Ardinger Hh
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
-
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
-
- 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)Pagon Ra (251 shared papers)Bean Ljh (251 shared papers)A Amemiya (251 shared papers)Mefford Hc (239 shared papers)Bird Td (242 shared papers)Smith Rjh (208 shared papers)Fong Ct (185 shared papers)
- Journals
- Memory & Cognition (1 paper)PLoS ONE (1 paper)Research Padua Archive (University of Padua) (1 paper)PubMed (1 paper)Research Explorer (The University of Manchester) (1 paper)
- Partner nations
- United States
In The Last Decade
Ardinger Hh
233 papers receiving 395 citations
Peers
Comparison fields: 5 of 72
- Clinical Biochemistry 56
- Genetics 124
- Molecular Biology 192
- Developmental Biology 6
- Neurology 22
Countries citing papers authored by Ardinger Hh
This map shows the geographic impact of Ardinger Hh'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 Ardinger Hh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ardinger Hh more than expected).
Fields of papers citing papers by Ardinger Hh
This network shows the impact of papers produced by Ardinger Hh. 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 Ardinger Hh. The network helps show where Ardinger Hh may publish in the future.
Co-authors
The 14 scholars most cited alongside Ardinger Hh, 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 287 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Microcephaly in familial holoprosencephaly. | 1988 | 14 |
| 2 | Neurodegeneration with Brain Iron Accumulation Disorders Overview -- GeneReviews(®) | 2016 | 7 |
| 3 | Neurofibromatosis 1 -- GeneReviews(®) | 2016 | 6 |
| 4 | Classic Galactosemia and Clinical Variant Galactosemia -- GeneReviews(®) | 2016 | 5 |
| 5 | Fibrous Dysplasia/McCune-Albright Syndrome -- GeneReviews(®) | 2016 | 5 |
| 6 | Juvenile Polyposis Syndrome -- GeneReviews(®) | 2016 | 5 |
| 7 | Mitochondrial Disorders Overview -- GeneReviews(®) | 2016 | 5 |
| 8 | AP-4-Associated Hereditary Spastic Paraplegia -- GeneReviews® | 2019 | 5 |
| 9 | Barth Syndrome -- GeneReviews® | 2016 | 5 |
| 10 | Prader-Willi Syndrome -- GeneReviews® | 2016 | 4 |
| 11 | Gaucher Disease -- GeneReviews(®) | 2016 | 4 |
| 12 | Disorders of Intracellular Cobalamin Metabolism -- GeneReviews® | 2016 | 4 |
| 13 | Hereditary Paraganglioma-Pheochromocytoma Syndromes -- GeneReviews® | 2016 | 4 |
| 14 | PTEN Hamartoma Tumor Syndrome -- GeneReviews® | 2016 | 4 |
| 15 | Spinocerebellar Ataxia Type 8 -- GeneReviews(®) | 2016 | 4 |
| 16 | Urea Cycle Disorders Overview -- GeneReviews(®) | 2016 | 4 |
| 17 | Niemann-Pick Disease Type C -- GeneReviews® | 2016 | 4 |
| 18 | Mitochondrial DNA Deletion Syndromes -- GeneReviews® | 2016 | 4 |
| 19 | Wilson Disease -- GeneReviews(®) | 2016 | 3 |
| 20 | Diamond-Blackfan Anemia -- GeneReviews® | 2016 | 3 |
About Ardinger Hh
Ardinger Hh is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cellular and Molecular Neuroscience and Rheumatology, having authored 287 papers that have together received 402 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 (124 citations), Molecular Biology (192 citations), Developmental Biology (6 citations) and Neurology (22 citations). Ardinger Hh has collaborated with scholars based in United States. Frequent co-authors include Adam Mp, Pagon Ra, Bean Ljh, 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), PubMed 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.