Maladies Rares: Génétique et Métabolisme
Impact in
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- Cancer, Hypoxia, and Metabolism
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- melanin and skin pigmentation
Papers in
- Cell Biology 33
- melanin and skin pigmentation 23
- Top scholars
- Rodrigue RossignolCaroline JoséCyril GoizetNadège BellancéPatrick J. BabinDidier LacombeMichael P. MurphyCindy E. Dieteren
- Journals
- European Journal of Medical Genetics (10 papers)Clinical Genetics (8 papers)Pigment Cell & Melanoma Research (8 papers)European Journal of Human Genetics (8 papers)PLoS ONE (6 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Maladies Rares: Génétique et Métabolisme
209 papers receiving 6.4k citations
Peers
Comparison fields: 5 of 150
- Cancer Research 802
- Cell Biology 923
- Molecular Biology 3.1k
- Genetics 349
- Physiology 780
Countries citing scholars working at Maladies Rares: Génétique et Métabolisme
This map shows the geographic impact of research produced by authors working at Maladies Rares: Génétique et Métabolisme. 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 produced at Maladies Rares: Génétique et Métabolisme with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maladies Rares: Génétique et Métabolisme more than expected).
Fields of papers published by authors at Maladies Rares: Génétique et Métabolisme
This network shows the impact of papers affiliated with Maladies Rares: Génétique et Métabolisme at the time of their publication. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers affiliated with Maladies Rares: Génétique et Métabolisme at the time of their publication.
About Maladies Rares: Génétique et Métabolisme
In recent decades, authors affiliated with Maladies Rares: Génétique et Métabolisme have published 244 papers, which have received a total of 7.0k indexed citations . Scholars at this organization have produced 8 papers in Developmental Biology, 33 papers in Cell Biology, 99 papers in Molecular Biology, 7 papers in Anesthesiology and Pain Medicine and 39 papers in Genetics on the topics of Mitochondrial Function and Pathology (27 papers), melanin and skin pigmentation (23 papers), Lysosomal Storage Disorders Research (17 papers), Cancer, Hypoxia, and Metabolism (14 papers), RNA regulation and disease (13 papers), RNA modifications and cancer (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetic Neurodegenerative Diseases (11 papers). Their work is cited by papers focused on Cancer Research (802 citations), Cell Biology (923 citations), Molecular Biology (3.1k citations), Genetics (349 citations) and Physiology (780 citations). Authors at Maladies Rares: Génétique et Métabolisme collaborate with scholars in France, United States and Germany and have published in prestigious journals including European Journal of Medical Genetics, Clinical Genetics, Pigment Cell & Melanoma Research, European Journal of Human Genetics and PLoS ONE. Some of Maladies Rares: Génétique et Métabolisme's most productive authors include Rodrigue Rossignol, Caroline José, Cyril Goizet, Nadège Bellancé, Patrick J. Babin, Didier Lacombe, Michael P. Murphy, Cindy E. Dieteren, Werner J.H. Koopman and Peter H.G.M. Willems.
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.