 781 citations David J. Birnkrant, K. Bushby et al. The Lancet Neurology profile →
Evidence‐based path to newborn screening for duchenne muscular dystrophy

2012 607 citations Jerry R. Mendell, Chris Shilling et al. Annals of Neurology profile →
Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan

2018 278 citations David J. Birnkrant, K. Bushby et al. The Lancet Neurology profile →

Peers

Natalie Street

GENET

CCM

PHYSI

Susan Apkon United States

Carolyn M. Constantin United States

Erik Henricson United States

James Poysky United States

Kathi Kinnett United States

Valeria Ricotti United Kingdom

Emma Ciafaloni United States

Jean Tomezsko United States

Rosaline C. M. Quinlivan United Kingdom

David D. Kilmer United States

Susan Apkon United States

Natalie Street

1.6k ×0.9

533 ×1.2

GENET

414 ×1.0

CCM

297 ×0.9

PHYSI

403 ×1.2

Citations per year, relative to Natalie Street Natalie Street (= 1×) peers Susan Apkon

Countries citing papers authored by Natalie Street

Since Specialization

Citations

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

Fields of papers citing papers by Natalie Street

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalie Street

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

All Works

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20 of 20 papers shown

Thomas, Shiny, et al.. (2025). Hearing Loss, Retinal Abnormality, and Seizures in People With Facioscapulohumeral Muscular Dystrophy. Muscle & Nerve. 72(5). 1156–1160. 1 indexed citations

Tavakoli, Norma P., Sunju Park, Michele Caggana, et al.. (2023). Multi-Laboratory Evaluation of Prototype Dried Blood Spot Quality Control Materials for Creatine Kinase-MM Newborn Screening Assays. International Journal of Neonatal Screening. 9(1). 13–13. 3 indexed citations

Thomas, Shiny, Kristin M. Conway, Natalie Street, et al.. (2022). Time to diagnosis of Duchenne muscular dystrophy remains unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000‐2015. Muscle & Nerve. 66(2). 193–197. 34 indexed citations

Conway, Kristin M., Scott D. Grosse, Lijing Ouyang, Natalie Street, & Paul A. Romitti. (2022). Direct costs of adhering to selected Duchenne muscular dystrophy Care Considerations: Estimates from a midwestern state. Muscle & Nerve. 65(5). 574–580. 2 indexed citations

Mathews, Katherine D., Kristin M. Conway, Nicholas E. Johnson, et al.. (2021). Characteristics of Clinical Trial Participants with Duchenne Muscular Dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet). Children. 8(10). 835–835. 4 indexed citations

Wallace, Bailey, Shiny Thomas, Kristin M. Conway, et al.. (2020). Characterization of individuals with selected muscular dystrophies from the expanded pilot of the Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet) in the United States. Birth Defects Research. 113(7). 560–569. 3 indexed citations

Ciafaloni, Emma, Kristin M. Conway, Natalie Street, et al.. (2020). DMD & BMD – CLINICAL. Neuromuscular Disorders. 30. S63–S63. 1 indexed citations

Birnkrant, David J., K. Bushby, Carla Bann, et al.. (2018). Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan. The Lancet Neurology. 17(5). 445–455. 278 indexed citations breakdown →

Birnkrant, David J., K. Bushby, Carla Bann, et al.. (2018). Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. The Lancet Neurology. 17(3). 251–267. 781 indexed citations breakdown →

10.

Ong, Katherine, Kathi Kinnett, Ann Martin, et al.. (2018). Evaluating Implementation of the Updated Care Considerations for Duchenne Muscular Dystrophy. PEDIATRICS. 142(Supplement 2). S118–S128. 7 indexed citations

11.

Street, Natalie, Melissa M. Adams, Christopher Cunniff, et al.. (2018). Muscular Dystrophy Surveillance, Tracking, and Research Network pilot: Population‐based surveillance of major muscular dystrophies at four U.S. sites, 2007–2011. Birth Defects Research. 110(19). 1404–1411. 11 indexed citations

12.

Ouyang, Lijing, Rodolfo Valdéz, Nicholas E. Johnson, et al.. (2018). Gender difference in clinical conditions among hospitalized adults with myotonic dystrophy. Muscle & Nerve. 59(3). 348–353. 5 indexed citations

13.

Andrews, Jennifer, Molly M. Lamb, Kristin M. Conway, et al.. (2018). Diagnostic Accuracy of Phenotype Classification in Duchenne and Becker Muscular Dystrophy Using Medical Record Data1. Journal of Neuromuscular Diseases. 5(4). 481–495. 13 indexed citations

14.

Street, Natalie, Christopher Cunniff, Joyce Oleszek, et al.. (2017). Secondary Conditions Among Males With Duchenne or Becker Muscular Dystrophy. Journal of Child Neurology. 32(7). 663–670. 47 indexed citations

15.

Pabayo, Roman, Beth E. Molnar, Natalie Street, & Ichiro Kawachi. (2014). The relationship between social fragmentation and sleep among adolescents living in Boston, Massachusetts. Journal of Public Health. 36(4). 587–598. 42 indexed citations

16.

Zhu, Yong, Paul A. Romitti, Kristin M. Conway, et al.. (2014). Complementary and Alternative Medicine for Duchenne and Becker Muscular Dystrophies: Characteristics of Users and Caregivers. Pediatric Neurology. 51(1). 71–77. 14 indexed citations

17.

Mendell, Jerry R., Chris Shilling, Nancy D. Leslie, et al.. (2012). Evidence‐based path to newborn screening for duchenne muscular dystrophy. Annals of Neurology. 71(3). 304–313. 607 indexed citations breakdown →

18.

Nabukera, Sarah K., Paul A. Romitti, Kristin Caspers, et al.. (2012). Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophy. American Journal of Medical Genetics Part A. 161(1). 70–75. 4 indexed citations

19.

McConkie‐Rosell, Allyn, Liane Abrams, Brenda Finucane, et al.. (2007). Recommendations from Multi‐disciplinary Focus Groups on Cascade Testing and Genetic Counseling for Fragile X‐associated Disorders. Journal of Genetic Counseling. 16(5). 593–606. 48 indexed citations

20.

Street, Natalie, Michael Yi, Laurie Bailey, & Robert J. Hopkin. (2006). Comparison of health-related quality of life between heterozygous women with Fabry disease, a healthy control population, and patients with other chronic disease. Genetics in Medicine. 8(6). 346–353. 40 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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