World's Best Scientists 2026 revealed!
Journal of Neuromuscular Diseases
H-index 24

Journal of Neuromuscular Diseases

Ranking & Metrics

Discipline name Position Best Scientists Publications D-Index
Medicine 1017 72 144 23

Additional Metrics

Number of Best Scientists*: 180
Documents by Best Scientists*: 221
Top 100 Ranked Scientists*: 6
SCIMAGO H-index: 43
SCIMAGO SJR: 1.016
Impact Factor: 3.4

Overview

Top Research Topics at Journal of neuromuscular diseases?

The primary areas of discussion in the journal are Disease, Internal medicine, Duchenne muscular dystrophy, Pediatrics and Physical therapy. Journal of neuromuscular diseases explores topics in Disease which can be helpful for research in disciplines like MEDLINE and Bioinformatics. In it, Gastroenterology, Endocrinology and Cardiology are investigated in conjunction with one another to address concerns in Internal medicine research.

The concepts on Duchenne muscular dystrophy presented in it can also apply to other research fields, including Exon skipping, Muscular dystrophy and Pathology. Studies on Pediatrics discussed in the journal link to the field of Cohort. Physical therapy research presented in the journal encompasses a variety of subjects, including Quality of life and Clinical trial.

Spinal muscular atrophy research discussed connects with the study of Nusinersen. The research on Nusinersen discussed in Journal of neuromuscular diseases draws on the closely related field of SMA*. Discussions in Journal of neuromuscular diseases are anchored in the subject of SMA* and the similar topic of Physical medicine and rehabilitation.

  • Disease (22.33%)
  • Internal medicine (19.92%)
  • Duchenne muscular dystrophy (17.51%)

What are the most cited papers published in the journal?

  • The Epidemiology of Neuromuscular Disorders: A Comprehensive Overview of the Literature. (112 citations)
  • Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening. (90 citations)
  • Skeletal Muscle Quantitative Nuclear Magnetic Resonance Imaging and Spectroscopy as an Outcome Measure for Clinical Trials. (87 citations)

Research areas of the most cited articles at Journal of neuromuscular diseases:

The most cited publications mostly deal with topics like Duchenne muscular dystrophy, Disease, Pediatrics, Bioinformatics and Spinal muscular atrophy. The journal publications explore topics in Disease which can be helpful for research in disciplines like Muscular dystrophy, Database, Myositis and Myopathy. The journal papers address concerns in Pediatrics which are intertwined with other disciplines, such as Physical therapy and Incidence (epidemiology).

What topics the last edition of the journal is best known for?

  • Internal medicine
  • Gene
  • Disease

The previous edition focused in particular on these issues:

Journal of neuromuscular diseases is mainly concerned with subjects like Duchenne muscular dystrophy, Internal medicine, Disease, Dystrophin and Clinical trial. The Duchenne muscular dystrophy works featured in it incorporate elements from Bioinformatics, Exon skipping, Muscular dystrophy, Pathophysiology and Simvastatin. Topics in Internal medicine were tackled in line with various other fields like Gastroenterology, Genotype and Cardiology.

The journal explores issues in Disease which can be linked to other research areas like Physical therapy, Pediatrics and Cohort. Many of the research works in Dystrophin, specifically Dystrophin gene, closely connected to disciplines like In patient. The journal addresses concerns in Clinical trial which are intertwined with other disciplines, such as Evidence-based medicine and MEDLINE.

The most cited articles from the last journal are:

  • Mechanisms and Clinical Applications of Glucocorticoid Steroids in Muscular Dystrophy (7 citations)
  • Molecular Mechanisms of Skeletal Muscle Hypertrophy. (7 citations)
  • Beyond the Traditional Clinical Trials for Amyotrophic Lateral Sclerosis and The Future Impact of Gene Therapy. (5 citations)

Papers citation over time

A key indicator for each journal is its effectiveness in reaching other researchers with the papers published at that venue.

