Orphanet Journal of Rare Diseases

107.4k citations
4.1k papers · · active since 1950

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

Orphanet Journal of Rare Diseases

3.3k papers receiving 96.8k citations

Peers

Orphanet Journal of Rare Diseases
Comparison fields: 5 of 218
  • Clinical Biochemistry 7.0k
  • Genetics 9.6k
  • Rheumatology 10.1k
  • Physiology 16.4k
  • Genetics 17.6k
Replace European Journal of Pediatrics with:
European Journal of Pediatrics Germany
Journal of Internal Medicine Sweden
European Journal of Clinical Investigation United States
Journal of Molecular Medicine Germany
Annual Review of Medicine United States
Scandinavian Journal of Clinical and Laboratory Investigation Denmark
Genetics in Medicine United States
Clinical Chemistry and Laboratory Medicine (CCLM) Germany
Clinical Genetics United States
Clinical Biochemistry Canada
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 4.1k papers published in Orphanet Journal of Rare Diseases in the last decades have received a total of 107.4k indexed citations . Papers published in Orphanet Journal of Rare Diseases usually cover Clinical Biochemistry (234 papers), Physiology (633 papers), Genetics (256 papers), Genetics (639 papers) and Rheumatology (214 papers) specifically the topics of Lysosomal Storage Disorders Research (439 papers), Genomics and Rare Diseases (284 papers), Metabolism and Genetic Disorders (234 papers), Connective tissue disorders research (133 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (116 papers), Health Systems, Economic Evaluations, Quality of Life (108 papers), Neurogenetic and Muscular Disorders Research (101 papers) and Mitochondrial Function and Pathology (93 papers). The most active scholars publishing in Orphanet Journal of Rare Diseases are Dominique P. Germain, Marie T. Vanier, Raymund A.C. Roos, Christian Hamel, Renzo Galanello, Raffaella Origa, Philip R Cohen, Piero Picci, P. Nigel Leigh and Lokesh Wijesekera.

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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