Patricia Kramer

6.4k total citations · 1 hit paper
21 papers, 1.9k citations indexed

About

Patricia Kramer is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Patricia Kramer has authored 21 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 9 papers in Cellular and Molecular Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Patricia Kramer's work include Neurological disorders and treatments (8 papers), Genetic Neurodegenerative Diseases (8 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Patricia Kramer is often cited by papers focused on Neurological disorders and treatments (8 papers), Genetic Neurodegenerative Diseases (8 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Patricia Kramer collaborates with scholars based in United States, Italy and Germany. Patricia Kramer's co-authors include M. Litt, John G. Nutt, E. R. Brunt, D.L. Browne, Stephen T. Gancher, Eric A. Smith, Laurie J. Ozelius, Susan Bressman, Stanley Fahn and Deborah de Leon and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Annals of Neurology.

In The Last Decade

Patricia Kramer

21 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

1994 561 citations D.L. Browne, Stephen T. Gancher et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Patricia Kramer United States	15	927	853	848	299	270	21	1.9k
M. Ben Hamida Tunisia	22	1.3k 1.4×	681 0.8×	1.2k 1.4×	182 0.6×	492 1.8×	43	2.4k
Torbjoern G. Nygaard United States	30	1.2k 1.3×	1.6k 1.8×	676 0.8×	188 0.6×	350 1.3×	45	2.6k
Denise M. Kay United States	25	534 0.6×	1.2k 1.4×	736 0.9×	294 1.0×	525 1.9×	54	2.4k
Larry H. Yamaoka United States	23	631 0.7×	325 0.4×	1.1k 1.3×	392 1.3×	196 0.7×	64	2.1k
Maurizio De Fusco Italy	19	770 0.8×	351 0.4×	1.3k 1.5×	319 1.1×	455 1.7×	32	2.8k
Patrícia de Carvalho Aguiar Brazil	18	573 0.6×	871 1.0×	397 0.5×	158 0.5×	133 0.5×	51	1.4k
Lis Hasholt Denmark	24	823 0.9×	412 0.5×	835 1.0×	149 0.5×	152 0.6×	86	1.6k
Viviana Caputo Italy	23	439 0.5×	643 0.8×	863 1.0×	298 1.0×	208 0.8×	52	1.8k
Tu‐Hsueh Yeh Taiwan	29	875 0.9×	903 1.1×	1.2k 1.4×	95 0.3×	373 1.4×	74	2.3k
Emilia Bellone Italy	24	1.0k 1.1×	787 0.9×	681 0.8×	176 0.6×	405 1.5×	100	1.8k

Countries citing papers authored by Patricia Kramer

Since Specialization

Citations

This map shows the geographic impact of Patricia 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 Patricia Kramer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patricia Kramer more than expected).

Fields of papers citing papers by Patricia Kramer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patricia 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 Patricia Kramer. The network helps show where Patricia Kramer may publish in the future.

Co-authorship network of co-authors of Patricia Kramer

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia Kramer. A scholar is included among the top collaborators of Patricia Kramer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Patricia Kramer. Patricia Kramer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Firoozabadi, Reza, et al.. (2022). Prospective Study Investigating the Prevalence and Evolution of Malnourishment in the Acute Orthopaedic Trauma Patient.. PubMed. 10(7). 592–600. 2 indexed citations

Erten‐Lyons, Deniz, Hiroko H. Dodge, Randall L. Woltjer, et al.. (2013). Neuropathologic Basis of Age-Associated Brain Atrophy. JAMA Neurology. 70(5). 616–616. 81 indexed citations

Erten‐Lyons, Deniz, Beth Wilmot, Pavana Anur, et al.. (2011). Microcephaly Genes and Risk of Late-onset Alzheimer Disease. Alzheimer Disease & Associated Disorders. 25(3). 276–282. 5 indexed citations

Kaye, Jeffrey, et al.. (2009). Exceptional Brain Aging in a Rural Population‐Based Cohort. The Journal of Rural Health. 25(3). 320–325. 13 indexed citations

Summers, Hobie, Patricia Kramer, & Stephen K. Benirschke. (2009). Pediatric calcaneal fractures. Orthopedic Reviews. 1(1). e9–e9. 12 indexed citations

Erten‐Lyons, Deniz, Anne Jacobson, Patricia Kramer, Andrew Grupe, & Jeffrey Kaye. (2009). The FAS gene, brain volume, and disease progression in Alzheimer's disease. Alzheimer s & Dementia. 6(2). 118–124. 28 indexed citations

Saunders‐Pullman, Rachel, Deborah Raymond, Geetha Senthil, et al.. (2007). Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish–Mennonites. American Journal of Medical Genetics Part A. 143A(18). 2098–2105. 48 indexed citations

Kay, Denise M., Cyrus P. Zabetian, Stewart A. Factor, et al.. (2005). Parkinson's disease and LRRK2: Frequency of a common mutation in U.S. movement disorder clinics. Movement Disorders. 21(4). 519–523. 73 indexed citations

Zaremba, Jacek, et al.. (2004). Rapid‐onset dystonia–parkinsonism: A fourth family consistent with linkage to chromosome 19q13. Movement Disorders. 19(12). 1506–1510. 24 indexed citations

10.

Hedrich, Katja, Beth Wilmot, Karen Marder, et al.. (2004). Distribution, type, and origin of Parkin mutations: Review and case studies. Movement Disorders. 19(10). 1146–1157. 165 indexed citations

11.

Diamond, Bruce J., et al.. (2003). Complementary and Alternative Medicines in the Treatment of Dementia. Drugs & Aging. 20(13). 981–998. 27 indexed citations

12.

Leung, Joanne, Christine Klein, Jennifer Friedman, et al.. (2001). Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism. Neurogenetics. 3(3). 133–143. 126 indexed citations

13.

Jakobs, Petra, John F. Hess, Paul G. Fitzgerald, et al.. (2000). Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2. The American Journal of Human Genetics. 66(4). 1432–1436. 137 indexed citations

14.

Nygaard, Torbjoern G., Deborah Raymond, Caiping Chen, et al.. (1999). Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31. Annals of Neurology. 46(5). 794–798. 71 indexed citations

15.

Klein, Christine, Mitchell F. Brin, Patricia Kramer, et al.. (1999). Association of a missense change in the D2 dopamine receptor with myoclonus dystonia. Proceedings of the National Academy of Sciences. 96(9). 5173–5176. 90 indexed citations

16.

Ozelius, Laurie J., Jeffrey Hewett, Patricia Kramer, et al.. (1997). Fine Localization of the Torsion Dystonia Gene (DYT1) on Human Chromosome 9q34: YAC Map and Linkage Disequilibrium. Genome Research. 7(5). 483–494. 50 indexed citations

17.

Taylor, Todd D., M. Litt, Patricia Kramer, et al.. (1996). Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13. Nature Genetics. 14(4). 479–481. 103 indexed citations

18.

Risch, Neil, Deborah de Leon, Laurie J. Ozelius, et al.. (1995). Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. Nature Genetics. 9(2). 152–159. 318 indexed citations

19.

Browne, D.L., Stephen T. Gancher, John G. Nutt, et al.. (1994). Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nature Genetics. 8(2). 136–140. 561 indexed citations breakdown →

20.

Olzak, Lynn A. & Patricia Kramer. (1984). Inhibition between spatially tuned mechanisms: temporal influences (A). 1. 1290. 2 indexed citations

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.

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