The chart below presents the interquartile range (first quartile 25%, median 50% and third quartile 75%) of the number of citations of articles over time.

The top authors publishing in Journal of neuromuscular diseases (based on the number of publications) are:

  • Hanns Lochmüller (29 papers) published 9 papers at the last edition, 5 more than at the previous edition,
  • Annemieke Aartsma-Rus (12 papers) published 3 papers at the last edition, 2 more than at the previous edition,
  • Jan J.G.M. Verschuuren (11 papers) published 2 papers at the last edition, 1 more than at the previous edition,
  • Anthony Behin (10 papers) published 2 papers at the last edition, 1 more than at the previous edition,
  • Rita Horvath (10 papers) published 3 papers at the last edition, 1 more than at the previous edition.

The overall trend for top authors publishing in this journal is outlined below. The chart shows the number of publications at each edition of the journal for top authors.

Only papers with recognized affiliations are considered

The top affiliations publishing in Journal of neuromuscular diseases (based on the number of publications) are:

  • Boston Children's Hospital (38 papers) published 11 papers at the last edition, 4 more than at the previous edition,
  • Newcastle University (34 papers) published 4 papers at the last edition, 2 less than at the previous edition,
  • Leiden University Medical Center (29 papers) published 7 papers at the last edition, 4 more than at the previous edition,
  • Radboud University Nijmegen (26 papers) published 7 papers at the last edition, 1 more than at the previous edition,
  • University of Paris (21 papers) published 8 papers at the last edition, 5 more than at the previous edition.

The overall trend for top affiliations publishing in this journal is outlined below. The chart shows the number of publications at each edition of the journal for top affiliations.

Publication chance based on affiliation

The publication chance index shows the ratio of articles published by the best research institutions in the journal edition to all articles published within that journal. The best research institutions were selected based on the largest number of articles published during all editions of the journal.

The chart below presents the percentage ratio of articles from top institutions (based on their ranking of total papers).Top affiliations were grouped by their rank into the following tiers: top 1-10, top 11-20, top 21-50, and top 51+. Only articles with a recognized affiliation are considered.

During the most recent 2021 edition, 5.69% of publications had an unrecognized affiliation. Out of the publications with recognized affiliations, 40.52% were posted by at least one author from the top 10 institutions publishing in the journal. Another 3.45% included authors affiliated with research institutions from the top 11-20 affiliations. Institutions from the 21-50 range included 23.28% of all publications and 32.76% were from other institutions.

Returning Authors Index

A very common phenomenon observed among researchers publishing scientific articles is the intentional selection of journals they have already attended in the past. In particular, it is worth analyzing the case when the authors participate in the same journal from year to year.

The Returning Authors Index presented below illustrates the ratio of authors who participated in both a given as well as the previous edition of the journal in relation to all participants in a given year.

Returning Institution Index

The graph below shows the Returning Institution Index, illustrating the ratio of institutions that participated in both a given and the previous edition of the conference in relation to all affiliations present in a given year.

The experience to innovation index

Our experience to innovation index was created to show a cross-section of the experience level of authors publishing in a journal. The index includes the authors publishing at the last edition of a journal, grouped by total number of publications throughout their academic career (P) and the total number of citations of these publications ever received (C).

The group intervals were selected empirically to best show the diversity of the authors' experiences, their labels were selected as a convenience, not as judgment. The authors were divided into the following groups:

  • Novice - P < 5 or C < 25 (the number of publications less than 5 or the number of citations less than 25),
  • Competent - P < 10 or C < 100 (the number of publications less than 10 or the number of citations less than 100),
  • Experienced - P < 25 or C < 625 (the number of publications less than 25 or the number of citations less than 625),
  • Master - P < 50 or C < 2500 (the number of publications less than 50 or the number of citations less than 2500),
  • Star - P ≥ 50 and C ≥ 2500 (both the number of publications greater than 50 and the number of citations greater than 2500).

The chart below illustrates experience levels of first authors in cases of publications with multiple authors.

