Pagon Ra
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Neurogenetic and Muscular Disorders Research
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
Papers in
-
- Mitochondrial Function and Pathology 19
- RNA regulation and disease 11
- Genetics 58
- Genetics and Neurodevelopmental Disorders 14
- Genetic Syndromes and Imprinting 13
- Neurogenetic and Muscular Disorders Research 12
- Co-authors
- Adam Mp (251 shared papers)Ardinger Hh (251 shared papers)Bean Ljh (251 shared papers)Uta Francke (1 shared paper)HD Ochs (1 shared paper)Christine M. Distèche (1 shared paper)Joseph C. Giacalone (1 shared paper)Pearson Pl (1 shared paper)
- Journals
- Memory & Cognition (1 paper)PLoS ONE (1 paper)Research Padua Archive (University of Padua) (1 paper)ACTA THERIOLOGICA (1 paper)Research Explorer (The University of Manchester) (1 paper)
- Partner nations
- United States
In The Last Decade
Pagon Ra
237 papers receiving 768 citations
Peers
Comparison fields: 5 of 76
- Genetics 243
- Clinical Biochemistry 54
- Molecular Biology 423
- Genetics 59
- Hematology 50
Countries citing papers authored by Pagon Ra
This map shows the geographic impact of Pagon Ra'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 Pagon Ra with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pagon Ra more than expected).
Fields of papers citing papers by Pagon Ra
This network shows the impact of papers produced by Pagon Ra. 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 Pagon Ra. The network helps show where Pagon Ra may publish in the future.
Co-authors
The 24 scholars most cited alongside Pagon Ra, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 291 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome. | 1985 | 364 |
| 2 | Trisomy 3 (p23-pter) resulting from maternal translocation, t (3 ; 4)(p23 ; q35). | 1978 | 19 |
| 3 | Teschler-Nicola/Killian syndrome. | 1983 | 10 |
| 4 | Neurodegeneration with Brain Iron Accumulation Disorders Overview -- GeneReviews(®) | 2016 | 7 |
| 5 | Neurofibromatosis 1 -- GeneReviews(®) | 2016 | 6 |
| 6 | Classic Galactosemia and Clinical Variant Galactosemia -- GeneReviews(®) | 2016 | 5 |
| 7 | Mitochondrial Disorders Overview -- GeneReviews(®) | 2016 | 5 |
| 8 | Barth Syndrome -- GeneReviews® | 2016 | 5 |
| 9 | Informed consent for research publication of patient-related data. | 1984 | 5 |
| 10 | Fibrous Dysplasia/McCune-Albright Syndrome -- GeneReviews(®) | 2016 | 5 |
| 11 | AP-4-Associated Hereditary Spastic Paraplegia -- GeneReviews® | 2019 | 5 |
| 12 | Juvenile Polyposis Syndrome -- GeneReviews(®) | 2016 | 5 |
| 13 | Prader-Willi Syndrome -- GeneReviews® | 2016 | 4 |
| 14 | Hereditary Paraganglioma-Pheochromocytoma Syndromes -- GeneReviews® | 2016 | 4 |
| 15 | Mitochondrial DNA Deletion Syndromes -- GeneReviews® | 2016 | 4 |
| 16 | Spinocerebellar Ataxia Type 8 -- GeneReviews(®) | 2016 | 4 |
| 17 | Gaucher Disease -- GeneReviews(®) | 2016 | 4 |
| 18 | Urea Cycle Disorders Overview -- GeneReviews(®) | 2016 | 4 |
| 19 | PTEN Hamartoma Tumor Syndrome -- GeneReviews® | 2016 | 4 |
| 20 | Niemann-Pick Disease Type C -- GeneReviews® | 2016 | 4 |
About Pagon Ra
Pagon Ra is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cellular and Molecular Neuroscience and Rheumatology, having authored 291 papers that have together received 790 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (39 papers), Mitochondrial Function and Pathology (19 papers), Genetic Neurodegenerative Diseases (15 papers), Genetics and Neurodevelopmental Disorders (14 papers), Genetic Syndromes and Imprinting (13 papers), Neurogenetic and Muscular Disorders Research (12 papers), RNA regulation and disease (11 papers) and Lysosomal Storage Disorders Research (10 papers). The work is most often cited by research in Genetics (243 citations), Clinical Biochemistry (54 citations), Molecular Biology (423 citations), Genetics (59 citations) and Hematology (50 citations). Pagon Ra has collaborated with scholars based in United States. Frequent co-authors include Adam Mp, Ardinger Hh, Bean Ljh, Uta Francke, HD Ochs, Christine M. Distèche, Joseph C. Giacalone, Pearson Pl, Lindgren and van Ommen Gj. Their work appears in journals such as Memory & Cognition, PLoS ONE, Research Padua Archive (University of Padua), ACTA THERIOLOGICA and Research Explorer (The University of Manchester).
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.