Orphanet Journal of Rare Diseases

130.7k citations
4.6k papers · · active since 2016

Impact in

    • Metabolism and Genetic Disorders
  • Genetics top 2%
    • Genomics and Rare Diseases
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders
    • Connective tissue disorders research

Papers in

    • Metabolism and Genetic Disorders 272
    • Genomics and Rare Diseases 303
    • Connective tissue disorders research 144
    • Neurogenetic and Muscular Disorders Research 113

Orphanet Journal of Rare Diseases

3.6k papers receiving 116.3k citations

Peers

Orphanet Journal of Rare Diseases
Comparison fields: 5 of 223
  • Clinical Biochemistry 9.5k
  • Genetics 11.8k
  • Physiology 20.6k
  • Rheumatology 11.8k
  • Genetics 21.9k
Replace European Journal of Pediatrics with:
European Journal of Pediatrics Germany
Journal of Molecular Medicine Germany
Journal of Internal Medicine Sweden
European Journal of Clinical Investigation Germany
Scandinavian Journal of Clinical and Laboratory Investigation Denmark
Genetics in Medicine United States
Clinical Genetics United States
Annual Review of Medicine United States
Clinical Chemistry and Laboratory Medicine (CCLM) Germany
Journal of Leukocyte Biology United States
Orphanet Journal of Rare Diseases relative to European Journal of Pediatrics Germany European Journal of Pediatrics's profile →
Citations per field
00.5×1.6×
European Journal of Pediatrics · 1×
Citations per year

Countries where authors publish in Orphanet Journal of Rare Diseases

Since Specialization
Citations

This map shows the geographic impact of research published in Orphanet Journal of Rare Diseases. 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 papers published in Orphanet Journal of Rare Diseases with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Orphanet Journal of Rare Diseases more than expected).

Fields of papers published in Orphanet Journal of Rare Diseases

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers published in Orphanet Journal of Rare Diseases. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers published in Orphanet Journal of Rare Diseases.

About Orphanet Journal of Rare Diseases

The 4.6k papers published in Orphanet Journal of Rare Diseases in the last decades have received a total of 130.7k indexed citations . Papers published in Orphanet Journal of Rare Diseases usually cover Clinical Biochemistry (272 papers), Genetics (291 papers), Physiology (698 papers), Genetics (705 papers) and Rheumatology (247 papers) specifically the topics of Lysosomal Storage Disorders Research (484 papers), Genomics and Rare Diseases (303 papers), Metabolism and Genetic Disorders (272 papers), Connective tissue disorders research (144 papers), Neurogenetic and Muscular Disorders Research (113 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (109 papers), Mitochondrial Function and Pathology (108 papers) and Health Systems, Economic Evaluations, Quality of Life (97 papers). The most active scholars publishing in Orphanet Journal of Rare Diseases are Dominique Paul Germain, Marie Therese Vanier, Raymund A.C. Roos, Christian Hamel, Philip R Cohen, Raffaella Origa, Renzo Galanello, Lokesh C. Wijesekera, P. Nigel Leigh and Piero Picci.

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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