Applications of Research into Neuromuscular Diseases

One crucial aspect we must discuss is how the findings from the research into neuromuscular diseases have been applied in various fields, especially in the healthcare sector. Researchers and medical professionals have utilized the knowledge generated to improve disease management and patient outcomes significantly. For instance, the discoveries in Duchenne muscular dystrophy, such as exon skipping and pathophysiology, have led to the development of new therapies and drug treatments, reducing the disease's progression and improving patients' quality of life. The methods and techniques used in these studies are also relevant to other research areas, possibly opening new avenues for investigation. Insights drawn from research in internal medicine, particularly in gastroenterology, endocrinology, and cardiology, have been influential in managing patients with neuromuscular conditions who also have corresponding complications in these medical fields. Similarly, the field of pediatrics has immensely benefited from the research findings, particularly spinal muscular atrophy's early diagnosis and treatment, leading to better prognoses for affected children. Interestingly, the research findings have also had implications beyond the field of healthcare. For instance, the discipline of bioinformatics has drawn from the vast databases developed from neuromuscular diseases research to come up with new algorithms and models, fostering advancements in big data analysis and artificial intelligence. Lastly, the training and professional development of healthcare providers also owe a lot to these research findings. For example, physical therapy education, particularly in colleges and universities offering health-related degree programs such as the best nursing schools in Georgia, have integrated these research findings into their curricula, equipping future therapists with the knowledge and competencies to deliver evidence-based care to their patients with neuromuscular conditions. As we push the boundaries of scientific knowledge with ongoing research, more applications of these findings across diverse fields are projected, holding even greater promise for the future.

Top Publications

  • Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2

    Jacqueline Glascock;Jacinda Sampson;Anne M. Connolly;Basil T. Darras

    (2020)
    128 Citations
  • Open-Label Evaluation of Eteplirsen in Patients with Duchenne Muscular Dystrophy Amenable to Exon 51 Skipping: PROMOVI Trial.

    Craig M McDonald;Perry B Shieh;Hoda Z Abdel-Hamid;Anne M Connolly

    (2021)
    73 Citations
  • Long-Term Functional Efficacy and Safety of Viltolarsen in Patients with Duchenne Muscular Dystrophy

    (2022)
    66 Citations
  • Molecular Mechanisms of Skeletal Muscle Hypertrophy.

    Stefano Schiaffino;Carlo Reggiani;Takayuki Akimoto;Bert Blaauw

    (2021)
    62 Citations
  • Advancements in AAV-mediated Gene Therapy for Pompe Disease.

    S.M. Salabarria;J. Nair;N. Clement;B.K. Smith

    (2020)
    58 Citations
  • Mechanisms and Clinical Applications of Glucocorticoid Steroids in Muscular Dystrophy

    Mattia Quattrocelli;Mattia Quattrocelli;Aaron S. Zelikovich;Isabella M. Salamone;Julie A. Fischer

    (2021)
    50 Citations
  • Measuring Outcomes in Adults with Spinal Muscular Atrophy - Challenges and Future Directions - Meeting Report.

    V A Sansone;M C Walter;S Attarian;S Delstanche

    (2020)
    50 Citations
  • A Combined Prospective and Retrospective Comparison of Long-Term Functional Outcomes Suggests Delayed Loss of Ambulation and Pulmonary Decline with Long-Term Eteplirsen Treatment.

    Olga Mitelman;Hoda Z. Abdel-Hamid;Barry J. Byrne;Anne M. Connolly

    (2021)
    36 Citations
  • Burden of Spinal Muscular Atrophy (SMA) on Patients and Caregivers in Canada.

    H.J. McMillan;B. Gerber;T. Cowling;W. Khuu

    (2021)
    35 Citations
  • Intrathecal Onasemnogene Abeparvovec for Sitting, Nonambulatory Patients with Spinal Muscular Atrophy: Phase I Ascending-Dose Study (STRONG)

    (2023)
    35 Citations

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Best Scientists Contributing to This Journal