P. L. Kramer
Impact in
- Neurology top 1%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
- Botulinum Toxin and Related Neurological Disorders
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Papers in
-
- Genetic Neurodegenerative Diseases 12
- Hereditary Neurological Disorders 10
- Neurology 18
- Neurological disorders and treatments 17
- Botulinum Toxin and Related Neurological Disorders 3
- Co-authors
- Laurie J. Ozelius (15 shared papers)Susan Bressman (11 shared papers)Neil Risch (11 shared papers)D. de Leon (10 shared papers)Mitchell F. Brin (8 shared papers)M. Litt (6 shared papers)Stanley Fahn (12 shared papers)Christine Klein (7 shared papers)
- Journals
- Neurology (9 papers)Human Molecular Genetics (3 papers)Genomics (3 papers)Annals of Neurology (2 papers)Genetic Epidemiology (2 papers)
- Partner nations
- United StatesGermanySweden
In The Last Decade
P. L. Kramer
41 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 70
- Neurology 938
- Cellular and Molecular Neuroscience 731
- Ophthalmology 258
- Neurology 118
- Genetics 249
Countries citing papers authored by P. L. Kramer
This map shows the geographic impact of P. L. Kramer'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 P. L. Kramer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. L. Kramer more than expected).
Fields of papers citing papers by P. L. Kramer
This network shows the impact of papers produced by P. L. Kramer. 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 P. L. Kramer. The network helps show where P. L. Kramer may publish in the future.
Co-authors
The 25 scholars most cited alongside P. L. Kramer, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 242 | |
| 2 | 1997 | 191 | |
| 3 | Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q. | 1997 | 168 |
| 4 | 1993 | 130 | |
| 5 | 1997 | 116 | |
| 6 | Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews. | 1992 | 97 |
| 7 | 2002 | 90 | |
| 8 | The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews. | 1994 | 89 |
| 9 | 2009 | 75 | |
| 10 | A gene for episodic ataxia/myokymia maps to chromosome 12p13. | 1994 | 69 |
| 11 | 2011 | 62 | |
| 12 | 1994 | 54 | |
| 13 | 1996 | 48 | |
| 14 | 2006 | 43 | |
| 15 | The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family. | 1998 | 41 |
| 16 | Clinical-genetic spectrum of primary dystonia. | 1998 | 36 |
| 17 | 1984 | 33 | |
| 18 | 1993 | 31 | |
| 19 | 1996 | 31 | |
| 20 | 1995 | 30 |
About P. L. Kramer
P. L. Kramer is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Genetics and Ophthalmology, having authored 41 papers that have together received 1.9k indexed citations. Recurring topics across this work include Neurological disorders and treatments (17 papers), Genetic Neurodegenerative Diseases (12 papers), Hereditary Neurological Disorders (10 papers), Genetics and Neurodevelopmental Disorders (5 papers), Glaucoma and retinal disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Botulinum Toxin and Related Neurological Disorders (3 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). The work is most often cited by research in Neurology (938 citations), Cellular and Molecular Neuroscience (731 citations), Ophthalmology (258 citations), Neurology (118 citations) and Genetics (249 citations). P. L. Kramer has collaborated with scholars based in United States, Germany and Sweden. Frequent co-authors include Laurie J. Ozelius, Susan Bressman, Neil Risch, D. de Leon, Mitchell F. Brin, M. Litt, Stanley Fahn, Christine Klein, Deborah Raymond and Irene H. Maumenee. Their work appears in journals such as Neurology, Human Molecular Genetics, Genomics, Annals of Neurology and Genetic Epidemiology.
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.