Patricia L. Kramer

3.7k total citations · 1 hit paper
31 papers, 2.3k citations indexed

About

Patricia L. Kramer is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Patricia L. Kramer has authored 31 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Neurology, 12 papers in Cellular and Molecular Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Patricia L. Kramer's work include Neurological disorders and treatments (12 papers), Parkinson's Disease Mechanisms and Treatments (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Patricia L. Kramer is often cited by papers focused on Neurological disorders and treatments (12 papers), Parkinson's Disease Mechanisms and Treatments (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Patricia L. Kramer collaborates with scholars based in United States, Germany and Italy. Patricia L. Kramer's co-authors include Laurie J. Ozelius, Xandra O. Breakefield, Susan Bressman, Deborah de Leon, Mitchell F. Brin, Stanley Fahn, Neil Risch, James F. Gusella, Jeffrey Hewett and Alan Buckler and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and Nature Genetics.

In The Last Decade

Patricia L. Kramer

31 papers receiving 2.3k 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.

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

1997 770 citations Laurie J. Ozelius, Jeffrey Hewett 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 L. Kramer United States	20	1.6k	1.3k	483	264	220	31	2.3k
Satoshi Goto Japan	32	1.6k 1.0×	1.3k 1.0×	557 1.2×	355 1.3×	249 1.1×	144	2.7k
Patricia Kramer United States	15	853 0.5×	927 0.7×	848 1.8×	270 1.0×	137 0.6×	21	1.9k
M. Ben Hamida Tunisia	22	681 0.4×	1.3k 1.0×	1.2k 2.5×	492 1.9×	106 0.5×	43	2.4k
Tinmarla F. Oo United States	21	789 0.5×	900 0.7×	666 1.4×	221 0.8×	242 1.1×	27	1.8k
Katrin Bürk Germany	37	1.6k 1.0×	2.8k 2.1×	2.4k 5.0×	477 1.8×	175 0.8×	73	3.7k
Kay Seidel Germany	30	1.1k 0.7×	1.7k 1.3×	1.5k 3.1×	350 1.3×	392 1.8×	50	2.7k
Sharon Vinsant United States	20	480 0.3×	965 0.7×	619 1.3×	259 1.0×	155 0.7×	22	1.8k
Jenny Sassone Italy	25	554 0.4×	991 0.7×	1.0k 2.1×	117 0.4×	253 1.1×	46	1.7k
Maurizio De Fusco Italy	19	351 0.2×	770 0.6×	1.3k 2.7×	455 1.7×	315 1.4×	32	2.8k
Milena Cannella Italy	29	1.1k 0.7×	1.5k 1.2×	1.3k 2.7×	177 0.7×	270 1.2×	60	2.4k

Countries citing papers authored by Patricia L. Kramer

Since Specialization

Citations

This map shows the geographic impact of Patricia 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 Patricia 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 Patricia L. Kramer more than expected).

Fields of papers citing papers by Patricia L. Kramer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patricia L. Kramer

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia L. Kramer. A scholar is included among the top collaborators of Patricia L. 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 L. Kramer. Patricia L. 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

Erten‐Lyons, Deniz, Andrea M. Piccinin, Scott M. Hofer, et al.. (2012). Review of selected databases of longitudinal aging studies. Alzheimer s & Dementia. 8(6). 584–589. 12 indexed citations

Shulman, Joshua M., Portia Chipendo, Lori B. Chibnik, et al.. (2011). Functional Screening of Alzheimer Pathology Genome-wide Association Signals in Drosophila. The American Journal of Human Genetics. 88(2). 232–238. 64 indexed citations

Kramer, Patricia L., et al.. (2010). Reconstructability Analysis as a Tool for Identifying Gene-Gene Interactions in Studies of Human Diseases. Statistical Applications in Genetics and Molecular Biology. 9(1). Article18–Article18. 8 indexed citations

Kramer, Patricia L., Haiyan Xu, Randall L. Woltjer, et al.. (2010). Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. Neurobiology of Aging. 32(12). 2113–2122. 82 indexed citations

Charlesworth, Jac, Patricia L. Kramer, Tom Dyer, et al.. (2010). The Path to Open-Angle Glaucoma Gene Discovery: Endophenotypic Status of Intraocular Pressure, Cup-to-Disc Ratio, and Central Corneal Thickness. Investigative Ophthalmology & Visual Science. 51(7). 3509–3509. 72 indexed citations

Tian, Wei, Yi Fu, Anna García-Elías, et al.. (2009). A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia. Proceedings of the National Academy of Sciences. 106(33). 14034–14039. 79 indexed citations

Gordon, Derek, Chad Haynes, Yaning Yang, Patricia L. Kramer, & Stephen J. Finch. (2007). Linear trend tests for case–control genetic association that incorporate random phenotype and genotype misclassification error. Genetic Epidemiology. 31(8). 853–870. 25 indexed citations

Wilmot, Beth, Shannon K. McWeeney, Randal R. Nixon, et al.. (2006). Translational gene mapping of cognitive decline. Neurobiology of Aging. 29(4). 524–541. 29 indexed citations

Djarmati, Ana, Kemal Kabakci, Irene Pichler, et al.. (2005). Co‐occurrence of restless legs syndrome and Parkin mutations in two families. Movement Disorders. 21(2). 258–263. 26 indexed citations

10.

Pramstaller, Peter P., Michael G. Schlossmacher, Thomas S. Jacques, et al.. (2005). Lewy body Parkinson's disease in a large pedigree with 77Parkin mutation carriers. Annals of Neurology. 58(3). 411–422. 187 indexed citations

11.

Klein, Christine, Liu Liu, Dana Doheny, et al.. (2002). ε‐sarcoglycan mutations found in combination with other dystonia gene mutations. Annals of Neurology. 52(5). 675–679. 69 indexed citations

12.

Kitsos, George, Hans Eiberg, E Economou-Petersen, et al.. (2001). Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree. European Journal of Human Genetics. 9(6). 452–457. 23 indexed citations

13.

Kramer, Patricia L., et al.. (2000). A new locus for autosomal dominant congenital cataracts maps to chromosome 3.. PubMed. 41(1). 36–9. 18 indexed citations

14.

Kramer, Patricia L., Mari Mineta, Christine Klein, et al.. (1999). Rapid-onset dystonia-parkinsonism: Linkage to chromosome 19q13. Annals of Neurology. 46(2). 176–182. 52 indexed citations

15.

Ozelius, Laurie J., Jeffrey Hewett, Susan Bressman, et al.. (1997). The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nature Genetics. 17(1). 40–48. 770 indexed citations breakdown →

16.

Bressman, Susan, Ann Hunt, Gary A. Heiman, et al.. (1994). Exclusion of the DYT1 locus in a non‐Jewish family with early‐onset dystonia. Movement Disorders. 9(6). 626–632. 29 indexed citations

17.

Kramer, Patricia L., Deborah de Leon, Laurie J. Ozelius, et al.. (1990). Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34. Annals of Neurology. 27(2). 114–120. 109 indexed citations

18.

Ozelius, Laurie J., Patricia L. Kramer, Carol Moskowitz, et al.. (1989). Human gene for torsion dystonia located on chromosome 9q32-q34. Neuron. 2(5). 1427–1434. 186 indexed citations

19.

Kramer, Patricia L., Lindsay A. Farrer, A.J. Pakstis, & Kenneth K. Kídd. (1986). Development of a map of chromosome 11p. Genetic Epidemiology. 3(S1). 153–158. 5 indexed citations

20.

Kramer, Patricia L.. (1983). Adolescent growth patterns in a northern Italian community.. PubMed. 55(3). 687–706. 3 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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