Bean Ljh
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
Papers in
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- Mitochondrial Function and Pathology 19
- RNA regulation and disease 11
- Genetics 55
- Genetics and Neurodevelopmental Disorders 14
- Neurogenetic and Muscular Disorders Research 12
- Genetic Syndromes and Imprinting 12
- Co-authors
- Adam Mp (251 shared papers)Ardinger Hh (251 shared papers)Pagon Ra (251 shared papers)A Amemiya (251 shared papers)Mefford Hc (239 shared papers)Bird Td (241 shared papers)Smith Rjh (207 shared papers)Fong Ct (184 shared papers)
- Journals
- Memory & Cognition (1 paper)PLoS ONE (1 paper)Research Padua Archive (University of Padua) (1 paper)Research Explorer (The University of Manchester) (1 paper)ACTA THERIOLOGICA (1 paper)
In The Last Decade
Bean Ljh
231 papers receiving 379 citations
Peers
Comparison fields: 5 of 72
- Clinical Biochemistry 56
- Genetics 113
- Molecular Biology 180
- Neurology 21
- Genetics 26
Countries citing papers authored by Bean Ljh
This map shows the geographic impact of Bean Ljh'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 Bean Ljh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bean Ljh more than expected).
Fields of papers citing papers by Bean Ljh
This network shows the impact of papers produced by Bean Ljh. 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 Bean Ljh. The network helps show where Bean Ljh may publish in the future.
Co-authors
The 14 scholars most cited alongside Bean Ljh, 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 285 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Neurodegeneration with Brain Iron Accumulation Disorders Overview -- GeneReviews(®) | 2016 | 7 |
| 2 | Neurofibromatosis 1 -- GeneReviews(®) | 2016 | 6 |
| 3 | Classic Galactosemia and Clinical Variant Galactosemia -- GeneReviews(®) | 2016 | 5 |
| 4 | Fibrous Dysplasia/McCune-Albright Syndrome -- GeneReviews(®) | 2016 | 5 |
| 5 | Juvenile Polyposis Syndrome -- GeneReviews(®) | 2016 | 5 |
| 6 | Mitochondrial Disorders Overview -- GeneReviews(®) | 2016 | 5 |
| 7 | AP-4-Associated Hereditary Spastic Paraplegia -- GeneReviews® | 2019 | 5 |
| 8 | Barth Syndrome -- GeneReviews® | 2016 | 5 |
| 9 | Prader-Willi Syndrome -- GeneReviews® | 2016 | 4 |
| 10 | Gaucher Disease -- GeneReviews(®) | 2016 | 4 |
| 11 | Disorders of Intracellular Cobalamin Metabolism -- GeneReviews® | 2016 | 4 |
| 12 | Hereditary Paraganglioma-Pheochromocytoma Syndromes -- GeneReviews® | 2016 | 4 |
| 13 | PTEN Hamartoma Tumor Syndrome -- GeneReviews® | 2016 | 4 |
| 14 | Spinocerebellar Ataxia Type 8 -- GeneReviews(®) | 2016 | 4 |
| 15 | Urea Cycle Disorders Overview -- GeneReviews(®) | 2016 | 4 |
| 16 | Niemann-Pick Disease Type C -- GeneReviews® | 2016 | 4 |
| 17 | Mitochondrial DNA Deletion Syndromes -- GeneReviews® | 2016 | 4 |
| 18 | Wilson Disease -- GeneReviews(®) | 2016 | 3 |
| 19 | Diamond-Blackfan Anemia -- GeneReviews® | 2016 | 3 |
| 20 | Mitochondrial DNA-Associated Leigh Syndrome and NARP -- GeneReviews® | 2016 | 3 |
About Bean Ljh
Bean Ljh is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cellular and Molecular Neuroscience and Rheumatology, having authored 285 papers that have together received 386 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), Neurogenetic and Muscular Disorders Research (12 papers), Genetic Syndromes and Imprinting (12 papers), RNA regulation and disease (11 papers) and Lysosomal Storage Disorders Research (10 papers). The work is most often cited by research in Clinical Biochemistry (56 citations), Genetics (113 citations), Molecular Biology (180 citations), Neurology (21 citations) and Genetics (26 citations). Frequent co-authors include Adam Mp, Ardinger Hh, Pagon Ra, A Amemiya, Mefford Hc, Bird Td, Smith Rjh, Fong Ct, K Stephens and Adam C. Smith. Their work appears in journals such as Memory & Cognition, PLoS ONE, Research Padua Archive (University of Padua), Research Explorer (The University of Manchester) and ACTA THERIOLOGICA.
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.